Journal of Obesity & Metabolic Syndrome

Search

Article

J Obes Metab Syndr 2022; 31(2): 100-122

Published online June 30, 2022 https://doi.org/10.7570/jomes22009

Copyright © Korean Society for the Study of Obesity.

Effect of Carbohydrate-Restricted Diets and Intermittent Fasting on Obesity, Type 2 Diabetes Mellitus, and Hypertension Management: Consensus Statement of the Korean Society for the Study of Obesity, Korean Diabetes Association, and Korean Society of Hypertension

Jong Han Choi1, Yoon Jeong Cho2, Hyun-Jin Kim3, Seung-Hyun Ko4, Suk Chon5, Jee-Hyun Kang6, Kyoung-Kon Kim7, Eun Mi Kim8, Hyun Jung Kim9, Kee-Ho Song1,* , Ga Eun Nam10,* , Kwang Il Kim11,* , Committee of Clinical Practice Guidelines, Korean Society for the Study of Obesity (KSSO), Committee of Clinical Practice Guidelines and Committee of Food and Nutrition, Korean Diabetes Association (KDA), Policy Committee of Korean Society of Hypertension (KSH), Policy Development Committee of National Academy of Medicine of Korea (NAMOK)

1Division of Endocrinology and Metabolism, Department of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul; 2Department of Family Medicine, Daegu Catholic University School of Medicine, Daegu; 3Division of Cardiology, Department of Internal Medicine, Hanyang University College of Medicine, Seoul; 4Division of Endocrinology and Metabolism, Department of Internal Medicine, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Seoul; 5Department of Endocrinology and Metabolism, College of Medicine, Kyung Hee University, Seoul; 6Department of Family Medicine, Konyang University College of Medicine, Daejeon; 7Department of Family Medicine, Gachon University College of Medicine, Incheon; 8Department of Dietetics, Kangbuk Samsung Hospital, Seoul; 9Institute for Evidence-based Medicine, Cochrane Korea, Department of Preventive Medicine, Korea University College of Medicine, Seoul; 10Department of Family Medicine, Korea University College of Medicine, Seoul; 11Division of Geriatrics, Department of Internal Medicine, Seoul National University School of Medicine, Seoul, Korea

Correspondence to:
Kee-Ho Song https://orcid.org/0000-0001-9276-6860
Division of Endocrinology and Metabolism, Department of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, 120-1 Neungdong-ro, Gwangjin-gu, Seoul 05030, Korea
Tel: +82-2-2030-7533, Fax: +82-2-2030-7748
E-mail: skh2k@kuh.ac.kr

Ga Eun Nam https://orcid.org/0000-0002-6739-9904
Department of Family Medicine, Korea University Guro Hospital, Korea University College of Medicine, 148 Gurodong-ro, Guro-gu, Seoul 08308, Korea
Tel: +82-2-2626-1540, Fax: +82-2-2626-1545
E-mail: namgaaa@hanmail.net

Kwang Il Kim https://orcid.org/0000-0002-6658-047X
Division of Geriatrics, Department of Internal Medicine, Seoul National University Bundang Hospital, 82 Gumi-ro 173beon-gil, Bundang-gu, Seongnam 13620, Korea
Tel: +82-31-787-7032, Fax: +82-31-787-4052
E-mail: kikim907@gmail.com

Jong Han Choi, Yoon Jeong Cho, and Hyun-Jin Kim contributed equally to this study as first authors.

This manuscript is simultaneously published in the Journal of Obesity & Metabolic Syndrome, Diabetes and Metabolism Journal, and Clinical Hypertension by the Korean Society for the Study of Obesity, Korean Diabetes Association, and the Korean Society of Hypertension.

Received: February 12, 2022; Reviewed : March 15, 2022; Accepted: May 4, 2022

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Carbohydrate-restricted diets and intermittent fasting (IF) have been rapidly gaining interest among the general population and patients with cardiometabolic disease, such as overweight or obesity, diabetes, and hypertension. However, there are limited expert recommendations for these dietary regimens. This study aimed to evaluate the level of scientific evidence on the benefits and harms of carbohydrate-restricted diets and IF to make responsible recommendations. A meta-analysis and systematic literature review of 66 articles on 50 randomized controlled trials (RCTs) of carbohydrate-restricted diets and 10 articles on eight RCTs of IF was performed. Based on the analysis, the following recommendations are suggested. In adults with overweight or obesity, a moderately-low carbohydrate or low carbohydrate diet (mLCD) can be considered as a dietary regimen for weight reduction. In adults with type 2 diabetes mellitus, mLCD can be considered as a dietary regimen for improving glycemic control and reducing body weight. In contrast, a very-low carbohydrate diet (VLCD) and IF are recommended against in patients with diabetes. Furthermore, no recommendations are suggested for VLCD and IF in adults with overweight or obesity, and carbohydrate-restricted diets and IF in patients with hypertension. Here, we describe the results of our analysis and the evidence for these recommendations.

Keywords: Carbohydrates, Diabetes mellitus, Diet, Hypertension, Obesity

Obesity, type 2 diabetes mellitus (T2DM), and hypertension are the most important risk factors for cardiovascular disease and are the most common causes of morbidity and mortality.1-4 Structured dietary intervention plays a crucial role in preventing and managing these cardiometabolic diseases. Major clinical practice guidelines commonly recommend losing more than 5% of body weight and reducing total caloric intake.5-8 Nevertheless, reducing total caloric intake enough to lose weight requires tremendous effort, and maintaining it over the long-term is much more challenging. Alternatively, carbohydrate-restricted diets and intermittent fasting (IF) are emerging as relatively easy and effective popular dietary regimens for reducing body weight.9

Carbohydrates make up more than half of an individual’s calorie intake, and restricting them can be critical in reducing total calories and body weight.10 Obesity, T2DM, and hypertension constitute metabolic syndrome, and glucose-stimulated hyperinsulinemia and insulin resistance are major contributors to the pathogenesis of these diseases.11 Reducing carbohydrate that is absorbed in the form of glucose or fructose and leading to immediate hyperglycemia may help prevent and improve these conditions.12 However, clinical evidence on the benefits and harms of carbohydrate-restricted diets in these diseases remains insufficient.5-8

IF is a generic term for a variety of eating methods involving fasting for different periods, such as several hours a day, 1 day every several days, or several days a week.13 In some studies, IF is known to be effective in preventing diabetes, cardiovascular disease, cancer, and degenerative brain disease, as well as weight loss in overweight or obese people.14 However, these studies were conducted for a short period with a small number of subjects, and results were heterogeneous among studies.14 Moreover, since most studies evaluated effects in healthy adults, applying the impact on patients with cardiometabolic diseases such as morbid obesity, diabetes, and hypertension is challenging.15

For these reasons, the principal clinical practice guidelines for managing obesity, T2DM, and hypertension do not provide specific recommendations for carbohydrate-restricted diets or IF.5-8 Notably, the dietary approaches that lack evidence for benefits but are potentially harmful are rapidly spreading to the public without clear guidance from experts. Therefore, we aimed to conduct a meta- analysis and systematic literature review to examine the benefits and harms of these dietary regimens in adults with obesity, T2DM, and hypertension and develop recommendations based on the high-level evidence by the results.

A systematic literature search was performed by a professional librarian for the meta-analysis with the key question, “Are carbohydrate- restricted diets or IF helpful in the management of patients with overweight or obesity, diabetes, and hypertension?” MEDLINE (via PubMed), Embase, Cochrane, and KoreaMed databases were used, and among the literature published in English and Korean from January 1, 2000, to June 8, 2021, only randomized controlled trials (RCTs) that tested the effectiveness of carbohydraterestricted diets or IF with a study period of more than 8 weeks were included. The search strategy in MEDLINE is shown in Supplementary Table 1. Further, the framework of the population, intervention, comparator, and outcomes (PICO) in developing the focused question (Supplementary Table 2), and literature selection and exclusion process (Supplementary Fig. 1), as well as the summary of studies included in the meta-analysis consisting of 50 RCTs (66 articles) on carbohydrate-restricted diets (Supplementary Table 3),16-81 and eight RCTs (10 articles) on IF (Supplementary Table 4),82-91 are presented in the supplementary data.

In most clinical studies, carbohydrate-restricted diets are classified as moderately-low carbohydrate diets (MCD) with carbohydrates accounting for 26% to 45% of total caloric intake, low carbohydrate diets (LCD) with carbohydrates accounting for 10% to 25%, and very-low carbohydrate diets (VLCD) with carbohydrates accounting for less than 10%.92 Considering that the average carbohydrate intake rate is about 65% in South Korea, which is significantly higher than that of other countries, and that the greater the restriction, the lower the adherence.93 Thus, we evaluated MCD and LCD as a combined category, moderately-low carbohydrate or low carbohydrate diets (mLCD) (Supplementary Table 5). IF includes several different dietary regimens, such as time-restricted feeding, alternate-day fasting, and intermittent energy restriction, as well as those with similar meanings. The comparative diets were diets with calorie restriction equivalent to those of the intervention diets, and most were included in a calorie-restricted diet and a low fat diet. Even if it was indicated as a standard diet, it was included in the analysis if the same degree of caloric restriction was achieved.

Outcome variables included anthropometric measurements like body weight, glycemic control indicators like glycosylated hemoglobin (HbA1c), and cardiovascular risk factors like blood pressure and lipid profiles. Detailed primary and secondary outcome variables will be described in each recommendation for each study population. The analysis of outcome variables was performed by classifying as follows according to the duration of the intervention: for 6 months or less (9 to 24 weeks), for more than 6 months to 1 year or less (36 to 52 weeks), and for more than 1 year. The quality of evidence for key outcome variables was evaluated and presented within 6 months since most of the results were performed within this period, and the recommendations were provided in a shortterm period of 6 months or less.

We assessed the risk of bias in the included trials using the revised Cochrane risk of bias tool for RCTs.94 Each trial was assessed by two independent observers, and any differences were resolved by a third observer. The final grade of recommendation and level of evidence for each statement was determined using the Grading of Recommendations Assessment, Development and Evaluation system.95 All subcommittee members participated in the joint production of each part of the guideline, from inception to publication. When the agreement was incomplete regarding the final grade of recommendation and level of evidence, consensus from the chair, vice-chair, and two assigned reviewers of the subcommittee have made the outcome. Recommendations formulated by the subcommittees were reviewed by the entire members of all five committees from the four academic societies that participated in this study.

Recommendation

In adults with overweight or obesity, a mLCD can be considered a dietary regimen for weight reduction since similar or greater effects on weight loss are observed than the generally recommended diets [Conditional recommendation, moderate quality of evidence].

1. A low carbohydrate diet does not imply an extreme reduction in carbohydrate and increase in fat intake, and must not be practiced indiscriminately.
2. A low carbohydrate diet should reduce total caloric intake while avoiding an increase in the intake of saturated and trans fatty acids.
3. After considering sustainability and balance between benefits and risks, we decided not to provide a recommendation for VLCD.

Level of evidence

In the meta-analysis, 63 articles from 47 RCTs were included. While overweight or obesity was an inclusion criterion for the meta-analysis, obese patients with a body mass index (BMI) of ≥30 kg/m2 were included in many cases, and a small number of studies included patients with T2DM. Although studies were conducted in various countries, no studies were conducted in South Korea, and only few targeted Asians. However, studies conducted in China, Japan, and Taiwan, which have similar demographic characteristics to South Korea, had similar overall results. Due to the nature of the studies, in most cases, participants were not blinded, or related information was not described. Low fat (44.7%) and calorie- restricted (29.8%) diets were the most common control diets. The dropout rate of participants was within 20% to 30%. Although the risk of bias differed depending on the study, it was generally low (Supplementary Fig. 2). If the sufficient effect (clinical decision threshold) was not reached, it was judged that there was imprecision. Since the dropout rate was high and the two groups were heterogenous, it was judged that there was indirectness, and thus, the level of evidence was downgraded and evaluated as either low or moderate (Supplementary Tables 6 and 7).

Benefits (advantages)

In the meta-analysis, the primary outcomes for assessing the benefit of a carbohydrate-restricted diet in adults with overweight or obesity included body weight, BMI, waist circumference (WC), fat mass, body fat percentage, and fat-free mass. Secondary outcomes included blood pressure, lipid profile, fasting blood glucose, HbA1c, fasting serum insulin, adiponectin, C-reactive protein (CRP), and adverse effects. Table 1 summarizes the results of the meta-analysis and the level of evidence for each outcome of mLCD and VLCD.

Body weight and BMI

The result of a meta-analysis of 24 articles with a study period of 6 months or less (8 to 24 weeks) showed mLCD had a significant decrease in body weight (mean difference, –1.03; 95% confidence interval [CI], –1.68 to –0.39), compared to the control diet (Fig. 1A). A meta-analysis of 17 studies with a study period of more than 6 months to 1 year or less (36 to 52 weeks) also showed a significant decrease in body weight (mean difference, –0.72; 95% CI, –1.25 to –0.20) compared to the control diet, but no significant weight loss was observed for more than 1 year (Fig. 1A). Compared to the control diet, VLCD significantly decreased body weight by 3.67 kg (95% CI, –4.84 to –2.51) for the study duration of 6 months or less (8 to 24 weeks), 1.87 kg (95% CI, –3.00 to –0.74) for more than 6 months to 1 year or less (36 to 52 weeks), and 1.51 kg (95% CI, –2.88 to –0.14) for more than 1 year, but the difference in weight loss decreased as the study period increased (Fig. 1B).

In all study periods, mLCD lowered the BMI compared to the control diet, but it was not statistically significant (Supplementary Fig. 3A). VLCD significantly decreased the BMI by 1.88 kg/m2 (95% CI, –3.11 to –0.65) for study period of 6 months or less, and 0.82 kg/m2 (95% CI, –1.44 to –0.19) for more than 6 months to 1 year or less compared to the control diet (Supplementary Fig. 3B).

Waist circumference

mLCD showed a significant decrease in WC (mean difference, –0.65; 95% CI, –1.16 to –0.14) for the study period of 6 months or less compared to the control diet, but there was no significant difference for a study period of more than 6 months to 1 year or less (36 to 52 weeks), and more than 1 year (Supplementary Fig. 4A). VLCD showed a decrease in WC compared to the control diet, but there was no statistically significant difference (Supplementary Fig. 4B).

Fat mass and fat percentage

mLCD significantly decreased the fat mass by 0.44 kg (95% CI, –0.83 to –0.04) for the study period of 6 months or less compared to the control diet, and 0.77 kg (95% CI, –1.29 to –0.25) for the study period of more than 6 months to 1 year or less. However, there was no significant decrease in a study period of more than 1 year (Supplementary Fig. 5A). VLCD led to a decreasing trend in the fat mass compared with the control diet in all studies, but it was not statistically significant (Supplementary Fig. 5B).

In all studies, mLCD did not lead to any significant change in body fat percentage compared with the control diet (Supplementary Fig. 6A). VLCD resulted to a significant decrease in body fat percentage by 1.88% (95% CI, –2.87 to –0.89) for 6 months or less compared to the control diet, and 1.56% (95% CI, –2.41 to –0.71) for more than 6 months to 1 year or less (Supplementary Fig. 6B).

Lipid profile, blood pressure, glycemic control, and other metabolic parameters

Triglyceride (TG), high-density lipoprotein cholesterol (HDLC), and low-density lipoprotein cholesterol (LDL-C) levels were evaluated. In mLCD, the TG level decreased by 13.76 mg/dL (95% CI, –19.78 to –7.74) for 6 months or less compared to the control diet (Supplementary Fig. 7A). In VLCD, the TG level significantly decreased by 21.33 mg/dL (95% CI, –30.46 to –12.21) for 6 months or less, and 22.52 mg/dL (95% CI, –31.01 to –14.03) for more than 6 months to 1 year or less (Supplementary Fig. 7B). mLCD showed a significant increase in HDL-C level compared to control diet in all periods (6 months or less [2.61 mg/dL; 95% CI, 1.34 to 3.89], more than 6 months to 1 year or less [1.45 mg/dL; 95% CI, 0.53 to 2.37], more than 1 year [2.84 mg/dL; 95% CI, 1.63 to 4.05]) (Supplementary Fig. 7C). Compared to the control diet, VLCD showed an increase in the HDL-C level for the study period of 1 year or less (6 months or less [4.30 mg/dL; 95% CI, 1.79 to 6.82] and more than 6 months to 1 year or less [4.86 mg/ dL; 95% CI, 2.16 to 7.56]) (Supplementary Fig. 7D). As for LDLC levels, possible risks were identified, and are discussed further in the “Harms” section (Supplementary Fig. 7E and F).

mLCD reduced the systolic blood pressure (SBP) for all study periods compared to the control diet, but it was not statistically significant (Supplementary Fig. 8A). For diastolic blood pressure (DBP), there was a statistically significant but minimal decrease only for the study period of more than 6 months to 1 year or less (mean difference, –0.66; 95% CI, –1.26 to –0.05) (Supplementary Fig. 8B). VLCD decreased the SBP by 1.97 mmHg (95% CI, –3.68 to –0.25) for 6 months or less, and 8.1 mmHg (95% CI, –13.35 to –2.85) for more than 6 months to 1 year or less (Supplementary Fig. 8C) compared to the control diet, but did not significantly decrease DBP (Supplementary Fig. 8D).

In mLCD, the fasting blood glucose level was significantly decreased by –1.62 mg/dL (95% CI, –2.69 to –0.55) compared to the control diet but only for the study period of more than 6 months to 1 year or less (Supplementary Fig. 9A). In VLCD, the fasting blood glucose level did not decrease significantly compared to the control diet, irrespective of the study period (Supplementary Fig. 9B). mLCD significantly decreased the HbA1c level by 0.2% (95% CI, –0.39 to –0.01) compared to the control diet for the study period of 6 months or less. There was also a decreasing trend over a longer period, but it was not statistically significant (Supplementary Fig. 9C). VLCD decreased the HbA1c level by 0.27% (95% CI, –0.50 to –0.03) compared with the control diet for an intervention period of 6 months or less (Supplementary Fig. 9D). mLCD led to decreasing trends in the fasting insulin levels in all studies compared to the control diet, but it was statistically significant only for 6 months or less (mean difference, –0.94; 95% CI, –1.73 to –0.16) (Supplementary Fig. 9E). VLCD decreased the fasting insulin levels in all studies compared to the control diet, but it was not statistically significant (Supplementary Fig. 9F).

In mLCD, the serum adiponectin level increased in all study periods compared to the control diet, with a significant increase of 0.45 μU/mL (95% CI, 0.15 to 0.76) for 6 months or less, and 0.73 μU/mL (95% CI, 0.29 to 1.16) for more than 6 months to 1 year or less (Supplementary Fig. 10A). In VLCD, the serum adiponectin level increased in all study periods compared to the control diet, with a significant increase of 0.75 μg/mL (95% CI, 0.29 to 1.21) for 6 months or less in two studies, and 1.30 μg/mL (95% CI, 0.34 to 2.26) for more than 1 year in two studies (Supplementary Fig. 10B).

In terms of CRP levels, mLCD showed a significant decrease of 0.34 mg/L (95% CI, –0.67 to –0.01) for 6 months or less compared to the control diet (Supplementary Fig. 10C). VLCD showed a decrease in all studies, but it was not statistically significant (Supplementary Fig. 10D).

Summary and conclusion of benefits

In adults with overweight or obesity, the carbohydrate-restricted diets led to weight loss similar to or greater than that of the control diet. As the proportion of carbohydrates decreased, body weight and BMI reduction became greater. When used for 6 months or less, reduction in body weight and BMI was greatest, and the reduction effect decreased as the study period increased. Compared to the control diet, WC is significantly reduced for the study period of 6 months or less in mLCD. Compared to the control diet, fat mass was significantly reduced for the study period of more than 6 months to 1 year or less in mLCD, and body fat percentage was significantly reduced in VLCD. Therefore, a reduction in weight and BMI, as well as WC and body fat mass, can be expected through a short-term carbohydrate-restricted diet for 6 months. Additional effects of TG reduction and HDL-C increase for 1 year or less could also be expected.

Harms (risks)

Fat-free mass

While mLCD led to decreasing trends in fat-free mass in all studies compared to the control diet, it was not statistically significant (Supplementary Fig. 11A). VLCD significantly decreased the body fat-free mass by 1.05 kg (95% CI, –1.75 to –0.35) compared to the control diet for a study period of 6 months or less in three studies (Supplementary Fig. 11B).

Lipid profiles and other adverse effects

While mLCD had an increasing trend in LDL-C levels in all studies compared to the control diet, it was not statistically significant (Supplementary Fig. 7E). VLCD significantly increase the LDL-C by 7.52 mg/dL (95% CI, 3.34 to 11.70) for 6 months or less (Supplementary Fig. 7F).

There was limited literature directly describing the adverse events. In some studies, carbohydrate-restricted diets increase the incidence of nausea, vomiting, headache, and constipation, although it was not statistically significant compared to the control diet in a period of 6 months or less (Supplementary Fig. 12). Although there is no causal relationship with dietary intervention, two cases of death and one case of coronary artery disease occurred 5 to 10 months after the beginning of research in the LCD group of the two studies.

Summary and conclusion of harms

In adults with overweight or obesity, VLCD has been found to cause a decrease in fat-free mass and an increase in LDL-C level compared to the control diet for the study period of 6 months or less. Moreover, caution is required as carbohydrate-restricted diets tend to increase adverse effects such as nausea, vomiting, constipation, and headache during the early period.

Balance of benefits and risks

In adults with overweight or obesity, carbohydrate-restricted diets led to weight loss similar to or greater than that of the control diet, and the effect was greater as the proportion of carbohydrates decreased. Remarkably, the effect was greatest in a short period of 6 months, and the effect decreased as the period increased. WC is significantly decreased in mLCD compared to the control diet within 6 months, a decrease in fat mass within 1 year, a decrease in TG, and an increase in HDL-C within 6 months. VLCD lowered the fat percentage within 1 year, but an increase in LDL-C, along with a decrease in fat-free mass, within 6 months, requires careful discernment on their application. Moreover, caution is required as carbohydrate-restricted diets tended to increase the incidence of nausea, vomiting, constipation, and headaches during the early period.

Considerations in the use of the recommendation

1. To reduce body weight in adults with overweight or obesity, a balanced and high quality diet with carbohydrate restriction and reduced caloric intake is recommended. Recent guidelines for obesity management allow the individualized use of carbohydrate-restricted diets for obesity treatment,5 and most of the carbohydrate-restricted diets included in this study involved a decrease in total calorie intake.

2. Carbohydrate-restricted diets should reduce total caloric intake while avoiding an increase in saturated and trans-fatty acids intake. In a cohort study examining the association between a carbohydrate-restricted diet and the mortality risk, an animal product-based carbohydrate-restricted diet was associated with increased all-cause mortality both in men and women. In contrast, a vegetable-based carbohydrate-restricted diet was associated with reduced all-cause mortality and cardiovascular mortality.95

3. The results should be interpreted with caution because the types and amount of carbohydrates, fats, and total calories ingested and the control diet varied across studies. The benefits and risks of the long-term use of these dietary regimens are incompletely understood. In addition, it is necessary to consider the dietary patterns in South Korea, characterized by a much higher rate of carbohydrate intake than in other countries, to improve adherence to these regimens.

The recommendation for IF in adults with overweight or obesity will be withheld due to the lack of long-term studies and the heterogeneity of previous studies.

Level of evidence

In the meta-analysis, ten articles from eight RCTs were included. The analysis included studies conducted with participants classified as overweight or obese, with BMI of ≥23 kg/m2, which is the Korean obesity criteria, and most participants in the studies had a mean BMI of ≥30 kg/m2. While the risk of bias in individual studies was generally low (Supplementary Fig. 13), there was a high risk of bias in several items, including indirectness and imprecision. Therefore, the level of evidence for the overall evaluation indicators was evaluated as “very-low evidence” (Supplementary Table 8).

Benefits (advantages)

The primary outcomes for assessing the benefit of IF in adults with overweight or obesity included body weight, BMI, WC, fat mass, body fat percentage, and fat-free mass. The secondary outcomes included TG, HDL-C, LDL-C, HbA1c, fasting blood glucose, fasting serum insulin, homeostatic model assessment for insulin resistance (HOMA-IR), SBP, and DBP.

Body weight, body mass index, and body composition

The intervention group, in whom IF was implemented showed no statistically significant difference in body weight (mean difference, –1.22 kg; 95% CI, –3.49 to 1.05), BMI (mean difference, –0.49 kg/m2; 95% CI, –1.13 to 0.14), WC (mean difference, –1.95 cm; 95% CI, –4.09 to 0.20), fat-free mass (mean difference, –0.35 kg; 95% CI, –0.87 to 0.18), fat mass (mean difference, –0.67 kg; 95% CI, –1.95 to 0.62), and fat mass percentage (mean difference, 0.27%; 95% CI, –0.48 to 1.01), compared to the control group, within 6 months (12 to 24 weeks). The results of the meta-analysis showed that there was no statistically significant difference in body weight, fat-free mass, and fat mass between the intervention and control group within the 1 year intervention period (Supplementary Fig. 14).

Lipid profile, blood pressure, glycemic control, and other metabolic parameters

As for the secondary outcomes of the meta-analysis of the studies conducted in a period of 12 to 24 weeks, the intervention group showed no statistically significant difference in TG (mean difference, –1.51 mg/dL; 95% CI, –17.06 to 14.04), HDL-C (mean difference, –0.17 mg/dL; 95% CI, –3.27 to 2.92), LDL-C (mean difference, –0.24 mg/dL; 95% CI, –5.08 to 4.59), HbA1c (mean difference, 0.11%; 95% CI, –0.04 to 0.26), fasting blood glucose (mean difference, –0.89 mg/dL; 95% CI, –4.30 to 2.53), fasting serum insulin (mean difference, –0.43 μU/mL; 95% CI, –1.99 to 1.14), HOMA-IR (mean difference, –0.22; 95% CI, –1.48 to 1.05), SBP (mean difference, 0.87 mmHg; 95% CI, –2.65 to 4.39), and DBP (mean difference, –0.16 mmHg; 95% CI, –2.89 to 2.56), compared to the control group. There was no statistically significant difference in TG, HDL-C, HbA1c, fasting blood glucose, fasting serum insulin, HOMA-IR, SBP, and DBP between the intervention and control group during the 6 months to 1 year intervention period (Supplementary Fig. 15).

Harms (risks)

A study reported mild headache and constipation in a patient undergoing alternate-day fasting. Nonetheless, the risks and adverse effects of this intervention were not reported in other studies.

Balance of benefits and harms

As a result of the IF in adults with overweight or obesity, an increase in LDL-C was observed in the studies conducted for more than 6 months to 1 year or less compared to the control diet. In addition, there were no significant differences in obesity-related outcomes such as body weight, BMI, and WC, as well as glycemic control and lipid profiles. However, an additional analysis of the changes in the intervention group alone revealed that significant reductions in body weight, BMI, WC, body fat mass, and fat-free mass were observed before and after the intervention in all studies. IF for 1 year or less in overweight or obese adults could help reduce body weight similar to the control diet, the continuous calorie restriction diet, or the Dietary Approaches to Stop Hypertension (DASH) diet, but also decrease the fat-free mass, requiring caution. In the studies included in the analysis, no serious adverse event was observed with IF other than a subtle headache and constipation. Nevertheless, there are limitations in interpreting and evaluating the overall benefits and risks of IF in adults with overweight or obesity for the following reasons.

1. The studies included in the analysis were very heterogeneous. The studies were conducted in a variety of countries and races, and limited studies were conducted on Asians. Due to the nature of diet research, there were many studies in which blinding was not performed or related information was not described, and the dropout rate of the study also varied from 6% to 31%. Although the analysis was performed under the integrated concept of IF, various heterogeneous dietary regimens such as time-restricted feeding and alternate-day fasting were included. Even within the dietary regimen of the same name, there was a limitation in evaluating the overall effect due to heterogeneity in the period or cycle of fasting. In the studies that conducted alternate-day fasting, the intervention was mostly performed with a modified IF method that did not perform complete fasting on the day of IF but reduced the intake of calories by about 70% to 75%. As for the dietary method on the day of intake, there were studies that restricted caloric intake, and there were studies that implemented a standard diet. In two studies, time-restricted feeding was implemented as an intervention, and these studies also divided the time of the day and implemented different feeding and fasting times of 16:8 and 12:12.

2. Long-term researches were scarce. The study periods varied from 3 months to a maximum of 1 year, and only one study was conducted for 1 year. Therefore, there is a lack of studies to evaluate the long-term effects of IF.

Considerations in the use of the recommendation

Considering the results of the analysis on benefits and harms as well as the limitations of the above-mentioned studies, recommendation on IF for weight management, diabetes prevention, and cardiovascular risk management in adults with overweight or obesity has been withheld.

Recommendation 1.

In adults with T2DM, a mLCD can be considered a dietary regimen for improving glycemic control and reducing body weight since similar or greater effects on blood glucose-lowering and weight loss are observed compared to generally recommended diets [Conditional recommendation, moderate quality of evidence].

1. A low carbohydrate diet does not imply an extreme reduction in carbohydrate and increase in fat intake, and must not be practiced indiscriminately.
2. A low carbohydrate diet should reduce caloric intake while avoiding an increase in the intake of saturated and trans fatty acids.

Recommendation 2.

In adults with T2DM, the strong recommendation against a VLCD as the risks of hypoglycemia and elevated LDL-C levels outweigh the benefits of blood glucose-lowering and weight loss [Strong recommendation against, moderate quality of evidence].

Level of evidence

A meta-analysis was performed on the key question, “Are carbohydrate- restricted diets helpful in improving glycemic control in diabetic patients?” Twenty-three articles from 18 RCTs on benefits were included in the analysis. In principle, studies in which more than 50% of all subjects had diabetes were included in the analysis. In 15 studies, 100% of the participants had diabetes29-31,45-48,51,56,59, 62,65,68,74-78,80,96 and 50% or more had diabetes in two studies.38,67 Although less than 50% were diabetic, one study was included in the analysis since the outcomes could be analyzed only for diabetic patients.69,70 There were 13 studies on mLCD and five studies on VLCD. Most studies were conducted in Western countries, and no studies were conducted in South Korea. Five studies were conducted in East Asian countries (China, Japan, and Taiwan), with similar demographic characteristics to South Korea. Of 1,282 subjects, 369 (28.8%) were from East Asian countries. The risk of bias in individual studies was evaluated as “low” or “some concern” (Supplementary Fig. 16). However, in evaluating the level of evidence for the key question, the overall dropout rate was high, with heterogeneity in the two groups, with an apparent indirectness. After rating down, the level of evidence for the change in HbA1c level was evaluated as “moderate evidence.” The level of evidence and evaluation results for all variables other than HbA1c can also be seen in Supplementary Tables 9 and 10.

Benefits (advantages)

The primary outcome for assessing the benefit of carbohydraterestricted diets in diabetic adults for blood glucose control was the change in HbA1c. The secondary outcomes for evaluating the metabolic and cardiovascular benefits of carbohydrate-restricted diets in diabetic adults included body weight, blood pressure, lipid profiles, fasting blood glucose, and HOMA-IR. Table 2 summarizes the meta-analysis results and level of evidence for primary and secondary outcomes.

HbA1 reduction

Compared to the control diets, mLCD (12 studies) and VLCD (five studies) reduced the HbA1c levels by 0.21% (95% CI, –0.32 to –0.10) and 0.36% (95% CI, –0.54 to –0.19) within 6 months, respectively. However, no additional benefit was observed for periods exceeding 6 months (Fig. 2). In addition, the results of five studies conducted in East Asia also showed similar results (within 6 months, mean difference, –0.26; 95% CI, –0.44 to –0.07) (Supplementary Fig. 17). Compared to before the intervention, mLCD lowered the HbA1c by 0.50% (95% CI, –0.63 to –0.37), and VLCD lowered the HbA1c by 0.60% (95% CI, –1.12 to –0.08) within 6 months after the intervention. Therefore, both mLCD and VLCD additionally improved glycemic control within 6 months in adults with T2DM compared to the control diet with an equivalent reduction in caloric intake.

Body weight, blood pressure, lipid profiles, fasting blood glucose, and insulin resistance

In body weight, mLCD (11 studies) reduced by 1.54 kg (95% CI, –3.11 to 0.02) within 6 months compared to the control diets, although it was not statistically significant. A weight loss of 3.84 kg (95% CI, –7.55 to –0.13) was also observed in VLCD (five studies). However, no additional benefit was observed for periods exceeding 6 months (Supplementary Fig. 18). These benefits were consistent with the meta-analysis results, including more studies in obese adults. Hence, mLCD and VLCD elicit additional weight loss within 6 months in diabetic patients compared to the control diet.

In blood pressure, mLCD (seven studies) reduced the SBP by 2.99 mmHg (95% CI, –5.48 to –0.49) was observed within 6 months compared to the control diets, but no such benefit was observed with VLCD (three studies). For DBP, both diets did not show any blood pressure-lowering effect in any period (Supplementary Fig. 19). These results were inconsistent with the meta-analysis results, including more studies in obese adults. Hence, the additional blood pressure-lowering effect of mLCD and VLCD compared to control diets in diabetic patients is inconclusive.

In lipid profiles, TG, HDL-C, and LDL-C levels were evaluated as outcomes. Compared to the control diets, mLCD (11 studies) decrease in TG level by 17.22 mg/dL (95% CI, –34.27 to –0.18) within 6 months, and 17.85 mg/dL (95% CI, –32.08 to –3.62) for 1 year or less. It also resulted to an additional increase in HDL-C level of 2.30 mg/dL (95% CI, 0.23 to 4.37) for 6 months or less, and 1.77 mg/dL (95% CI, 0.01 to 3.53) for 1 year or less. However, for LDL-C levels, no additional reduction was confirmed in all periods. In VLCD, no benefits in TG and HDL-C levels were observed (five studies). Rather, an additional increase in LDL-C level of 7.19 mg/dL (95% CI, 0.02 to 14.36) was observed within 6 months (Supplementary Fig. 20). These findings were consistent with the meta-analysis results, including more studies in obese adults. Hence, even in diabetic patients, mLCD has additional benefits of improving TG and HDL-C levels within 1 year, whereas VLCD has a risk of increasing LDL-C levels within 6 months compared to the control diets.

In fasting blood glucose, mLCD (seven studies) caused an additional reduction of 9.88 mg/dL (95% CI, –18.04 to –1.71) within 6 months compared to the control diet. Although not statistically significant, VLCD (three studies) also reduced blood glucose level by 9.64 mg/dL (95% CI, –19.54 to 0.26). However, no additional benefits were observed for periods exceeding 6 months (Supplementary Fig. 21). These findings were consistent with the meta-analysis results, including more studies in obese adults. Hence, mLCD and VLCD additionally improved fasting blood glucose levels within 6 months compared to the control diets.

HOMA-IR was examined as an outcome for the evaluation of insulin resistance. In the five studies included in the HOMA-IR analysis, mLCD (three studies) led to an additional reduction of 0.53 (95% CI, –0.96 to –0.11) within 6 months compared to the control diets. At the same time, VLCD (two studies) reduced HOMA-IR by 1.07 (95% CI, –3.13 to 0.98), although it was not statistically significant (Supplementary Fig. 22). Hence, mLCD additionally improved insulin resistance within 6 months compared to the control diets.

Summary and conclusion of benefits

In adults with T2DM, mLCD and VLCD were more effective in reducing body weight and improving glycemic control than equivalent calorie-restricted diets within 6 months. The benefits were greater in VLCD than in mLCD. In addition, mLCD improved insulin resistance and lipid profile (decreased TG and increased HLD-C levels).

Harms (risks)

Of the 18 studies, eight studies mentioned risks, and five of them stated that there were “no serious adverse events.” Three studies reported adverse events, but they were evaluated to not be associated with the intervention. Gastrointestinal disturbance, such as nausea, vomiting, and constipation, tended to increase within a short period but decreased afterward in two VLCD studies for the risk assessment in obese adults (Supplementary Fig. 12).17,45

Hypoglycemia is the most concerning complication of reducing total calorie intake or carbohydrate-restricted diets in diabetic patients. There was no direct evidence that carbohydrate-restricted diets were more likely to cause hypoglycemia than a calorie-restricted diet. However, patients with type 1 diabetes mellitus or a history of severe hypoglycemia, or patients using insulin or sulfonylureas at a higher risk of hypoglycemia were also excluded in several studies.38,45,51,59,67,74-78 Furthermore, it is clear that the risk of hypoglycemia increase with a greater degree of carbohydrate or calorie restriction.96 Indeed, only two of 13 mLCD studies (15.4%) excluded patients at a higher risk of hypoglycemia with type 1 diabetes mellitus or those using insulin or sulfonylureas,59,74-78 compared to four of five VLCD studies (75.0%)38,45,51,67 in our analysis. Therefore, carbohydrate-restricted diets may increase the risk of hypoglycemia, which was greater in VLCD.

LDL-C level was statistically significantly increased by VLCD compared to the control diet in the meta-analysis results. These results were consistent with the meta-analysis results, including more studies in obese adults. Hence, VLCD is likely to increase the risk of LDL-C.

Summary and conclusion of harms

Many studies excluded patients with a higher risk of hypoglycemia, and this risk is higher as the degree of carbohydrate restriction increases.97 Therefore, VLCD is associated with the highest risk of hypoglycemia. LDL-C levels, an important risk factor for cardiovascular disease, increased significantly in VLCD but not in mLCD. Diabetes is a significant contributor to cardiovascular disease, and the prevalence of cardiovascular disease is two to four times higher in patients with diabetes than in those without diabetes.98 Therefore, elevated LDL-C in VLCD is a potential risk factor for cardiovascular disease.

Balance of benefits and harms

In adults with T2DM, carbohydrate-restricted diets improved glycemic control and reduced body weight to a level similar to or greater than that of the control diets, and the effects were greater as carbohydrate intake decreased. Moreover, the effects were greatest within 6 months and decreased as the intervention period increased. mLCD decreased TG, increased HDL-C. VLCD elevated LDL-C and significantly increased the risk of hypoglycemia. Therefore, mLCD was evaluated as beneficial with the minor risks of harm to adults with T2DM. In contrast, VLCD was evaluated that the benefits did not significantly outweigh the risks of serious harm.

Considerations in the use of the recommendation

Participants with malignancies or serious medical conditions in the cardiovascular system, kidney, gastrointestinal tract, and pancreas; pregnant or lactating women; psychiatric disorders including eating disorders or drug abuse; acute illnesses such as infections, were excluded due to the greater risk of harm in most studies, because carbohydrate-restricted diets have a high potential for harm in such patients and inconclusive benefits. Therefore, it is inappropriate to recommend a carbohydrate-restricted diet to those patients.

Recently popular dietary approaches, such as extremely low carbohydrate and high-fat diets, focus only on lowering the carbohydrate ratio, neglecting the total caloric intake and fat quality. Since reducing carbohydrate intake inevitably leads to an increase in fat intake, we should also be concerned about total fat intake and fat quality. Fortunately, the researchers in most studies tried to minimize the increase in fat intake while reducing the total caloric intake included in the analysis. Simultaneously, they attempted to decrease the intake of saturated and trans-fatty acids, with potential harm to cardiovascular disease. Therefore, carbohydrate-restricted diets should reduce total caloric intake while avoiding an increase in the intake of saturated and trans-fatty acids.

Since most studies are focused on evaluating the benefits of carbohydrate- restricted diets, with a scarcity of research on risk assessment, further studies are required. Furthermore, well-designed RCTs in Korean patients are also needed. Considering that the carbohydrate intake rate of Koreans is about 65%, which is significantly higher than that of other countries,93 future studies must evaluate (1) whether this benefit can be maintained even after adjusting the carbohydrate restriction rate to 45%–55%, which is higher than that of MCD, and (2) whether carbohydrate restriction to the level of MCD or LCD would be harmful to Koreans.

Recommendation

In adults with T2DM, strong recommendation against IF due to the lack of evidence on its benefits and harms, and risk of hypoglycemia [Strong recommendation against, low quality of evidence].

Level of evidence

Eight RCTs in 10 articles were conducted for evaluating the benefits of IF in overweight and obese adults, but only one study was conducted with T2DM patients. Table 2 shows the results in two literature of one research85,86 and the assessment of the level of evidence performed in diabetic patients. The risk of bias in the study was evaluated as “low” or “some concern” (Supplementary Fig. 13). However, there was only one study to be analyzed, the number of subjects was too small, and the effect of outcome was insufficient, with apparent imprecision. After rating down, the level of evidence for the change in HbA1c level was evaluated as “low evidence.”

Benefits (advantages)

No additional benefit was identified in one study on patients with T2DM compared to a control diet.

Harms (risks)

The single study conducted on patients with T2DM had no description of the risks. In other studies, diabetes itself is often used as an exclusion criterion of participants due to the associated risks, including hypoglycemia, in diabetic patients during the fasting period.

Balance of benefits and harms

In adults with T2DM, IF has no evidence of benefit for metabolic outcomes such as glycemic control and weight loss, and no evidence of harm has been identified. However, there is a high risk of harm such as hypoglycemia during the fasting period. Therefore, IF was evaluated as having the risk of harm while the evidence for the benefit was insufficient. Accordingly, this committee decided that IF was a “strong recommendation against” in adults with T2DM.

Considerations in the use of the recommendation

Additional research is needed to establish sufficient evidence, considering the continuing and high interest in IF as an attractive diet regimen among the general population with some studies publishing beneficial results. Although few studies have been conducted in diabetic patients due to hypoglycemia, research on these patients can be possible with the widespread use of various antidiabetic drugs with a low risk of hypoglycemia.

1. As there is insufficient evidence to support carbohydrate-restricted diets in adults with hypertension, it has been decided not to present a recommendation.

2. As there is insufficient evidence to support IF in adults with hypertension, it has been decided not to present a recommendation.

Level of evidence

Carbohydrate-restricted diets

The inclusion criteria were studies conducted on patients with hypertension; studies in which ≥50% of participants were diagnosed with hypertension; studies in which ≥50% of participants were taking antihypertensive drugs; and studies with patients having SBP of 140 mmHg or higher, or DBP of 90 mmHg or higher at baseline. In the meta-analysis, 14 articles from six RCTs on benefit were included. There were three studies each on both mLCD and VLCD. Each study was evaluated to be designed with low or some concerns (Supplementary Fig. 23). In the evaluation of the level of evidence with respect to the key question, however, there was a high risk of bias in several items, including indirectness and imprecision with no studies targeting only patients with hypertension, with the absence of blinding in most of the studies due to the nature of the research, high dropout rates, and heterogeneity between groups. Therefore, the level of evidence was downgraded to “verylow evidence” (Supplementary Tables 11 and 12).

Intermittent fasting

There have been no studies on the benefits of IF conducted on the included studies. Therefore, the evidence for IF was not evaluated.

Benefits (advantages)

Changes in SBP and DBP were the primary outcomes to determine the benefits of carbohydrate-restricted diets in adults with hypertension. The secondary outcomes for assessing the metabolic and cardiovascular benefits of carbohydrate-restricted diets included body weight, lipid profiles of cholesterol and TG. Table 3 summarizes the level of evidence and meta-analysis results for primary and secondary outcomes.

Blood pressure control

Compared to the control diet, mLCD significantly decreased SBP in 8 to 24 weeks and marginally decreased SBP in intervention periods longer than 36 weeks (Fig. 3A). mLCD did not significantly affect DBP (Fig. 3A). However, with mLCD, there was a significant reduction in BP levels compared to the baseline within 1 year (SBP: 6 months or less [mean difference, –9.28; 95% CI, –13.76 to –4.80], more than 6 months to 1 year or less [mean difference, –7.10; 95% CI, –10.37 to –3.83], more than 1 year [mean difference, –5.27; 95% CI, –11.44 to 0.90]) (DBP: 6 months or less [mean difference, –8.20; 95% CI, –9.82 to –6.58], more than 6 months to 1 year or less [mean difference, –6.20; 95% CI, –8.16 to –4.24], more than 1 year [mean difference, –3.14; 95% CI, –6.86 to 0.58]). The absence of a difference between the intervention group and the control group did not necessarily mean that the LCD did not have a benefit associated with blood pressure. VLCD marginally decreased SBP compared with the control diet (Fig. 3B). VLCD did not lead to a significant difference in DBP compared to the control diet (Fig. 3B).

Body weight, lipid profile, fasting blood glucose, and insulin resistance

In terms of body weight, mLCD and VLCD did not show an additional reduction effect than the control diet (Supplementary Fig. 24). mLCD significantly decreased TG levels compared with the control diet; however, the significant difference between the two groups disappeared in intervention periods longer than 1 year. mLCD significantly increased the HDL-C levels by 3.36 mg/dL (95% CI, 0.71 to 6.00) after 1 year relative to the control diet. VLCD did not significantly change the body weight and TG compared to the control diet. However, there is a significant increase in HDL-C level by 4.11 mg/dL (95% CI, 0.81 to 7.42) for more than 6 months to 1 year or less, which disappeared after 1 year (Supplementary Fig. 25).

Harms (risks)

mLCD marginally increased LDL-C levels, whereas VLCD significantly increased LDL-C in an intervention period of 6 months to 1 year compared with the control diet (Supplementary Fig. 25). High participant dropout was observed during the study period, suggesting difficulty in maintaining carbohydrate-restricted diets. In addition, although rare, deaths have been reported in the VLCD group during the observation period in some studies. During the 24-month observation period, one patient died from myocardial infarction in both the intervention and control groups. During the 12-month observation period, there was one death due to ischemic cardiomyopathy and one death due to hyperosmolar coma in the intervention group, and one patient was hospitalized with noncardiac chest pain. Although it has not been proven that each death is directly related to a VLCD, further assessment of the risk will be needed. In some LCD studies, 14.0% of musculoskeletal disorders occurred in the low carbohydrate intervention group during the observation period, and 22.4% of musculoskeletal disorders occurred in the control group. Although rare, during the 52-week observation period, one patient in the intervention group was hospitalized for arrhythmia suspected of heart failure, and one patient underwent a hypoglycemic event without being hospitalized. Although it has not been proven that each event is directly caused by a LCD, further assessment of the risk is needed.

Balance of benefits and risks

For obese adults with hypertension, carbohydrate-restricted diets had no additional benefit in reducing blood pressure and weight compared to calorie-restricted or low fat diets when maintained for 1 year or longer. While TG levels decreased within 1 year, such a benefit reduced after 1 year. There was a risk of increasing LDL-C for less than 1 year in VLCD, but thereafter, the risk disappeared. Although it has not been proven as a direct result of carbohydraterestricted diets, cardiovascular death and hospitalization have been reported. Therefore, the selection of such methods should be made by fully considering the potential benefits and risks according to the condition of each patient. Accordingly, the benefits and risks remain unclear. Additional research results in patients with hypertension will be needed in the future.

Considerations in the use of the recommendation

Further research is needed to establish the evidence, as there is insufficient evidence to prove the effectiveness of LCD in adults with hypertension, and there are no RCTs targeting only patients with hypertension, with no studies presenting the change in blood pressure as a primary outcome.

Fig. 1. Effects of carbohydrate-restricted diets on body weight in adults with overweight/obesity. (A) Moderately-low carbohydrate or low carbohydrate diet (mLCD). (B)
Very-low carbohydrate diet (VLCD). WMD, weighted mean difference; CI, confidence interval.
Fig. 2. Effects of carbohydrate-restricted diets on glycosylated hemoglobin (HbA1c) in adults with type 2 diabetes mellitus. (A) Moderately-low carbohydrate or low carbohydrate diet (mLCD). (B) Very-low carbohydrate diet (VLCD). WMD, weighted mean difference; CI, confidence interval.
Fig. 3. Effects of carbohydrate-restricted diets on systolic and diastolic blood pressure in adults with hypertension. (A) Moderately-low carbohydrate or low carbohydrate diet (mLCD). (B) Very-low carbohydrate diet (VLCD). WMD, weighted mean difference; CI, confidence interval.

Summary of findings for effects of carbohydrate-restricted diets and intermittent fasting in adults with overweight/obesity

Outcome Illustrative comparative risk* (95% CI) No. of participants Quality of the evidence (GRADE)

Assumed risk(control) Corresponding risk

Intervention Mean difference
mLCD
Body weight (kg, follow-up: 8–24 wk) –3.74 –4.77 –1.03 (–1.68 to –0.39) 3,660 (24 studies) Low
Body mass index (kg/m2, follow-up: 8–24 wk) –1.5 –1.73 –0.23 (–0.46 to 0.00) 2,750 (15 studies) Very low
Waist circumference (cm, follow-up: 12–24 wk) –4.83 –5.48 –0.65 (–1.16 to –0.14) 2,340 (15 studies) Moderate
Fat mass (kg, follow-up: 12–24 wk) –2.92 –3.36 –0.44 (–0.83 to –0.04) 2,080 (14 studies) Moderate
Fat-free mass (kg, follow-up: 12–24 wk) 0.17 0.00 –0.17 (–0.49 to 0.14) 1,139 (10 studies) Low
Fat mass (%, follow-up: 12–24 wk) –2.7 –2.61 0.09 (–0.45 to 0.64) 445 (4 studies) Low
Systolic blood pressure (mmHg, follow-up: 8–24 wk) –4.0 –4.56 –0.56 (–1.69 to 0.56) 2,612 (19 studies) Low
Diastolic blood pressure (mmHg, follow-up: 8–24 wk) –2.5 –3.19 –0.69 (–1.39 to 0.01) 2,615 (19 studies) Low
Triglyceride (mg/dL, follow-up: 8–24 wk) –11.8 –25.56 –13.76 (–19.78 to –7.74) 2,896 (24 studies) Low
LDL-C (mg/dL, follow-up: 12–24 wk) –4.6 –2.31 2.29 (–0.41 to 4.99) 2,721 (21 studies) Very low
HDL-C (mg/dL, follow-up: 8–24 wk) –0.8 1.81 2.61 (1.34 to 3.89) 2,448 (20 studies) Moderate
HbA1c (%, follow-up: 8–24 wk) –0.2 –0.40 –0.20 (–0.39 to –0.01) 739 (8 studies) Low
Fasting insulin (μU/mL, follow-up: 12–24 wk) –0.9 –1.84 –0.94 (–1.73 to –0.16) 1,855 (13 studies) Moderate
Fasting glucose (mg/dL, follow-up: 8–24 wk) –3.1 –3.42 –0.32 (–1.23 to 0.58) 2,143 (17 studies) Low
C-reactive protein (mg/L, follow-up: 8–24 wk) –0.1 –0.44 –0.34 (–0.67 to –0.01) 1,391 (11 studies) Low
Adiponectin (μg/mL, follow-up: 8–24 wk) 0.2 0.65 0.45 (0.15 to 0.76) 1,356 (8 studies) Moderate
VLCD
Body weight (kg, follow-up: 8–24 wk) –3.75 –7.42 –3.67 (–4.84 to –2.51) 1,266 (14 studies) Moderate
Body mass index (kg/m2, follow-up: 8–24 wk) –1.0 –2.88 –1.88 (–3.11 to –0.65) 388 (5 studies) Moderate
Waist circumference (cm, follow-up: 8–24 wk) –4.7 –8.81 –4.11 (–8.70 to 0.49) 233 (2 studies) Low
Fat mass (kg, follow-up: 8–24 wk) –4.8 –7.81 –3.01 (–6.29 to 0.27) 168 (3 studies) Low
Fat-free mass (kg, follow-up: 8–24 wk) –0.3 –1.35 –1.05 (–1.75 to –0.35) 168 (3 studies) Low
Fat mass (%, follow-up: 8–24 wk) –1.45 –3.33 –1.88 (–2.87 to –0.89) 515 (4 studies) Moderate
Systolic blood pressure (mmHg, follow-up: 8–24 wk) –3.0 –4.97 –1.97 (–3.68 to –0.25) 506 (9 studies) Moderate
Diastolic blood pressure (mmHg, follow-up: 8–24 wk) –2.1 –2.78 –0.68 (–1.79 to 0.44) 906 (9 studies) Low
Triglyceride (mg/dL, follow-up: 8–24 wk) –11.9 –33.23 –21.33 (–30.46 to –12.21) 1,059 (13 studies) Low
LDL-C (mg/dL, follow-up: 8–24 wk) –5.1 2.42 7.52 (3.34 to 11.70) 1,023 (12 studies) Moderate
HDL-C (mg/dL, follow-up: 8–24 wk) 0.0 4.30 4.30 (1.79 to 6.82) 1,058 (13 studies) Low
HbA1c (%, follow-up: 8–24 wk) –0.15 –0.42 –0.27 (–0.50 to –0.03) 354 (6 studies) Low
Fasting insulin (μU/mL, follow-up: 8–24 wk) –1.55 –2.92 –1.37 (–2.89 to 0.15) 603 (6 studies) Low
Fasting glucose (mg/dL, follow-up: 8–24 wk) –2.9 –3.34 –0.44 (–2.66 to 1.78) 730 (9 studies) Low
C-reactive protein (mg/L, follow-up: 8–24 wk) –0.2 –0.83 –0.63 (–1.41 to 0.15) 371 (5 studies) Low
Adiponectin (μg/mL, follow-up: 8–24 wk) 0.4 1.15 0.75 (0.29 to 1.21) 181 (2 studies) Low
Intermittent fasting§
Body weight (kg, follow-up: 12–24 wk) –3.62 –4.84 –1.22 (–3.49 to 1.05) 554 (8 studies) Very low
Body mass index (kg/m2, follow-up: 12–24 wk) –1.46 –1.95 –0.49 (–1.13 to 0.14) 380 (5 studies) Low
Waist circumference (cm, follow-up: 12–24 wk) –2.28 –4.23 –1.95 (–4.09 to 0.2) 180 (3 studies) Very low
Fat mass (kg, follow-up: 12–24 wk) –1.1 –1.46 –0.36 (–0.87 to 0.16) 540 (8 studies) Very low
Fat-free mass (kg, follow-up: 12–24 wk) –3.7 –4.37 –0.67 (–1.95 to 0.62) 540 (8 studies) Very low
Fat mass (%, follow-up: 12–24 wk) –0.9 –0.63 0.27 (–0.48 to 1.01) 142 (3 studies) Very low
Systolic blood pressure (mmHg, follow-up: 12–24 wk) –5.7 –4.83 0.87 (–2.56 to 4.39) 404 (6 studies) Very low
Diastolic blood pressure (mmHg, follow-up: 12–24 wk) –3.4 –3.56 –0.16 (–2.89 to 2.56) 404 (6 studies) Very low
Triglyceride (mg/dL, follow-up: 12–24 wk) –22.0 –23.51 –1.51 (–17.06 to 14.04) 432 (6 studies) Very low
LDL-C (mg/dL, follow-up: 12–24 wk) –12.48 –12.72 –0.24 (–5.08 to 4.59) 387 (5 studies) Very low
HDL-C (mg/dL, follow-up: 12–24 wk) 0.0 –0.17 –0.17 (–3.27 to 2.89) 432 (6 studies) Very low
HbA1c (%, follow-up: 12–24 wk) –0.31 –0.20 0.11 (–0.04 to 0.26) 173 (3 studies) Very low
Fasting glucose (mg/dL, follow-up: 12–24 wk) –3.00 –3.89 –0.89 (–4.30 to 2.53) 359 (5 studies) Low
Fasting insulin (μU/mL, follow-up: 12–24 wk) –2.6 –3.03 –0.43 (–1.99 to 1.14) 314 (4 studies) Low
HOMA-IR (follow-up: 12–24 wk) –0.94 –1.16 –0.22 (–1.48 to 1.05) 119 (2 studies) Very low

GRADE Working Group grades of evidence: High quality (Further research is very unlikely to change our confidence in the estimate of effect); Moderate quality (Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate); Low quality (Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate); Very low quality (We are very uncertain about the estimate).

*The basis for the assumed risk is the mean change of outcomes compared to baseline in the control group across studies, and the corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group; mLCD for overweight/obesity: Patient or population (patients with overweight/obese), Intervention (mLCD); VLCD for overweight/obese: Patient or population (patients with overweight/obesity), Intervention (VLCD); §Intermittent fasting for overweight/obesity: Patient or population (patients with overweight/obesity), Intervention (intermittent fasting).

CI, confidence interval; GRADE, Grading of Recommendations Assessment, Development and Evaluation; mLCD, moderately-low carbohydrate or low carbohydrate diet; LDL-C, lowdensity lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; HbA1c, glycosylated hemoglobin; VLCD, very-low carbohydrate diet; HOMA-IR, homeostatic model assessment for insulin resistance.

Summary of findings for effects of carbohydrate-restricted diets in adults with type 2 diabetes mellitus

Outcome Illustrative comparative risk* (95% CI) No. of participants Quality of the evidence (GRADE)

Assumed risk(control) Corresponding risk

Intervention Mean difference
mLCD
HbA1c (%, follow-up: 8–24 wk) –0.2 –0.41 –0.21 (–0.32 to –0.10) 758 (10 studies) Moderate
HOMA-IR (follow-up: 8–24 wk) –0.4 –0.93 –0.53 (–0.96 to –0.11) 248 (3 studies) Low
Fasting glucose (mg/dL, follow-up: 8–24 wk) 4.65 –5.23 –9.88 (–18.04 to –1.71) 337 (6 studies) Low
Body weight (kg, follow-up: 8–24 wk) –1.45 –2.99 –1.54 (–3.11 to 0.02) 619 (8 studies) Low
Systolic blood pressure (mmHg, follow-up: 8–24 wk) –0.25 –3.24 –2.99 (–5.48 to –0.49) 510 (6 studies) Moderate
Diastolic blood pressure (mmHg, follow-up: 8–24 wk) 0.55 –0.52 –1.07 (–2.43 to 0.29) 513 (6 studies) Low
Triglyceride (mg/dL, follow-up: 8–24 wk) –4.0 –21.22 –17.22 (–34.27 to –0.18) 742 (10 studies) Low
LDL-C (mg/dL, follow-up: 8–24 wk) –3.6 –3.25 0.35 (–3.03 to 3.72) 607 (8 studies) Low
HDL-C (mg/dL, follow-up: 8–24 wk) 0.2 2.50 2.30 (0.23 to 4.37) 547 (8 studies) Moderate
Hypoglycemia There is no study directly evaluated the risk of hypoglycemia. Patients at high risk of hypoglycemia were excluded in 2 out of 13 studies.
VLCD
HbA1c (%, follow-up: 12–24 wk) –0.2 –0.56 –0.36 (–0.54 to –0.19) 321 (5 studies) Moderate
HOMA-IR (follow-up: 12–24 wk) –0.45 –1.52 –1.07 (–3.13 to 0.98) 119 (2 studies) Low
Fasting glucose (mg/dL, follow-up: 12–24 wk) –17.2 –26.84 –9.64 (–19.54 to 0.26) 267 (3 studies) Low
Body weight (kg, follow-up: 12–24 wk) –3.4 –7.24 –3.84 (–7.55 to –0.13) 291 (4 studies) Moderate
Systolic blood pressure (mmHg, follow-up: 12–24 wk) –1.7 –1.36 0.34 (–3.61 to 4.28) 218 (3 studies) Low
Diastolic blood pressure (mmHg, follow-up: 12–24 wk) –2.5 –1.12 1.38 (–0.90 to 3.67) 218 (3 studies) Low
Triglyceride (mg/dL, follow-up: 12–24 wk) –15.7 –27.10 –11.40 (–27.01 to 4.22) 313 (5 studies) Low
LDL-C (mg/dL, follow-up: 12–24 wk) –1.35 5.84 7.19 (0.02 to 14.36) 277 (4 studies) Moderate
HDL-C (mg/dL, follow-up: 12–24 wk) 2.3 2.73 0.43 (–1.98 to 2.84) 312 (5 studies) Low
Hypoglycemia Although no study directly evaluated the risk of hypoglycemia, patients at high risk of hypoglycemia were excluded in 4 out of 5 studies.
Intermittent fasting§
HbA1c (%, follow-up: 24 wk) –0.6 –0.5 0.10 (–0.35 to 0.55) 63 (1 study) Low
HbA1c (%, follow-up: 52 wk) –0.5 –0.3 0.20 (–0.22 to 0.62) 137 (1 study) Low
Body weight (kg, follow-up: 24 wk) –4.0 –5.0 –1.00 (–6.94 to 4.94) 63 (1 study) Low
Fat-free mass (kg, follow-up: 24 wk) –1.1 –2.2 –1.10 (–2.22 to 0.02) 49 (1 study) Low
Fat mass (kg, follow-up: 24 wk) –4.0 –3.8 0.20 (–1.46 to 1.86) 49 (1 study) Low
Fat mass (%, follow-up: 24 wk) –2.1 –1.7 0.40 (–0.86 to 1.66) 49 (1 study) Low
Hypoglycemia Although no study directly evaluated the risk of hypoglycemia, most studies in obese or overweight adults have excluded patients with diabetes as an exclusion criterion.

GRADE Working Group grades of evidence: High quality (Further research is very unlikely to change our confidence in the estimate of effect); Moderate quality (Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate); Low quality (Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate); Very low quality (We are very uncertain about the estimate).

*The basis for the assumed risk is the mean change of outcomes compared to baseline in the control group across studies, and the corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group; mLCD for type 2 diabetes mellitus: Patient or population (patients with type 2 diabetes mellitus), Intervention (mLCD); VLCD for type 2 diabetes mellitus: Patient or population (patients with type 2 diabetes mellitus), Intervention (VLCD); §Intermittent fasting for type 2 diabetes mellitus: Patient or population (patients with type 2 diabetes mellitus), Intervention (intermittent fasting).

CI, confidence interval; GRADE, Grading of Recommendations Assessment, Development and Evaluation; mLCD, moderately-low carbohydrate or low carbohydrate diet; HbA1c, glycosylated hemoglobin; HOMA-IR, homeostatic model assessment for insulin resistance; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; VLCD, very-low carbohydrate diet.

Summary of findings for effects of carbohydrate-restricted diet in adults with hypertension

Outcome Illustrative comparative risk* (95% CI) No. of participants Quality of the evidence (GRADE)

Assumed risk(control) Corresponding risk

Intervention Mean difference
mLCD
Systolic blood pressure (mmHg, follow-up: 8–24 wk) –4.55 –7.80 –3.25 (–7.28 to 0.77) 195 (2 studies) Very low
Diastolic blood pressure (mmHg, follow-up: 8–24 wk) –4.00 –5.80 –1.80 (–4.56 to 0.96) 93 (1 study) Very low
Triglyceride (mg/dL, follow-up: 8–24 wk) –15.48 –51.06 –35.58 (–52.84 to –18.33) 195 (2 studies) Very low
LDL-C (mg/dL, follow-up: 8–24 wk) –0.30 –0.30 0.00 (–9.55 to 9.55) 93 (1 study) Very low
HDL-C (mg/dL, follow-up: 36–52 wk) 2.3 3.90 1.60 (–1.13 to 4.33) 93 (1 study) Very low
Body weight (kg, follow-up: 8–24 wk) –6.2 –8.01 –1.81 (–3.93 to 0.30) 195 (2 studies) Very low
FMD (%, follow-up: 36–52 wk) –0.6 –0.30 0.30 (–0.58 to 1.18) 93 (1 study) Very low
VLCD
Systolic blood pressure (mmHg, follow-up: 8–24 wk) –6.3 –7.64 –1.34 (–5.20 to 2.51) 232 (2 studies) Very low
Diastolic blood pressure (mmHg, follow-up: 8–24 wk) –4.0 –1.99 2.01 (–0.61 to 4.63) 232 (2 studies) Very low
Triglyceride (mg/dL, follow-up: 8–24 wk) –19.95 –30.12 –10.17 (–43.00 to 22.67) 232 (2 studies) Very low
LDL-C (mg/dL, follow-up: 8–24 wk) –6.75 2.16 8.91 (–9.27 to 27.08) 232 (2 studies) Very low
HDL-C (mg/dL, follow-up: 8–24 wk) 2.75 4.60 1.85 (–5.98 to 9.69) 232 (2 studies) Very low
Body weight (kg, follow-up: 8–24 wk) –6.05 –7.21 –1.16 (–2.65 to 0.34) 232 (2 studies) Very low
FMD (%, follow-up: 36–52 wk) –0.3 –2.10 –1.80 (–3.48 to –0.12) 49 (1 study) Very low

GRADE Working Group grades of evidence: High quality (Further research is very unlikely to change our confidence in the estimate of effect); Moderate quality (Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate); Low quality (Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate); Very low quality (We are very uncertain about the estimate).

*The basis for the assumed risk is the mean change of outcomes compared to baseline in the control group across studies, and the corresponding risk (and its 95% CI) is based on the assumed risk in the comparison group; mLCD for hypertension: Patient or population (patients with hypertension), Intervention (mLCD); VLCD for hypertension: Patient or population (patients with hypertension), Intervention (VLCD).

CI, confidence interval; GRADE, Grading of Recommendations Assessment, Development and Evaluation; mLCD, moderately-low carbohydrate or low carbohydrate diet; LDL-C, lowdensity lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; FMD, flow-mediated dilatation; VLCD, very-low carbohydrate diet.

  1. Nam GE, Kim YH, Han K, Jung JH, Rhee EJ, Lee WY, et al. Obesity fact sheet in Korea, 2020: prevalence of obesity by obesity class from 2009 to 2018. J Obes Metab Syndr 2021;30:141-8.
    Pubmed KoreaMed CrossRef
  2. Jung CH, Son JW, Kang S, Kim WJ, Kim HS, Kim HS, et al. Diabetes fact sheets in Korea, 2020: an appraisal of current status. Diabetes Metab J 2021;45:1-10.
    Pubmed KoreaMed CrossRef
  3. Kim HC, Cho SM, Lee H, Lee HH, Baek J, Heo JE, et al. Korea hypertension fact sheet 2020: analysis of nationwide population-based data. Clin Hypertens 2021;27:8.
    Pubmed KoreaMed CrossRef
  4. Huh Y and Nam GE. Overcoming increasing morbid obesity in Korea. J Obes Metab Syndr 2021;30:77-80.
    Pubmed KoreaMed CrossRef
  5. Kim BY, Kang SM, Kang JH, Kang SY, Kim KK, Kim KB, et al. 2020 Korean Society for the Study of Obesity guidelines for the management of obesity in Korea. J Obes Metab Syndr 2021;30:81-92.
    Pubmed KoreaMed CrossRef
  6. Hur KY, Moon MK, Park JS, Kim SK, Lee SH, Yun JS, et al. 2021 Clinical practice guidelines for diabetes mellitus of the Korean Diabetes Association. Diabetes Metab J 2021;45:461-81.
    Pubmed KoreaMed CrossRef
  7. Evert AB, Dennison M, Gardner CD, Garvey WT, Lau KH, MacLeod J, et al. Nutrition therapy for adults with diabetes or prediabetes: a consensus report. Diabetes Care 2019;42:731-54.
    Pubmed KoreaMed CrossRef
  8. Shim JS, Heo JE, Kim HC. Factors associated with dietary adherence to the guidelines for prevention and treatment of hypertension among Korean adults with and without hypertension. Clin Hypertens 2020;26:5.
    Pubmed KoreaMed CrossRef
  9. Kim JY. Optimal diet strategies for weight loss and weight loss maintenance. J Obes Metab Syndr 2021;30:20-31.
    Pubmed KoreaMed CrossRef
  10. Seidelmann SB, Claggett B, Cheng S, Henglin M, Shah A, Steffen LM, et al. Dietary carbohydrate intake and mortality: a prospective cohort study and meta-analysis. Lancet Public Health 2018;3:e419-28.
    CrossRef
  11. Zhang AM, Wellberg EA, Kopp JL, Johnson JD. Hyperinsulinemia in obesity, inflammation, and cancer. Diabetes Metab J 2021;45:285-311.
    Pubmed KoreaMed CrossRef
  12. Volek JS, Fernandez ML, Feinman RD, Phinney SD. Dietary carbohydrate restriction induces a unique metabolic state positively affecting atherogenic dyslipidemia, fatty acid partitioning, and metabolic syndrome. Prog Lipid Res 2008;47:307-18.
    Pubmed CrossRef
  13. Patterson RE, Laughlin GA, LaCroix AZ, Hartman SJ, Natarajan L, Senger CM, et al. Intermittent fasting and human metabolic health. J Acad Nutr Diet 2015;115:1203-12.
    Pubmed KoreaMed CrossRef
  14. de Cabo R and Mattson MP. Effects of intermittent fasting on health, aging, and disease. N Engl J Med 2019;381:2541-51.
    Pubmed CrossRef
  15. St-Onge MP, Ard J, Baskin ML, Chiuve SE, Johnson HM, Kris-Etherton P, et al. Meal timing and frequency: implications for cardiovascular disease prevention: a scientific statement from the American Heart Association. Circulation 2017;135:e96-121.
    Pubmed KoreaMed CrossRef
  16. Aronica L, Rigdon J, Offringa LC, Stefanick ML, Gardner CD. Examining differences between overweight women and men in 12-month weight loss study comparing healthy low-carbohydrate vs. low-fat diets. Int J Obes (Lond) 2021;45:225-34.
    Pubmed KoreaMed CrossRef
  17. Bazzano LA, Hu T, Reynolds K, Yao L, Bunol C, Liu Y, et al. Effects of low-carbohydrate and low-fat diets: a randomized trial. Ann Intern Med 2014;161:309-18.
    Pubmed KoreaMed CrossRef
  18. Hu T, Yao L, Reynolds K, Whelton PK, Niu T, Li S, et al. The effects of a low-carbohydrate diet vs. a low-fat diet on novel cardiovascular risk factors: a randomized controlled trial. Nutrients 2015;7:7978-94.
    Pubmed KoreaMed CrossRef
  19. Bhattacharyya S, Pradhan R, Mondal S, Pathak H, Mandal SK. Effect of modified Atkins diet on short term and intermediate term weight loss. Res J Pharm Biol Chem Sci 2012;3:929-35.
  20. Brinkworth GD, Noakes M, Keogh JB, Luscombe ND, Wittert GA, Clifton PM. Long-term effects of a high-protein, low-carbohydrate diet on weight control and cardiovascular risk markers in obese hyperinsulinemic subjects. Int J Obes Relat Metab Disord 2004;28:661-70.
    Pubmed CrossRef
  21. Brinkworth GD, Noakes M, Buckley JD, Keogh JB, Clifton PM. Long-term effects of a very-low-carbohydrate weight loss diet compared with an isocaloric low-fat diet after 12 mo. Am J Clin Nutr 2009;90:23-32.
    Pubmed CrossRef
  22. Brinkworth GD, Buckley JD, Noakes M, Clifton PM. Renal function following long-term weight loss in individuals with abdominal obesity on a very-low-carbohydrate diet vs highcarbohydrate diet. J Am Diet Assoc 2010;110:633-8.
    Pubmed CrossRef
  23. Brinkworth G, Noakes M, Buckley J, Clifton P. Long-term effects of a moderate energy restricted, very low carbohydrate diet on bone health in abdominally obese individuals. FASEB J 2011;25(S1):774.16.
  24. Wycherley TP, Buckley JD, Noakes M, Clifton PM, Brinkworth GD. Long-term effects of a very low-carbohydrate weight loss diet on exercise capacity and tolerance in overweight and obese adults. J Am Coll Nutr 2014;33:267-73.
    Pubmed CrossRef
  25. Tay J, Brinkworth GD, Noakes M, Keogh J, Clifton PM. Metabolic effects of weight loss on a very-low-carbohydrate diet compared with an isocaloric high-carbohydrate diet in abdominally obese subjects. J Am Coll Cardiol 2008;51:59-67.
    Pubmed CrossRef
  26. Wycherley TP, Brinkworth GD, Keogh JB, Noakes M, Buckley JD, Clifton PM. Long-term effects of weight loss with a very low carbohydrate and low fat diet on vascular function in overweight and obese patients. J Intern Med 2010;267:452-61.
    Pubmed CrossRef
  27. Cardillo S, Seshadri P, Iqbal N. The effects of a low-carbohydrate versus low-fat diet on adipocytokines in severely obese adults: three-year follow-up of a randomized trial. Eur Rev Med Pharmacol Sci 2006;10:99-106.
  28. Zinn C, McPhee J, Harris N, Williden M, Prendergast K, Schofield G. A 12-week low-carbohydrate, high-fat diet improves metabolic health outcomes over a control diet in a randomised controlled trial with overweight defence force personnel. Appl Physiol Nutr Metab 2017;42:1158-64.
    Pubmed CrossRef
  29. Chen CY, Huang WS, Chen HC, Chang CH, Lee LT, Chen HS, et al. Effect of a 90 g/day low-carbohydrate diet on glycaemic control, small, dense low-density lipoprotein and carotid intima-media thickness in type 2 diabetic patients: an 18-month randomised controlled trial. PLoS One 2020;15:e0240158.
    Pubmed KoreaMed CrossRef
  30. Daly ME, Paisey R, Paisey R, Millward BA, Eccles C, Williams K, et al. Short-term effects of severe dietary carbohydrate-restriction advice in type 2 diabetes: a randomized controlled trial. Diabet Med 2006;23:15-20.
    Pubmed CrossRef
  31. Davis NJ, Tomuta N, Schechter C, Isasi CR, Segal-Isaacson CJ, Stein D, et al. Comparative study of the effects of a 1-year dietary intervention of a low-carbohydrate diet versus a lowfat diet on weight and glycemic control in type 2 diabetes. Diabetes Care 2009;32:1147-52.
    Pubmed KoreaMed CrossRef
  32. de Jonge L, Bray GA, Smith SR, Ryan DH, de Souza RJ, Loria CM, et al. Effect of diet composition and weight loss on resting energy expenditure in the POUNDS LOST study. Obesity (Silver Spring) 2012;20:2384-9.
    Pubmed KoreaMed CrossRef
  33. de Luis DA, Aller R, Izaola O, Gonzalez Sagrado M, Bellioo D, Conde R. Effects of a low-fat versus a low-carbohydrate diet on adipocytokines in obese adults. Horm Res 2007;67:296-300.
    Pubmed CrossRef
  34. de Luis DA, Izaola O, de la Fuente B, Primo D, Romero E. Role of fatty acid-binding protein 2 Ala54Thr genotype on weight loss and cardiovascular risk factors after a high-protein/low-carbohydrate versus a standard hypocaloric diet during 9 months. Ann Nutr Metab 2015;67:81-6.
    Pubmed CrossRef
  35. de Luis DA, Aller R, Izaola O, Primo D, Urdiales S, Romero E. Effects of a high-protein/low-carbohydrate diet versus a standard hypocaloric diet on weight and cardiovascular risk factors: role of a genetic variation in the rs9939609 FTO gene variant. J Nutrigenet Nutrigenomics 2015;8:128-36.
    Pubmed CrossRef
  36. de Luis DA, Aller R, Izaola O, Romero E. Effect of -55CT polymorphism of UCP3 on insulin resistance and cardiovascular risk factors after a high protein/low carbohydrate versus a standard hypocaloric diet. Ann Nutr Metab 2016;68:157-63.
    Pubmed CrossRef
  37. de Luis DA, Izaola O, Primo D, Aller R. Different effects of high-protein/low-carbohydrate versus standard hypocaloric diet on insulin resistance and lipid profile: role of rs16147 variant of neuropeptide Y. Diabetes Res Clin Pract 2019;156:107825.
    Pubmed CrossRef
  38. Dyson PA, Beatty S, Matthews DR. A low-carbohydrate diet is more effective in reducing body weight than healthy eating in both diabetic and non-diabetic subjects. Diabet Med 2007;24:1430-5.
    Pubmed CrossRef
  39. Foraker RE, Pennell M, Sprangers P, Vitolins MZ, DeGraffinreid C, Paskett ED. Effect of a low-fat or low-carbohydrate weight-loss diet on markers of cardiovascular risk among premenopausal women: a randomized trial. J Womens Health (Larchmt) 2014;23:675-80.
    Pubmed KoreaMed CrossRef
  40. Forsythe CE, Phinney SD, Fernandez ML, Quann EE, Wood RJ, Bibus DM, et al. Comparison of low fat and low carbohydrate diets on circulating fatty acid composition and markers of inflammation. Lipids 2008;43:65-77.
    Pubmed CrossRef
  41. Friedman AN, Ogden LG, Foster GD, Klein S, Stein R, Miller B, et al. Comparative effects of low-carbohydrate high-protein versus low-fat diets on the kidney. Clin J Am Soc Nephrol 2012;7:1103-11.
    Pubmed KoreaMed CrossRef
  42. Foster GD, Wyatt HR, Hill JO, Makris AP, Rosenbaum DL, Brill C, et al. Weight and metabolic outcomes after 2 years on a low-carbohydrate versus low-fat diet. Obstet Gynecol Surv 2010;65:769-70.
    CrossRef
  43. Foster GD, Wyatt HR, Hill JO, McGuckin BG, Brill C, Mohammed BS, et al. A randomized trial of a low-carbohydrate diet for obesity. N Engl J Med 2003;348:2082-90.
    Pubmed CrossRef
  44. Frisch S, Zittermann A, Berthold HK, Gotting C, Kuhn J, Kleesiek K, et al. A randomized controlled trial on the efficacy of carbohydrate-reduced or fat-reduced diets in patients attending a telemedically guided weight loss program. Cardiovasc Diabetol 2009;8:36.
    Pubmed KoreaMed CrossRef
  45. Gardner CD, Kiazand A, Alhassan S, Kim S, Stafford RS, Balise RR, et al. Comparison of the Atkins, Zone, Ornish, and LEARN diets for change in weight and related risk factors among overweight premenopausal women. The A to Z weight loss study:. a randomized trial Obstet Gynecol Surv 2007;62:454.
    CrossRef
  46. Goday A, Bellido D, Sajoux I, Crujeiras AB, Burguera B, Garcia-Luna PP, et al. Short-term safety, tolerability and efficacy of a very low-calorie-ketogenic diet interventional weight loss program versus hypocaloric diet in patients with type 2 diabetes mellitus. Nutr Diabetes 2016;6:e230.
    Pubmed KoreaMed CrossRef
  47. Goldstein T, Kark JD, Berry EM, Adler B, Ziv E, Raz I. The effect of a low carbohydrate energy-unrestricted diet on weight loss in obese type 2 diabetes patients: a randomized controlled trial. E Spen Eur E J Clin Nutr Metab 2011;6:e178-86.
    CrossRef
  48. Guldbrand H, Dizdar B, Bunjaku B, Lindstrom T, Bachrach-Lindstrom M, Fredrikson M, et al. In type 2 diabetes, randomisation to advice to follow a low-carbohydrate diet transiently improves glycaemic control compared with advice to follow a low-fat diet producing a similar weight loss. Diabetologia 2012;55:2118-27.
    Pubmed KoreaMed CrossRef
  49. Jonasson L, Guldbrand H, Lundberg AK, Nystrom FH. Advice to follow a low-carbohydrate diet has a favourable impact on low-grade inflammation in type 2 diabetes compared with advice to follow a low-fat diet. Ann Med 2014;46:182-7.
    Pubmed KoreaMed CrossRef
  50. Haufe S, Engeli S, Kast P, Bohnke J, Utz W, Haas V, et al. Randomized comparison of reduced fat and reduced carbohydrate hypocaloric diets on intrahepatic fat in overweight and obese human subjects. Hepatology 2011;53:1504-14.
    Pubmed CrossRef
  51. Haufe S, Utz W, Engeli S, Kast P, Bohnke J, Pofahl M, et al. Left ventricular mass and function with reduced-fat or reducedcarbohydrate hypocaloric diets in overweight and obese subjects. Hypertension 2012;59:70-5.
    Pubmed CrossRef
  52. Iqbal N, Vetter ML, Moore RH, Chittams JL, Dalton-Bakes CV, Dowd M, et al. Effects of a low-intensity intervention that prescribed a low-carbohydrate vs. a low-fat diet in obese, diabetic participants. Obesity (Silver Spring) 2010;18:1733-8.
    Pubmed CrossRef
  53. Jabekk PT, Moe IA, Meen HD, Tomten SE, Hostmark AT. Resistance training in overweight women on a ketogenic diet conserved lean body mass while reducing body fat. Nutr Metab (Lond) 2010;7:17.
    Pubmed KoreaMed CrossRef
  54. Jenkins DJ, Wong JM, Kendall CW, Esfahani A, Ng VW, Leong TC, et al. Effect of a 6-month vegan low-carbohydrate ('Eco-Atkins') diet on cardiovascular risk factors and body weight in hyperlipidaemic adults: a randomised controlled trial. BMJ Open 2014;4:e003505.
    Pubmed KoreaMed CrossRef
  55. Keogh JB, Brinkworth GD, Clifton PM. Effects of weight loss on a low-carbohydrate diet on flow-mediated dilatation, adhesion molecules and adiponectin. Br J Nutr 2007;98:852-9.
    Pubmed CrossRef
  56. Kimura M, Kondo Y, Aoki K, Shirakawa J, Kamiyama H, Kamiko K, et al. A randomized controlled trial of a mini lowcarbohydrate diet and an energy-controlled diet among Japanese patients with type 2 diabetes. J Clin Med Res 2018;10:182-8.
    Pubmed KoreaMed CrossRef
  57. Kreider RB, Rasmussen C, Kerksick CM, Wilborn C, Taylor L 4th, Campbell B, et al. A carbohydrate-restricted diet during resistance training promotes more favorable changes in body composition and markers of health in obese women with and without insulin resistance. Phys Sportsmed 2011;39:27-40.
    Pubmed CrossRef
  58. Larsen RN, Mann NJ, Maclean E, Shaw JE. The effect of high-protein, low-carbohydrate diets in the treatment of type 2 diabetes: a 12 month randomised controlled trial. Diabetologia 2011;54:731-40.
    Pubmed CrossRef
  59. Liu K, Wang B, Zhou R, Lang HD, Ran L, Wang J, et al. Effect of combined use of a low-carbohydrate, high-protein diet with omega-3 polyunsaturated fatty acid supplementation on glycemic control in newly diagnosed type 2 diabetes: a randomized, double-blind, parallel-controlled trial. Am J Clin Nutr 2018;108:256-65.
    Pubmed CrossRef
  60. Liu X, Zhang G, Ye X, Li H, Chen X, Tang L, et al. Effects of a low-carbohydrate diet on weight loss and cardiometabolic profile in Chinese women: a randomised controlled feeding trial. Br J Nutr 2013;110:1444-53.
    Pubmed CrossRef
  61. Meckling KA, O'Sullivan C, Saari D. Comparison of a low-fat diet to a low-carbohydrate diet on weight loss, body composition, and risk factors for diabetes and cardiovascular disease in free-living, overweight men and women. J Clin Endocrinol Metab 2004;89:2717-23.
    Pubmed CrossRef
  62. Morris E, Aveyard P, Dyson P, Noreik M, Bailey C, Fox R, et al. A food-based, low-energy, low-carbohydrate diet for people with type 2 diabetes in primary care: a randomized controlled feasibility trial. Diabetes Obes Metab 2020;22:512-20.
    Pubmed KoreaMed CrossRef
  63. Noakes M, Foster PR, Keogh JB, James AP, Mamo JC, Clifton PM. Comparison of isocaloric very low carbohydrate/high saturated fat and high carbohydrate/low saturated fat diets on body composition and cardiovascular risk. Nutr Metab (Lond) 2006;3:7.
    Pubmed KoreaMed CrossRef
  64. Lim SS, Noakes M, Keogh JB, Clifton PM. Long-term effects of a low carbohydrate, low fat or high unsaturated fat diet compared to a no-intervention control. Nutr Metab Cardiovasc Dis 2010;20:599-607.
    Pubmed CrossRef
  65. Perna S, Alalwan TA, Gozzer C, Infantino V, Peroni G, Gasparri C, et al. Effectiveness of a hypocaloric and low-carbohydrate diet on visceral adipose tissue and glycemic control in overweight and obese patients with type 2 diabetes. Bahrain Med Bull 2019;41:159-64.
  66. Ruth MR, Port AM, Shah M, Bourland AC, Istfan NW, Nelson KP, et al. Consuming a hypocaloric high fat low carbohydrate diet for 12 weeks lowers C-reactive protein, and raises serum adiponectin and high density lipoprotein-cholesterol in obese subjects. Metabolism 2013;62:1779-87.
    Pubmed KoreaMed CrossRef
  67. Saslow LR, Daubenmier JJ, Moskowitz JT, Kim S, Murphy EJ, Phinney SD, et al. Twelve-month outcomes of a randomized trial of a moderate-carbohydrate versus very low-carbohydrate diet in overweight adults with type 2 diabetes mellitus or prediabetes. Nutr Diabetes 2017;7:304.
    Pubmed KoreaMed CrossRef
  68. Sato J, Kanazawa A, Makita S, Hatae C, Komiya K, Shimizu T, et al. A randomized controlled trial of 130 g/day low-carbohydrate diet in type 2 diabetes with poor glycemic control. Clin Nutr 2017;36:992-1000.
    Pubmed CrossRef
  69. Shai I, Schwarzfuchs D, Henkin Y, Shahar DR, Witkow S, Greenberg I, et al. Weight loss with a low-carbohydrate, Mediterranean, or low-fat diet. N Engl J Med 2008;359:229-41.
    Pubmed CrossRef
  70. Yokose C, McCormick N, Rai SK, Lu N, Curhan G, Schwarzfuchs D, et al. Effects of low-fat, Mediterranean, or low-carbohydrate weight loss diets on serum urate and cardiometabolic risk factors: a secondary analysis of the Dietary Intervention Randomized Controlled Trial (DIRECT). Diabetes Care 2020;43:2812-20.
    Pubmed KoreaMed CrossRef
  71. Soenen S, Bonomi AG, Lemmens SG, Scholte J, Thijssen MA, van Berkum F, et al. Relatively high-protein or 'low-carb' energy-restricted diets for body weight loss and body weight maintenance? Physiol Behav 2012;107:374-80.
    Pubmed CrossRef
  72. Stern L, Iqbal N, Seshadri P, Chicano KL, Daily DA, McGrory J, et al. The effects of low-carbohydrate versus conventional weight loss diets in severely obese adults: one-year follow-up of a randomized trial. Ann Intern Med 2004;140:778-85.
    Pubmed CrossRef
  73. Samaha FF, Iqbal N, Seshadri P, Chicano KL, Daily DA, Mc-Grory J, et al. A low-carbohydrate as compared with a low-fat diet in severe obesity. N Engl J Med 2003;348:2074-81.
    Pubmed CrossRef
  74. Struik NA, Brinkworth GD, Thompson CH, Buckley JD, Wittert G, Luscombe-Marsh ND. Very low and higher carbohydrate diets promote differential appetite responses in adults with type 2 diabetes: a randomized trial. J Nutr 2020;150:800-5.
    Pubmed CrossRef
  75. Wycherley TP, Thompson CH, Buckley JD, Luscombe-Marsh ND, Noakes M, Wittert GA, et al. Long-term effects of weight loss with a very-low carbohydrate, low saturated fat diet on flow mediated dilatation in patients with type 2 diabetes: a randomised controlled trial. Atherosclerosis 2016;252:28-31.
    Pubmed CrossRef
  76. Tay J, Luscombe-Marsh ND, Thompson CH, Noakes M, Buckley JD, Wittert GA, et al. Comparison of low- and highcarbohydrate diets for type 2 diabetes management: a randomized trial. Am J Clin Nutr 2015;102:780-90.
    Pubmed CrossRef
  77. Tay J, Thompson CH, Luscombe-Marsh ND, Wycherley TP, Noakes M, Buckley JD, et al. Effects of an energy-restricted low-carbohydrate, high unsaturated fat/low saturated fat diet versus a high-carbohydrate, low-fat diet in type 2 diabetes: a 2-year randomized clinical trial. Diabetes Obes Metab 2018;20:858-71.
    Pubmed CrossRef
  78. Tay J, Luscombe-Marsh ND, Thompson CH, Noakes M, Buckley JD, Wittert GA, et al. A very low-carbohydrate, lowsaturated fat diet for type 2 diabetes management: a randomized trial. Diabetes Care 2014;37:2909-18.
    Pubmed CrossRef
  79. Tsai AG, Glick HA, Shera D, Stern L, Samaha FF. Cost-effectiveness of a low-carbohydrate diet and a standard diet in severe obesity. Obes Res 2005;13:1834-40.
    Pubmed CrossRef
  80. Wang LL, Wang Q, Hong Y, Ojo O, Jiang Q, Hou YY, et al. The effect of low-carbohydrate diet on glycemic control in patients with type 2 diabetes mellitus. Nutrients 2018;10:661.
    Pubmed KoreaMed CrossRef
  81. Yancy WS Jr, Olsen MK, Guyton JR, Bakst RP, Westman EC. A low-carbohydrate, ketogenic diet versus a low-fat diet to treat obesity and hyperlipidemia: a randomized, controlled trial. Ann Intern Med 2004;140:769-77.
    Pubmed CrossRef
  82. Barnosky A, Kroeger CM, Trepanowski JF, Klempel MC, Bhutani S, Hoddy KK, et al. Effect of alternate day fasting on markers of bone metabolism: an exploratory analysis of a 6-month randomized controlled trial. Nutr Healthy Aging 2017;4:255-63.
    Pubmed KoreaMed CrossRef
  83. Trepanowski JF, Kroeger CM, Barnosky A, Klempel MC, Bhutani S, Hoddy KK, et al. Effect of alternate-day fasting on weight loss, weight maintenance, and cardioprotection among metabolically healthy obese adults: a randomized clinical trial. JAMA Intern Med 2017;177:930-8.
    Pubmed KoreaMed CrossRef
  84. Bowen J, Brindal E, James-Martin G, Noakes M. Randomized trial of a high protein, partial meal replacement program with or without alternate day fasting: similar effects on weight loss, retention status, nutritional, metabolic, and behavioral outcomes. Nutrients 2018;10:1145.
    Pubmed KoreaMed CrossRef
  85. Carter S, Clifton PM, Keogh JB. Effect of intermittent compared with continuous energy restricted diet on glycemic control in patients with type 2 diabetes: a randomized noninferiority trial. JAMA Netw Open 2018;1:e180756.
    Pubmed KoreaMed CrossRef
  86. Carter S, Clifton PM, Keogh JB. The effects of intermittent compared to continuous energy restriction on glycaemic control in type 2 diabetes; a pragmatic pilot trial. Diabetes Res Clin Pract 2016;122:106-12.
    Pubmed CrossRef
  87. Kunduraci YE and Ozbek H. Does the energy restriction intermittent fasting diet alleviate metabolic syndrome biomarkers?: a randomized controlled trial. Nutrients 2020;12:3213.
    Pubmed KoreaMed CrossRef
  88. Panizza CE, Lim U, Yonemori KM, Cassel KD, Wilkens LR, Harvie MN, et al. Effects of intermittent energy restriction combined with a Mediterranean diet on reducing visceral adiposity: a randomized active comparator pilot study. Nutrients 2019;11:1386.
    Pubmed KoreaMed CrossRef
  89. Phillips NE, Mareschal J, Schwab N, Manoogian EN, Borloz S, Ostinelli G, et al. The effects of time-restricted eating versus standard dietary advice on weight, metabolic health and the consumption of processed food: a pragmatic randomised controlled trial in community-based adults. Nutrients 2021;13:1042.
    Pubmed KoreaMed CrossRef
  90. Razavi R, Parvaresh A, Abbasi B, Yaghoobloo K, Hassanzadeh A, Mohammadifard N, et al. The alternate-day fasting diet is a more effective approach than a calorie restriction diet on weight loss and hs-CRP levels. Int J Vitam Nutr Res 2021;91:242-50.
    Pubmed CrossRef
  91. Varady KA, Bhutani S, Klempel MC, Kroeger CM, Trepanowski JF, Haus JM, et al. Alternate day fasting for weight loss in normal weight and overweight subjects: a randomized controlled trial. Nutr J 2013;12:146.
    Pubmed KoreaMed CrossRef
  92. Feinman RD, Pogozelski WK, Astrup A, Bernstein RK, Fine EJ, Westman EC, et al. Dietary carbohydrate restriction as the first approach in diabetes management: critical review and evidence base. Nutrition 2015;31:1-13.
    Pubmed CrossRef
  93. Ha K and Song Y. Low-carbohydrate diets in Korea: why does it matter, and what is next? J Obes Metab Syndr 2021;30:222-32.
    Pubmed KoreaMed CrossRef
  94. Sterne JAC, Savovic J, Page MJ, Elbers RG, Blencowe NS, Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in randomized trials. BMJ 2019;366:l4898.
    Pubmed CrossRef
  95. Guyatt G, Gutterman D, Baumann MH, Addrizzo-Harris D, Hylek EM, Phillips B, et al. Grading strength of recommendations and quality of evidence in clinical guidelines: report from an American College of Chest Physicians task force. Chest 2006;129:174-81.
    Pubmed CrossRef
  96. Larsen RN, Mann NJ, Maclean E, Shaw JE. The effect of high-protein, low-carbohydrate diets in the treatment of type 2 diabetes: a 12 month randomized controlled trial. Diabetologia 2011;54:731-40.
    Pubmed CrossRef
  97. Hall KD, Guo J, Courville AB, Boring J, Brychta R, Chen KY, et al. Effect of a plant-based, low-fat diet versus an animalbased, ketogenic diet on ad libitum energy intake. Nat Med 2021;27:344-53.
    Pubmed CrossRef
  98. Bertoluci MC and Rocha VZ. Cardiovascular risk assessment in patients with diabetes. Diabetol Metab Syndr 2017;9:25.
    Pubmed KoreaMed CrossRef