The Canadian Trial of Carbohydrates in Diabetes (CCD), a 1-y controlled trial of low-glycemic-index dietary carbohydrate in type 2 diabetes: no effect on glycated hemoglobin but reduction in C-reactive protein
Open accessAbstract
Background The optimal source and amount of dietary carbohydrate for managing type 2 diabetes (T2DM) are unknown.Objective We aimed to compare the effects of altering the glycemic index or the amount of carbohydrate on glycated hemoglobin (HbA1c), plasma glucose, lipids, and C-reactive protein (CRP) in T2DM patients.Design Subjects with T2DM managed by diet alone (n=162) were randomly assigned to receive high-carbohydrate, high-glycemic-index (high-GI), high-carbohydrate, low-glycemic-index (low-GI), or low-carbohydrate, high-monounsaturated-fat (low-CHO) diets for 1 y.Results The high-GI, low-GI, and low-CHO diets contained, respectively, 47%, 52%, and 39% of energy as carbohydrate and 31%, 27%, and 40% of energy as fat; they had GIs of 63, 55, and 59, respectively. Body weight and HbA1c did not differ significantly between diets. Fasting glucose was higher (P=0.041), but 2-h postload glucose was lower (P=0.010) after 12 mo of the low-GI diet. With the low-GI diet, overall mean triacylglycerol was 12% higher and HDL cholesterol 4% lower than with the low-CHO diet (P<0.05), but the difference in the ratio of total to HDL cholesterol disappeared by 6 mo (time x diet interaction, P=0.044). Overall mean CRP with the low-GI diet, 1.95 mg/L, was 30% less than that with the high-GI diet, 2.75 mg/L (P=0.0078); the concentration with the low-CHO diet, 2.35 mg/L, was intermediate.Conclusions In subjects with T2DM managed by diet alone with optimal glycemic control, long-term HbA1c was not affected by altering the GI or the amount of dietary carbohydrate. Differences in total:HDL cholesterol among diets had disappeared by 6 mo. However, because of sustained reductions in postprandial glucose and CRP, a low-GI diet may be preferred for the dietary management of T2DM.
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Reducing GI or GL in the context of diets low in saturated fat can improve CHD risk factors including BMI, blood pressure, and serum cholesterol.
“Over the last 3 decades, clinical trials have demonstrated that reducing the GI or glycemic load (GL), the product of GI and the available carbohydrate content of a food,13 in the context of diets low in saturated fat, can improve CHD risk factors including body mass index (BMI), blood pressure, and serum cholesterol.14–24”
From Associations of Glycemic Index and Load With Coronary Heart Disease Events: A Systematic Review and Meta‐Analysis of Prospective Cohorts (2012) · cites this paper as [22]
There is emerging evidence on positive effects of low-GI diets on CHD risk factors such as oxidative damage and inflammation in overweight/obese and type 2 diabetic individuals.
“There has also been emerging evidence on the positive effects of low-GI diets on CHD risk factors such as oxidative damage58 and inflammation22 in overweight/obese and type 2 diabetic individuals, respectively.”
From Associations of Glycemic Index and Load With Coronary Heart Disease Events: A Systematic Review and Meta‐Analysis of Prospective Cohorts (2012) · cites this paper as [22]
Fructose metabolism is relatively unregulated compared with glucose metabolism, which is regulated in part by phosphofructokinase.
“In contrast to glucose metabolism, which is regulated in part by phosphofructokinase, fructose metabolism is relatively unregulated.425”
From Triglycerides and Cardiovascular Disease: A Scientific Statement From the American Heart Association (2011) · cites this paper as [425]
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References 77 · Cited by 333
Research works printed but not linked: 6
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- [58]58. Rizkalla SW, Taghrid L, Laromiguiere M, et al. Improved plasma glucose control, whole-body glucose utilization, and lipid profile on a lowglycemicindexdietintype2diabeticmen:arandomizedcontrolledtrial. Diabetes Care 2004;27:1866-72.
- Authors
- Wolever, T. M., Gibbs, A. L., Mehling, C., Chiasson, J.-L., Connelly, P. W., Josse, R. G., Leiter, L. A., Maheux, P., Rabasa-Lhoret, R., Rodger, N. W., & Ryan, E. A.
- Affiliations
- Western University (CA)
- Corresponding author
- Wolever, Thomas MS
- ORCID
- Venue
- The American Journal of Clinical Nutrition
- Publisher
- Elsevier BV
- Published
- 2008-01
- Volume
- 87
- Issue
- 1
- Pages
- 114-125
- ISSN
- 0002-9165 (ISSN-L)
- OpenAlex
- W2135769210
- Cited by
- 333
- References
- 77
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 8 · 2023: 6 · 2022: 13 · 2021: 9 · 2020: 6 · 2019: 18 · 2018: 20 · 2017: 22 · 2016: 11 · 2015: 18 · 2014: 31 · 2013: 33 · 2012: 27
- FWCI
- 22.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- American Journal of Clinical Nutrition (publishedVersion)
- PubMed (publishedVersion)
- TSpace (University of Toronto) (submittedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Diet and metabolism studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Keywords
- type 2 diabetes, glycemic index, dietary carbohydrates, low glycemic index diet, low-carbohydrate diet, monounsaturated fatty acids, C-reactive protein, HbA1c, postprandial blood glucose, lipid profile, TC/HDL-C ratio, dietary intervention, glycemic control, inflammation, weight management
- MeSH terms
- Adult, Aged, Blood Glucose, C-Reactive Protein, Cholesterol, Diabetes Mellitus, Type 2, Dietary Carbohydrates, Dietary Fats, Female, Glycated Hemoglobin, Humans, Lipids, Cholesterol, HDL, Male, Middle Aged, Area Under Curve, Glycemic Index
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