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Effect of low glycaemic index or load dietary patterns on glycaemic control and cardiometabolic risk factors in diabetes: systematic review and meta-analysis of randomised controlled trials
L. Chiavaroli, D. Lee, A. Ahmed, A. Cheung, TA. Khan, S. Blanco, . Mejia, A. Mirrahimi, DJA. Jenkins, G. Livesey, TMS. Wolever, D. Rahelić, H. Kahleová, J. Salas-Salvadó, CWC. Kendall, JL. Sievenpiper
Language English Country Great Britain
Document type Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't, Systematic Review
NLK
ProQuest Central
from 1996-01-01
Nursing & Allied Health Database (ProQuest)
from 1996-01-01
Health & Medicine (ProQuest)
from 1996-01-01
PubMed
34348965
DOI
10.1136/bmj.n1651
Knihovny.cz E-resources
- MeSH
- Diabetes Mellitus, Type 1 prevention & control MeSH
- Diabetes Mellitus, Type 2 prevention & control MeSH
- Diet, Diabetic MeSH
- Glycemic Load * MeSH
- Glycemic Index * MeSH
- Cardiometabolic Risk Factors MeSH
- Humans MeSH
- Glycemic Control MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Meta-Analysis MeSH
- Research Support, Non-U.S. Gov't MeSH
- Systematic Review MeSH
OBJECTIVE: To inform the update of the European Association for the Study of Diabetes clinical practice guidelines for nutrition therapy. DESIGN: Systematic review and meta-analysis of randomised controlled trials. DATA SOURCES: Medline, Embase, and the Cochrane Library searched up to 13 May 2021. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Randomised controlled trials of three or more weeks investigating the effect of diets with low glycaemic index (GI)/glycaemic load (GL) in diabetes. OUTCOME AND MEASURES: The primary outcome was glycated haemoglobin (HbA1c). Secondary outcomes included other markers of glycaemic control (fasting glucose, fasting insulin); blood lipids (low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C), non-HDL-C, apo B, triglycerides); adiposity (body weight, BMI (body mass index), waist circumference), blood pressure (systolic blood pressure (SBP) and diastolic blood pressure (DBP)), and inflammation (C reactive protein (CRP)). DATA EXTRACTION AND SYNTHESIS: Two independent reviewers extracted data and assessed risk of bias. Data were pooled by random effects models. GRADE (grading of recommendations assessment, development, and evaluation) was used to assess the certainty of evidence. RESULTS: 29 trial comparisons were identified in 1617 participants with type 1 and 2 diabetes who were predominantly middle aged, overweight, or obese with moderately controlled type 2 diabetes treated by hyperglycaemia drugs or insulin. Low GI/GL dietary patterns reduced HbA1c in comparison with higher GI/GL control diets (mean difference −0.31% (95% confidence interval −0.42 to −0.19%), P<0.001; substantial heterogeneity, I2=75%, P<0.001). Reductions occurred also in fasting glucose, LDL-C, non-HDL-C, apo B, triglycerides, body weight, BMI, systolic blood pressure (dose-response), and CRP (P<0.05), but not blood insulin, HDL-C, waist circumference, or diastolic blood pressure. A positive dose-response gradient was seen for the difference in GL and HbA1c and for absolute dietary GI and SBP (P<0.05). The certainty of evidence was high for the reduction in HbA1c and moderate for most secondary outcomes, with downgrades due mainly to imprecision. CONCLUSIONS: This synthesis suggests that low GI/GL dietary patterns result in small important improvements in established targets of glycaemic control, blood lipids, adiposity, blood pressure, and inflammation beyond concurrent treatment with hyperglycaemia drugs or insulin, predominantly in adults with moderately controlled type 1 and type 2 diabetes. The available evidence provides a good indication of the likely benefit in this population. STUDY REGISTRATION: ClinicalTrials.gov NCT04045938.
College of Pharmacy and Nutrition University of Saskatchewan SK Canada
Department of Medical Imaging Faculty of Medicine University of Toronto Toronto ON Canada
Department of Medicine Temerty Faculty of Medicine University of Toronto Toronto ON Canada
Independent Nutrition Logic Wymondham UK
INQUIS Clinical Research Toronto ON Canada
Institut d'Investigació Sanitària Pere Virgili Hospital Universitari San Joan de Reus Reus Spain
Institute for Clinical and Experimental Medicine Diabetes Centre Prague Czech Republic
Li Ka Shing Knowledge Institute St Michael's Hospital Toronto ON Canada
Physicians Committee for Responsible Medicine Washington DC USA
School of Medicine Josip Juraj Strossmayer University of Osijek Osijek Croatia
References provided by Crossref.org
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