Effect of Total and Partial Meal Replacements on Factors Related to Glucose Metabolism: A Systematic Review and Meta-analysis of Randomized Controlled Trials

医学 糖化血红素 内科学 胰岛素抵抗 荟萃分析 子群分析 随机对照试验 胰岛素 背景(考古学) 餐食 糖尿病 碳水化合物代谢 血糖性 血糖 内分泌学 2型糖尿病 胃肠病学 生物 古生物学
作者
Niloofar Sadat Maddahi,Mohammad Hassan Sohouli,Elma Izze da Silva Magalhães,Neda Ezoddin,Azadeh Nadjarzadeh
出处
期刊:Nutrition Reviews [Oxford University Press]
标识
DOI:10.1093/nutrit/nuae206
摘要

Abstract Context Although some evidence shows the beneficial effects of meal replacements (MRs) on glucose metabolism as one of the main factors of diabetes, there are still no comprehensive findings in this field. Objective We investigated the effects of total and partial MRs on fasting blood sugar (FBS), insulin, glycated hemoglobin (HbA1c), and homeostatic model assessment for insulin resistance (HOMA-IR) in this comprehensive study and meta-analysis. Data Sources To find pertinent randomized controlled trials (RCTs) up to March 2024, databases including PubMed/Medline, Web of Science, Scopus, and Embase were searched. Data Extraction This study included all RCTs investigating the effects of MRs on factors related to glucose metabolism. The pooled weighted mean difference (WMD) and 95% CIs were computed using the random-effects model. Data Analysis The findings from 52 studies indicated significant reductions in FBS (WMD: –3.10 mg/dL; 95% CI: –4.99, –1.20; P < .001), insulin (WMD: –1.79 μU/mL; 95% CI: –3.51, –0.08; P = .40), HOMA-IR (WMD: –0.86; 95% CI: –1.68, –0.04; P = .040), and HbA1c (WMD: –0.24%; 95% CI: –0.35%, –0.13%; P < .001) levels following MR consumption compared with the control group. The findings obtained from the subgroup analysis showed that MRs cause a greater decrease in FBS, insulin, and HOMA-IR in the >50-years age group compared with those aged ≤50 years and also during interventions ≤24 weeks compared with >24 weeks. Conclusion In conclusion, it appears that MRs, along with other lifestyle factors, can lead to significant improvements in glucose metabolism.

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