» Articles » PMID: 31398841

Metabolic Effects of Resistant Starch Type 2: A Systematic Literature Review and Meta-Analysis of Randomized Controlled Trials

Overview
Journal Nutrients
Date 2019 Aug 11
PMID 31398841
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Published evidence exploring the effects of dietary resistant starch (RS) on human cardiometabolic health is inconsistent. This review aimed to investigate the effect of dietary RS type 2 (RS2) supplementation on body weight, satiety ratings, fasting plasma glucose, glycated hemoglobin (HbA1c), insulin resistance and lipid levels in healthy individuals and those with overweight/obesity, the metabolic syndrome (MetS), prediabetes or type 2 diabetes mellitus (T2DM). Five electronic databases were searched for randomized controlled trials (RCTs) published in English between 1982 and 2018, with trials eligible for inclusion if they reported RCTs involving humans where at least one group consumed ≥ 8 g of RS2 per day and measured body weight, satiety, glucose and/or lipid metabolic outcomes. Twenty-two RCTs involving 670 participants were included. Meta-analyses indicated that RS2 supplementation significantly reduced serum triacylglycerol concentrations (mean difference (MD) = -0.10 mmol/L; 95% CI -0.19, -0.01, = 0.03) in healthy individuals ( = 269) and reduced body weight (MD = -1.29 kg; 95% CI -2.40, -0.17, = 0.02) in people with T2DM ( = 90). However, these outcomes were heavily influenced by positive results from a small number of individual studies which contradicted the conclusions of the majority of trials. RS2 had no effects on any other metabolic outcomes. All studies ranged from 1-12 weeks in duration and contained small sample sizes (10-60 participants), and most had an unclear risk of bias. Short-term RS2 supplementation in humans is of limited cardiometabolic benefit.

Citing Articles

Gut microbial features and dietary fiber intake predict gut microbiota response to resistant starch supplementation.

Devarakonda S, Superdock D, Ren J, Johnson L, Loinard-Gonzalez A, Poole A Gut Microbes. 2024; 16(1):2367301.

PMID: 38913541 PMC: 11197919. DOI: 10.1080/19490976.2024.2367301.


The role of carbohydrates in canine and feline nutrition.

Kayser E, Finet S, de Godoy M Anim Front. 2024; 14(3):28-37.

PMID: 38910951 PMC: 11188962. DOI: 10.1093/af/vfae017.


Dietary resistant starch enhances immune health of the kidney in diabetes via promoting microbially-derived metabolites and dampening neutrophil recruitment.

Snelson M, Deliyanti D, Tan S, Drake A, de Pasquale C, Kumar V Nutr Diabetes. 2024; 14(1):46.

PMID: 38902253 PMC: 11190267. DOI: 10.1038/s41387-024-00305-2.


The impact of slowly digestible and resistant starch on glucose homeostasis and insulin resistance.

Chisbert M, Castell A, Vinoy S, Nazare J Curr Opin Clin Nutr Metab Care. 2024; 27(4):338-343.

PMID: 38836807 PMC: 11155281. DOI: 10.1097/MCO.0000000000001044.


The effects of prebiotic, probiotic or synbiotic supplementation on overweight/obesity indicators: an umbrella review of the trials' meta-analyses.

Rasaei N, Heidari M, Esmaeili F, Khosravi S, Baeeri M, Tabatabaei-Malazy O Front Endocrinol (Lausanne). 2024; 15:1277921.

PMID: 38572479 PMC: 10987746. DOI: 10.3389/fendo.2024.1277921.


References
1.
Slavin J, Martini M, Jacobs Jr D, Marquart L . Plausible mechanisms for the protectiveness of whole grains. Am J Clin Nutr. 1999; 70(3 Suppl):459S-463S. DOI: 10.1093/ajcn/70.3.459s. View

2.
Liu S, Manson J, Lee I, Cole S, Hennekens C, Willett W . Fruit and vegetable intake and risk of cardiovascular disease: the Women's Health Study. Am J Clin Nutr. 2000; 72(4):922-8. DOI: 10.1093/ajcn/72.4.922. View

3.
Hu F, Manson J, Stampfer M, Colditz G, Liu S, Solomon C . Diet, lifestyle, and the risk of type 2 diabetes mellitus in women. N Engl J Med. 2001; 345(11):790-7. DOI: 10.1056/NEJMoa010492. View

4.
Kinoshita M, Suzuki Y, Saito Y . Butyrate reduces colonic paracellular permeability by enhancing PPARgamma activation. Biochem Biophys Res Commun. 2002; 293(2):827-31. DOI: 10.1016/S0006-291X(02)00294-2. View

5.
Batterham R, Cowley M, Small C, Herzog H, Cohen M, Dakin C . Gut hormone PYY(3-36) physiologically inhibits food intake. Nature. 2002; 418(6898):650-4. DOI: 10.1038/nature00887. View