Literature DB >> 35768556

The importance of molecular weight in determining the minimum dose of oat β-glucan required to reduce the glycaemic response in healthy subjects without diabetes: a systematic review and meta-regression analysis.

Jarvis C Noronha1,2, Andreea Zurbau1,3,4, Thomas M S Wolever5,6.   

Abstract

To determine the minimum amount of oat β-glucan (OBG) required to reduce glycaemic responses (MinDose), we conducted a systematic review and meta-regression analysis of acute, crossover, single-meal feeding trials that examined the effects of adding OBG or oat bran to a carbohydrate-containing test-meal versus a control test-meal containing an equivalent amount of available-carbohydrate (avCHO) from the same or similar source. Medline, Embase, and Cochrane Library were searched up to 18 August 2021. The primary outcome was glucose incremental-area-under-the-curve (iAUC). Secondary outcomes included insulin iAUC, and glucose and insulin incremental peak-rise (iPeak). Two independent reviewers extracted data. Results were expressed as ratio-of-means (RoM) with 95% confidence intervals (CIs). Linear associations were assessed by random effects meta-regression. MinDose was defined as the dose at which the upper 95% CI of the regression line cut the line of no effect (i.e., RoM = 1). Fifty-nine comparisons (n = 340) were included; 57 in healthy subjects without diabetes and two in subjects with diabetes; 24 high-MW (>1000 kg/mol), 22 medium-MW (300-1,000 kg/mol), and 13 low-MW (<300 kg/mol). In healthy subjects without diabetes the associations between OBG dose and glucose iAUC and iPeak were linear (non-linear p value >0.05). MinDoses for glucose iAUC for high-MW, medium-MW and low-MW OBG, respectively, were estimated to be 0.2 g, 2.2 g and 3.2 g per 30 g avCHO; MinDoses for glucose iPeak were less than those for iAUC. Insufficient data were available to assess MinDose for insulin, however, there was no evidence of a disproportionate increase in insulin. More high-quality trials are needed to establish MinDose in individuals with diabetes.
© 2022. The Author(s).

Entities:  

Year:  2022        PMID: 35768556     DOI: 10.1038/s41430-022-01176-5

Source DB:  PubMed          Journal:  Eur J Clin Nutr        ISSN: 0954-3007            Impact factor:   4.016


  46 in total

1.  Influence of sterilization, drying and oat bran enrichment of pasta on glucose and insulin responses in healthy subjects and on the rate and extent of in vitro starch digestion.

Authors:  J Holm; B Koellreutter; P Würsch
Journal:  Eur J Clin Nutr       Date:  1992-09       Impact factor: 4.016

2.  Postprandial glucose, insulin, and incretin responses to grain products in healthy subjects.

Authors:  Katri S Juntunen; Leo K Niskanen; Kirsi H Liukkonen; Kaisa S Poutanen; Jens J Holst; Hannu M Mykkänen
Journal:  Am J Clin Nutr       Date:  2002-02       Impact factor: 7.045

Review 3.  The effect of oat β-glucan on LDL-cholesterol, non-HDL-cholesterol and apoB for CVD risk reduction: a systematic review and meta-analysis of randomised-controlled trials.

Authors:  Hoang V T Ho; John L Sievenpiper; Andreea Zurbau; Sonia Blanco Mejia; Elena Jovanovski; Fei Au-Yeung; Alexandra L Jenkins; Vladimir Vuksan
Journal:  Br J Nutr       Date:  2016-10-11       Impact factor: 3.718

Review 4.  Review of human studies investigating the post-prandial blood-glucose lowering ability of oat and barley food products.

Authors:  S M Tosh
Journal:  Eur J Clin Nutr       Date:  2013-02-20       Impact factor: 4.016

5.  Comparison of hormone and glucose responses of overweight women to barley and oats.

Authors:  Kay M Behall; Daniel J Scholfield; Judith Hallfrisch
Journal:  J Am Coll Nutr       Date:  2005-06       Impact factor: 3.169

6.  Barley β-glucan reduces blood cholesterol levels via interrupting bile acid metabolism.

Authors:  Yanan Wang; Scott V Harding; Sijo J Thandapilly; Susan M Tosh; Peter J H Jones; Nancy P Ames
Journal:  Br J Nutr       Date:  2017-11-08       Impact factor: 3.718

Review 7.  Role of dietary beta-glucans in the prevention of the metabolic syndrome.

Authors:  Lieselotte Cloetens; Matilda Ulmius; Anna Johansson-Persson; Björn Akesson; Gunilla Onning
Journal:  Nutr Rev       Date:  2012-08       Impact factor: 7.110

8.  Products based on a high fiber barley genotype, but not on common barley or oats, lower postprandial glucose and insulin responses in healthy humans.

Authors:  H G Liljeberg; Y E Granfeldt; I M Björck
Journal:  J Nutr       Date:  1996-02       Impact factor: 4.798

9.  Cholesterol-lowering effects of oat β-glucan: a meta-analysis of randomized controlled trials.

Authors:  Anne Whitehead; Eleanor J Beck; Susan Tosh; Thomas M S Wolever
Journal:  Am J Clin Nutr       Date:  2014-10-15       Impact factor: 7.045

Review 10.  The effect of oat β-glucan on postprandial blood glucose and insulin responses: a systematic review and meta-analysis.

Authors:  Andreea Zurbau; Jarvis C Noronha; Tauseef A Khan; John L Sievenpiper; Thomas M S Wolever
Journal:  Eur J Clin Nutr       Date:  2021-02-19       Impact factor: 4.016

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