4.4 Article

Effect of fat type in baked bread on amylose-lipid complex formation and glycaemic response

期刊

BRITISH JOURNAL OF NUTRITION
卷 115, 期 12, 页码 2122-2129

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114516001458

关键词

Glycaemic response; Amylose-lipid complex; Dietary fats; Breads

资金

  1. Agency for Science, Technology and Research Health and Lifestyle [1121770033]

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The formation of amylose-lipid complexes (ALC) had been associated with reduced starch digestibility. A few studies have directly characterised the extent of ALC formation with glycaemic response. The objectives of this study were to investigate the effect of using fats with varying degree of saturation and chain length on ALC formation as well as glycaemic and insulinaemic responses after consumption of bread. Healthy men consumed five test breads in a random order: control bread without any added fats (CTR) and breads baked with butter (BTR), coconut oil (COC), grapeseed oil (GRP) or olive oil (OLV). There was a significant difference in glycaemic response between the different test breads (P = 0.002), primarily due to COC having a lower response than CTR (P = 0.016), but no significant differences between fat types were observed. Insulinaemic response was not altered by the addition of fats/oils. Although BTR was more insulinotropic than GRP (P < 0.05), postprandial beta-cell function did not differ significantly. The complexing index (CI), a measure of ALC formation, was significantly higher for COC and OLV compared with BTR and GRP (P < 0.05). CI was significantly negatively correlated with incremental AUC (IAUC) of change in blood glucose concentrations over time (IAUC(glucose)) (r-0.365, P=0.001). Linear regression analysis showed that CI explained 13.3% of the variance and was a significant predictor of IAUC(glucose) (beta=-1.265, P=0.001), but IAUC(insulin) did not predict IAUC(glucose). Our study indicated that a simple way to modulate glycaemic response in bread could lie in the choice of fats/oils, with coconut oil showing the greatest attenuation of glycaemic response.

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