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Genetic predisposition to type 2 diabetes is associated with impaired insulin secretion but does not modify insulin resistance or secretion in response to an intervention to lower dietary saturated fat

机译:2型糖尿病的遗传易感性与胰岛素分泌受损有关但不会因降低饮食中的饱和脂肪而改变胰岛素抵抗或分泌

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摘要

Genome-wide association studies have identified SNPs reproducibly associated with type 2 diabetes (T2D). We examined the effect of genetic predisposition to T2D on insulin sensitivity and secretion using detailed phenotyping in overweight individuals with no diagnosis of T2D. Furthermore, we investigated whether this genetic predisposition modifies the responses in beta-cell function and insulin sensitivity to a 24-week dietary intervention. We genotyped 25 T2D-associated SNPs in 377 white participants from the RISCK study. Participants underwent an IVGTT prior to and following a dietary intervention that aimed to lower saturated fat intake by replacement with monounsaturated fat or carbohydrate. We composed a genetic predisposition score (T2D-GPS) by summing the T2D risk-increasing alleles of the 25 SNPs and tested for association with insulin secretion and sensitivity at baseline, and with the change in response to the dietary intervention. At baseline, a higher T2D-GPS was associated with lower acute insulin secretion (AIRg 4% lower/risk allele, P = 0.006) and lower insulin secretion for a given level of insulin sensitivity, assessed by the disposition index (DI 5% lower/risk allele, P = 0.002), but not with insulin sensitivity (Si). T2D-GPS did not modify changes in insulin secretion, insulin sensitivity or the disposition index in response to the dietary interventions to lower saturated fat. Participants genetically predisposed to T2D have an impaired ability to compensate for peripheral insulin resistance with insulin secretion at baseline, but this does not modify the response to a reduction in dietary saturated fat through iso-energetic replacement with carbohydrate or monounsaturated fat.Electronic supplementary materialThe online version of this article (doi:10.1007/s12263-012-0284-8) contains supplementary material, which is available to authorized users.
机译:全基因组关联研究已确定与2型糖尿病(T2D)可重复相关的SNP。我们在没有诊断为T2D的超重患者中使用详细的表型分析了T2D遗传易感性对胰岛素敏感性和分泌的影响。此外,我们调查了这种遗传易感性是否改变了针对24周饮食干预的β细胞功能和胰岛素敏感性的反应。我们对RISCK研究中的377名白人参与者的25个T2D相关SNP进行了基因分型。参与者在饮食干预之前和之后进行了IVGTT,该干预旨在通过用单不饱和脂肪或碳水化合物替代来降低饱和脂肪的摄入。我们通过对25个SNP的增加T2D风险的等位基因进行求和,组成了遗传易感评分(T2D-GPS),并测试了其与基线时胰岛素分泌和敏感性以及饮食干预反应的变化之间的相关性。在基线时,较高的T2D-GPS与较低的急性胰岛素分泌相关(AIRg降低4%/风险等位基因,P = 0.006),并且在给定的胰岛素敏感性水平下,胰岛素分泌较低(通过处置指数评估)(DI降低5%) /风险等位基因,P = 0.002),但不具有胰岛素敏感性(Si)。 T2D-GPS并没有响应于降低饱和脂肪的饮食干预而改变胰岛素分泌,胰岛素敏感性或处置指数的变化。基因上易患T2D的参与者在基线时通过胰岛素分泌来补偿外周胰岛素抵抗的能力受损,但这不会通过碳水化合物或单不饱和脂肪的等能量替代来改变饮食中饱和脂肪减少的反应。本文的版本(doi:10.1007 / s12263-012-0284-8)包含补充材料,可供授权用户使用。

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