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基于液体混合餐的早期胰岛素反应的全基因组关联研究:来自 NEO 研究的结果。

Genome-Wide Association Study on the Early-Phase Insulin Response to a Liquid Mixed Meal: Results From the NEO Study.

机构信息

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands

Division of Nephrology, Department of Internal Medicine, Leiden University Medical Center, Leiden, the Netherlands.

出版信息

Diabetes. 2019 Dec;68(12):2327-2336. doi: 10.2337/db19-0378. Epub 2019 Sep 19.

Abstract

Early-phase insulin secretion is a determinant of postprandial glucose homeostasis. In this study, we aimed to identify novel genetic variants associated with the early-phase insulin response to a liquid mixed meal by a genome-wide association study using a discovery and replication design embedded in the Netherlands Epidemiology of Obesity (NEO) study. The early-phase insulin response was defined as the difference between the natural logarithm-transformed insulin concentrations of the postprandial state at 30 min after a meal challenge and the fasting state (Δinsulin). After Bonferroni correction, rs505922 (β: -6.5% [minor allele frequency (MAF) 0.32, = 3.3 × 10]) located in the gene reached genome-wide significant level ( < 5 × 10) and was also replicated successfully (β: -7.8% [MAF 0.32, = 7.2 × 10]). The function of the gene was assessed using in vitro shRNA-mediated knockdown of gene expression in the murine pancreatic β-cell line MIN6. Knocking down the gene led to decreased insulin secretion in the murine pancreatic β-cell line. These data indicate that the previously identified elevated risk of type 2 diabetes for carriers of the rs505922:C allele may be caused by decreased early-phase insulin secretion.

摘要

早期胰岛素分泌是餐后血糖稳态的决定因素。在这项研究中,我们旨在通过一项全基因组关联研究,使用嵌入荷兰肥胖症流行病学研究(NEO)的发现和复制设计,确定与液体混合餐餐后早期胰岛素反应相关的新型遗传变异。早期胰岛素反应定义为餐后 30 分钟餐后状态与空腹状态(Δ胰岛素)的自然对数转化胰岛素浓度之间的差异。经过 Bonferroni 校正后,位于基因中的 rs505922(β:-6.5%[次要等位基因频率(MAF)为 0.32,= 3.3×10])达到全基因组显著水平(<5×10),并且成功复制(β:-7.8%[MAF 0.32,= 7.2×10])。通过在小鼠胰腺β细胞系 MIN6 中使用体外 shRNA 介导的基因表达敲低来评估基因的功能。敲低基因导致小鼠胰腺β细胞系胰岛素分泌减少。这些数据表明,携带 rs505922:C 等位基因的个体患 2 型糖尿病的风险增加,可能是由于早期胰岛素分泌减少所致。

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