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