Ma Yujia, Zhou Zechen, Li Xiaoyi, Yan Zeyu, Ding Kexin, Xiao Han, Wu Yiqun, Wu Tao, Chen Dafang
Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China.
Biomedicines. 2022 Feb 2;10(2):368. doi: 10.3390/biomedicines10020368.
Accumulating evidence suggests a relationship between type 2 diabetes mellitus and sleep problems. A comprehensive study is needed to decipher whether shared polygenic risk variants exist between diabetic traits and sleep traits.
We integrated summary statistics from different genome-wide association studies and investigated overlap in single-nucleotide polymorphisms (SNPs) associated with diabetes-related traits (type 2 diabetes, fasting glucose, fasting insulin, and glycated hemoglobin) and sleep traits (insomnia symptoms, sleep duration, and chronotype) using a conditional/conjunctional false discovery rate approach. Pleiotropic genes were further evaluated for differential expression analysis, and we assessed their expression pattern effects on type 2 diabetes by Mendelian randomization (MR) analysis.
We observed extensive polygenic pleiotropy between diabetic traits and sleep traits. Fifty-eight independent genetic loci jointly influenced the risk of type 2 diabetes and the sleep traits of insomnia, sleep duration, and chronotype. The strongest shared locus between type 2 diabetes and sleep straits was (lead SNP rs8047587). Type 2 diabetes (z score, 16.19; P = 6.29 × 10) and two sleep traits, sleep duration (z score, -6.66; P = 2.66 × 10) and chronotype (z score, 7.42; P = 1.19 × 10), were shared. Two of the pleiotropic genes, and , were validated to be differentially expressed in type 2 diabetes, and showed a slight protective effect on type 2 diabetes in MR analysis.
Our study provided evidence for the polygenic overlap between diabetic traits and sleep traits, of which the expression of may play a crucial role and provide support of the hazardous effect of being an "evening" person on diabetes risk.
越来越多的证据表明2型糖尿病与睡眠问题之间存在关联。需要进行一项全面研究来解读糖尿病特征和睡眠特征之间是否存在共同的多基因风险变异。
我们整合了来自不同全基因组关联研究的汇总统计数据,并使用条件/联合错误发现率方法研究了与糖尿病相关特征(2型糖尿病、空腹血糖、空腹胰岛素和糖化血红蛋白)和睡眠特征(失眠症状、睡眠时间和生物钟类型)相关的单核苷酸多态性(SNP)的重叠情况。对多效性基因进行进一步评估以进行差异表达分析,并通过孟德尔随机化(MR)分析评估它们对2型糖尿病的表达模式影响。
我们观察到糖尿病特征和睡眠特征之间存在广泛的多基因多效性。58个独立的基因位点共同影响2型糖尿病风险以及失眠、睡眠时间和生物钟类型等睡眠特征。2型糖尿病与睡眠特征之间最强的共同位点是(领先SNP rs8047587)。2型糖尿病(z值,16.19;P = 6.29×10)与两个睡眠特征,即睡眠时间(z值,-6.66;P = 2.66×10)和生物钟类型(z值,7.42;P = 1.19×10)存在共同之处。两个多效性基因, 和 ,在2型糖尿病中被验证存在差异表达,并且 在MR分析中对2型糖尿病显示出轻微的保护作用。
我们的研究为糖尿病特征和睡眠特征之间的多基因重叠提供了证据,其中 的表达可能起关键作用,并为“夜型人”对糖尿病风险的有害影响提供了支持。