Lin Eugene, Tsai Shih-Jen, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Feng, Yang Cheng-Hung
Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Vita Genomics, Inc., Taipei, Taiwan.
PLoS One. 2017 Feb 22;12(2):e0172440. doi: 10.1371/journal.pone.0172440. eCollection 2017.
Evidence indicates that the pathophysiologic mechanisms associated with insulin resistance may contribute to cognitive aging and Alzheimer's diseases. In this study, we hypothesize that single nucleotide polymorphisms (SNPs) within insulin resistance-associated genes, such as the ADAM metallopeptidase with thrombospondin type 1 motif 9 (ADAMTS9), glucokinase regulator (GCKR), and peroxisome proliferator activated receptor gamma (PPARG) genes, may be linked with cognitive aging independently and/or through complex interactions in an older Taiwanese population. A total of 547 Taiwanese subjects aged over 60 years from the Taiwan Biobank were analyzed. Mini-Mental State Examinations (MMSE) were administered to all subjects, and MMSE scores were used to measure cognitive functions. Our data showed that four SNPs (rs73832338, rs9985304, rs4317088, and rs9831846) in the ADAMTS9 gene were significantly associated with cognitive aging among the subjects (P = 1.5 x 10-6 ~ 0.0002). This association remained significant after performing Bonferroni correction. Additionally, we found that interactions between the ADAMTS9 rs9985304 and ADAMTS9 rs76346246 SNPs influenced cognitive aging (P < 0.001). However, variants in the GCKR and PPARG genes had no association with cognitive aging in our study. Our study indicates that the ADAMTS9 gene may contribute to susceptibility to cognitive aging independently as well as through SNP-SNP interactions.
有证据表明,与胰岛素抵抗相关的病理生理机制可能导致认知衰老和阿尔茨海默病。在本研究中,我们假设胰岛素抵抗相关基因内的单核苷酸多态性(SNP),如含血小板反应蛋白基序的解聚素金属蛋白酶9(ADAMTS9)、葡萄糖激酶调节蛋白(GCKR)和过氧化物酶体增殖物激活受体γ(PPARG)基因,可能独立地和/或通过复杂的相互作用与台湾老年人群的认知衰老相关联。对来自台湾生物银行的547名60岁以上的台湾受试者进行了分析。对所有受试者进行简易精神状态检查(MMSE),并使用MMSE评分来测量认知功能。我们的数据显示,ADAMTS9基因中的四个SNP(rs73832338、rs9985304、rs4317088和rs9831846)与受试者的认知衰老显著相关(P = 1.5×10-6至0.0002)。在进行Bonferroni校正后,这种关联仍然显著。此外,我们发现ADAMTS9 rs9985304和ADAMTS9 rs76346246 SNP之间的相互作用影响认知衰老(P < 0.001)。然而,在我们的研究中,GCKR和PPARG基因的变异与认知衰老无关。我们的研究表明ADAMTS9基因可能独立地以及通过SNP-SNP相互作用导致认知衰老易感性。