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Replicative association analysis of genetic markers of cognitive traits with Alzheimer's disease in the Russian population

机译:俄罗斯人群认知特征与阿尔茨海默氏病遗传标记的复制关联分析

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摘要

A replicative association analysis of Alzheimer's disease (AD) was carried out for 15 genetic markers that have been associated with cognitive disorders in genome-wide association studies. In the Russian population, AD was associated with CSMD1 rs2616984 (OR = 1.50, 95% CI 1.07-2.09, p-value = 0.018) and, potentially, with NOTCH4 rs313296 (OR = 1.53, 95% CI 0.98-2.39, p-value = 0.06) and NRIP1 rs2229741 (OR = 1.35, 95% CI 0.99-1.85, p-value = 0.061). Combinations of epistatically interacting genes (CSMD1 and NRIP1; NOTCH4, CSMD1, and NRIP1; and TLR4, CSMD1, and NRIP1) were identified, along with their genotype combinations that showed a significant association with AD and the highest predictive values. Possible molecular mechanisms of the gene involvement in AD pathogenesis are discussed. A bioinformatics analysis of the biological processes, molecular functions, and protein-protein interactions for the AD genes indicated that the genes may play a modulating or modifying role, acting together in various regulatory and signaling pathways involved in AD.
机译:对与全基因组关联研究中的认知障碍相关的15个遗传标记进行了阿尔茨海默氏病(AD)的复制关联分析。在俄罗斯人群中,AD与CSMD1 rs2616984(OR = 1.50,95%CI 1.07-2.09,p值= 0.018)相关,并可能与NOTCH4 rs313296(OR = 1.53,95%CI 0.98-2.39,p-值= 0.06)和NRIP1 rs2229741(OR = 1.35,95%CI 0.99-1.85,p值= 0.061)。鉴定了上位相互作用基因(CSMD1和NRIP1; NOTCH4,CSMD1和NRIP1;以及TLR4,CSMD1和NRIP1)的组合,以及它们的基因型组合,这些组合显示出与AD的显着相关性和最高的预测值。讨论了基因参与AD发病机制的可能分子机制。对AD基因的生物学过程,分子功能和蛋白质-蛋白质相互作用的生物信息学分析表明,这些基因可能发挥调节或修饰作用,共同参与AD涉及的各种调节和信号通路。

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