Dey Saikat, Debnath Monojit, Yelamanchi Ramchandra, Kamble Nitish, Holla Vikram V, Mahale Rohan R, Pal Pramod Kumar, Yadav Ravi
Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bangalore, India.
Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.
J Neurogenet. 2025 May 14:1-7. doi: 10.1080/01677063.2025.2500953.
Genes play an important role in the risk of Progressive Supranuclear Palsy (PSP). Some of the major risk genes identified for PSP include , , , and in several ethnic groups. However, the interactions among these genes have not been explored in PSP. Therefore, this prospective case-control study aimed to explore the impact of gene-gene interactions in patients with PSP (n = 106) and healthy subjects (n = 109) of Indian ethnicity. Eight single nucleotide polymorphisms (SNPs) of gene (rs1467967, rs242557, rs3785883, rs2471738, rs8070723, rs7521, rs12185268, and rs62063857, and two SNPs of gene (rs3747957 and rs1411478), one SNP each from (rs1768208) and (rs7571971) genes were genotyped by TaqMan Alleleic Discrimination Assay in all the study participants. Gene-gene interactions among these 12 SNPs were performed using the multi-dimensionality reduction (MDR) test. The combination of SNPs from the gene (rs1467967, rs242557, rs3785883), along with (rs1411478) and (rs1768208), appeared to be the best five-locus model ( < 0.001), suggesting strong interactions among , and genes in modulating the risk of PSP. Strong synergistic interactions were observed within gene (rs1467967, rs244557, rs3785883, rs7521, and rs2471738), and between (rs7521) and (rs1768208). Additionally, moderately strong synergistic interactions were found between (i) (rs1768208) and (rs1411478), and (ii) (rs1768208) and (rs3785883) genes. The findings of this study suggest significant impact of gene-gene interactions amongst , , and genes in modulating the risk of PSP. This implies that epistatic interactions might constitute an important mechanism in delineating the genetic basis of PSP.
基因在进行性核上性麻痹(PSP)的发病风险中起着重要作用。在多个种族群体中,已确定的一些主要PSP风险基因包括[具体基因1]、[具体基因2]、[具体基因3]和[具体基因4]。然而,这些基因之间的相互作用在PSP中尚未得到研究。因此,这项前瞻性病例对照研究旨在探讨基因 - 基因相互作用对印度裔PSP患者(n = 106)和健康受试者(n = 109)的影响。通过TaqMan等位基因鉴别分析对所有研究参与者进行了[具体基因1]的8个单核苷酸多态性(SNP)(rs1467967、rs242557、rs3785883、rs2471738、rs8070723、rs7521、rs12185268和rs62063857)、[具体基因2]的2个SNP(rs3747957和rs1411478)、[具体基因3]的1个SNP(rs1768208)和[具体基因4]的1个SNP(rs7571971)的基因分型。使用多维度约简(MDR)测试对这12个SNP之间的基因 - 基因相互作用进行了分析。来自[具体基因1]的SNP(rs1467967、rs242557、rs3785883)与[具体基因2](rs1411478)和[具体基因3](rs1768208)的组合似乎是最佳的五位点模型(P < 0.001),表明[具体基因1]、[具体基因2]和[具体基因3]在调节PSP风险方面存在强烈相互作用。在[具体基因1]内(rs1467967、rs244557、rs3785883、rs7521和rs2471738)以及[具体基因1](rs7521)与[具体基因3](rs1768208)之间观察到了强烈的协同相互作用。此外,在(i)[具体基因3](rs1768208)与[具体基因2](rs1411478)以及(ii)[具体基因3](rs1768208)与[具体基因1](rs3785883)基因之间发现了中等强度的协同相互作用。本研究结果表明,[具体基因1]、[具体基因2]和[具体基因3]之间的基因 - 基因相互作用对调节PSP风险具有显著影响。这意味着上位性相互作用可能是阐明PSP遗传基础的重要机制。