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DPYSL2 基因多态性与白种人群酒精依赖的相关性研究。

Association between DPYSL2 gene polymorphisms and alcohol dependence in Caucasian samples.

机构信息

Department of Biostatistics and Epidemiology, College of Public Health, East Tennessee State University, PO Box 70259, Lamb Hall, Johnson City, TN, 37614-1700, USA.

出版信息

J Neural Transm (Vienna). 2014 Jan;121(1):105-11. doi: 10.1007/s00702-013-1065-2. Epub 2013 Jul 12.

Abstract

The DPYSL2 gene at 8p22-p21 is expressed widely in neuronal tissues and has been implicated in multiple psychiatric disorders such as Alzheimer's disease and schizophrenia. We therefore hypothesized that DPYSL2 gene polymorphisms may play a role in alcohol dependence (AD). We investigated the genetic associations of 57 single-nucleotide polymorphisms (SNPs) within the DPYSL2 gene with AD using two Caucasian samples-the Collaborative Study on the Genetics of Alcoholism (COGA) sample (660 AD cases and 400 controls), and the Study of Addiction: Genetics and Environment (SAGE) sample (623 cases and 1,016 controls). The SNP rs11995227 was most significantly associated with AD (p = 0.000122) in the COGA sample while one flanking SNP rs7832576 revealed the second most significant association with AD (p = 0.00163) in the COGA sample and association with AD (p = 0.0195) in the SAGE sample. Meta-analysis of two samples showed both rs119952227 and rs7832576 were associated with AD (p = 0.000363 and 0.000184, respectively). Furthermore, the C-A haplotype from rs11995227 and rs7832576 revealed significant association with AD (p = 0.0000899) in the COGA sample while the T-G haplotype revealed association with AD both in the COGA and SAGE samples (p = 0.00098 and 0.021, respectively). These findings suggest that genetic variants in DPYSL2 may play a role in susceptibility to AD.

摘要

DPYSL2 基因位于 8p22-p21,广泛表达于神经元组织中,与多种精神疾病相关,如阿尔茨海默病和精神分裂症。因此,我们假设 DPYSL2 基因多态性可能与酒精依赖(AD)有关。我们使用两个白种人样本——酒精遗传合作研究(COGA)样本(660 例 AD 病例和 400 例对照)和成瘾研究:遗传学与环境(SAGE)样本(623 例病例和 1016 例对照),研究了 DPYSL2 基因内 57 个单核苷酸多态性(SNP)与 AD 的遗传相关性。在 COGA 样本中,SNP rs11995227 与 AD 最显著相关(p = 0.000122),而侧翼 SNP rs7832576 与 AD 相关性第二显著(p = 0.00163),且与 SAGE 样本的 AD 相关(p = 0.0195)。两个样本的荟萃分析表明,rs11995227 和 rs7832576 均与 AD 相关(p = 0.000363 和 0.000184)。此外,rs11995227 和 rs7832576 的 C-A 单倍型与 COGA 样本中的 AD 显著相关(p = 0.0000899),而 T-G 单倍型在 COGA 和 SAGE 样本中均与 AD 相关(p = 0.00098 和 0.021)。这些发现表明,DPYSL2 基因中的遗传变异可能与 AD 的易感性有关。

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