Suppr超能文献

阿尔茨海默病患者中SOD2 rs4880基因变异的分析

Analysis of SOD2 rs4880 Genetic Variant in Patients with Alzheimer's Disease.

作者信息

Siokas Vasileios, Stamati Polyxeni, Pateraki Georgia, Liampas Ioannis, Aloizou Athina-Maria, Tsirelis Daniil, Nousia Anastasia, Sgantzos Markos, Nasios Grigorios, Bogdanos Dimitrios P, Dardiotis Efthimios

机构信息

Laboratory of Neurogenetics, Department of Neurology, University Hospital of Larissa, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41100 Larissa, Greece.

Department of Speech and Language Therapy, University of Ioannina, 45500 Ioannina, Greece.

出版信息

Curr Issues Mol Biol. 2022 Sep 21;44(10):4406-4414. doi: 10.3390/cimb44100302.

Abstract

A few gene loci that contribute to Alzheimer's Disease (AD) onset have been identified. Few studies have been published about the relationship between SOD2 rs4880 single nucleotide variant and AD, revealing inconsistent results. Therefore, the aim of the current study is to further examine the role of the SOD2 rs4880 in AD. We performed a case-control study with a total of 641 subjects (320 patients with probable AD, and 321 healthy controls). The statistical analysis was performed assuming five genetic models. The threshold for statistical significance was set at 0.05. The results revealed no association between SOD2 rs4880 and AD in any of the assumed genetic models that were examined [log-additive OR = 0.95 (0.76-1.19), over-dominant OR = 1.15 (0.85-1.57), recessive OR = 0.85 (0.59-1.22), dominant OR = 1.03 (0.72-1.47), and co-dominant OR1 = 1.10 (0.75-1.60) and OR2 = 0.90 (0.58-1.40)]. Adjustment for sex and subgroup analyses based on sex did not reveal any statistically significant results either. Based on our findings, SOD2 rs4880 does not appear to play a determining role in the risk of developing AD. Larger studies are warranted to elucidate the connection between rs4880 and AD.

摘要

已经确定了一些与阿尔茨海默病(AD)发病相关的基因位点。关于超氧化物歧化酶2(SOD2)基因rs4880单核苷酸变异与AD之间的关系,发表的研究较少,且结果不一致。因此,本研究的目的是进一步探讨SOD2基因rs4880在AD中的作用。我们进行了一项病例对照研究,共纳入641名受试者(320例可能患有AD的患者和321名健康对照)。在五种遗传模型下进行了统计分析。统计学显著性阈值设定为0.05。结果显示,在所检测的任何假定遗传模型中,SOD2基因rs4880与AD之间均无关联[对数相加模型的比值比(OR)=0.95(0.76 - 1.19),超显性模型OR = 1.15(0.85 - 1.57),隐性模型OR = 0.85(0.59 - 1.22),显性模型OR = 1.03(0.72 - 1.47),共显性模型OR1 = 1.10(0.75 - 1.60),OR2 = 0.90(0.58 - 1.40)]。对性别进行校正以及基于性别的亚组分析也未显示出任何具有统计学显著性的结果。基于我们的研究结果,SOD2基因rs4880似乎在AD发病风险中不起决定性作用。需要开展更大规模的研究来阐明rs4880与AD之间的联系。

相似文献

本文引用的文献

8
SLC2A3 rs12842 polymorphism and risk for Alzheimer's disease.SLC2A3 rs12842 多态性与阿尔茨海默病风险。
Neurol Res. 2020 Oct;42(10):853-861. doi: 10.1080/01616412.2020.1786973. Epub 2020 Jul 4.
9
Pesticides, cognitive functions and dementia: A review.农药、认知功能与痴呆:综述
Toxicol Lett. 2020 Jun 15;326:31-51. doi: 10.1016/j.toxlet.2020.03.005. Epub 2020 Mar 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验