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肿瘤坏死因子-α(-238G/A和-308G/A)基因多态性可能与缺血性中风风险无关。

TNF-a (-238G/A and -308G/A) gene polymorphisms may not contribute to the risk of ischemic stroke.

作者信息

Gu Lian, Wu Guangliang, Su Li, Yan Yan, Liang Baoyun, Tan Jinjing, Cai Haiyan, Jiang Haiyun, Wei Qiugui, Shen Tingting, Wei Ailing

机构信息

a First Affiliated Hospital , Guangxi University of Chinese Medicine , Nanning , Guangxi , China.

b School of Public Health of Guangxi Medical University , Nanning , Guangxi , China.

出版信息

Int J Neurosci. 2016;126(3):219-26. doi: 10.3109/00207454.2015.1010200. Epub 2015 May 22.

Abstract

BACKGROUND

The common and major pathological change in ischemic stroke is atherosclerosis in the artery. Tumor necrosis factor-a (TNF-a) is closely related to the pathogenesis of atherosclerosis. The aim of our study was to investigate whether TNF-a gene variants (-238G/A and -308G/A) are associated with ischemic stroke.

METHODS

A total of 619 ischemic stroke patients and 612 controls were recruited to estimate the frequencies of two TNF-a (-238G/A and -308G/A) single nucleotide polymorphisms using a Sequenom MassARRAY time-of-flight mass spectrometer. The association between TNF-a gene polymorphisms and ischemic stroke risk was evaluated by computing the odds ratio (OR) and 95% Confidence Interval with multivariate unconditional logistic regression analyses.

RESULTS

The OR results indicated that no significant associations were found between TNF-a gene (-238G/A and -308G/A) polymorphisms and the risk of ischemic stroke using five genetic models, including the allele model (A vs. G), co-dominant model 1 (GA vs. GG), co-dominant model 2 (AA vs. GG), the dominant model (AA+GA vs. GG), and the recessive model (GG+GA vs. AA).

CONCLUSIONS

The TNF-a (-238G/A and -308G/A) gene polymorphisms may not be a susceptible predictor of ischemic stroke in Chinese populations.

摘要

背景

缺血性卒中常见且主要的病理变化是动脉粥样硬化。肿瘤坏死因子-α(TNF-α)与动脉粥样硬化的发病机制密切相关。我们研究的目的是调查TNF-α基因变异(-238G/A和-308G/A)是否与缺血性卒中相关。

方法

共招募了619例缺血性卒中患者和612例对照,使用Sequenom MassARRAY飞行时间质谱仪估计两种TNF-α(-238G/A和-308G/A)单核苷酸多态性的频率。通过多变量无条件逻辑回归分析计算比值比(OR)和95%置信区间,评估TNF-α基因多态性与缺血性卒中风险之间的关联。

结果

OR结果表明,使用五种遗传模型,包括等位基因模型(A对G)、共显性模型1(GA对GG)、共显性模型2(AA对GG)、显性模型(AA + GA对GG)和隐性模型(GG + GA对AA),未发现TNF-α基因(-238G/A和-308G/A)多态性与缺血性卒中风险之间存在显著关联。

结论

TNF-α(-238G/A和-308G/A)基因多态性可能不是中国人群缺血性卒中的易感预测指标。

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