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β-纤维蛋白原基因-455G/A 的遗传多态性可能与缺血性脑卒中的发病风险相关。

Genetic polymorphism of β-fibrinogen gene-455G/A can contribute to the risk of ischemic stroke.

机构信息

First Affiliated Hospital, Guangxi University of Chinese Medicine, 89-9 Dong Ge Road, Nanning, 530023, Guangxi, China.

出版信息

Neurol Sci. 2014 Feb;35(2):151-61. doi: 10.1007/s10072-013-1608-1. Epub 2013 Dec 24.

Abstract

Many studies have investigated the association between the β-fibrinogen gene-455G/A (FGβ-455G/A) polymorphism and the risk of ischemic stroke. However, these evidences were inadequate to provide stronger conclusions because most studies were generally small. To shed light on these inconclusive findings, we conducted a large sample size meta-analysis of studies relating to the FGβ-455G/A polymorphism and the risk of ischemic stroke. Odds ratios with a 95 % confidence interval were used to investigate the association between FGβ-455G/A polymorphism and ischemic stroke. Publication bias was tested by Egger's test and funnel plot. Inconsistency index and Cochran's Q statistic were used to check heterogeneity. Cumulative and recursive cumulative meta-analyses were performed to provide a framework for updating a genetic effect from all of the included studies. Twenty-six independent publications with 4,070 cases and 4,649 controls were included in this meta-analysis. Results showed that the β-fibrinogen-455G/A polymorphism was significantly associated with the risk of ischemic stroke. The FGβ-455G/A polymorphism was found to be a risk factor for ischemic stroke in Asians and adults, while association was not observed for Caucasians and juveniles based on the small size and it may be necessary to conduct larger studies on them to investigate the association in the future. The cumulative meta-analysis indicated a decline from 1998 to 2003, and the results remained stable during the period 2004-2012. The results indicate that FGβ-455G/A polymorphism may be a susceptible predictor of ischemic stroke. More studies are needed to elucidate the relationship further.

摘要

许多研究调查了β-纤维蛋白原基因-455G/A(FGβ-455G/A)多态性与缺血性卒中风险之间的关系。然而,由于大多数研究规模较小,这些证据不足以得出更强有力的结论。为了阐明这些不确定的发现,我们对与 FGβ-455G/A 多态性和缺血性卒中风险相关的研究进行了大规模样本量的荟萃分析。使用比值比和 95%置信区间来研究 FGβ-455G/A 多态性与缺血性卒中之间的关联。使用 Egger 检验和漏斗图检验发表偏倚。使用不一致指数和 Cochran's Q 统计量检查异质性。进行累积和递归累积荟萃分析,为从所有纳入研究中更新遗传效应提供框架。这项荟萃分析纳入了 26 项独立出版物,包括 4070 例病例和 4649 例对照。结果表明,β-纤维蛋白原-455G/A 多态性与缺血性卒中风险显著相关。FGβ-455G/A 多态性被发现是亚洲人和成年人缺血性卒中的危险因素,但根据样本量较小,未观察到白人和青少年存在相关性,未来可能有必要对其进行更大规模的研究以进一步探讨相关性。累积荟萃分析表明,1998 年至 2003 年呈下降趋势,2004 年至 2012 年期间结果保持稳定。结果表明,FGβ-455G/A 多态性可能是缺血性卒中的易感预测因子。需要进一步的研究来阐明这种关系。

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