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中国人群中亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与缺血性脑卒中的关联:一项荟萃分析。

Association between the methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and ischemic stroke in the Chinese population: a meta-analysis.

作者信息

Zhu Xiao-Yan, Hou Rong-Yao, Pan Xu-Dong, Wang Yu-Chun, Zhang Zheng-Shou, Guo Rui-You

机构信息

a Department of Critical Care Medicine, the Affiliated Hiser Hospital of Qingdao University , Qingdao , China.

b Department of Neurology, the Affiliated Hiser Hospital of Qingdao University , Qingdao , China.

出版信息

Int J Neurosci. 2015;125(12):885-94. doi: 10.3109/00207454.2014.984295. Epub 2014 Nov 21.

Abstract

PURPOSE

The association between the methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and ischemic stroke (IS) has been extensively studied; however, the results from genetic association studies have been inconsistent even in the Chinese population. As far as we know, there was no previous meta-analysis concerning this association in the Chinese population. Therefore, the aim of our meta-analysis was to further evaluate the association in the Chinese population.

METHODS

We collected all of the relevant studies from Pubmed, OVID, Embase, Chinese Wan Fang database, CNKI, Chongqing VIP database and CBM up to August 2014. The available data was analyzed by Stata (version 12.0). We used odds ratios (ORs) and corresponding 95% confidence intervals (CIs) to present the strength of the association. Heterogeneity was evaluated by the Q-test and I(2) statistic. Different genetic models, subgroup analysis, publication bias and sensitivity analysis were used to improve the comprehensive understanding.

RESULTS

The results showed a significant association between the MTHFR gene C677T polymorphism and IS in six genetic models (additive model: OR = 1.34, 95%CI: 1.17 ∼ 1.54, p < 0.001; dominant model: OR = 1.44, 95% CI:1.26 ∼ 1.64, p < 0.001; recessive model: OR = 1.45, 95% CI: 1.15 ∼ 1.83, p = 0.001; heterozygote model: OR = 1.35, 95% CI: 1.18 ∼ 1.55, p < 0.001; homozygote model: OR = 1.80, 95% CI: 1.34 ∼ 2.41, p < 0.001; and allelic model: OR = 1.34, 95% CI: 1.17 ∼ 1.53, p < 0.001) based on the overall population, as well as subgroup analysis. In addition, the similar results were obtained in the sensitivity analysis based on studies with the high quality.

CONCLUSIONS

This meta-analysis presented a significant association between the MTHFR gene C677T polymorphism and IS, the T allele might be a risk factor for IS in the Chinese population.

摘要

目的

亚甲基四氢叶酸还原酶(MTHFR)基因C677T多态性与缺血性卒中(IS)之间的关联已得到广泛研究;然而,即使在中国人群中,基因关联研究的结果也不一致。据我们所知,此前尚无关于中国人群中这种关联的荟萃分析。因此,我们进行荟萃分析的目的是进一步评估中国人群中的这种关联。

方法

我们收集了截至2014年8月来自PubMed、OVID、Embase、中国万方数据库、CNKI、重庆维普数据库和CBM的所有相关研究。利用Stata(12.0版)对可得数据进行分析。我们使用比值比(OR)和相应的95%置信区间(CI)来表示关联强度。通过Q检验和I²统计量评估异质性。采用不同的遗传模型、亚组分析、发表偏倚分析和敏感性分析来增进全面理解。

结果

结果显示,基于总体人群以及亚组分析,MTHFR基因C6T多态性与IS在六种遗传模型中存在显著关联(加性模型:OR = 1.34,95%CI:1.17~1.54,p < 0.001;显性模型:OR = 1.44,95%CI:l.26~1.64,p < 0.001;隐性模型:OR = 1.45,95%CI:1.15~1.83,p = 0.001;杂合子模型:OR = 1.35,95%CI:1.18~1.55,p < 0.001;纯合子模型:OR = 1.80,95%CI:1.34~2.41,p < 0.001;等位基因模型:OR = 1.34,95%CI:1.17~1.53,p < 0.001)。此外,在基于高质量研究的敏感性分析中也获得了类似结果。

结论

这项荟萃分析表明MTHFR基因C677T多态性与IS之间存在显著关联,T等位基因可能是中国人群中IS的一个危险因素。

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