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亚甲基四氢叶酸还原酶基因多态性与静脉血栓栓塞的相关性:99 项遗传关联研究的荟萃分析。

Correlations between methylenetetrahydrofolate reductase gene polymorphisms and venous thromboembolism: A meta-analysis of 99 genetic association studies.

机构信息

Center of General Practice, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, China.

出版信息

Eur J Prev Cardiol. 2019 Jan;26(2):120-134. doi: 10.1177/2047487318799467. Epub 2018 Nov 22.

Abstract

We performed this meta-analysis to better assess the relationship between methylenetetrahydrofolate reductase gene ( MTHFR) polymorphisms and the risk of venous thromboembolism. Eligible studies were searched in PubMed, Medline, Embase, and Web of Science. Odds ratios with 95% confidence intervals were used to assess associations of MTHFR polymorphisms with venous thromboembolism. A total of 99 genetic association studies were enrolled for analyses. Although no positive results were detected in overall analyses for the rs1801131 polymorphism. Further subgroup analyses according to ethnicity of participants and type of disease revealed that the rs1801131 polymorphism was significantly correlated with the risk of pulmonary embolism. For the rs1801133 polymorphism, significant association with the risk of venous thromboembolism was found in the dominant, recessive, and allele models. Further subgroup analyses according to ethnicity of participants revealed that the rs1801133 polymorphism was significantly associated with the risk of venous thromboembolism in Caucasians, East Asians, and West Asians. When we stratified available data according to type of disease, we found that the rs1801133 polymorphism was also significantly correlated with the risk of deep vein thrombosis and pulmonary embolism. In conclusion, our findings indicate that the MTHFR rs1801133 polymorphism may serve as a potential biological marker for venous thromboembolism in Caucasians, East Asians, and West Asians. Moreover, the MTHFR rs1801133 polymorphism may be implicated in the development of deep vein thrombosis and pulmonary embolism, while the MTHFR rs1801131 polymorphism may contribute to the development of pulmonary embolism.

摘要

我们进行了这项荟萃分析,以更好地评估亚甲基四氢叶酸还原酶基因(MTHFR)多态性与静脉血栓栓塞风险之间的关系。在 PubMed、Medline、Embase 和 Web of Science 中搜索了合格的研究。使用优势比和 95%置信区间来评估 MTHFR 多态性与静脉血栓栓塞的关联。共有 99 项遗传关联研究被纳入分析。尽管在总体分析中未检测到 rs1801131 多态性的阳性结果。根据参与者的种族和疾病类型进一步进行亚组分析表明,rs1801131 多态性与肺栓塞风险显著相关。对于 rs1801133 多态性,在显性、隐性和等位基因模型中发现与静脉血栓栓塞风险显著相关。根据参与者的种族进一步进行亚组分析表明,rs1801133 多态性与高加索人、东亚人和西亚人的静脉血栓栓塞风险显著相关。当我们根据疾病类型对可用数据进行分层时,我们发现 rs1801133 多态性也与深静脉血栓形成和肺栓塞的风险显著相关。总之,我们的研究结果表明,MTHFR rs1801133 多态性可能是高加索人、东亚人和西亚人静脉血栓栓塞的潜在生物学标志物。此外,MTHFR rs1801133 多态性可能与深静脉血栓形成和肺栓塞的发展有关,而 MTHFR rs1801131 多态性可能与肺栓塞的发展有关。

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