首页> 外文期刊>Cerebrovascular diseases >Meta-analysis of genetic studies from journals published in China of ischemic stroke in the han chinese population.
【24h】

Meta-analysis of genetic studies from journals published in China of ischemic stroke in the han chinese population.

机译:来自中国汉族人群缺血性中风的中国期刊发表的遗传研究的荟萃分析。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: The aim of this study was to confirm the nature and number of genes contributing to stroke risk and qualify the genetic risk of each susceptibility gene in the Han Chinese population. METHODS: After collecting all case-control studies related to DNA polymorphism of any candidate gene for ischemic stroke in Han Chinese, strict selection criteria and exclusion criteria were determined and different effect models were used according to the difference in heterogeneity. Meta-analyses were carried out by Revman 4.0 software and the publication bias was further evaluated through calculation of fail-safe numbers in the included gene polymorphisms. RESULTS: Seventy-six studies were included in the meta-analyses which were all published in mainland China and referred to 6 candidate genes and 7 polymorphisms. Among the gene polymorphisms tested in the study, association of gene polymorphisms with increasing risk of ischemic stroke was confirmed in 6 polymorphisms including angiotensin-converting enzyme insertion/deletion (ACE I/D; OR = 1.87, 95% CI = 1.45-2.42), methylenetetrahydrofolate reductase (MTHFR) C677T (OR = 1.55, 95% CI = 1.26-1.90), plasminogen activator inhibitor 1 (PAI-1) 4G/5G (OR = 1.79, 95% CI = 1.20-2.67), beta-fibrinogen (beta-Fg) -455A/G (OR = 1.48, 95% CI = 1.14-1.92), beta-Fg -148T/C (OR = 1.72, 95% CI = 1.42-2.07), apolipoprotein E (ApoE) epsilon2-4 (OR = 2.39, 95% CI = 1.94-2.95). Because of the obvious publication bias, the association between paraoxonase 1 (PON-1) polymorphisms and stroke risk was not established although the OR of the meta-analysis suggested a positive result (OR = 1.14, 95% CI = 1.01-1.35). CONCLUSIONS: ACE D/I, MTHFR C677T, beta-Fg -455A/G, beta-Fg -148T/C, PAI-1 4G/5G, and ApoE epsilon2-4 were associated with risk of ischemic stroke in Han Chinese.
机译:背景:这项研究的目的是确定导致中风风险的基因的性质和数量,并确定汉族人群中每个易感基因的遗传风险。方法:收集汉族人缺血性卒中候选基因DNA多态性的所有病例对照研究后,确定严格的选择标准和排除标准,并根据异质性差异使用不同的疗效模型。通过Revman 4.0软件进行荟萃分析,并通过计算包含的基因多态性中的故障安全编号进一步评估发布偏倚。结果:荟萃分析共纳入76项研究,这些研究全部发表在中国大陆,涉及6个候选基因和7个多态性。在该研究测试的基因多态性中,证实了6种多态性与多态性与缺血性卒中风险的相关性,包括血管紧张素转换酶的插入/缺失(ACE I / D; OR = 1.87,95%CI = 1.45-2.42)。 ,亚甲基四氢叶酸还原酶(MTHFR)C677T(OR = 1.55,95%CI = 1.26-1.90),纤溶酶原激活物抑制剂1(PAI-1)4G / 5G(OR = 1.79,95%CI = 1.20-2.67),β-纤维蛋白原(β-Fg)-455A / G(OR = 1.48,95%CI = 1.14-1.92),β-Fg-148T / C(OR = 1.72,95%CI = 1.42-2.07),载脂蛋白E(ApoE)epsilon2 -4(OR = 2.39,95%CI = 1.94-2.95)。由于明显的出版偏倚,尽管荟萃分析的OR显示阳性结果,但对氧磷酶1(PON-1)多态性与中风风险之间的关联尚未建立(OR = 1.14,95%CI = 1.01-1.35)。结论:ACE D / I,MTHFR C677T,β-Fg-455A / G,β-Fg-148T / C,PAI-1 4G / 5G和ApoE epsilon2-4与中国汉族缺血性中风的风险有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号