Cao Yuezhou, Fan Xinying, Zhu Wusheng, Ni Guihua, Qian Yun, Han Yunfei, Ma Minmin
a 1 Department of Neurology, Jinling Hospital , Southern Medical University , Nanjing , China.
b 2 Department of Geriatiric Neurology , First Affiliated Hospital of Nanjing Medical University , Nanjing , China.
Int J Neurosci. 2016;126(7):584-92. doi: 10.3109/00207454.2015.1052429. Epub 2015 Aug 18.
Epidemiological studies have evaluated the association between the C7673T polymorphism in apolipoprotein B (apoB) gene and ischemic stroke (IS), but the results are still debatable even in the Chinese population. This meta-analysis was therefore designed to clarify these controversies.
All of the relevant studies were identified from PubMed, Embase, Chinese National Knowledge Infrastructure database and Chinese Wanfang database up to 31 October 2014. Statistical analyses were conducted with Revman 5.2 and STATA 12.0 software. Odds ratio (OR) with 95% confidence interval (CI) values were applied to evaluate the strength of the association. A fixed or random effect model was selected for pooling data based on the heterogeneity test. Publication bias was assessed by Begg's test and Egger's test.
A significant association was found between the C7673T polymorphism in apoB gene and IS under the heterozygous genetic model (OR = 1.868, 95% CI = 1.160-3.007) and the allelic genetic model (OR = 1.742, 95% CI = 1.294-2.346), respectively. In the subgroup analysis by the geographic region, T allele could increase the risk of IS in northern Chinese (OR = 2.359, 95% CI: 1.425-3.907), but not in southern Chinese individuals (OR = 1.485, 95% CI: 0.778-2.832). Further stratification for source of controls showed that statistical significance was found among the population-based studies.
Our meta-analysis revealed that C7673T polymorphism in apoB gene was significantly associated with increased IS risk in the Chinese population.
流行病学研究评估了载脂蛋白B(apoB)基因C7673T多态性与缺血性脑卒中(IS)之间的关联,但即便在中国人群中,研究结果仍存在争议。因此,本荟萃分析旨在阐明这些争议。
截至2014年10月31日,从PubMed、Embase、中国知网数据库和中国万方数据库中检索所有相关研究。使用Revman 5.2和STATA 12.0软件进行统计分析。采用比值比(OR)及95%置信区间(CI)评估关联强度。根据异质性检验结果选择固定效应模型或随机效应模型合并数据。采用Begg检验和Egger检验评估发表偏倚。
分别在杂合子遗传模型(OR = 1.868,95%CI = 1.160 - 3.007)和等位基因遗传模型(OR = 1.742,95%CI = 1.294 - 2.346)下发现apoB基因C7673T多态性与IS之间存在显著关联。在按地理区域进行的亚组分析中,T等位基因可增加中国北方人群患IS的风险(OR = 2.359,95%CI:1.425 - 3.907),但在中国南方人群中未发现此关联(OR = 1.485,95%CI:0.778 - 2.832)。进一步按对照来源分层显示,基于人群的研究中有统计学意义。
我们的荟萃分析表明,apoB基因C7673T多态性与中国人群IS风险增加显著相关。