Department of Epidemiology and Health Statistics, Qingdao University Medical College, Qingdao, People's Republic of China.
Am J Alzheimers Dis Other Demen. 2013 Aug;28(5):517-23. doi: 10.1177/1533317513494450. Epub 2013 Jun 28.
The association between urokinase-plasminogen activator (PLAU) gene rs2227564 polymorphism and Alzheimer's disease (AD) risk has been widely reported across different ethnic populations, with inconsistent results. Thus, we performed a meta-analysis to assess the association between PLAU rs2227564 polymorphism and AD risk.
Fixed or random effect model was used as the pooling method to assess the basis of homogeneity test among studies. Summarized estimation of odds ratio (OR) and 95% confidence interval (CI) were calculated. Heterogeneity among studies was evaluated using Q test and I (2). Publication bias was estimated using Harbord's test.
A total of 27 studies (comprising 6100 AD cases and 5718 controls) were included in this meta-analysis. The present meta-analysis showed a significant increased effect of T allele on risk of AD in dominant model (fixed effect model [FEM] OR 1.123, 95% CI 1.025-1.231) and heterozygote comparison (CT vs CC; FEM OR 1.126, 95% CI 1.027-1.235). No publication bias was detected.
This meta-analysis showed that T allele of rs2227564 polymorphism in PLAU gene could increase the effects on risk of AD, and this result needs to be confirmed by further studies.
尿激酶型纤溶酶原激活物(PLAU)基因 rs2227564 多态性与阿尔茨海默病(AD)风险之间的关联已在不同种族人群中广泛报道,但结果不一致。因此,我们进行了一项荟萃分析,以评估 PLAU rs2227564 多态性与 AD 风险之间的关联。
使用固定效应模型或随机效应模型作为合并方法,根据研究之间的同质性检验来评估基础。汇总了优势比(OR)和 95%置信区间(CI)的估计值。使用 Q 检验和 I (2)评估研究之间的异质性。使用 Harbord 检验估计发表偏倚。
共有 27 项研究(包括 6100 例 AD 病例和 5718 例对照)纳入本荟萃分析。本荟萃分析显示,T 等位基因在显性模型(固定效应模型 [FEM] OR 1.123,95%CI 1.025-1.231)和杂合子比较(CT 与 CC;FEM OR 1.126,95%CI 1.027-1.235)中对 AD 风险的影响显著增加。未发现发表偏倚。
本荟萃分析表明,PLAU 基因 rs2227564 多态性的 T 等位基因可能增加 AD 发病风险,这一结果需要进一步研究证实。