Department of Pharmacology, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Department of Neurology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China (mainland).
Med Sci Monit. 2016 Oct 19;22:3820-3827. doi: 10.12659/MSM.896904.
BACKGROUND Recent studies demonstrated that polymorphisms in the PDE4D gene were associated with several processes involved in the occurrence of ischemic stroke (IS). The association between specific PDE4D single-nucleotide polymorphism 56 (SNP56) and IS risk was initially identified via genome-wide association studies (GWAS), although the GWAS in different populations produced inconclusive results. Thus, we performed a meta-analysis to better explain the association between PDE4D SNP56 and IS risk. MATERIAL AND METHODS A literature search was conducted using PubMed, Embase, and Web of Science up to June 1, 2015. A fixed-effects or random-effects model was used to calculate the pooled odds ratios (ORs) based on the results from the heterogeneity tests. RESULTS Finally, we performed a meta-analysis of 15 studies, involving 8731 IS patients and 10,756 controls. The results showed nonsignificant association between PDE4D SNP56 and IS risk (T vs. A: OR=1.01, 95%CI=0.88-1.15, P=0.90). Similarly, in the subgroup analysis by ethnicity, no significant association was observed in Asian (T vs. A: OR=1.08, 95%CI=0.80-1.44, P=0.62) or European (T vs. A: OR=0.96, 95%CI=0.86-1.08, P=0.54) population. Moreover, funnel plots and Egger regression testing showed no evidence of publication bias. CONCLUSIONS In summary, current evidence suggested that PDE4D SNP56 might not be associated with an increased susceptibility to IS. However, this conclusion needs further validation by well-designed studies with large sample sizes.
最近的研究表明,PDE4D 基因的多态性与缺血性中风(IS)发生过程中的几个过程有关。通过全基因组关联研究(GWAS)最初确定了 PDE4D 特定单核苷酸多态性 56(SNP56)与 IS 风险之间的关联,尽管不同人群中的 GWAS 得出了不一致的结果。因此,我们进行了荟萃分析以更好地解释 PDE4D SNP56 与 IS 风险之间的关联。
我们使用 PubMed、Embase 和 Web of Science 进行了文献检索,截至 2015 年 6 月 1 日。根据异质性检验的结果,使用固定效应或随机效应模型计算汇总的优势比(OR)。
最后,我们对 15 项研究进行了荟萃分析,涉及 8731 例 IS 患者和 10756 例对照。结果显示 PDE4D SNP56 与 IS 风险之间无显著关联(T 对 A:OR=1.01,95%CI=0.88-1.15,P=0.90)。同样,在按种族进行的亚组分析中,在亚洲人群(T 对 A:OR=1.08,95%CI=0.80-1.44,P=0.62)或欧洲人群(T 对 A:OR=0.96,95%CI=0.86-1.08,P=0.54)中也未观察到显著关联。此外,漏斗图和 Egger 回归检验均未显示存在发表偏倚的证据。
总之,目前的证据表明 PDE4D SNP56 与 IS 的易感性增加可能无关。但是,需要进一步通过设计良好、样本量大的研究来验证这一结论。