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血清素转运体(SERT)基因多态性与特发性肺动脉高压的相关性:荟萃分析和文献回顾。

Association between serotonin transporter (SERT) gene polymorphism and idiopathic pulmonary arterial hypertension: a meta-analysis and review of the literature.

机构信息

Affiliated Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Ave, Qiaokou district, Wuhan City, Hubei Province 430030, China.

出版信息

Metabolism. 2013 Dec;62(12):1867-75. doi: 10.1016/j.metabol.2013.08.012. Epub 2013 Sep 24.

DOI:10.1016/j.metabol.2013.08.012
PMID:24075737
Abstract

OBJECTIVE

Idiopathic pulmonary arterial hypertension (IPAH) is a rare and often fatal disease of unknown etiology. Serotonin transporter (SERT) protein, whose genes can have two allelic forms, namely long (L) and short (S), is suspected to be related to IPAH risk. Several studies have investigated the association between SERT's different allelic forms and IPAH but showed conflicting results. A meta-analysis of published studies was performed to allow a more reliable estimate of this association.

METHODS

Relevant databases were searched to identify eligible studies published from 2000 to 2013. Odds ratios (OR) and 95% confidence intervals (CI) were determined for the gene-disease association using fixed or random effects models.

RESULTS

A total of 6 studies with 451 IPAH subjects and 664 controls were included in this meta-analysis. A significant difference was found in the comparison between IPAH subjects and controls with LL vs. SS genotypes, and the pooled odds ratio (OR) with the fixed effects model was 1.446 (95% CI=1.036-2.018, p=0.030, I(2)=38.8%). However, no statistically significant differences were observed for LL vs. LS or LL vs. LS+SS. The pooled OR indicated no significant differences in IPAH risk between carriers of SERT L and S alleles (ORL VS. S=1.327, 95% CI=0.933-1.886, p=0.115).

CONCLUSION

This meta-analysis provides evidence suggesting an association between the SERT L/S polymorphism and IPAH. Individuals with the LL genotype have an obviously higher risk of developing IPAH than those with the SS genotype.

摘要

目的

特发性肺动脉高压(IPAH)是一种病因不明的罕见且常致命的疾病。血清素转运体(SERT)蛋白的基因有两种等位基因形式,即长(L)和短(S),疑似与 IPAH 风险有关。几项研究已经调查了 SERT 的不同等位基因形式与 IPAH 之间的关联,但结果存在矛盾。对已发表的研究进行了荟萃分析,以更可靠地估计这种关联。

方法

搜索了相关数据库,以确定 2000 年至 2013 年期间发表的符合条件的研究。使用固定或随机效应模型确定基因-疾病关联的比值比(OR)和 95%置信区间(CI)。

结果

共有 6 项研究,涉及 451 名 IPAH 患者和 664 名对照者,纳入了本荟萃分析。与 SS 基因型相比,IPAH 患者与对照组之间的 LL 与 SS 基因型之间存在显着差异,固定效应模型的汇总比值比(OR)为 1.446(95%CI=1.036-2.018,p=0.030,I(2)=38.8%)。然而,LL 与 LS 或 LL 与 LS+SS 之间未观察到统计学显着差异。SERT L 和 S 等位基因携带者的 IPAH 风险无显着差异(ORL VS. S=1.327,95%CI=0.933-1.886,p=0.115)。

结论

本荟萃分析提供了证据,表明 SERT L/S 多态性与 IPAH 之间存在关联。与 SS 基因型相比,LL 基因型的个体发生 IPAH 的风险明显更高。

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