Department of Internal Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Urol J. 2020 Apr 18;18(1):1-10. doi: 10.22037/uj.v0i0.5437.
The association of rs1982073 (codon 10) polymorphism at Transforming Growth Factor- β1 (TGF-β1) gene with acute renal rejection (ARR) has been reported by several studies. However, the results were controversial. To derive a more precise estimation of this association, a meta-analysis was performed.
The eligible literatures were identified through PubMed, Scopus, Web of Science, EMBASE, SciELO, WanFang, and CNKI databases up to July 01, 2019. The pooled odds ratios (ORs) with corresponding 95% confidence intervals (CIs) were used to calculate the strength of the association.
A total of 23 case-control studies with 795 ARR cases and 1,562 non-AR controls were selected. Pooled data revealed that there was no significant association between TGF-β1 codon 10 polymorphism and an increased risk of ARR in the overall population (C vs. T: OR=0.908, 95% CI 0.750-1.099, p = 0.322; CT vs. TT: OR=1.074, 95% CI 0.869-1.328, p = 0.507; CC vs.TT: OR=0.509, 95% CI=0.738-1.253, p = 0.770; CC+CT vs. TT: OR = 0.917, 95% CI 0.756-1.112, p = 0.376, and CC vs. CT+TT: OR=0.995, 95% CI 0.809-1.223, p = 0.959). Moreover, stratified analysis revealed no significant association between the TGF-β1 rs1982073 polymorphism and ARR risk by ethnicity and cases type (recipient and donor).
The current meta-analysis demonstrated that the TGF-β1 rs1982073 polymorphism was not significantly associated with increased risk of ARR. However, studies with a larger number of subjects among different ethnic groups are needed to further validate the results.
已有多项研究报道转化生长因子-β1(TGF-β1)基因 rs1982073(密码子 10)多态性与急性肾排斥反应(ARR)之间存在关联。然而,研究结果存在争议。为了更准确地评估这种关联,进行了荟萃分析。
通过 PubMed、Scopus、Web of Science、EMBASE、SciELO、WanFang 和 CNKI 数据库,检索至 2019 年 7 月 1 日的相关文献。采用合并优势比(OR)及其 95%置信区间(CI)来评估关联强度。
共纳入 23 项病例对照研究,包含 795 例 ARR 病例和 1562 例非 ARR 对照。汇总数据显示,在总体人群中,TGF-β1 密码子 10 多态性与 ARR 风险增加无关(C 对 T:OR=0.908,95%CI 0.750-1.099,p=0.322;CT 对 TT:OR=1.074,95%CI 0.869-1.328,p=0.507;CC 对 TT:OR=0.509,95%CI=0.738-1.253,p=0.770;CC+CT 对 TT:OR=0.917,95%CI=0.756-1.112,p=0.376;CC 对 CT+TT:OR=0.995,95%CI=0.809-1.223,p=0.959)。此外,分层分析显示,TGF-β1 rs1982073 多态性与种族和病例类型(受者和供者)之间的 ARR 风险无显著关联。
本荟萃分析表明,TGF-β1 rs1982073 多态性与 ARR 风险增加无显著相关性。然而,需要在不同种族群体中开展更多具有较大样本量的研究来进一步验证结果。