Department of Pharmacy, Changzhou No. 2 People's Hospital, The Affiliated Hospital of Nanjing Medical University, Changzhou, China.
Department of Pharmacy, The Third Affiliated Hospital of Soochow University, The First People's Hospital of Changzhou, Changzhou, China.
Int J Clin Pract. 2022 Mar 8;2022:7140024. doi: 10.1155/2022/7140024. eCollection 2022.
The purpose of this study was to clarify the role of genetic factors on posttransplant diabetes mellitus (PTDM) risk.
Relevant publications were systematically retrieved from PubMed, EMBASE, and the Cochrane Library up to December 2020. Data from eligible case-control and cohort studies were extracted for qualitative and quantitative analyses. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the association between gene polymorphisms and PTDM in the quantitative meta-analysis.
A total of 43 eligible articles were identified, and 16 studies on 9 DNA variants from 8 genes were included in the meta-analysis. rs7903146 was significantly associated with PTDM risk in 5 genetic models (OR (95% CI): allelic: 1.59 (1.17-2.16), =0.003; dominant recessive: 1.62 (1.14, 2.31), =0.007; recessive: 1.87 (1.18, 2.94), =0.007; homozygote: 2.21 (1.23, 3.94), =0.008; and heterozygote 1.50 (1.08, 2.10), =0.017). rs2237892 was significantly correlated with PTDM risk in 3 genetic models (allelic: 0.68 (0.58, 0.81), < 0.001; dominant: 0.6 (049, 0.74), < 0.001; and heterozygote: 0.61 (0.48, 0.76), < 0.001). rs5219 was significantly linked with PTDM in the recessive genetic model (1.59 (1.01, 2.50), =0.047). No significant correlations of PTDM with rs12255372, rs13266634, rs1801282, rs10811661, rs1111875, and rs4402960 polymorphisms were found.
The gene polymorphisms of rs7903146, rs2237892, and rs5219 may predispose kidney transplant recipients to PTDM. Large sample size studies on diverse ethnic populations were warranted to confirm our findings.
本研究旨在阐明遗传因素在移植后糖尿病(PTDM)风险中的作用。
系统检索了PubMed、EMBASE 和 Cochrane 图书馆截至 2020 年 12 月的相关文献。提取合格的病例对照和队列研究的数据进行定性和定量分析。采用比值比(ORs)和 95%置信区间(CIs)来估计基因多态性与 PTDM 之间的关联。
共确定了 43 篇符合条件的文章,其中 16 项研究涉及 8 个基因的 9 个 DNA 变体,纳入了荟萃分析。在 5 种遗传模型中,rs7903146 与 PTDM 风险显著相关(OR(95%CI):等位基因:1.59(1.17-2.16),=0.003;显性隐性:1.62(1.14-2.31),=0.007;隐性:1.87(1.18-2.94),=0.007;纯合子:2.21(1.23-3.94),=0.008;杂合子 1.50(1.08-2.10),=0.017)。rs2237892 在 3 种遗传模型中与 PTDM 风险显著相关(等位基因:0.68(0.58-0.81),<0.001;显性:0.6(049-0.74),<0.001;杂合子:0.61(0.48-0.76),<0.001)。rs5219 与隐性遗传模型中的 PTDM 显著相关(1.59(1.01-2.50),=0.047)。rs12255372、rs13266634、rs1801282、rs10811661、rs1111875 和 rs4402960 多态性与 PTDM 无显著相关性。
rs7903146、rs2237892 和 rs5219 的基因多态性可能使肾移植受者易患 PTDM。需要对不同种族人群进行更大样本量的研究来证实我们的发现。