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A model integrating donor gene polymorphisms predicts fibrosis after liver transplantation

机译:集成供体基因多态性的模型预测肝移植后的纤维化

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摘要

Post-transplant liver fibrosis (PTLF) is a common and severe complication in liver recipients. In this study, we assessed the impact of donor liver genetics on the development of PTLF. A total of 232 patients undergoing liver transplantation were included. Twenty-two single nucleotide polymorphisms (SNPs) associated with liver fibrosis were analyzed. Univariate analysis revealed seven donor SNPs to be associated with PTLF. In a multivariate analysis, independent risk factors of PTLF were genetic variation of donor GRP78 rs430397 (OR = 8.99, p = 0.003), GSTP1 rs1695 (OR = 0.13, p = 0.021), miRNA-196a rs12304647 (OR = 16.01, p =0.001), and TNF-α rs1800630 (OR = 79.78, p = 0.001); blood tacrolimus levels at maintenance > 7 ng/ml (OR =7.48, p <0.001); and post-transplant diabetes mellitus (OR = 7.50, p = 0.001). A predictive model that included donor SNPs showed better prognostic ability for PTLF than a model with only clinical parameters (AUROC: 0.863 vs 0.707, P < 0.001). Given that donor gene SNPs are associated with an increased risk of PTLF, this model integrated with donor gene polymorphisms may help clinicians predict PTLF.
机译:移植后肝纤维化(PTLF)是肝脏受体中的常见和严重的并发症。在这项研究中,我们评估了供体肝遗传学对PTLF发育的影响。共用了232例接受肝移植的患者。分析了与肝纤维化相关的二十二种单核苷酸多态性(SNP)。单变量分析显示七种供体SNP与PTLF相关。在多变量分析中,PTLF的独立危险因素是供体GRP78 RS430397(或= 8.99,P = 0.003)的遗传变异,GSTP1 RS1695(或= 0.13,P = 0.021),miRNA-196A RS12304647(或= 16.01,P = 0.001),TNF-αrs1800630(或= 79.78,p = 0.001);维持血喉水平> 7 ng / ml(或= 7.48,p <0.001);和移植后糖尿病(或= 7.50,P = 0.001)。包括供体SNP的预测模型表明PTLF的预后能力比仅具有临床参数的模型(Auroc:0.863 Vs 0.707,P <0.001)。鉴于供体基因SNP与PTLF的风险增加相关,该模型与供体基因多态性集成的这种模型可以帮助临床医生预测PTLF。

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