Phagura Nuvreen, Hussain Azm, Culliford Alice, Hodson James, Evison Felicity, Gallier Suzy, Borrows Richard, Lane Hanna A, Briggs David, Sharif Adnan
College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Department of Nephrology and Transplantation, University Hospitals Birmingham, Birmingham, United Kingdom.
Transplant Direct. 2021 Jul 23;7(8):e737. doi: 10.1097/TXD.0000000000001188. eCollection 2021 Aug.
The association between specific HLA alleles and risk for posttransplantation diabetes (PTDM) in a contemporary and multiethnic kidney transplant recipient cohort is not clear.
In this single-center analysis, data were retrospectively analyzed for 1560 nondiabetic kidney transplant recipients at a single center between 2007 and 2018, with median follow-up of 33 mo (interquartile range 8-73). HLA typing methodology was by DNA analysis and reported at the resolution required for the national allocation scheme. Diagnosis of PTDM was aligned with International Consensus recommendations.
PTDM developed in 231 kidney transplant recipients. Exploring 99 HLA alleles, the presence of Cw12, B52, B38, B58, DQ4, A80, and DR13 and the absence of DQ3 and DR04 were associated with significant increases in PTDM risk. In a multivariable Cox regression model, adjusting for other clinical risk factors for PTDM, the presence of Cw12 (hazard ratio [HR], 1.57; 95% CI, 1.08-2.27; = 0.017) and DQ4 (HR, 1.78; 95% CI, 1.07-2.96; = 0.026) were found to be independent risk factors for PTDM. There was also evidence that the presence of B58 increases PTDM risk within the subgroup of recipients of White ethnicity (HR, 5.01; 95% CI, 2.20-11.42; < 0.001).
Our data suggest that specific HLA alleles can be associated with PTDM risk, which can be used pretransplantation for PTDM risk stratification. However, association is not causality, and this work requires replication and further investigation to understand underlying biological mechanisms.
在当代多民族肾移植受者队列中,特定HLA等位基因与移植后糖尿病(PTDM)风险之间的关联尚不清楚。
在这项单中心分析中,对2007年至2018年期间一个中心的1560例非糖尿病肾移植受者的数据进行回顾性分析,中位随访时间为33个月(四分位间距8 - 73)。HLA分型方法采用DNA分析,并按照国家分配方案要求的分辨率报告。PTDM的诊断符合国际共识建议。
231例肾移植受者发生了PTDM。在对99个HLA等位基因进行探索时,发现Cw12、B52、B38、B58、DQ4、A80和DR13的存在以及DQ3和DR04的缺失与PTDM风险显著增加相关。在多变量Cox回归模型中,在对其他PTDM临床风险因素进行校正后,发现Cw12(风险比[HR],1.57;95%置信区间,1.08 - 2.27;P = 0.017)和DQ4(HR,1.78;95%置信区间,1.07 - 2.96;P = 0.026)是PTDM的独立风险因素。还有证据表明,在白人种族受者亚组中,B58的存在会增加PTDM风险(HR,5.01;95%置信区间,2.20 - 11.42;P < 0.001)。
我们的数据表明,特定HLA等位基因可能与PTDM风险相关,可在移植前用于PTDM风险分层。然而,关联并不等同于因果关系,这项工作需要重复和进一步研究以了解潜在的生物学机制。