供肾组织病理学病变对肾移植术后BK病毒感染及其进展风险的影响

Impact of donor kidney histopathological lesions on BK virus infection and its progression risk after kidney transplantation

  • 摘要:
    目的  探讨供肾组织病理学病变对肾移植术后BK病毒(BKV)感染及进展的风险影响。
    方法  回顾性分析郑州大学第一附属医院肾移植科2019年1月至2020年6月实施的326例公民逝世后器官捐献肾移植供、受者临床资料。根据受者肾移植术后是否发生BKV感染分为BKV感染组(145例)和BKV未感染组(181例)。分析肾移植供肾零点活组织检查组织病理结果与BKV感染的相关性及对其风险的影响,以及对BKV感染进展的影响。
    结果  326例肾移植受者中BKV感染发生率为44.4%(145/326),感染后BKV清除率为82.1%(119/145),进展为BKV血症为17.9%(26/145)。326例合格肾穿刺标本中,肾小管轻度萎缩32例,轻度急性肾小管损伤324例,轻度小动脉玻璃样变27例,中度及重度小动脉玻璃样变10例,轻度间质炎7例,轻度间质纤维化23例,轻度动脉内膜纤维化6例,中度及重度动脉内膜纤维化1例。多因素logistic回归分析显示男性受者、供者年龄、肾小管萎缩均是BKV感染的独立危险因素(均为P<0.05)。肾小管萎缩是BKV尿症进展为BKV血症的独立危险因素(P<0.05)。
    结论  供肾组织病理学病变对肾移植术后BKV病毒感染及其进展具有一定影响,尤其是肾小管萎缩程度较重的患者,其在肾移植术后发生BKV感染的风险更高,且更容易进展为BKV血症。

     

    Abstract:
    Objective  To investigate the impact of donor kidney histopathological lesions on the risk of BK virus (BKV) infection and progression after kidney transplantation.
    Methods  A retrospective analysis was conducted on the clinical data of 326 kidney transplant recipients from deceased donors at the Department of Kidney Transplantation, the First Affiliated Hospital of Zhengzhou University, from January 2019 to June 2020. The recipients were divided into two groups based on whether BKV infection occurred after kidney transplantation: the BKV infection group (145 cases) and the non-BKV infection group (181 cases). The correlation between donor kidney histopathological findings from zero-hour biopsy and BKV infection, as well as the impact on the risk and progression of BKV infection, was analyzed.
    Results  The incidence of BKV infection among the 326 kidney transplant recipients was 44.4% (145/326). The clearance rate of BKV after infection was 82.1% (119/145), while 17.9% (26/145) progressed to BKV viremia. Among the 326 qualified kidney biopsy specimens, 32 cases showed mild tubular atrophy, 324 cases had mild acute tubular injury, 27 cases exhibited mild hyaline arteriosclerosis, 10 cases had moderate to severe hyaline arteriosclerosis, 7 cases showed mild interstitial inflammation, 23 cases had mild interstitial fibrosis, 6 cases exhibited mild arterial intimal fibrosis, and 1 case had moderate to severe arterial intimal fibrosis. Multivariate logistic regression analysis revealed that male recipients, donor age and tubular atrophy were independent risk factors for BKV infection (all P<0.05). Tubular atrophy was also an independent risk factor for the progression from BKV uria to BKV viremia (P<0.05).
    Conclusions  Donor kidney histopathological lesions have a certain impact on BKV infection and progression after kidney transplantation. Patients with more severe tubular atrophy in donor kidneys have a higher risk of BKV infection after kidney transplantation and are more likely to progress to BKV viremia.

     

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