Abudayyeh A, Hamdi A, Lin H, Abdelrahim M, Rondon G, Andersson B S, Afrough A, Martinez C S, Tarrand J J, Kontoyiannis D P, Marin D, Gaber A O, Salahudeen A, Oran B, Chemaly R F, Olson A, Jones R, Popat U, Champlin R E, Shpall E J, Winkelmayer W C, Rezvani K
Division of Internal Medicine, Section of Nephrology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.
Am J Transplant. 2016 May;16(5):1492-502. doi: 10.1111/ajt.13635. Epub 2016 Mar 2.
Nephropathy due to BK virus (BKV) infection is an evolving challenge in patients undergoing hematopoietic stem cell transplantation (HSCT). We hypothesized that BKV infection was a marker of kidney function decline and a poor prognostic factor in HSCT recipients who experience this complication. In this retrospective study, we analyzed all patients who underwent their first allogeneic HSCT at our institution between 2004 and 2012. We evaluated the incidence of persistent kidney function decline, which was defined as a confirmed reduction in estimated glomerular filtration rate of at least 25% from baseline using the Chronic Kidney Disease Epidemiology equation. Cox proportional hazard regression was used to model the cause-specific hazard of kidney function decline, and the Fine-Gray method was used to account for the competing risks of death. Among 2477 recipients of a first allogeneic HSCT, BK viruria was detected in 25% (n = 629) and kidney function decline in 944 (38.1%). On multivariate analysis, after adjusting for age, sex, acute graft-versus-host disease (GVHD), chronic GVHD, preparative conditioning regimen, and graft source, BK viruria remained a significant risk factor for kidney function decline (p < 0.001). In addition, patients with BKV infection and kidney function decline experienced worse overall survival. After allogeneic HSCT, BKV infection was strongly and independently associated with subsequent kidney function decline and worse patient survival after HSCT.
BK病毒(BKV)感染所致肾病是接受造血干细胞移植(HSCT)患者面临的一个不断演变的挑战。我们推测,BKV感染是肾功能下降的一个标志物,也是经历这种并发症的HSCT受者预后不良的一个因素。在这项回顾性研究中,我们分析了2004年至2012年期间在我们机构接受首次异基因HSCT的所有患者。我们评估了持续性肾功能下降的发生率,持续性肾功能下降定义为使用慢性肾脏病流行病学方程证实估算肾小球滤过率较基线至少降低25%。采用Cox比例风险回归对肾功能下降的病因特异性风险进行建模,并使用Fine-Gray方法考虑死亡的竞争风险。在2477例首次接受异基因HSCT的受者中,25%(n = 629)检测到BK病毒尿,944例(38.1%)出现肾功能下降。多因素分析显示,在调整年龄、性别、急性移植物抗宿主病(GVHD)、慢性GVHD、预处理方案和移植物来源后,BK病毒尿仍然是肾功能下降的一个显著危险因素(p < 0.001)。此外,发生BKV感染且肾功能下降的患者总生存期较差。异基因HSCT后,BKV感染与随后的肾功能下降以及HSCT后患者较差的生存情况密切且独立相关。