Department of Pharmacy, University of Wisconsin Hospital and Clinics, Madison, Wisconsin, USA.
Department of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Clin Transplant. 2019 Aug;33(8):e13636. doi: 10.1111/ctr.13636. Epub 2019 Jul 1.
The risk of cytomegalovirus infection (CMV) after rejection treatment is poorly understood. To investigate this, we conducted a case/control (1:2) analysis of adult renal transplant recipients between January 1, 2005 and December 31, 2015, via incidence density sampling and survival analysis. Our objective was to evaluate the association of prior acute rejection with subsequent CMV, including epidemiology and outcomes. There were 2481 eligible renal transplants within the study period and 251 distinct CMV infections. Despite the use of antiviral prophylaxis rejection was a significant risk factor for CMV on unadjusted (HR 1.73 [1.34, 2.24] P < 0.05) and adjusted analysis (HR 1.46 [1.06, 2.04] P < 0.05). When matching cases to controls patients with CMV had significantly more rejection prior to CMV diagnosis (26.7% vs 14.2%, P < 0.01). CMV was associated with a twofold increased risk of prior rejection on unadjusted (OR 1.94, 95%CI: 1.28-2.96, P < 0.01) and adjusted analysis (OR 2.16, 95% CI: 1.31-3.58, P < 0.01). Patients with rejection preceding CMV had significantly increased graft loss (HR 2.89, 95% CI: 1.65-5.09, P < 0.01) and mortality (HR 1.82, 95% CI: 1.12-4.24, P = 0.03) as compared to those CMV cases without rejection. In conclusion, rejection is a risk factor for CMV infection that appears to persist for 1 year. Preceding rejection events increased risk of graft loss and mortality in CMV patients. Given this, prolonged surveillance monitoring for CMV after rejection may be warranted. Studies are needed investigating optimal monitoring strategies.
巨细胞病毒感染(CMV)的风险在接受排斥治疗后仍不明确。为了研究这个问题,我们进行了一项病例对照(1:2)分析,纳入 2005 年 1 月 1 日至 2015 年 12 月 31 日期间的成年肾移植受者,采用发病率密度抽样和生存分析。我们的目的是评估先前的急性排斥与随后的 CMV 的关系,包括流行病学和结果。在研究期间,有 2481 例符合条件的肾移植,251 例明确的 CMV 感染。尽管使用了抗病毒预防,但在未调整(HR 1.73[1.34,2.24],P<0.05)和调整分析(HR 1.46[1.06,2.04],P<0.05)中,排斥反应仍然是 CMV 的显著危险因素。在匹配病例和对照时,CMV 诊断前有 CMV 的患者的排斥反应明显更多(26.7%比 14.2%,P<0.01)。CMV 与未调整(OR 1.94,95%CI:1.28-2.96,P<0.01)和调整分析(OR 2.16,95%CI:1.31-3.58,P<0.01)上先前排斥反应的风险增加两倍相关。与无排斥反应的 CMV 病例相比,CMV 前发生排斥反应的患者移植肾丢失(HR 2.89,95%CI:1.65-5.09,P<0.01)和死亡率(HR 1.82,95%CI:1.12-4.24,P=0.03)显著增加。总之,排斥是 CMV 感染的危险因素,这种关联似乎持续 1 年。先前的排斥事件增加了 CMV 患者移植肾丢失和死亡率的风险。鉴于此,在排斥反应后可能需要对 CMV 进行长期监测。需要研究确定最佳监测策略。