Gordon Fredric D, Goldberg David S, Goodrich Nathan P, Lok Anna S F, Verna Elizabeth C, Selzner Nazia, Stravitz R Todd, Merion Robert M
Department of Hepatobiliary Surgery and Transplantation, Lahey Hospital and Medical Center, Burlington, MA.
Division of Gastroenterology, University of Pennsylvania, Philadelphia, PA.
Liver Transpl. 2016 Sep;22(9):1214-22. doi: 10.1002/lt.24496. Epub 2016 Aug 2.
Primary sclerosing cholangitis (PSC) recurs in 15%-25% of patients transplanted for PSC. In the United States, PSC transplant patients are more likely to receive an organ from a living donor (LD) than patients without PSC. Our aims were to (1) compare risk of PSC recurrence in LD versus deceased donor recipients and (2) identify risk factors for PSC recurrence. There were 241 living donor liver transplantations (LDLTs) and 65 deceased donor liver transplantation (DDLT) patients transplanted between 1998 and 2013 enrolled in the Adult-to-Adult Living Donor Liver Transplantation Cohort Study who were evaluated. PSC recurrence risk for LDLT and DDLT recipients was compared using Kaplan-Meier survival curves and log-rank tests. Cox models were used to evaluate PSC risk factors. Overall PSC recurrence probabilities were 8.7% and 22.4% at 5 and 10 years after liver transplantation (LT), respectively. The risk of PSC recurrence was not significantly different for DDLT versus LDLT recipients (P = 0.36). For DDLT versus LDLT recipients, unadjusted 5- and 10-year PSC recurrence was 9.4% versus 9.5% and 36.9% versus 21.1%. Higher laboratory Model for End-Stage Liver Disease (MELD) score at LT, onset of a biliary complication, cholangiocarcinoma, and higher donor age were associated with increased risks of PSC recurrence: for MELD (hazard ratio [HR] = 1.06; 95% confidence interval [CI] 1.02-1.10 per MELD point, P = 0.002); for biliary complication (HR, 2.82; 95% CI, 1.28-6.25; P = 0.01); for cholangiocarcinoma (HR, 3.98; 95% CI, 1.43-11.09; P = 0.008); for donor age (per 5-years donor age; HR, 1.17; 95% CI, 1.02-1.35; P = 0.02). Factors not significantly associated with PSC recurrence included the following: first-degree relative donor (P = 0.11), post-LT cytomegalovirus infection (P = 0.38), and acute rejection (P = 0.22). Risk of recurrent PSC was not significantly different for DDLT and LDLT recipients. Biliary complications, cholangiocarcinoma, MELD, and donor age were significantly associated with risk of PSC recurrence. Liver Transplantation 22 1214-1222 2016 AASLD.
原发性硬化性胆管炎(PSC)患者接受移植后,15%-25%会复发。在美国,与非PSC患者相比,PSC移植患者更有可能接受活体供体(LD)的器官。我们的目的是:(1)比较LD供体受者和已故供体受者中PSC复发的风险;(2)确定PSC复发的风险因素。在1998年至2013年间接受评估的成人间活体供肝移植队列研究中,有241例活体供肝移植(LDLT)患者和65例已故供肝移植(DDLT)患者。使用Kaplan-Meier生存曲线和对数秩检验比较LDLT和DDLT受者的PSC复发风险。采用Cox模型评估PSC风险因素。肝移植(LT)后5年和10年,PSC总体复发概率分别为8.7%和22.4%。DDLT受者与LDLT受者的PSC复发风险无显著差异(P = 0.36)。对于DDLT与LDLT受者,未经调整的5年和10年PSC复发率分别为9.4%对9.5%和36.9%对21.1%。LT时终末期肝病模型(MELD)评分较高、出现胆道并发症、胆管癌以及供体年龄较大与PSC复发风险增加相关:对于MELD(风险比[HR]=1.06;每增加1个MELD点,95%置信区间[CI]为1.02-1.10,P = 0.002);对于胆道并发症(HR,2.82;95%CI,1.28-6.25;P = 0.01);对于胆管癌(HR,3.98;95%CI,1.43-11.09;P = 0.008);对于供体年龄(每增加5岁供体年龄;HR,1.17;95%CI,1.02-1.35;P = 0.02)。与PSC复发无显著相关的因素包括:一级亲属供体(P = 0.11)、LT后巨细胞病毒感染(P = 0.38)和急性排斥反应(P = 0.22)。DDLT和LDLT受者复发性PSC的风险无显著差异。胆道并发症、胆管癌、MELD和供体年龄与PSC复发风险显著相关。《肝移植》2016年第22卷1214 - 1222页,美国肝病研究学会。