Department of Surgery, University of California San Francisco, San Francisco, CA.
Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Transplantation. 2022 Jan 1;106(1):106-116. doi: 10.1097/TP.0000000000003681.
Deceased donor and recipient predictors of posttransplant steatosis/steatohepatitis and fibrosis are not well known. Our aim was to evaluate the prevalence and assess donor and recipient predictors of steatosis, steatohepatitis, and fibrosis in liver transplantation recipients.
Using the immune tolerance network A-WISH multicenter study (NCT00135694), donor and recipient demographic and clinical features were collected. Liver biopsies were taken from the donor liver at transplant, and from recipients per protocol and for-cause (ie, abnormal transaminases and to rule out rejection) and were interpreted by a central pathologist.
One hundred eighty-three paired donor/recipients liver biopsies at the time of transplant and posttransplant follow-up (median time 582 d; average time to last biopsies was 704 d [SD ± 402 d]) were analyzed. Donor steatosis did not influence recipient steatosis or fibrosis. Ten of 183 recipients had steatohepatitis on the last biopsy. Recipient body mass index at the time of liver biopsy was the most influential factor associated with posttransplant steatosis. Both donor and recipient metabolic syndrome features were not associated with graft steatosis. Untreated hepatitis C viral (HCV) infection was the most influential factor associated with the development of allograft fibrosis.
In a large experience evaluating paired donor and recipient characteristics, recipient body mass index at the time of liver biopsy was most significantly associated with posttransplant steatosis. Untreated HCV etiology influenced graft fibrosis. Thus relative to untreated HCV, hepatic fibrosis in those with steatosis/steatohepatitis is less common though long-term follow-up is needed to determine the course of posttransplant fibrosis. Emphasis on recipient weight control is essential.
移植后脂肪变性/脂肪性肝炎和纤维化的供体和受体预测因子尚不清楚。我们的目的是评估肝移植受者脂肪变性、脂肪性肝炎和纤维化的患病率,并评估供体和受体的预测因子。
使用免疫耐受网络 A-WISH 多中心研究(NCT00135694),收集供体和受体的人口统计学和临床特征。在移植时和移植后随访期间(中位时间 582 天;最后一次活检的平均时间为 704 天[SD ± 402 天]),对 183 对供体/受体肝活检进行了分析。
分析了 183 对供体/受体肝移植时和移植后随访(中位时间 582 天;最后一次活检的平均时间为 704 天[SD ± 402 天])的肝活检。供体脂肪变性并不影响受体脂肪变性或纤维化。183 例受检者中,有 10 例在最后一次活检时发生脂肪性肝炎。肝活检时受体体重指数是与移植后脂肪变性最相关的因素。供体和受体代谢综合征特征均与移植物脂肪变性无关。未经治疗的丙型肝炎病毒(HCV)感染是与同种异体纤维化发展最相关的因素。
在评估供体和受体特征的大量经验中,肝活检时受体体重指数与移植后脂肪变性最显著相关。未经治疗的 HCV 病因影响移植物纤维化。因此,与未经治疗的 HCV 相比,脂肪变性/脂肪性肝炎患者的肝纤维化较少见,但需要长期随访来确定移植后纤维化的病程。强调受体体重控制至关重要。