Donor age (≥45 years) and reduced immunosuppression are associated with the recurrent primary sclerosing cholangitis after liver transplantation - a multicenter retrospective study

被引:5
作者
Akamatsu, Nobuhisa [1 ]
Hasegawa, Kiyoshi [1 ]
Egawa, Hiroto [2 ]
Ohdan, Hideki [3 ]
Yoshizawa, Atsushi [4 ]
Kokudo, Norihiro [5 ]
Tazuma, Susumu [6 ]
Tanaka, Atsushi [7 ]
Takikawa, Hajime [7 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Surg, Artificial Organ & Transplantat Div, Tokyo, Japan
[2] Tokyo Womens Med Univ, Inst Gastroenterol, Dept Surg, Tokyo, Japan
[3] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Gastroenterol & Transplant Surg, Appl Life Sci, Hiroshima, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Surg, Div Hepatobiliary Pancreat & Transplant Surg, Kyoto, Japan
[5] Natl Ctr Global Hlth & Med, Dept Surg, Tokyo, Japan
[6] Hiroshima Univ Hosp, Grad Sch Biomed & Hlth Sci, Dept Gen Internal Med, Hiroshima, Japan
[7] Teikyo Univ, Dept Med, Sch Med, Tokyo, Japan
关键词
disease recurrence; living donor liver transplantation; primary sclerosing cholangitis; risk factor;
D O I
10.1111/tri.13852
中图分类号
R61 [外科手术学];
学科分类号
摘要
The present study investigated the possible risk factors, including relationship/HLA matching between donor and recipient, and immunosuppressive therapies on the recurrence of primary sclerosing cholangitis (PSC) after liver transplantation (LT). Subjects were 197 recipients of LT for PSC, among whom 180 surviving more than 1 year after LT were further analyzed for risk factors of recurrence. The 5- and 10-year patient- and graft survival rates were 83% and 68%, and 71% and 62%, respectively. The overall PSC recurrence rate was 25% with a 5- and 10-year graft survival rate of 34% and 18%, which was significantly lower than the survival rate of those without recurrence (P < 0.001). Univariate analysis identified the following as risk factors for recurrence: donor age (P < 0.001), cyclosporine use (P = 0.012), mono or no immunosuppressive agent (P < 0.001), postoperative biliary complication (P < 0.001), and active intestinal bowel disease after LT (P < 0.001). Among these factors, donor age >= 45 years [hazard ratio (HR), 1.65; 95% confidence interval (CI), 1.21-2.69; P = 0.003] and mono or no immunosuppressive agent 1-year after LT (HR, 2.38; 95% CI, 1.23-3.45; P = 0.011) were identified as independent risk factors in the final multivariate Cox regression model. The results were similar in sub-analysis for ABO-identical/compatible adult living donor LT cases.
引用
收藏
页码:916 / 929
页数:14
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