Fattahi Mohammad Reza, Malek-Hosseini Seyyed Ali, Sivandzadeh Gholam Reza, Safarpour Ali Reza, Bagheri Lankarani Kamran, Taghavi Ali Reza, Ejtehadi Fardad
*Department of Digestive Diseases, Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Namazi Hospital, Shiraz, Iran; †Department of Surgery, Transplant Research Center, Shiraz University of Medical Sciences, Namazi Hospital, Shiraz, Iran; ‡Department of Internal Medicine, Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Namazi Hospital, Shiraz, Iran; §Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; and ‖Department of Internal Medicine, Healthcare Policy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Inflamm Bowel Dis. 2017 Jul;23(7):1160-1167. doi: 10.1097/MIB.0000000000001105.
The natural history of ulcerative colitis (UC) after liver transplantation (LT) for primary sclerosing cholangitis (PSC) remains ill defined. This study aimed to evaluate the course of UC after LT for PSC.
The course of UC, including the clinical colitis severity index, was evaluated in patients with concomitant PSC and UC who received LT for PSC-induced end-stage liver disease. A total of 167 (55.4%) patients with PSC had concurrent inflammatory bowel disease (IBD). Of 159 cases of IBD that started before LT, 152 (95.5%) had UC and 7 (4.5%) had Crohn's disease.
The mean duration of patient follow-up after LT was 47.7 ± 33.5 months. The simple clinical colitis activity index scores after LT showed no change in 15.8% of patients, decreased in 78.3%, and increased in 5.9%. Seventy-one (46.7%) patients required no change in their specific UC treatment after LT, whereas 12 (7.9%) had to use more aggressive treatments after LT. In 69 (45.4%) patients, treatment could be tapered although not discontinued. Multiple logistic regression analysis demonstrated that the duration of LT (odds ratio = 1.02; 95% confidence interval, 1.00-1.05, P = 0.03) was significantly associated with aggravation in the clinical course of UC after LT. Posttransplant cyclosporine exposure (odds ratio = 0.14; 95% confidence interval, 0.015-0.79, P = 0.028) and pretransplant body weight (odds ratio = 0.81; 95% confidence interval, 0.71-0.93, P = 0.003) demonstrated a protective effect.
Although the clinical course of UC remains unchanged or even improves in the majority of patients after LT, some may experience an aggressive course. The type of immunosuppression after transplantation can affect UC activity after LT. Cyclosporine may have some protective effects post-LT.
肝移植(LT)治疗原发性硬化性胆管炎(PSC)后溃疡性结肠炎(UC)的自然病程仍不明确。本研究旨在评估LT治疗PSC后UC的病程。
对因PSC导致终末期肝病而接受LT的合并PSC和UC的患者,评估其UC病程,包括临床结肠炎严重程度指数。共有167例(55.4%)PSC患者合并炎症性肠病(IBD)。在LT前发病的159例IBD中,152例(95.5%)为UC,7例(4.5%)为克罗恩病。
LT后患者的平均随访时间为47.7±33.5个月。LT后简单临床结肠炎活动指数评分显示,15.8%的患者无变化,78.3%的患者下降,5.9%的患者上升。71例(46.7%)患者LT后无需改变其特定的UC治疗,而12例(7.9%)患者LT后不得不采用更积极的治疗。69例(45.4%)患者的治疗虽不能停药但可减量。多因素logistic回归分析表明,LT持续时间(比值比=1.02;95%置信区间,1.00 - 1.05,P = 0.03)与LT后UC临床病程加重显著相关。移植后环孢素暴露(比值比=0.14;95%置信区间,0.015 - 0.79,P = 0.028)和移植前体重(比值比=0.81;95%置信区间,0.71 - 0.93,P = 0.003)显示出保护作用。
虽然大多数患者LT后UC的临床病程保持不变甚至改善,但部分患者可能经历进展性病程。移植后免疫抑制类型可影响LT后UC的活动。环孢素在LT后可能具有一定保护作用。