Schmeltzer Paul A, Russo Mark W
Division of Hepatology Atrium Health, Wake Forest University School of Medicine, Charlotte, NC 28204, USA.
J Clin Med. 2021 Sep 28;10(19):4476. doi: 10.3390/jcm10194476.
Primary sclerosing cholangitis (PSC) is a cholestatic liver disease with a variable clinical course that can ultimately lead to end-stage liver disease, cholangiocarcinoma, and the need for liver transplantation. Several prognostic models have been developed to predict clinical outcomes and have been compared to the revised Mayo Risk Score (rMRS).
To conduct a systematic review comparing the rMRS to other non-invasive prognostic tests for PSC.
A systematic review of studies from 2000 to 2020 was performed that compared non-invasive biochemical prognostic models to the rMRS in predicting outcomes in patients with PSC.
Thirty-seven studies were identified, of which five studies that collectively included 3230 patients were reviewed. Outcomes included transplant-free survival or composite clinical outcomes. The rMRS was better than the Amsterdam-Oxford model for predicting 1-year transplant-free survival, c-statistics 0.75 and 0.70, respectively. The UK-PSC score outperformed the rMRS for 10-year transplant-free survival, c-statistics 0.85 and 0.69, respectively. An enhanced liver fibrosis score was independently associated with transplant-free survival after adjusting for rMRS. PREsTo predicts 5-year hepatic decompensation with a c-statistic modestly higher than rMRS; 0.90 and 0.85, respectively.
Newer prognostic models, including the UK-PSC score and PREsTo, are more accurate at predicting clinical endpoints in PSC compared to the rMRS. Time frames and clinical endpoints are not standard among studies.
原发性硬化性胆管炎(PSC)是一种胆汁淤积性肝病,临床病程多变,最终可导致终末期肝病、胆管癌以及肝移植需求。已经开发了几种预后模型来预测临床结局,并与修订的梅奥风险评分(rMRS)进行了比较。
进行一项系统评价,比较rMRS与其他用于PSC的非侵入性预后检测方法。
对2000年至2020年的研究进行系统评价,这些研究比较了非侵入性生化预后模型与rMRS在预测PSC患者结局方面的情况。
共识别出37项研究,其中对5项共纳入3230例患者的研究进行了综述。结局包括无移植生存或综合临床结局。在预测1年无移植生存方面,rMRS优于阿姆斯特丹-牛津模型,c统计量分别为0.75和0.70。在预测10年无移植生存方面,英国PSC评分优于rMRS,c统计量分别为0.85和0.69。在调整rMRS后,增强肝纤维化评分与无移植生存独立相关。PREsTo预测5年肝失代偿的c统计量略高于rMRS;分别为0.90和0.85。
与rMRS相比,包括英国PSC评分和PREsTo在内的新型预后模型在预测PSC临床终点方面更准确。各研究中的时间框架和临床终点并不标准。