Hilscher Moira, Enders Felicity B, Carey Elizabeth J, Lindor Keith D, Tabibian James H
Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Division of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, MN, USA.
Ann Hepatol. 2016 Mar-Apr;15(2):246-53. doi: 10.5604/16652681.1193721.
Introduction. Recent studies suggest that serum alkaline phosphatase may represent a prognostic biomarker in patients with primary sclerosing cholangitis. However, this association remains poorly understood. Therefore, the aim of this study was to investigate the prognostic significance and clinical correlates of alkaline phosphatase normalization in primary sclerosing cholangitis.
This was a retrospective cohort study of patients with a new diagnosis of primary sclerosing cholangitis made at an academic medical center. The primary endpoint was time to hepatobiliaryneoplasia, liver transplantation, or liver-related death. Secondary endpoints included occurrence of and time to alkaline phosphatase normalization. Patients who did and did not achieve normalization were compared with respect to clinical characteristics and endpoint-free survival, and the association between normalization and the primary endpoint was assessed with univariate and multivariate Cox proportional-hazards analyses.
Eighty six patients were included in the study, with a total of 755 patient-years of follow-up. Thirty-eight patients (44%) experienced alkaline phosphatase normalization within 12 months of diagnosis. Alkaline phosphatase normalization was associated with longer primary endpoint-free survival (p = 0.0032) and decreased risk of requiring liver transplantation (p = 0.033). Persistent normalization was associated with even fewer adverse endpoints as well as longer survival. In multivariate analyses, alkaline phosphatase normalization (adjusted hazard ratio 0.21, p = 0.012) and baseline bilirubin (adjusted hazard ratio 4.87, p = 0.029) were the only significant predictors of primary endpoint-free survival.
Alkaline phosphatase normalization, particularly if persistent, represents a robust biomarker of improved long-term survival and decreased risk of requiring liver transplantation in patients with primary sclerosing cholangitis.
引言。近期研究表明,血清碱性磷酸酶可能是原发性硬化性胆管炎患者的一种预后生物标志物。然而,这种关联仍未得到充分理解。因此,本研究的目的是探讨碱性磷酸酶正常化在原发性硬化性胆管炎中的预后意义及临床相关性。
这是一项对在一所学术医疗中心新诊断为原发性硬化性胆管炎患者的回顾性队列研究。主要终点是发生肝胆肿瘤、肝移植或肝相关死亡的时间。次要终点包括碱性磷酸酶正常化的发生情况及时间。对实现和未实现正常化的患者在临床特征和无终点生存期方面进行比较,并通过单因素和多因素Cox比例风险分析评估正常化与主要终点之间的关联。
86例患者纳入研究,共随访755患者年。38例患者(44%)在诊断后12个月内碱性磷酸酶实现正常化。碱性磷酸酶正常化与更长的无主要终点生存期相关(p = 0.0032),且肝移植需求风险降低(p = 0.033)。持续正常化与更少的不良终点以及更长的生存期相关。在多因素分析中,碱性磷酸酶正常化(调整后风险比0.21,p = 0.012)和基线胆红素(调整后风险比4.87,p = 0.029)是无主要终点生存期的仅有的显著预测因素。
碱性磷酸酶正常化,尤其是持续正常化,是原发性硬化性胆管炎患者长期生存改善及肝移植需求风险降低的有力生物标志物。