Yu Haitian, Lv Tingting, Li Shuxiang, Chen Sha, Li Min, Liu Jimin, Duan Weijia, Jia Jidong, Zhao Xinyan
Department of Liver Research Center, Beijing Friendship Hospital, Capital Medical University; National Clinical Research Center for Digestive Diseases, Beijing, China.
Department of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Am J Surg Pathol. 2025 Mar 1;49(3):265-272. doi: 10.1097/PAS.0000000000002343. Epub 2024 Dec 20.
Primary biliary cholangitis (PBC) with early cholestasis and extensive bile duct loss but no significant fibrosis or cirrhosis is rare and underrecognized. We aimed to clarify the clinicopathology features and prognosis of these variants of patients with early-stage PBC with ductopenia. From January 2009 to January 2023, we retrospectively collected the laboratory and pathologic data of patients with early-stage PBC and recorded their liver-related events with a median follow-up of 4.5 years. Finally, a total of 141 patients with PBC in the early stage were included and divided into 2 groups: one with ductopenia (n = 36) and the other without ductopenia (n = 105). The median age of the participants was 50 years, with 90.8% being female. The ductopenia group exhibited significantly elevated alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma-glutamyl transpeptidase, total bilirubin, total bile acid, and total cholesterol (CHOL). Conversely, they showed a reduced biochemical response to ursodeoxycholic acid according to the Paris II, Barcelona, and Rotterdam criteria. A relatively poorer prognosis was observed in patients with early-stage PBC with ductopenia but with no statistical difference (11.8% vs 4.9%, P = 0.352). Baseline total CHOL levels were identified as an independent factor for the presence of ductopenia in early-stage PBC (odds ratio = 1.771, 95% CI: 1.264-2.479, P = 0.001). In conclusion, ductopenia was a significant risk factor for worse biochemical profiles and poor treatment response in patients with early-stage PBC. High levels of total CHOL at baseline are associated with the presence of ductopenia in early-stage PBC.
原发性胆汁性胆管炎(PBC)伴有早期胆汁淤积和广泛胆管丢失但无明显纤维化或肝硬化的情况罕见且未得到充分认识。我们旨在阐明这些早期PBC伴胆管减少患者的临床病理特征及预后。2009年1月至2023年1月,我们回顾性收集了早期PBC患者的实验室和病理数据,并记录其肝脏相关事件,中位随访时间为4.5年。最终,共纳入141例早期PBC患者,分为两组:一组有胆管减少(n = 36),另一组无胆管减少(n = 105)。参与者的中位年龄为50岁,女性占90.8%。胆管减少组的丙氨酸氨基转移酶、天冬氨酸氨基转移酶、碱性磷酸酶、γ-谷氨酰转肽酶、总胆红素、总胆汁酸和总胆固醇(CHOL)显著升高。相反,根据巴黎II、巴塞罗那和鹿特丹标准,他们对熊去氧胆酸的生化反应降低。早期PBC伴胆管减少的患者预后相对较差,但无统计学差异(11.8%对4.9%,P = 0.352)。基线总CHOL水平被确定为早期PBC中存在胆管减少的独立因素(比值比 = 1.771,95%CI:1.264 - 2.4