[1] Onofrio FQ, Hirshfield GM, Gulamhusein AF. A practical review of primary biliary cholangitis for the gastroenterologist.Gastroenterol Hepatol (N Y),2019,15(3):145-154. [2] Lindor KD, Bowlus CL, Boyer J, et al. Primary biliary cholangitis: 2018 practice guidance from the american association for the study of liver diseases. Hepatology,2019,69(1):394-419. [3] Trivedi PJ, Lammers WJ, Van Buuren HR, et al. Stratification of hepatocellular carcinoma risk in primary biliary cirrhosis: a multicentre international study. Gut,2016,65(2):321-329. [4] Galoosian A, HanlonC, Zhang J, et al. Clinical updates in primary biliary cholangitis: trends, epidemiology, diagnostics, and new therapeutic approaches.J Clin Transl Hepatol,2020,8(1):49-60. [5] 徐小元,丁惠国,李文刚,等. 肝硬化诊治指南.实用肝脏病杂志,2019,22(6):770-786. [6] Boonstra K, Beuers U, Ponsioen CY. Epidemiology of primary sclerosing cholangitis and primary biliary cirrhosis:a systematic review.J Hepatol,2012,56(5):1181-1188. [7] Carey EJ, Ali AH, Lindor KD. Primary biliary cirrhosis.Lancet,2015,386(10003): 1565-1575. [8] Lleo A, Wang GQ, Gershwin ME, et al. Primary biliary cholangitis. Lancet,2020,396(10266):1915-1926. [9] Wang Z, Peng C, Wang P, et al. Serum vitamin D level is related to disease progression in primary biliary cholangitis.Scand J Gastroenterol,2020,55(11): 1333-1340. [10] Poupon R. Liver alkaline phosphatase: a missing link between choleresis and biliary inflammation.Hepatology,2015,61(6):2080-2090. [11] Leuschner M, Dietrich CF, You T, et al. Characterisation of patients with primary biliary cirrhosis responding to long term ursodeoxycholic acid treatment. Gut,2000,46(1):121-126. [12] Corpechot C, Abenavoli L, Rabahi N, et al. Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis. Hepatology,2008,48(3):871-877. [13] Lammers WJ, Van Buuren HR, Hirschfield GM, et al. Levels of alkaline phosphatase and bilirubin are surrogate end points of outcomes of patients with primary biliary cirrhosis: an international follow-up study. Gastroenterology,2014,147(6):1338-1349,e5; quiz e15. [14] Kamath PS, Wiesner RH, Malinchoc M, et al. A model to predict survival in patients with end-stage liver disease.Hepatology,2001,33(2):464-470. [15] Selmi C, Bowlus CL, Gershwin ME, et al. Primary biliary cirrhosis. Lancet,2011,377(9777):1600-1609. [16] Beck M, Hurt E. The nuclear pore complex: understanding its function through structural insight.Nat Rev Mol Cell Biol,2017,18(2):73-89. [17] Nakamura M. Clinical significance of autoantibodies in primary biliary cirrhosis. Semin Liver Dis,2014,34(3):334-340. [18] Huang C, Han W, Wang C, et al. Early prognostic utility of gp210 antibody-positive rate in primary biliary cholangitis: a meta-analysis.Dis Markers,2019,2019:9121207. [19] You Z, Wang Q, Bian Z, et al. The immunopathology of liver granulomas in primary biliary cirrhosis.J Autoimmun,2012,39(3):216-221. [20] Takano K, Saeki C, Oikawa T, et al. IgM response is a prognostic biomarker of primary biliary cholangitis treated with ursodeoxycholic acid and bezafibrate.J Gastroenterol Hepatol,2020,35(4):663-672. [21] Garred P, Tenner AJ, Mollnes TE. Therapeutic targeting of the complement system: from rare diseases to pandemics.Pharmacol Rev,2021,73(2):792-827. [22] Gialeli C, Gungor B, Blom AM. Novel potential inhibitors of complement system and their roles in complement regulation and beyond.Mol Immunol,2018,102:73-83. |