Extrahepatic autoimmune diseases in primary biliary cholangitis: Prevalence and significance for clinical presentation and disease outcomeUniversity of Alberta Division of Gastroenterology and Liver Unit, Edmonton AB, Canada.
Division of GI and Hepatology, Beth Israel Medical Center, Harvard Medical School, Boston MA, United States.
Department of Gastroenterology, Medical Faculty, Uludag University, Bursa, Turkey.
Division of Gastroenterology, Clinic and Polyclinic for Oncology, Hepatology, Infectious Diseases and Pneumology, University Clinic Leipzig, Leipzig, Germany.
Center for the Study and Treatment of Autoimmune Diseases of the Liver and Biliary System, University of Bologna, Bologna, Italy.
Department of Gastroenterology, Hacettepe University, Ankara, Turkey.
Center for the Study and Treatment of Autoimmune Diseases of the Liver and Biliary System, University of Bologna, Bologna, Italy.
Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Center for the Study and Treatment of Autoimmune Diseases of the Liver and Biliary System, University of Bologna, Bologna, Italy.
Department of Gastroenterology and Hepatology, Uppsala University Hospital, Uppsala, Sweden.
Department of Gastroenterology and Hepatology, Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Gastroenterology Division, Skåne University Hospital, Lund, Sweden.
Department of Hepato-Gastroenterology, CHU Reims, Reims, France.
Department of Gastroenterology, Gazi Yaşargil Education and Research Hospital, Diyarbakir, Turkey.
Division of Gastroenterology and Hepatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Department of Gastroenterology, Medical Faculty, Uludag University, Bursa, Turkey.
Division of Liver Diseases, The Mount Sinai Medical Center, New York NY, United States.
University of Alberta Division of Gastroenterology and Liver Unit, Edmonton AB, Canada.
Division of Gastroenterology, Clinic and Polyclinic for Oncology, Hepatology, Infectious Diseases and Pneumology, University Clinic Leipzig, Leipzig, Germany.
Department of Gastroenterology, Ankara City Hospital, Ankara, Turkey.
Division of Gastroenterology, University of British Columbia and Vancouver General Hospital, Vancouver BC, Canada.
Division of GI and Hepatology, Beth Israel Medical Center, Harvard Medical School, Boston MA, United States.
Department of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Epatocentro Ticino, Lugano, Switzerland.
Hepatology Division, Centre for Digestive Diseases, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
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2021 (English)In: Journal of Gastroenterology and Hepatology, ISSN 0815-9319, E-ISSN 1440-1746, Vol. 36, no 4, p. 936-942Article in journal (Refereed) Published
Abstract [en]
Background and Aim: The prevalence and clinical significance of extrahepatic autoimmune diseases (EHAIDs) have not been evaluated in a large cohort of primary biliary cholangitis (PBC).
Methods: The medical records of 1554 patients with PBC from 20 international centers were retrospectively reviewed. Development of decompensated cirrhosis (ascites, variceal bleeding, and/or hepatic encephalopathy) and hepatocellular carcinoma were considered clinical endpoints.
Results: A total of 35 different EHAIDs were diagnosed in 440 (28.3%) patients with PBC. Patients with EHAIDs were more often female (92.5% vs 86.1%, P < 0.001) and seropositive for anti-mitochondrial antibodies (88% vs 84%, P = 0.05) and antinuclear antibodies and/or smooth muscle antibodies (53.8% vs 43.6%, P = 0.005). At presentation, patients with EHAIDs had significantly lower levels of alkaline phosphatase (1.76 vs 1.98 x upper limit of normal [ULN], P = 0.006), aspartate aminotransferase (1.29 vs 1.50 x ULN, P < 0.001), and total bilirubin (0.53 vs 0.58 x ULN, P = 0.002). Patients with EHAIDs and without EHAIDs had similar rates of GLOBE high-risk status (12.3% vs 16.1%, P = 0.07) and Paris II response (71.4% vs 69.4%, P = 0.59). Overall, event-free survival was not different in patients with and without EHAIDs (90.8% vs 90.7%, P = 0.53, log rank). Coexistence of each autoimmune thyroid diseases (10.6%), Sjogren disease (8.3%), systemic sclerosis (2.9%), rheumatoid arthritis (2.7%), systemic lupus erythematosus (1.7%), celiac disease (1.7%), psoriasis (1.5%), and inflammatory bowel diseases (1.3%) did not influence the outcome.
Conclusions: Our study confirms that EHAIDs are frequently diagnosed in patients with PBC. The presence of EHAIDs may influence the clinical phenotype of PBC at presentation but has no impact on PBC outcome.
Place, publisher, year, edition, pages
John Wiley & Sons, 2021. Vol. 36, no 4, p. 936-942
Keywords [en]
Ankylosing spondylitis, Anti-phospholipid syndrome, Autoimmune hemolytic anemia, Idiopathic thrombocytopenic purpura, IgA nephropathy, Multiple sclerosis, Polyarteritis nodosa, Polymyositis, Sarcoidosis, Temporal arteritis
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-85420DOI: 10.1111/jgh.15214ISI: 000561706700001PubMedID: 32790935Scopus ID: 2-s2.0-85089706815OAI: oai:DiVA.org:oru-85420DiVA, id: diva2:1464208
2020-09-042020-09-042025-02-11Bibliographically approved