AASLD AGA clinical Practice Guideline on management of primary biliary cholangitis

Background & Aims: Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease associated with progressive fibrosis, cirrhosis, liver transplantation, and premature mortality. Despite effective therapies, important challenges remain in the diagnosis and management of PBC, including identification of antimitochondrial antibody–negative disease, assessment of response to ursodeoxycholic acid (UDCA), risk stratification, treatment of patients with inadequate response, management of cholestatic pruritus, and prevention of recurrent disease after liver transplantation. The aim of this guideline was to develop evidence-based recommendations addressing these key areas of clinical care. Methods: The American Gastroenterological Association (AGA) and the American Association for the Study of Liver Diseases (AASLD) convened a multidisciplinary panel to develop clinical practice recommendations for adults with PBC. Systematic reviews were performed for 6 prioritized clinical questions. The Grading of Recommendations Assessment, Development and Evaluation framework was used to prioritize clinical outcomes and assess evidence, and its Evidence to Decision Framework was used to develop recommendations. Results: The guideline panel agreed on 6 recommendations. These recommendations address the use of PBC-specific antinuclear antibodies in antimitochondrial antibody–negative suspected PBC, UDCA as first-line therapy, liver stiffness measurement for prognostication, peroxisome proliferator–activated receptor agonists for patients with inadequate response or intolerance to UDCA, linerixibat for moderate to severe pruritus, and UDCA prophylaxis post-transplantation to reduce disease recurrence. The certainty of evidence ranged from moderate to very low. Conclusions: The guideline emphasizes early diagnosis, optimization of first-line therapy, risk-based treatment escalation, symptom management, and prevention of post-transplantation disease recurrence to improve patient outcomes and quality of life.

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Publication Details

Journal
Hepatology
Published
2026-10-22
DOI
https://doi.org/10.1097/hep.0000000000001875
Primary Topic
Liver Diseases and Immunity
Type
article
Field-Weighted Citation Impact
0.00
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article

AASLD AGA clinical Practice Guideline on management of primary biliary cholangitis

Elizabeth J. Carey, Perica Davitkov, Marlyn J. Mayo, David N. Assis et al.
Hepatology
Liver Diseases and Immunity
article

AASLD AGA clinical Practice Guideline on management of primary biliary cholangitis

Elizabeth J. Carey, Perica Davitkov, Marlyn J. Mayo, David N. Assis, Tamar Hamosh Taddei, Shahnaz Sultan, Mai Sedki, Aparna Goel, Therese Bittermann, Vincent Lingzhi Chen, Cynthia Levy
article en

Abstract

Background & Aims: Primary biliary cholangitis (PBC) is a chronic cholestatic liver disease associated with progressive fibrosis, cirrhosis, liver transplantation, and premature mortality. Despite effective therapies, important challenges remain in the diagnosis and management of PBC, including identification of antimitochondrial antibody–negative disease, assessment of response to ursodeoxycholic acid (UDCA), risk stratification, treatment of patients with inadequate response, management of cholestatic pruritus, and prevention of recurrent disease after liver transplantation. The aim of this guideline was to develop evidence-based recommendations addressing these key areas of clinical care. Methods: The American Gastroenterological Association (AGA) and the American Association for the Study of Liver Diseases (AASLD) convened a multidisciplinary panel to develop clinical practice recommendations for adults with PBC. Systematic reviews were performed for 6 prioritized clinical questions. The Grading of Recommendations Assessment, Development and Evaluation framework was used to prioritize clinical outcomes and assess evidence, and its Evidence to Decision Framework was used to develop recommendations. Results: The guideline panel agreed on 6 recommendations. These recommendations address the use of PBC-specific antinuclear antibodies in antimitochondrial antibody–negative suspected PBC, UDCA as first-line therapy, liver stiffness measurement for prognostication, peroxisome proliferator–activated receptor agonists for patients with inadequate response or intolerance to UDCA, linerixibat for moderate to severe pruritus, and UDCA prophylaxis post-transplantation to reduce disease recurrence. The certainty of evidence ranged from moderate to very low. Conclusions: The guideline emphasizes early diagnosis, optimization of first-line therapy, risk-based treatment escalation, symptom management, and prevention of post-transplantation disease recurrence to improve patient outcomes and quality of life.

Hepatology
University of Minnesota (US), University of Miami (US), University of California, San Francisco (US), QIMR Berghofer Medical Research Institute (AU), University of Michigan (US), Royal Brisbane and Women's Hospital (AU), Veterans Health Administration (US), Yale University (US), VA Connecticut Healthcare System (US), Northern California Research (US), Michigan Medicine (US), Minneapolis VA Health Care System (US), Mayo Clinic in Arizona (US), VA Northeast Ohio Healthcare System (US), VA Northern California Health Care System (US), Case Western Reserve University (US), The University of Texas Southwestern Medical Center (US), Stanford University (US)
Openalex Percentile: Top 14%
Liver Diseases and Immunity
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