Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases

Lindor, Keith D., Bowlus, Christopher L., Boyer, James, Levy, Cynthia, Mayo, Marlyn·2019·Hepatology

Cited by (924)

Items 101–200 of 924

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    Alena Laschtowitz, Rozanne C. de Veer, Adriaan J Van der Meer, Christoph Schramm · 2020 · United European Gastroenterology Journal
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  3. Obeticholic acid in primary biliary cholangitis
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  4. Open‐label, clinical trial extension: Two‐year safety and efficacy results of seladelpar in patients with primary biliary cholangitis
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  7. Management of Primary Biliary Cholangitis: Current Treatment and Future Perspectives
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  8. Single cell sequencing analysis identifies genetics-modulated ORMDL3+ cholangiocytes having higher metabolic effects on primary biliary cholangitis
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  10. Bezafibrate therapy in primary biliary cholangitis refractory to ursodeoxycholic acid: a longitudinal study of paired liver biopsies at 5 years of follow up
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  11. Primary biliary cholangitis: Personalizing second-line therapies
    Cynthia Levy, Christopher L. Bowlus · 2024 · Hepatology
  12. Understanding fatigue in primary biliary cholangitis: From pathophysiology to treatment perspectives
    Erica Nicola Lynch, Claudia Campani, Tommaso Innocenti, Gabriele Dragoni, Maria Rosa Biagini, Paolo Forte, Andrea Galli · 2022 · World Journal of Hepatology
  13. Emperipolesis mediated by CD8 + T cells correlates with biliary epithelia cell injury in primary biliary cholangitis
    Suxian Zhao, Wen‐cong Li, Na Fu, Guangde Zhou, Shu‐hong Liu, Lina Jiang, Yuguo Zhang, Rongqi Wang, Yuemin Nan, Jingmin Zhao · 2019 · Journal of Cellular and Molecular Medicine
  14. Treatment response to ursodeoxycholic acid in primary biliary cholangitis: A systematic review and meta-analysis.
    J. Gazda, Sylvia Dražilová, Matej Gazda, M. Janíčko, Tomas Koky, Marian Macej, M. Carbone, P. Jarčuška · 2022 · Digestive and Liver Disease
  15. Safety and tolerability of obeticholic acid in chronic liver disease: a pooled analysis of 1878 individuals
    Cheng Han Ng, Ansel Shao Pin Tang, Jieling Xiao, Zhen Yu Wong, Jie Ning Yong, Clarissa Elysia Fu, Rebecca Wenling Zeng, Caitlyn Tan, Gabriel Hong Zhe Wong, Margaret Li Peng Teng et al. · 2023 · Hepatology Communications
  16. High‐Resolution Exposomics and Metabolomics Reveals Specific Associations in Cholestatic Liver Diseases
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  17. Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study
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  18. The Role of Vitamin K in Cholestatic Liver Disease
    Halima Sultana, Michio Komai, Hitoshi Shirakawa · 2021 · Nutrients
  19. Additional fibrate treatment in UDCA‐refractory PBC patients
    Sung Won Chung, Jeong‐Hoon Lee, Minseok Albert Kim, Galam Leem, Sun Woong Kim, Young Woon Chang, Hyo Young Lee, Jun Sik Yoon, Jun Yong Park, Yun Bin Lee et al. · 2019 · Liver International
  20. Early Prognostic Utility of Gp210 Antibody-Positive Rate in Primary Biliary Cholangitis: A Meta-Analysis
    Huang, Chunyang, Han, Weijia, Wang, Chuanmin, Liu, Yanmin, Chen, Yue, Duan, Zhongping · 2019 · Disease Markers
  21. Application of the Latest Advances in Evidence-Based Medicine in Primary Biliary Cholangitis
    K. Kowdley, C. Bowlus, C. Levy, M. Mayo, D. Pratt, R. Vuppalanchi, Z. Younossi · 2022 · American Journal of Gastroenterology
  22. New Therapies on the Horizon for Primary Biliary Cholangitis
    Atsushi Tanaka · 2023 · Drugs
  23. Linerixibat in patients with primary biliary cholangitis and cholestatic pruritus (GLISTEN): a randomised, multicentre, double-blind, placebo-controlled, phase 3 trial
    Hirschfield, Gideon M, Bowlus, Christopher L, Jones, David E J, Kremer, Andreas E, Mayo, Marlyn J, Tanaka, Atsushi, Andreone, Pietro, Jia, Jidong, Jin, Qinglong, Macías-Rodríguez, Ricardo U et al. · 2026 · The Lancet Gastroenterology & Hepatology
  24. Increased p16INK4a-expressing senescent bile ductular cells are associated with inadequate response to ursodeoxycholic acid in primary biliary cholangitis
    Motoko Sasaki, Yasunori Sato, Yasuni Nakanuma · 2019 · Journal of Autoimmunity
  25. Nutrition as Therapy in Liver Disease.
    N. Shah, A. Barritt · 2022 · Clinical Therapeutics
  26. Evaluation of potential hepatic recompensation criteria in patients with PBC and decompensated cirrhosis
    Benedikt Hofer, Lukas Burghart, Emina Halilbasic, Benedikt Simbrunner, Oleksandr Petrenko, Mattias Mandorfer, Albert Friedrich Stättermayer, Michael A Trauner, Thomas Reiberger · 2024 · Alimentary Pharmacology & Therapeutics
  27. Cholestatic Pruritus Treatments in Primary Biliary Cholangitis and Primary Sclerosing Cholangitis: A Systematic Literature Review
    Helen T. Smith, Andréa Ribeiro de Souza, April H. Thompson, Megan McLaughlin, John J. Dever, Julie A. Myers, Jing Voon Chen · 2023 · Digestive Diseases and Sciences
  28. New treatments/targets for primary biliary cholangitis
    Christophe Corpechot, Raoul Y. Poupon, Olivier Chazouillères · 2019 · JHEP Reports
  29. The fecal microbiota of patients with primary biliary cholangitis (PBC) causes PBC-like liver lesions in mice and exacerbates liver damage in a mouse model of PBC
    Huiyong Jiang, Ying Yu, Xiaoxiang Hu, Bingbing Du, Yini Shao, Feiyu Wang, Lifeng Chen, Ren Yan, Lanjuan Li, Longxian Lv · 2024 · Gut Microbes
  30. Recent progress on the application of compound formulas of traditional Chinese medicine in clinical trials and basic research in vivo for chronic liver disease
    Feipeng Xu, Hua Zhang, Jiamei Chen, Junyi Zhan, Ping Liu, Wei Liu, Shenglan Qi, Yongping Mu · 2023 · Journal of Ethnopharmacology
  31. Pharmacokinetics and pharmacodynamics of HTD1801 (berberine ursodeoxycholate, BUDCA) in patients with hyperlipidemia
    Adrian M. Di Bisceglie, Gerald Francis Watts, Philip T. Lavin, Meng Yu, Ru Bai, Liping Liu · 2020 · Lipids in Health and Disease
  32. Therapeutic mechanisms and beneficial effects of non-antidiabetic drugs in chronic liver diseases
    Han Ah Lee, Young Woon Chang, Pil Soo Sung, Eileen Laureal Yoon, Hye Won Lee, Jeong‐Ju Yoo, Young‐Sun Lee, Jihyun An, Do Seon Song, Young Youn Cho et al. · 2022 · Clinical and Molecular Hepatology
  33. The Management of Cholestatic Liver Diseases: Current Therapies and Emerging New Possibilities
    Marta Mazzetti, Giulia Marconi, Martina Mancinelli, A. Benedetti, Marco Marzioni, Luca Maroni · 2021 · Journal of Clinical Medicine
  34. Emerging therapies for PBC
    David M. H. Chascsa, Keith D. Lindor · 2020 · Journal of Gastroenterology
  35. Osteoporosis in Primary Biliary Cholangitis: Prevalence, Impact and Management Challenges
    Hirsh D. Trivedi, Christopher J. Danford, Daniela Goyes, Alan Bonder · 2020 · Clinical and Experimental Gastroenterology
  36. Exploring Advanced Therapies for Primary Biliary Cholangitis: Insights from the Gut Microbiota–Bile Acid–Immunity Network
    Ziqi Guo, Kun He, Ke Pang, Daiyu Yang, Chengzhen Lyu, Haifeng Xu, Dong Wu · 2024 · International Journal of Molecular Sciences
  37. Role of ductular reaction and ductular–canalicular junctions in identifying severe primary biliary cholangitis
    Diletta Overi, Guido Carpino, Laura Cristoferi, Paolo Onori, Lindsey Leann Kennedy, Heather Francis, Nicola Zucchini, Cristina Rigamonti, Mauro Viganò, Annarosa Floreani et al. · 2022 · JHEP Reports
  38. Belimumab treatment in autoimmune hepatitis and primary biliary cholangitis – a case series
    Mirjam Kolev, Adela-Cristina Sarbu, Burkhard Möller, Britta Maurer, Florian Kollert, Nasser Semmo · 2023 · Journal of Translational Autoimmunity
  39. Guidelines on the Diagnosis and Management of Primary Biliary Cholangitis (2021)
    Hong You, Weijia Duan, Shuxiang Li, Tingting Lv, Sha Chen, Lungen Lu, Xiong Ma, Ying Han, Yuemin Nan, Xiaoyuan Xu et al. · 2023 · Journal of Clinical and Translational Hepatology
  40. Muscle pathological features and extra-muscle involvement in idiopathic inflammatory myopathies with anti-mitochondrial antibody
    Lu Zhang, Hanbo Yang, Jieping Lei · 2021 · Seminars in Arthritis and Rheumatism
  41. Genetic predisposition of the gastrointestinal microbiome and primary biliary cholangitis: a bi-directional, two-sample Mendelian randomization analysis
    Xin Luo, Xin You · 2023 · Frontiers in Endocrinology
  42. Treatment in primary biliary cholangitis: Beyond ursodeoxycholic acid
    Maria C. van Hooff, E. Werner, A.J. van der Meer · 2024 · European Journal of Internal Medicine
  43. Managing cognitive symptoms and fatigue in cholestatic liver disease
    Naw April Phaw, Jessica Leighton, Jessica Katharine Dyson, David E. Jones · 2020 · Expert Review of Gastroenterology & Hepatology
  44. Liver transplant‐free survival according to alkaline phosphatase and GLOBE score in patients with primary biliary cholangitis treated with ursodeoxycholic acid
    Rozanne C. de Veer, Maren H. Harms, Christophe Corpechot, Douglas Thorburn, Pietro Invernizzi, Harry L.A. Janssen, Pier Maria Battezzati, Frederik Nevens, Keith D. Lindor, Annarosa Floreani et al. · 2022 · Alimentary Pharmacology & Therapeutics
  45. Single-cell mass cytometry on peripheral blood identifies immune cell subsets associated with primary biliary cholangitis
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  46. Primary biliary cholangitis: treatment
    Nora Cazzagon, Annarosa Floreani · 2021 · Current Opinion in Gastroenterology
  47. Is liver biopsy still useful in the era of non-invasive tests?
    Tae Seop Lim, Ja Kyung Kim · 2020 · Clinical and Molecular Hepatology
  48. Practical strategies for pruritus management in the obeticholic acid-treated patient with PBC: proceedings from the 2018 expert panel
    Jennifer Pate, Juilo A Gutierrez, Catherine T Frenette, Aparna Goel, Sonal Rajesh Kumar, Richard A. Manch, Edward Mena, Paul J. Pockros, Sanjaya Kumar Satapathy, Kidist K. Yimam et al. · 2019 · BMJ Open Gastroenterology
  49. Meta-analysis of antinuclear antibodies in the diagnosis of antimitochondrial antibody-negative primary biliary cholangitis
    Zhang, Qian, Liu, Zhiqiang, Wu, Shanshan, Duan, Weijia, Chen, Sha, Ou, Xiaojuan, You, Hong, Kong, Yuanyuan, Jia, Jidong · 2019 · Gastroenterology Research and Practice
  50. Hepatocellular Carcinoma in Primary Biliary Cholangitis
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  51. Cholestatic Itch: Our Current Understanding of Pathophysiology and Treatments
    Ashley Vander Does, Cynthia Levy, Gil Yosipovitch · 2022 · American Journal of Clinical Dermatology
  52. The role of peroxisome proliferator‐activated receptors in the regulation of bile acid metabolism
    Yuqing Sun, Luyong Zhang, Zhenzhou Jiang · 2023 · Basic & Clinical Pharmacology & Toxicology
  53. Adjunct Fenofibrate Up‐regulates Bile Acid Glucuronidation and Improves Treatment Response For Patients With Cholestasis
    Gallucci, Gina M., Trottier, Jocelyn, Hemme, Christopher, Assis, David N., Boyer, James L., Barbier, Olivier, Ghonem, Nisanne S. · 2021 · Hepatology Communications
  54. Primary Biliary Cholangitis and Primary Sclerosing Cholangitis Therapy Landscape
    Sheena R. Bhushan, Aalam Sohal, Kris V. Kowdley · 2024 · The American Journal of Gastroenterology
  55. Prediction and evaluation of high-risk patients with primary biliary cholangitis receiving ursodeoxycholic acid therapy: an early criterion
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  56. A Multicenter, Open-Label, Single-Arm Study to Evaluate the Efficacy and Safety of Saroglitazar in Patients With Primary Biliary Cholangitis
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  57. Protective effect of ursodeoxycholic acid on COVID-19 in patients with chronic liver disease
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  58. Vitamin D Is Associated with Clinical Outcomes in Patients with Primary Biliary Cholangitis
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  59. Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis
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  61. Ursodeoxycholic Acid Treatment Preferentially Improves Overall Survival Among African Americans With Primary Biliary Cholangitis
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  63. Current Landscape and Evolving Therapies for Primary Biliary Cholangitis
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  68. The Emerging Role of Mitochondrial Dysfunction in the Pathogenesis of Idiopathic Inflammatory Myopathies
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  72. Concentration of Serum Matrix Metalloproteinase-3 in Patients With Primary Biliary Cholangitis
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  73. Pruritus in primary biliary cholangitis is under-recorded in patient medical records
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  78. Ubiquitin-Like Post-Translational Modifications (Ubl-PTMs): Small Peptides with Huge Impact in Liver Fibrosis
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  79. Liver Transplantation for Primary Biliary Cholangitis
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  80. Efficacy and Safety of Bezafibrate Alone or in Combination with Ursodeoxycholic Acid in Primary Biliary Cholangitis: Systematic Review and Meta-Analysis
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  81. Global Epidemiology of Primary Biliary Cholangitis: An Updated Systematic Review and Meta-Analysis
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  82. Widespread gaps in the quality of care for primary biliary cholangitis in UK
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  83. Integrated GWAS and mRNA Microarray Analysis Identified IFNG and CD40L as the Central Upstream Regulators in Primary Biliary Cholangitis
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  84. Shear wave-based sound touch elastography in liver fibrosis assessment for patients with autoimmune liver diseases
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  85. Diagnostic value of anti-mitochondrial antibody in patients with primary biliary cholangitis: A systemic review and meta-analysis
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  86. Multiple therapeutic targets in rare cholestatic liver diseases: Time to redefine treatment strategies
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  88. Reduction and stabilization of bilirubin with obeticholic acid treatment in patients with primary biliary cholangitis
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  89. The future risk of primary biliary cholangitis (PBC) is low among patients with incidental anti‐mitochondrial antibodies but without baseline PBC
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  90. Hypercholesterolemia Is Associated With Dysregulation of Lipid Metabolism and Poor Prognosis in Primary Biliary Cholangitis
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  91. Seladelpar: First Approval
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  92. Efficacy of ursodeoxycholic acid combined with prednisolone and immunosuppressant triple therapy in the treatment of refractory primary biliary cholangitis
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  93. The evolving role of liver biopsy: Current applications and future prospects
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  94. Ursodeoxycholic acid impairs liver‐infiltrating T‐cell chemotaxis through IFN‐γ and CX3CL1 production in primary biliary cholangitis
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  95. We Are Not Immune: Racial and Ethnic Disparities in Autoimmune Liver Diseases
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  96. Emerging novel treatments for autoimmune liver diseases
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  98. Ursodeoxycholic Acid Treatment–Induced GLOBE Score Changes Are Associated With Liver Transplantation-Free Survival in Patients With Primary Biliary Cholangitis
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  99. Use of Butorphanol as Treatment for Cholestatic Itch
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  100. Ethnicity, disease severity, and survival in Canadian patients with primary biliary cholangitis
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