Risk of liver disease in patients with psoriasis, psoriatic arthritis, and rheumatoid arthritis receiving methotrexate: A population-based study
- PMID: 33607181
- DOI: 10.1016/j.jaad.2021.02.019
Risk of liver disease in patients with psoriasis, psoriatic arthritis, and rheumatoid arthritis receiving methotrexate: A population-based study
Erratum in
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Correction.J Am Acad Dermatol. 2023 Nov;89(5):1089. doi: 10.1016/j.jaad.2023.07.1001. Epub 2023 Jul 20. J Am Acad Dermatol. 2023. PMID: 37486285 No abstract available.
Abstract
Background: Patients with psoriatic disease may be more susceptible to methotrexate hepatotoxicity than those with rheumatoid arthritis (RA); however, direct evidence supporting this notion is lacking.
Objective: To compare liver disease risk among patients with psoriasis (PsO), psoriatic arthritis (PsA), or RA receiving methotrexate.
Methods: In a population-based cohort study, Danish individuals with PsO, PsA, or RA receiving methotrexate between 1997 and 2015 were compared according to 4 disease outcomes: mild liver disease, moderate-to-severe liver disease, cirrhosis, and cirrhosis-related hospitalization.
Results: Among 5687, 6520, and 28,030 patients with PsO, PsA, and RA, respectively, the incidence rate of any liver disease was greatest for PsO, followed by PsA, and lowest for RA. Compared with patients with RA, patients with PsO were 1.6-3.4 times more likely to develop at least one of the liver disease outcomes, whereas those with PsA were 1.3-1.6 times more likely to develop mild liver disease and cirrhosis after adjusting for demographics, smoking, alcohol use, comorbidities, and methotrexate dose.
Limitations: Confounding due to unmeasured variables, misclassification, and surveillance bias.
Conclusion: PsO, PsA, and RA differentially influence liver disease risk in the setting of methotrexate use independent of other major risk factors. More conservative monitoring should be considered in patients receiving methotrexate for psoriatic disease, particularly in PsO patients.
Keywords: cirrhosis; hepatotoxicity; liver disesase; methotrexate; psoriasis; psoriatic arthritis; rheumatoid arthritis.
Copyright © 2021 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflict of interest Dr Gelfand has served as a consultant for Abcentra, BMS, Boehringer Ingelheim, Cara (DSMB), GSK, Lilly (DMC), Janssen Biologics, Novartis Corp, UCB (DSMB), Neuroderm (DSMB), Dr. Reddy's Labs, Pfizer Inc., and Sun Pharma, receiving honoraria; received research grants (to the Trustees of the University of Pennsylvania) from AbbVie, Boehringer Ingelheim, Janssen, Novartis Corp, Celgene, Ortho Dermatologics, and Pfizer Inc.; received payment for continuing medical education work related to psoriasis that was supported indirectly by Lilly, Ortho Dermatologics, and Novartis; is co-patent holder of resiquimod for treatment of cutaneous T cell lymphoma; serves as a deputy editor for the Journal of Investigative Dermatology, receiving honoraria from the Society for Investigative Dermatology; and is a member of the Board of Directors of the International Psoriasis Council, receiving no honoraria. Dr Wan has received a research grant and fellowship support (to the Trustees of the University of Pennsylvania) from Pfizer Inc. Dr Ogdie has served as a consultant for AbbVie, Amgen, BMS, Celgene, Corrona, Global Health Living Foundation, Janssen, Lilly, Novartis, Pfizer, and Takeda; received grants to the University of Pennsylvania from Pfizer and Novartis and to Forward from Amgen. Dr Syed has received fellowship support (to the Trustees of the University of Pennsylvania) from Pfizer Inc. Dr Egeberg has received research funding from Pfizer, Eli Lilly, Novartis, AbbVie, Janssen Pharmaceuticals, the Danish National Psoriasis Foundation, the Simon Spies Foundation, and the Kgl Hofbundtmager Aage Bang Foundation, and honoraria as consultant and/or speaker from AbbVie, Almirall, Leo Pharma, Samsung Bioepis Co., Ltd., Pfizer, Eli Lilly and Company, Novartis, Galderma, Dermavant, UCB, Mylan, Bristol-Myers Squibb, and Janssen Pharmaceuticals. Drs Zhang and Shin declare no conflicts of interest.
Comment in
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Methotrexate use and liver outcomes in psoriasis and rheumatoid arthritis patients: A commentary on "Risk of liver disease in patients with psoriasis, psoriatic arthritis and rheumatoid arthritis receiving methotrexate: A population-based study".J Am Acad Dermatol. 2021 Dec;85(6):e399-e400. doi: 10.1016/j.jaad.2021.07.069. Epub 2021 Aug 14. J Am Acad Dermatol. 2021. PMID: 34403710 No abstract available.
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Response to: "Methotrexate Use and Liver Outcomes in Psoriasis and Rheumatoid Arthritis Patients: A Commentary on 'Risk of liver disease in patients with psoriasis, psoriatic arthritis and rheumatoid arthritis receiving methotrexate: A population-based study'".J Am Acad Dermatol. 2021 Dec;85(6):e401. doi: 10.1016/j.jaad.2021.07.068. Epub 2021 Aug 14. J Am Acad Dermatol. 2021. PMID: 34403717 No abstract available.
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