Risk of liver disease in patients with psoriasis, psoriatic arthritis, and rheumatoid arthritis receiving methotrexate: A population-based study

被引:35
作者
Gelfand, Joel M. [1 ,2 ]
Wan, Joy [1 ,2 ]
Zhang, He [4 ]
Shin, Daniel B. [1 ,2 ]
Ogdie, Alexis [2 ,3 ]
Syed, Maha N. [1 ]
Egeberg, Alexander [4 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Dermatol, 3400 Civ Ctr Blvd,PCAM South Tower,7th Floor, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Epidemiol & Informat, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA
[4] Univ Copenhagen, Bispebjerg Hosp, Dept Dermatol, Copenhagen, Denmark
关键词
cirrhosis; hepatotoxicity; liver disesase; methotrexate; psoriasis; psoriatic arthritis; rheumatoid arthritis; EULAR RECOMMENDATIONS; MANAGEMENT; GUIDELINES; REGISTRY;
D O I
10.1016/j.jaad.2021.02.019
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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.
引用
收藏
页码:1636 / 1643
页数:8
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