Methotrexate and liver fibrosis in people with psoriasis: a systematic review of observational studies

被引:78
作者
Maybury, C. M. [1 ]
Jabbar-Lopez, Z. K. [2 ]
Wong, T. [3 ]
Dhillon, A. P. [5 ]
Barker, J. N. [1 ]
Smith, C. H. [1 ,4 ]
机构
[1] Kings Coll London, Div Genet & Mol Med, St Johns Inst Dermatol, London WC2R 2LS, England
[2] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Guys & St Thomas NHS Fdn Trust, Dept Gastroenterol, London, England
[4] Guys & St Thomas NHS Fdn Trust, St Johns Inst Dermatol, London, England
[5] UCL Med Sch, Dept Cellular Pathol, London, England
关键词
NONALCOHOLIC STEATOHEPATITIS; METABOLIC SYNDROME; PSORIATICS; RISK; HEPATOTOXICITY; PREVALENCE; BIOPSIES;
D O I
10.1111/bjd.12941
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Methotrexate (MTX) is an effective treatment for psoriasis but concerns regarding the development of liver fibrosis prevent optimal use. The primary objective of this systematic review was to assess whether MTX use increases the risk of developing fibrosis in people with psoriasis. Searches were performed on Medline, Embase, the Cochrane Database and Clinical Trials Register from inception until September 2013 for studies including at least two liver biopsies in people with psoriasis. Double extraction using predefined data fields was performed. Randomized controlled trials and observational studies were considered. Statistical analysis was performed using Review Manager 5. Quality of observational studies was assessed using a study quality bias checklist. Eight observational studies met the inclusion criteria (n = 429 patients). The pooled risk difference (RD) of developing significant liver fibrosis was 0.09 [95% confidence interval (CI) -0.03 to 0.20]. The RD for developing 'any fibrosis' was 0.22 (95% CI 0.04-0.41). The RD for cirrhosis was 0.04 (95% CI 0.02-0.07). There was no clear association between cumulative dose of MTX and fibrosis. Obesity, diabetes and alcohol use were under-reported. The quality of the included studies was weak and the degree of selection bias means the results are not generalizable to all patients with psoriasis taking MTX. High-quality, population-based studies that consider potential confounders common in psoriasis population are justified for better prediction of the subset of patients at risk of liver fibrosis. In this highly selected review population, MTX use appears to contribute to the development of 'any' fibrosis without clear evidence of risk stratifiers.
引用
收藏
页码:17 / 29
页数:13
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