The role of transient elastography and novel serum biomarkers in assessment of liver fibrosis in patients with psoriasis and rheumatic disease

Abstract

AbstractBackgroundMethotrexate (MTX) and leflunomide are commonly used among patients with psoriasis and rheumatoid arthritis (RA) and are implicated in hepatotoxicity. We aimed to determine the prevalence of significant liver fibrosis and its risk factors in patients with psoriasis and RA. We also explored the role of novel serum biomarkers to identify significant liver fibrosis in these patients.MethodsA total of 318 patients attending dermatology-rheumatology clinics in Queen Mary Hospital, with clinical diagnosis of psoriasis or RA were recruited from August 2020 to July 2022. Liver fibrosis was assessed by transient elastography (TE) and serum biomarkers for liver fibrosis, namely autotaxin and matrix metalloproteinase (MMP), were measured. Risk factors associated with significant liver fibrosis (defined as liver stiffness [LS] ≥7.1kPa) were analyzed by multivariate regression models.ResultsA total of 67 (21.1%) patients with psoriasis or RA had significant liver fibrosis. Body mass index (OR 1.14, 95%CI 1.04-1.24), diabetes mellitus (OR 1.93, 95%CI 1.25-2.98) and PASI (OR 1.13, 95%CI 1.05-1.27), but not cumulative dosage (CD) of MTX or leflunomide, were independently associated with significant liver fibrosis (all p<0.01). Serum MMP 3,8,9 and autotaxin levels were significantly higher among patients with advanced liver fibrosis (LS≥14 kPa). Serum autotaxin showed modest correlation with LS (r=0.31, p=0.026) and CD of MTX (r=0.30, p<0.001).ConclusionSignificant liver fibrosis in patients with psoriasis and RA is related to the underlying metabolic risk factors and independent of MTX and leflunomide CD. Minimising hepatic risks by tight control of metabolic risk factors should be considered.