We evaluated 61 patients (25 NASH and 36 CHC) who had undergone

liver biopsy for clinical purposes and 20 subjects without liver disease. Serum 25(OH)D3 was measured via colorimetric assay. Expression of VDR, CYP2R1, and CYP27A1 was evaluated via immunohistochemistry in hepatocytes, cholangiocytes, and liver inflammatory cells. Parenchymal and inflammatory cells from liver biopsies of patients with NASH and CHC expressed VDR, CYP2R1, and CYP27A1. In NASH patients, VDR expression on cholangiocytes was inversely correlated with steatosis severity Acalabrutinib supplier (P < 0.02), lobular inflammation (P < 0.01), and nonalcoholic fatty liver disease score (P < 0.03). Moreover, expression of CYP2R1 in hepatocytes correlated strongly with VDR positivity on liver inflammatory cells. In CHC subjects, fibrosis stage was associated with low hepatic CYP27A1 expression, whereas portal inflammation was significantly higher in patients with VDR-negative inflammatory cells (P < 0.009) and low VDR expression in hepatocytes (P < 0.03). Conclusion: VDR is widely expressed in the liver and inflammatory cells of chronic liver disease patients and its expression is negatively associated with the severity of liver histology in both NASH and CHC

patients. These data suggest that vitamin D/VDR system may play a role in the progression of metabolic and viral chronic liver damage. (HEPATOLOGY 2012;56:2180–2187) Recent studies have suggested a direct association between low serum 25-hydroxy-vitamin D3 [25(OH)D3] levels and the presence, severity, and prognosis of several liver diseases.1-7 Targher et al.1 and Manco et al.2 reported MCE公司 low serum 25(OH)D3 Apoptosis inhibitor concentrations among adults and children affected by

nonalcoholic steatohepatitis (NASH). Furthermore, we demonstrated the existence of a strong association between nonalcoholic fatty liver disease (NAFLD) and low 25(OH)D3 levels in a large adult population with normal serum liver enzymes.3 Recently, other studies have shown the presence of low serum 25(OH)D3 levels in patients affected by chronic hepatitis C (CHC) along with a failure to achieve sustained antiviral responses after standard therapy in CHC subjects with hypovitaminosis D.4-6 Vitamin D is present in the diet and dietary supplements, but its primary source is the photo-mediated conversion of 7-dehydrocholesterol in the skin.8 To become biologically active, vitamin D requires 25-hydroxylation in the liver and subsequent 1-hydroxylation in the kidney.9, 10 The 25-hydroxylation occurs exclusively in hepatocytes and is mediated by CYP27A1 and CYP2R1, two liver-expressed cytochromes characterized by different intracellular location, specificity, and affinity for vitamin D3.11, 12 Low serum 25(OH)D3 levels and hypovitaminosis D–related diseases have been shown to be associated with CYP2R1 polymorphisms by some authors,13, 14 but only one study to date has investigated liver 25-hydroxylase expression.