Abstract

Vitamin D deficiency is common in advanced liver disease but its clinical significance remains controversial. The aim of this study was to examine the correlation of 25-hydryoxyvitamin D levels with liver disease severity and calcium levels in adults with cirrhosis. This cross-sectional study included 180 adults with cirrhosis enrolled in a clinical cohort study at a single university hospital. The mean age was 58.8 (±9.2) years, and cirrhosis was attributed to alcohol use in 27.2%, hepatitis C in 35.0%, non-alcoholic steatohepatitis in 27.2%, and both alcohol and hepatitis C in 10.6%. The median model for end-stage liver disease-sodium (MELD-Na) score was 12.0 (interquartile range 9.0–16.0), and mean serum albumin levels were 3.4 (±0.7) gm/dl. Median serum 25-hydroxyvitamin D levels were 28.0 (interquartile range 20–38) ng/mL, with 16 patients (8.9%) having levels <12 ng/ml and 43 (23.9%) with 25(OH)D levels <20 ng/ml. No correlation was noted between levels of 25-hydroxyvitamin D and albumin-corrected calcium in the total group and in groups stratified by vitamin D supplementation. In contrast, both serum albumin (r = 0.32; P < 0.001) and MELD-Na scores were significantly correlated with 25-hydroxyvitamin D levels (r = –0.29; P < 0.001). Correlations between 25-hydroxyvitamin D levels and serum albumin (r = ?0.39; P < 0.001) and MELD-Na scores did not change substantially after excluding 67 patients receiving vitamin D supplementation (r = ?0.33; P = 0.009). In conclusion, total 25-hydroxyvitamin D levels correlate inversely with liver disease severity in adults with cirrhosis.

Highlights

  • Vitamin D impacts bone mineralization and calcium homeostasis by increasing intestinal calcium absorption [1, 2]

  • The aim of the study was to evaluate the association of 25(OH)D levels with liver disease severity measures and albumin-corrected serum calcium levels in patients with cirrhosis

  • This study examined the proportion of 25(OH)D variance attributed to the MELD-Na score, serum albumin levels, and demographic variables and the use of vitamin D supplements

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Summary

Introduction

Vitamin D impacts bone mineralization and calcium homeostasis by increasing intestinal calcium absorption [1, 2]. Without vitamin D, only 10% to 15% of dietary calcium and less than 60% of dietary phosphate is absorbed [3]. The liver plays an important role in vitamin D metabolism. Vitamins D2 and D3 derived from food and supplements, and vitamin D3 obtained via sunlight exposure, undergo hydroxylation in Journal of Renal and Hepatic Disorders 2017; 1(2): 1–9 Age (years) 58.8 ± 9.2 Male (%) Race (%) White African American Asian Pacific Islander Unknown. Cirrhosis etiology (%) Alcohol HCV NASH Both alcohol and HCV

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