Disturbances of parathyroid hormone–vitamin D axis in non-cholestatic chronic liver disease: a cross-sectional study
- 25 July 2010
- journal article
- research article
- Published by Springer Nature in Hepatology International
- Vol. 4 (3) , 634-640
- https://doi.org/10.1007/s12072-010-9194-2
Abstract
Purpose Liver has an important role in metabolism of vitamin D. This study aimed to evaluate the patterns of vitamin D–parathyroid hormone (PTH) disturbance and correlate it in patients with non-cholestatic chronic liver disease (CLD). Methods A total of 40 healthy controls and 90 consecutive patients with evidence of non-cholestatic CLD due to hepatitis C (n = 28), hepatitis B (n = 26), autoimmune hepatitis (n = 19), and cryptogenic causes (n = 17) were enrolled. Cirrhosis was evident in 51 patients. Serum concentrations of 25-hydroxy vitamin D, PTH, calcium, phosphate, and liver enzymes were measured. Child–Pugh classification was determined in cirrhotic patients. Results Vitamin D deficiency ( 6.8 pmol/l) was present in 6 (6.7%) patients. The prevalence of vitamin D deficiency was significantly higher in cirrhotic versus noncirrhotic patients (76.5 vs. 17.9%; P < 0.001), whereas there was no significant difference in serum calcium, phosphate, and PTH levels. Child–Pugh class B and C patients had significantly lower vitamin D level compared with class A patients (P < 0.001), whereas there was no significant difference in serum calcium, phosphate, and PTH levels. No significant correlation was seen between vitamin D and PTH, calcium or phosphate levels. Lower serum level of vitamin D was associated with coagulopathy, hyperbilirubinemia, hypoalbuminemia, anemia, and thrombocytopenia. Conclusions Vitamin D inadequacy and the severity of liver dysfunction move in parallel in patients with non-cholestatic CLD. Vitamin D assessment and replacement should be considered in the management of patients with non-cholestatic CLD.Keywords
This publication has 30 references indexed in Scilit:
- Bone mineral density and disorders of mineral metabolism in chronic liver diseaseWorld Journal of Gastroenterology, 2009
- Vitamin D reduces the expression of collagen and key profibrotic factors by inducing an antifibrotic phenotype in mesenchymal multipotent cellsJournal of Endocrinology, 2008
- 1,25-Dihydroxy Vitamin D3 Is an Autocrine Regulator of Extracellular Matrix Turnover and Growth Factor Release via ERp60-Activated Matrix Vesicle Matrix MetalloproteinasesCells Tissues Organs, 2008
- Vitamin D status in gastrointestinal and liver diseaseCurrent Opinion in Gastroenterology, 2008
- Estimates of optimal vitamin D statusOsteoporosis International, 2005
- AGA technical review on osteoporosis in hepatic disordersGastroenterology, 2003
- A Model to Predict Survival in Patients With End–Stage Liver DiseaseHepatology, 2001
- Bone mineral density, serum insulin-like growth factor I, and bone turnover markers in viral cirrhosisHepatology, 1998
- Metabolic bone disease of liver cirrhosis: Is it parallel to the clinical severity of cirrhosis?Journal of Gastroenterology and Hepatology, 1996
- Transection of the oesophagus for bleeding oesophageal varicesBritish Journal of Surgery, 1973