» Articles » PMID: 22359532

Serum Vitamin D Levels Are Not Predictive of the Progression of Chronic Liver Disease in Hepatitis C Patients with Advanced Fibrosis

Overview
Journal PLoS One
Date 2012 Feb 24
PMID 22359532
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

In animal models and human cross-sectional studies, vitamin D deficiency has been associated with liver disease progression. Vitamin D supplementation has been suggested as a treatment to prevent disease progression. We sought to evaluate the role of vitamin D levels in predicting chronic liver disease development. We conducted a nested case-control study of vitamin D levels in subjects with (cases) and without (controls) liver histologic progression or clinical decompensation over the course of the HALT-C Trial. Vitamin D levels were measured at 4 points over 45 months. 129 cases and 129 aged-matched controls were included. No difference in baseline vitamin D levels were found between cases and controls. (44.8 ng/mL vs. 44.0 ng/mL, P = 0.74). Vitamin D levels declined in cases and controls over time (P = 0.0005), however, there was no difference in the level of decline (P = 0.37). Among study subjects with diabetes mellitius, baseline vitamin D levels were higher in cases, 49.9 ng/mL, than controls, 36.3 ng/mL. (P = 0.03) In addition, baseline vitamin D levels were higher in black case subjects, 32.7 ng/mL, than in black control subjects, 25.2 ng/mL (P = 0.08) No difference in vitamin D levels was found between patients with and without progression of hepatitis C-associated liver disease over 4 years. Our data do not suggest any role for vitamin D supplementation in patients with advanced chronic hepatitis C and raise the possibility that higher vitamin D levels may be associated with disease progression.

Citing Articles

Investigation of the influential factors for hepatic osteodystrophy in chronic liver disease: A case-control survey among the patients attending a tertiary care hospital in a rural region of Northern India.

Yadav E, Kaur R, Sasan A, Garg S Tzu Chi Med J. 2023; 35(1):95-102.

PMID: 36866351 PMC: 9972938. DOI: 10.4103/tcmj.tcmj_27_22.


Prevalence and characteristics of bone disease in cirrhotic patients.

Gokcan H, Akdogan Kayhan M, Demir S, Kacar S, Cam P, Kaplan M Hepatol Forum. 2022; 1(2):48-52.

PMID: 35949442 PMC: 9349342. DOI: 10.14744/hf.2020.2020.0007.


Vitamin D supplementation for chronic liver diseases in adults.

Bjelakovic M, Nikolova D, Bjelakovic G, Gluud C Cochrane Database Syst Rev. 2021; 8:CD011564.

PMID: 34431511 PMC: 8407054. DOI: 10.1002/14651858.CD011564.pub3.


High Prevalent Hypovitaminosis D Is Associated with Dysregulation of Calcium-parathyroid Hormone-vitamin D Axis in Patients with Chronic Liver Diseases.

Narayanasamy K, Karthick R, Raj A J Clin Transl Hepatol. 2019; 7(1):15-20.

PMID: 30944814 PMC: 6441643. DOI: 10.14218/JCTH.2018.00018.


Vitamin D and Gastrointestinal Cancers: A Narrative Review.

Goyal H, Perisetti A, Rahman M, Levin A, Lippi G Dig Dis Sci. 2018; 64(5):1098-1109.

PMID: 30511197 DOI: 10.1007/s10620-018-5400-1.


References
1.
Fisher L, Fisher A . Vitamin D and parathyroid hormone in outpatients with noncholestatic chronic liver disease. Clin Gastroenterol Hepatol. 2007; 5(4):513-20. DOI: 10.1016/j.cgh.2006.10.015. View

2.
Petta S, Camma C, Di Marco V, Alessi N, Barbaria F, Cabibi D . Retinol-binding protein 4: a new marker of virus-induced steatosis in patients infected with hepatitis c virus genotype 1. Hepatology. 2008; 48(1):28-37. DOI: 10.1002/hep.22316. View

3.
Holick M, Matsuoka L, Wortsman J . Age, vitamin D, and solar ultraviolet. Lancet. 1989; 2(8671):1104-5. DOI: 10.1016/s0140-6736(89)91124-0. View

4.
Agborsangaya C, Toriola A, Grankvist K, Surcel H, Holl K, Parkkila S . The effects of storage time and sampling season on the stability of serum 25-hydroxy vitamin D and androstenedione. Nutr Cancer. 2010; 62(1):51-7. DOI: 10.1080/01635580903191460. View

5.
Svegliati-Baroni G, Ridolfi F, Di Sario A, Casini A, Marucci L, Gaggiotti G . Insulin and insulin-like growth factor-1 stimulate proliferation and type I collagen accumulation by human hepatic stellate cells: differential effects on signal transduction pathways. Hepatology. 1999; 29(6):1743-51. DOI: 10.1002/hep.510290632. View