1. Assessment of indicators of vitamin A status in non-cirrhotic chronic hepatitis C patients.
- Author
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Santana RC, Machado AA, Martinelli AL, Jordão AA, Ramalho LN, and Vannucchi H
- Subjects
- Adult, Aged, Biomarkers analysis, Biopsy, Body Mass Index, Cross-Sectional Studies, Dietary Supplements, Dose-Response Relationship, Drug, Female, Humans, Liver chemistry, Liver Cirrhosis pathology, Male, Middle Aged, Organ Dysfunction Scores, Overweight blood, Retinol-Binding Proteins analysis, Vitamin A Deficiency complications, Young Adult, Hepatitis C, Chronic complications, Vitamin A analysis, Vitamin A Deficiency diagnosis
- Abstract
Subjects with chronic liver disease are susceptible to hypovitaminosis A due to several factors. Therefore, identifying patients with vitamin deficiency and a requirement for vitamin supplementation is important. Most studies assessing vitamin A in the context of hepatic disorders are conducted using cirrhotic patients. A cross-sectional study was conducted in 43 non-cirrhotic patients with chronic hepatitis C to evaluate markers of vitamin A status represented by serum retinol, liver retinol, and serum retinol-binding protein levels. We also performed the relative dose-response test, which provides an indirect estimate of hepatic vitamin A reserves. These vitamin A indicators were assessed according to the stage of liver fibrosis using the METAVIR score and the body mass index. The sample study was predominantly composed of male subjects (63%) with mild liver fibrosis (F1). The relative dose-response test was <20% in all subjects, indicating vitamin A sufficiency. Overweight or obese patients had higher serum retinol levels than those with a normal body mass index (2.6 and 1.9 µmol/L, respectively; P<0.01). Subjects with moderate liver fibrosis (F2) showed lower levels of serum retinol (1.9 vs 2.5 µmol/L, P=0.01) and retinol-binding protein levels compared with those with mild fibrosis (F1) (46.3 vs 67.7 µg/mL, P<0.01). These results suggested an effect of being overweight on serum retinol levels. Furthermore, more advanced stages of liver fibrosis were related to a decrease in serum vitamin A levels.
- Published
- 2016
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