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Minerva Med ; 109(5): 352-357, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29963831

RESUMO

BACKGROUND: The liver is involved in the metabolism of vitamin D. The prevalence of osteopenia in alcoholic liver disease (ALD) patients is 34-48%, and the prevalence of osteoporosis is 11-36%. Advanced liver disease is considered a risk factor for the development of osteoporosis. The aim of this study was to establish the relationship between vitamin D level and Child-Pugh score in patients with alcoholic liver cirrhosis (ALC), and to evaluate the effects of oral vitamin D supplementation. METHODS: Seventy male ALC patients in the absence of active alcohol intake were enrolled and their clinical and laboratory data were recorded. A supplementation of cholecalciferol 1000 IU/day was administered. The vitamin D status was analyzed during the study, in patients stratified by Child-Pugh score. RESULTS: The study was completed by fifty patients. At the enrollment, the mean level of vitamin D was 60.73±28.02, 50.53±39.52 and 26.71±12.81 nmol/L, respectively for Child-Pugh score class A, B and C. During vitamin D supplementation it was found in all the patients a significant increase of its levels during the first six months (P<0.05). However, in class C the improvement was consistent also after year (P<0.05). At the end of the study, two of seven patients initially in class C changed in class A, four from class C to B, and one remained in class C (P=0.012). Out of seventeen patients initially in class B, eleven changed to class A, and six remained in class B. CONCLUSIONS: In patients with ALC, higher level of vitamin D level is related with lower Child-Pugh score. The supplementation of 1000 IU/day of vitamin D in these patients was optimal for a period of at least six months. A decrease in the Child-Pugh score was also found, with a redistribution of the patients in different classes.


Assuntos
Colecalciferol/uso terapêutico , Suplementos Nutricionais , Cirrose Hepática Alcoólica/complicações , Deficiência de Vitamina D/tratamento farmacológico , Vitamina D/sangue , Bilirrubina/sangue , Doenças Ósseas Metabólicas/etiologia , Doenças Ósseas Metabólicas/prevenção & controle , Colecalciferol/metabolismo , Humanos , Coeficiente Internacional Normatizado , Cirrose Hepática Alcoólica/sangue , Masculino , Pessoa de Meia-Idade , Osteoporose/etiologia , Osteoporose/prevenção & controle , Estudos Prospectivos , Albumina Sérica/análise , Índice de Gravidade de Doença , Resultado do Tratamento , Deficiência de Vitamina D/sangue , Deficiência de Vitamina D/etiologia
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