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Poor zinc and selenium status in phenylketonuric children and adolescents in Brazil
Authors:Junaura Rocha Barretto  Luciana Rodrigues Silva  Maria Efigênia Leite  Ney Boa-Sorte  Helena Pimentel  Antonio Conceição Purificação  Gildasio Carvalho  Maria Inês MM Fontes  Tatiana Amorim
Institution:1. Center of Study and Research on Pediatric Gastroenterology and Liver Disease at the Federal University of Bahia, Brazil;2. Reference Service of Neonatal Screening of Parents and Friends Association of Disabled Children, Salvador, Bahia, Brazil
Abstract:Because of the restricted intake of high-biologic-value protein, children with phenylketonuria (PKU) may have lower than normal plasma concentrations of copper, zinc, and selenium. The purpose of the present study was to investigate erythrocyte zinc levels and serum copper and selenium levels in children and adolescents with PKU by analyzing the relation between their diet and the laboratory profiles of these elements. The study was conducted in 32 children and adolescents with PKU, who were on a special diet. Dietary records and blood samples were collected from each subject. Erythrocyte zinc and serum selenium levels were below normal in 37.5% and 90.6% of the subjects, respectively. Plasma copper levels were normal. Metabolic formulas were the only source of 86.9% of the zinc, 65.6% of the copper, and 32.4% of the selenium. Despite this, there was no significant correlation between the zinc formula supply and erythrocyte zinc levels (ρ = −0.143, P = .435) or the supply and serum levels for copper (ρ = −0.117, P = .523) and selenium (ρ = 0.113, P = .538). These results suggest that Brazilian patients with PKU present with low ingestion levels, low serum selenium levels, and low erythrocyte zinc levels.
Keywords:Zinc  Selenium  Copper  Dietary therapy  Humans  Phenylketonuria
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