Literature DB >> 19083409

Poor zinc and selenium status in phenylketonuric children and adolescents in Brazil.

Junaura Rocha Barretto1, Luciana Rodrigues Silva, Maria Efigênia Leite, Ney Boa-Sorte, Helena Pimentel, Antonio Conceição Purificação, Gildasio Carvalho, Maria Inês M M Fontes, Tatiana Amorim.   

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 (rho = -0.143, P = .435) or the supply and serum levels for copper (rho = -0.117, P = .523) and selenium (rho = 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.

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Year:  2008        PMID: 19083409     DOI: 10.1016/j.nutres.2007.12.009

Source DB:  PubMed          Journal:  Nutr Res        ISSN: 0271-5317            Impact factor:   3.315


  5 in total

1.  Nutritional Management of Phenylketonuria.

Authors:  Erin L Macleod; Denise M Ney
Journal:  Ann Nestle Eng       Date:  2010-06

Review 2.  Oxidative stress in phenylketonuria: future directions.

Authors:  Júlio César Rocha; Maria João Martins
Journal:  J Inherit Metab Dis       Date:  2011-11-25       Impact factor: 4.982

Review 3.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

4.  Nutritional status of patients with phenylketonuria in Japan.

Authors:  Yoshiyuki Okano; Toshikazu Hattori; Hiroki Fujimoto; Kaori Noi; Miki Okamoto; Toshiaki Watanabe; Ryoko Watanabe; Rika Fujii; Tomoko Tamaoki
Journal:  Mol Genet Metab Rep       Date:  2016-08-20

5.  Micronutrient in hyperphenylalaninemia.

Authors:  Vanesa Crujeiras; Luís Aldámiz-Echevarría; Jaume Dalmau; Isidro Vitoria; Fernando Andrade; Iria Roca; Rosaura Leis; Ana Fermandez-Marmiesse; María L Couce
Journal:  Data Brief       Date:  2015-08-01
  5 in total

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