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Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?

BACKGROUND: A phenylalanine (Phe) restricted dietary management is required in phenylketonuria (PKU) to maintain good metabolic control. Nevertheless, five different models of dietary regimes, which differ in their accuracy of Phe documentation, are used. To investigate the effect of the dietary reg...

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Autores principales: Rohde, Carmen, Thiele, Alena Gerlinde, Och, Ulrike, Schönherr, Katrin, Meyer, Uta, Rosenbaum-Fabian, Stefanie, Maddalon, Cornelia, Matzken, Sabine, Blessing, Holger, Lang, Frauke, Jörg-Streller, Monika, Beblo, Skadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471407/
https://www.ncbi.nlm.nih.gov/pubmed/28649540
http://dx.doi.org/10.1016/j.ymgmr.2015.09.006
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author Rohde, Carmen
Thiele, Alena Gerlinde
Och, Ulrike
Schönherr, Katrin
Meyer, Uta
Rosenbaum-Fabian, Stefanie
Maddalon, Cornelia
Matzken, Sabine
Blessing, Holger
Lang, Frauke
Jörg-Streller, Monika
Beblo, Skadi
author_facet Rohde, Carmen
Thiele, Alena Gerlinde
Och, Ulrike
Schönherr, Katrin
Meyer, Uta
Rosenbaum-Fabian, Stefanie
Maddalon, Cornelia
Matzken, Sabine
Blessing, Holger
Lang, Frauke
Jörg-Streller, Monika
Beblo, Skadi
author_sort Rohde, Carmen
collection PubMed
description BACKGROUND: A phenylalanine (Phe) restricted dietary management is required in phenylketonuria (PKU) to maintain good metabolic control. Nevertheless, five different models of dietary regimes, which differ in their accuracy of Phe documentation, are used. To investigate the effect of the dietary regime on metabolic control, a multicenter evaluation was performed. PATIENTS/METHODS: 149 patients (max. 800 mg Phe-intake/day; 108 children aged 1–9 years and 41 adolescents aged 10–15 years) could be included. They were separated according to age and dietary regime, revealed by a questionnaire on dietary habits. Dietary regimes vary from daily strict calculation of all Phe-intake (group 1) to a rather loose regime only estimating Phe-intake and including high protein food (group 5). Data were analyzed with respect to metabolic control (Phe-concentrations, Phe-concentrations above upper recommended limit during 6 months before the interview), Phe-intake (mg/day) and age (years). RESULTS: Median Phe-concentrations in children did not differ significantly among diet groups (group 1: 161; 2: 229, 3: 236, 4: 249, 5: 288 μmol/l, p = 0.175). However, exact daily Phe calculation led to significantly lower percentage of Phe concentrations above the upper recommended limit (group 1: 17, 2: 50, 3: 42, 4: 50, 5: 75%, p = 0.035). All included patients showed good to acceptable metabolic control. Patients on the dietary regime with the least accuracy, consuming also high protein foods, showed the poorest metabolic control. Median Phe concentrations of all other groups remained within recommended ranges, including from groups not calculating special low protein foods, fruit and vegetables and using a simplified system of recording Phe-intake. In adolescents no significant differences among diet groups were revealed. CONCLUSION: Exact calculation of Phe content of all food is not necessary to achieve good metabolic control in children and adolescents with PKU. Excluding special low protein food, as well as fruit and vegetables from calculation of Phe-intake has no impact on metabolic control. However including protein rich food into the diet and simply estimating all Phe-intake appears insufficient. The simplification of dietary regime may be helpful in enhancing acceptability and feasibility.
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spelling pubmed-54714072017-06-23 Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary? Rohde, Carmen Thiele, Alena Gerlinde Och, Ulrike Schönherr, Katrin Meyer, Uta Rosenbaum-Fabian, Stefanie Maddalon, Cornelia Matzken, Sabine Blessing, Holger Lang, Frauke Jörg-Streller, Monika Beblo, Skadi Mol Genet Metab Rep Research Paper BACKGROUND: A phenylalanine (Phe) restricted dietary management is required in phenylketonuria (PKU) to maintain good metabolic control. Nevertheless, five different models of dietary regimes, which differ in their accuracy of Phe documentation, are used. To investigate the effect of the dietary regime on metabolic control, a multicenter evaluation was performed. PATIENTS/METHODS: 149 patients (max. 800 mg Phe-intake/day; 108 children aged 1–9 years and 41 adolescents aged 10–15 years) could be included. They were separated according to age and dietary regime, revealed by a questionnaire on dietary habits. Dietary regimes vary from daily strict calculation of all Phe-intake (group 1) to a rather loose regime only estimating Phe-intake and including high protein food (group 5). Data were analyzed with respect to metabolic control (Phe-concentrations, Phe-concentrations above upper recommended limit during 6 months before the interview), Phe-intake (mg/day) and age (years). RESULTS: Median Phe-concentrations in children did not differ significantly among diet groups (group 1: 161; 2: 229, 3: 236, 4: 249, 5: 288 μmol/l, p = 0.175). However, exact daily Phe calculation led to significantly lower percentage of Phe concentrations above the upper recommended limit (group 1: 17, 2: 50, 3: 42, 4: 50, 5: 75%, p = 0.035). All included patients showed good to acceptable metabolic control. Patients on the dietary regime with the least accuracy, consuming also high protein foods, showed the poorest metabolic control. Median Phe concentrations of all other groups remained within recommended ranges, including from groups not calculating special low protein foods, fruit and vegetables and using a simplified system of recording Phe-intake. In adolescents no significant differences among diet groups were revealed. CONCLUSION: Exact calculation of Phe content of all food is not necessary to achieve good metabolic control in children and adolescents with PKU. Excluding special low protein food, as well as fruit and vegetables from calculation of Phe-intake has no impact on metabolic control. However including protein rich food into the diet and simply estimating all Phe-intake appears insufficient. The simplification of dietary regime may be helpful in enhancing acceptability and feasibility. Elsevier 2015-10-22 /pmc/articles/PMC5471407/ /pubmed/28649540 http://dx.doi.org/10.1016/j.ymgmr.2015.09.006 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Rohde, Carmen
Thiele, Alena Gerlinde
Och, Ulrike
Schönherr, Katrin
Meyer, Uta
Rosenbaum-Fabian, Stefanie
Maddalon, Cornelia
Matzken, Sabine
Blessing, Holger
Lang, Frauke
Jörg-Streller, Monika
Beblo, Skadi
Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title_full Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title_fullStr Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title_full_unstemmed Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title_short Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
title_sort effect of dietary regime on metabolic control in phenylketonuria: is exact calculation of phenylalanine intake really necessary?
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471407/
https://www.ncbi.nlm.nih.gov/pubmed/28649540
http://dx.doi.org/10.1016/j.ymgmr.2015.09.006
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