Literature DB >> 12872834

Evaluation of nutritional status and pathophysiology of growth retardation in patients with phenylketonuria.

D Dobbelaere1, L Michaud, A Debrabander, S Vanderbecken, F Gottrand, D Turck, J P Farriaux.   

Abstract

Recent European studies have shown that growth retardation is com-mon in people with phenylketonuria (PKU) during the first years of life while they receive a low-phenylalanine (Phe) diet. The aims of the present study were to assess the growth of our PKU patients and to search for nutritional and hormonal explanations for the growth delay. Twenty PKU patients aged 8 months to 7 years entered the study. The design was cross-sectional, a longitudinal study having already been performed in our centre. The following data were recorded: weight/height (W/H), height/age (H/A), and weight/age (W/A) Z-scores; fat-free mass (measured from bioelectrical impedometry (FFM1), and skinfold thickness (FFMA). Thyroid hormones, insulin-like growth factor I (IGF1), insulin-like growth factor binding protein (IGFBP3), selenium, zinc, and Phe blood levels were measured. Dietary intake was also recorded over 4 days. PKU patients were moderately but significantly shorter (H/A Z-score varied from -2.12 to 1.61; mean -0.49) and lighter (W/A Z-score varied from -2.58 to 1.49; mean -0.71) than the French reference population. Body composition was not different from that of controls matched for age and sex. IGF1, IGFBP3, and thyroid hormone levels were within normal range. All children received more than two-thirds of the recommended daily allowances for energy (91% +/- 18%) and for proteins (146% +/- 26%). The mean daily intake of our patients was sufficient in selenium, but markedly deficient in zinc (2.4 +/- 2.2 mg/day). No correlation was found between zinc daily intake or zinc plasma levels and growth retardation. Moreover, no relation was found between the plasma Phe concentrations, protein or caloric intake and the presence of growth retardation. Our results show that growth retardation in PKU patients is not related to hormonal or caloric deficiencies. Further studies are needed to investigate the effect of various nutrient supplementation regimens (especially zinc) on the growth of PKU patients.

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Year:  2003        PMID: 12872834     DOI: 10.1023/a:1024063726046

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  14 in total

1.  Effect of foodstuffs on the absorption of zinc sulfate.

Authors:  A Pécoud; P Donzel; J L Schelling
Journal:  Clin Pharmacol Ther       Date:  1975-04       Impact factor: 6.875

2.  Serum insulin-like growth factors I and II concentrations and growth hormone and insulin responses to arginine infusion in children with protein-energy malnutrition before and after nutritional rehabilitation.

Authors:  A T Soliman; A E Hassan; M K Aref; R L Hintz; R G Rosenfeld; A D Rogol
Journal:  Pediatr Res       Date:  1986-11       Impact factor: 3.756

3.  Trace elements nutriture in hyperphenylalaninemic patients. Long-term follow up study.

Authors:  R Longhi; A Rottoli; A Vittorelli; G Zecchini; T Bonabitacola; F Bertassi; E Riva; M Giovannini
Journal:  Eur J Pediatr       Date:  1987       Impact factor: 3.183

Review 4.  Dietary interactions involving the trace elements.

Authors:  C F Mills
Journal:  Annu Rev Nutr       Date:  1985       Impact factor: 11.848

5.  Determination of body composition of children from skinfold measurements.

Authors:  C G Brook
Journal:  Arch Dis Child       Date:  1971-04       Impact factor: 3.791

6.  Usefulness of bioelectric impedance and skinfold measurements in predicting fat-free mass derived from total body potassium in children.

Authors:  F Schaefer; M Georgi; A Zieger; K Schärer
Journal:  Pediatr Res       Date:  1994-05       Impact factor: 3.756

7.  Growth in patients with phenylketonuria.

Authors:  J Weglage; J H Brämswig; H G Koch; S Karassalidou; K Ullrich
Journal:  Eur J Pediatr       Date:  1994-07       Impact factor: 3.183

Review 8.  Nutrition, physical growth, and bone density in treated phenylketonuria.

Authors:  H Przyrembel; H J Bremer
Journal:  Eur J Pediatr       Date:  2000-10       Impact factor: 3.183

9.  Zinc and copper status of treated children with phenylketonuria.

Authors:  P B Acosta; P M Fernhoff; H S Warshaw; K M Hambidge; A Ernest; E R McCabe; L J Elsas
Journal:  JPEN J Parenter Enteral Nutr       Date:  1981 Sep-Oct       Impact factor: 4.016

10.  Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee.

Authors:  P H Verkerk; F J van Spronsen; G P Smit; R C Sengers
Journal:  Arch Dis Child       Date:  1994-08       Impact factor: 3.791

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  26 in total

1.  New insights in growth of phenylketonuric patients.

Authors:  María L Couce; Ipek Guler; Andrés Anca-Couce; Marta Lojo; Alicia Mirás; Rosaura Leis; Alejandro Pérez-Muñuzuri; José M Fraga; Francisco Gude
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2.  The intake of total protein, natural protein and protein substitute and growth of height and head circumference in Dutch infants with phenylketonuria.

Authors:  M Hoeksma; M Van Rijn; P H Verkerk; A M Bosch; M F Mulder; J B C de Klerk; T J de Koning; E Rubio-Gozalbo; M de Vries; P J J Sauer; F J van Spronsen
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3.  The Validity of Bioelectrical Impedance Analysis to Measure Body Composition in Phenylketonuria.

Authors:  Maureen Evans; Kay Nguo; Avihu Boneh; Helen Truby
Journal:  JIMD Rep       Date:  2017-11-24

Review 4.  Up to date knowledge on different treatment strategies for phenylketonuria.

Authors:  Amaya Bélanger-Quintana; Alberto Burlina; Cary O Harding; Ania C Muntau
Journal:  Mol Genet Metab       Date:  2011-08-16       Impact factor: 4.797

5.  Predictive equations underestimate resting energy expenditure in female adolescents with phenylketonuria.

Authors:  Meghan E Quirk; Brian J Schmotzer; Rani H Singh
Journal:  J Am Diet Assoc       Date:  2010-06

6.  Transition of young adults with phenylketonuria from pediatric to adult care.

Authors:  Ulrike Mütze; Annika Roth; Johannes F W Weigel; Skadi Beblo; Christoph G Baerwald; Peter Bührdel; Wieland Kiess
Journal:  J Inherit Metab Dis       Date:  2011-02-09       Impact factor: 4.982

Review 7.  Growth and body composition in children with classical phenylketonuria: results in 34 patients and review of the literature.

Authors:  M Huemer; C Huemer; D Möslinger; D Huter; S Stöckler-Ipsiroglu
Journal:  J Inherit Metab Dis       Date:  2007-07-11       Impact factor: 4.982

Review 8.  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

Review 9.  Mild hyperphenylalaninemia: to treat or not to treat.

Authors:  Francjan J van Spronsen
Journal:  J Inherit Metab Dis       Date:  2011-02-24       Impact factor: 4.982

10.  A long-term study of bone mineral density in patients with phenylketonuria under diet therapy.

Authors:  Hala M Koura; Nagwa Abdallah Ismail; Ashraf F Kamel; Azza M Ahmed; Amal Saad-Hussein; Laila K Effat
Journal:  Arch Med Sci       Date:  2011-07-11       Impact factor: 3.318

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