Evidence map›Paper›PMID 40759975›Full record

ArticleOrphanet journal of rare diseases2025

Multicenter study on long-term growth in patients with phenylketonuria.

S Stanescu, A Belanger-Quintana, J C Rocha, M F Almeida, K Ahring, K Dokoupil, A M Lammardo, E van Dam, A Muriel, A MacDonald and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

S StanescuU. Enf. Metabolicas, Paediatric Department, MetabERN, Hospital Universitario Ramón y Cajal, Madrid, Spain. sinziana.stanescu@salud.madrid.org.ORCID http://orcid.org/0000-0003-0340-4580
A Belanger-QuintanaU. Enf. Metabolicas, Paediatric Department, MetabERN, Hospital Universitario Ramón y Cajal, Madrid, Spain.
J C RochaNutrition & Metabolism, NOVA Medical School, Faculdade de Ciências Médicas, NMS, FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
M F AlmeidaCentro de Referência Para As Doenças Hereditárias Do Metabolismo, Unidade Local de Saúde de Santo António, Porto, Portugal.
K AhringCenter for PKU, Kennedy Institute, Glostrup, Denmark.
K DokoupilDp Metab Nutr, Dr Hauner Child Hosp, Munich, Germany.
A M LammardoDp Pediatric, San Paolo Hosp, Univ Milan, Milan, Italy.
E van DamS. Metab Dis, Univ Med Centre Groningen, Groningen, Netherlands.
A MurielU. Bioestadística Clínica, Instituto Ramón y Cajal de Investigación Sanitaria, Hospital Universitario Ramón y Cajal, Madrid, Spain.
A MacDonaldDietetic Department, Birmingham Children's Hospital, Birmingham, UK.
ENEP group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMost of the studies on PKU have focused on the neurological development of patients. Studies regarding the physical development usually cover a short period of time, do not include dietary information, and results are contradictory. The aim of this study is to determine whether the patients with PKU have a normal growth, the incidence of obesity and the relationship of these parameters with diet and nutritional intake. MATERIAL AND

methodsThis is a retrospective, multicenter, multinational study including patients with PKU from 8 centers from different countries. Data of growth parameters and dietary regimes were collected from birth until the age of 18 years. Anthropometric tools of the WHO (Anthro version 3.2.2 and Anthro plus) were used to calculate z-score for weight-for-age, height-for-age and body mass index (BMI).

resultsData from 182 patients with classical PKU were included. The median height z-scores for both male and female patients showed a normal growth pattern according to the WHO charts. Significant positive correlation  was observed between height z-score and the Phe (mg/day) and natural protein (g/day) intakes in all ages, especially in children younger than 11 years. The amount of Phe-free amino acid mixture did not affect the height, but lower intakes were negative correlated with the BMI. Also, we detected a positive correlation between the median Phe levels and BMI, meaning that the poorer metabolic control was correlated with higher BMI.

conclusionsAn objective of PKU is that patients have satisfactory final physical development; the height prognosis seems to be associated with Phe and natural protein intake and therefore should be optimized. It is important to collect longitudinal growth data throughout childhood and adolescence in PKU that considers any change in growth in relationship to dietary patterns.

Indexed as

PhenylketonuriasAdolescentBody HeightBody Mass IndexBody WeightChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleRetrospective StudiesDietGrowthNatural protein intakePhenylketonuria

Identifiers

PMID40759975
PMCPMC12323032

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