Evidence map›Paper›PMID 41390423›Full record

ArticleOrphanet journal of rare diseases2025

Clinical assessment of growth patterns, weight, and dietary management in children and adults with phenylketonuria - a retrospective study.

Lionesa Bahtiri, Christine Jørgensen, Kirsten Ahring, Helle Rasmussen, Janne Meedon Hermansen, Olivia Welle Fjellbirkeland, Allan Meldgaard Lund, Mette Cathrine Ørngreen

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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

8 authors.

Lionesa BahtiriDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark. lionesa_@hotmail.com.ORCID 0000-0002-7502-9321
Christine JørgensenDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Kirsten AhringDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Helle RasmussenDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Janne Meedon HermansenDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Olivia Welle FjellbirkelandDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Allan Meldgaard LundDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.
Mette Cathrine ØrngreenDepartment of Clinical Genetics and of Pediatrics and Adolescent Medicine, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, 2100, København, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhenylketonuria (PKU) is an inherited metabolic disorder where the body cannot break down phenylalanine (Phe), leading to its harmful accumulation if left untreated. Concerns have been raised about growth and risk of overweight in PKU patients, with conflicting research findings. This retrospective study aims to assess growth patterns and the prevalence of overweight and obesity in Danish children and adults with PKU by comparing them with Danish growth charts and prevalence rates.

resultsData were collected from medical records of 291 Danish patients from the National PKU Clinic at Rigshospitalet in Copenhagen, including data on age, sex, PKU phenotype, Phe levels, and anthropometric measurements from their last clinic visit. Weight status for children was classified according to Danish guidelines, while World Health Organization criteria were used for adults. All data analyses were carried out separately for children and adults. A total of 291 PKU patients were included, 116 children and 175 adults. Children had normal growth patterns compared to Danish growth charts. The rates of overweight and obesity among children were 15% and 1%, respectively, while 32% of adults were overweight, and 28% were obese. Adults with classic PKU were significantly more obese and had higher BMI levels compared to other phenotypes. Additionally, a slight positive correlation was noted between high Phe levels and the risk of being overweight.

conclusionsChildren with phenylketonuria following a restricted diet achieve normal growth. However, overweight and obesity rates rise with age, particularly in adults with the most severe phenotype, suggesting disease severity may influence weight gain. The potential link between high phenylalanine levels and overweight requires further investigation. These findings highlight the need for ongoing weight and metabolic monitoring, as well as strategies to support weight management in adults with phenylketonuria.

Indexed as

Body WeightPhenylketonuriasAdolescentAdultChildChild, PreschoolDenmarkFemaleHumansInfantMaleMiddle AgedObesityOverweightPhenylalanineRetrospective StudiesPhenylalanine

Identifiers

PMID41390423
PMCPMC12713284

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