Social-cognitive functioning and social skills in patients with early treated phenylketonuria: a PKU-COBESO study.

Rianne Jahja, Francjan J van Spronsen, Leo M J de Sonneville, Jaap J van der Meere, Annet M Bosch, Carla E M Hollak, M Estela Rubio-Gozalbo, Martijn C G J Brouwers, Floris C Hofstede, Maaike C de Vries, Mirian C H Janssen, Ans T van der Ploeg, Janneke G Langendonk, Stephan C J Huijbregts

Journal: Journal of inherited metabolic disease 2017;39(3):355-362

PMID: 26914933

Abstract

OBJECTIVE

Early treatment of phenylketonuria (ET-PKU) prevents mental retardation, but many patients still show cognitive and mood problems. In this study, it was investigated whether ET-PKU-patients have specific phenylalanine (Phe-)related problems with respect to social-cognitive functioning and social skills.

METHODS

Ninety five PKU-patients (mean age 21.6 ± 10.2 years) and 95 healthy controls (mean age 19.6 ± 8.7 years) were compared on performance of computerized and paper-and-pencil tasks measuring social-cognitive abilities and on parent- and self-reported social skills, using multivariate analyses of variance, and controlling for general cognitive ability (IQ-estimate). Further comparisons were made between patients using tetrahydrobiopterin (BH4, N = 30) and patients not using BH4. Associations with Phe-levels on the day of testing, during childhood, during adolescence and throughout life were examined.

RESULTS

PKU-patients showed poorer social-cognitive functioning and reportedly had poorer social skills than controls (regardless of general cognitive abilities). Quality of social-cognitive functioning was negatively related to recent Phe-levels and Phe-levels between 8 and 12 years for adolescents with PKU. Quality of social skills was negatively related to lifetime phenylalanine levels in adult patients, and specifically to Phe-levels between 0 and 7, and between 8 and 12 years. There were no differences with respect to social outcome measures between the BH4 and non-BH4 groups.

CONCLUSION

PKU-patients have Phe-related difficulties with social-cognitive functioning and social skills. Problems seem to be more evident among adolescents and adults with PKU. High Phe-levels during childhood and early adolescence seem to be of greater influence than current and recent Phe-levels for these patients.

Address: University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, Division of Metabolic Diseases CA33, PO Box 30.001, 9700 RB, Groningen, The Netherlands. [email protected].; University of Groningen, University Medical Center Groningen, Beatrix Children's Hospital, Division of Metabolic Diseases CA33, PO Box 30.001, 9700 RB, Groningen, The Netherlands.; Department of Clinical Child and Adolescent Studies & Leiden Institute for Brain and Cognition, Leiden University, Leiden, The Netherlands.; Department of Developmental and Clinical Neuropsychology, University of Groningen, Groningen, The Netherlands.; Academic Medical Center, Amsterdam, The Netherlands.; Laboratory Genetics Metabolic Diseases, University Hospital Maastricht, Maastricht, The Netherlands.; Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.; University Medical Center St Radboud Nijmegen, Nijmegen, The Netherlands.; Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, Rotterdam, The Netherlands.
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