Cargando…

Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin

CONTEXT: Prader‐Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a typical behavioural phenotype, with characteristics of autism spectrum disorder (ASD) like stubbornness, temper tantrums and compulsivity. It has been suggested that the oxytocin system in patients w...

Descripción completa

Detalles Bibliográficos
Autores principales: Damen, Layla, Grootjen, Lionne N., Juriaans, Alicia F., Donze, Stephany H., Huisman, T. Martin, Visser, Jenny A., Delhanty, Patric J.D., Hokken‐Koelega, Anita C.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246775/
https://www.ncbi.nlm.nih.gov/pubmed/33296519
http://dx.doi.org/10.1111/cen.14387
_version_ 1783716383322800128
author Damen, Layla
Grootjen, Lionne N.
Juriaans, Alicia F.
Donze, Stephany H.
Huisman, T. Martin
Visser, Jenny A.
Delhanty, Patric J.D.
Hokken‐Koelega, Anita C.S.
author_facet Damen, Layla
Grootjen, Lionne N.
Juriaans, Alicia F.
Donze, Stephany H.
Huisman, T. Martin
Visser, Jenny A.
Delhanty, Patric J.D.
Hokken‐Koelega, Anita C.S.
author_sort Damen, Layla
collection PubMed
description CONTEXT: Prader‐Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a typical behavioural phenotype, with characteristics of autism spectrum disorder (ASD) like stubbornness, temper tantrums and compulsivity. It has been suggested that the oxytocin system in patients with PWS is dysfunctional. In ASD, intranasal oxytocin treatment has favourable effects on behaviour. OBJECTIVE: To evaluate the effects of 3 months of twice daily intranasal oxytocin (dose range 16‐40 IU/day), compared to placebo, on behaviour and hyperphagia in children with PWS. DESIGN: Randomized, double‐blind, placebo‐controlled, crossover study in the Dutch PWS Reference Center. PATIENTS: Twenty‐six children with PWS aged 3‐11 years. MAIN OUTCOME MEASURES: (Change in) behaviour and hyperphagia measured by Oxytocin Questionnaire and Dykens hyperphagia questionnaire. RESULTS: In the total group, no significant effects of oxytocin on social behaviour or hyperphagia were found. However, in boys, the Oxytocin Questionnaire scores improved significantly during oxytocin treatment, compared to a deterioration during placebo (4.5 (−0.8 to 15.3) vs. −4.0 (−11.3 to 0.8), P = .025). The Dykens hyperphagia questionnaire scores remained similar during oxytocin treatment, while there was a deterioration during placebo (0.0 (−0.8 to 4.3) vs. −3.5 (−6.0 to 0.0), P = .046). Patients with a deletion had significant improvements in both questionnaire scores during oxytocin treatment, but deteriorations during placebo. Oxytocin treatment was well tolerated, and there were no serious adverse events. CONCLUSIONS: Intranasal oxytocin treatment has positive effects on social and eating behaviour in 3‐11 years aged boys with PWS and in children with a deletion without safety concerns. Intranasal oxytocin in children with PWS might be considered, but individual effects should be carefully evaluated and treatment discontinued if no effects are found.
format Online
Article
Text
id pubmed-8246775
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-82467752021-07-02 Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin Damen, Layla Grootjen, Lionne N. Juriaans, Alicia F. Donze, Stephany H. Huisman, T. Martin Visser, Jenny A. Delhanty, Patric J.D. Hokken‐Koelega, Anita C.S. Clin Endocrinol (Oxf) ORIGINAL ARTICLES CONTEXT: Prader‐Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a typical behavioural phenotype, with characteristics of autism spectrum disorder (ASD) like stubbornness, temper tantrums and compulsivity. It has been suggested that the oxytocin system in patients with PWS is dysfunctional. In ASD, intranasal oxytocin treatment has favourable effects on behaviour. OBJECTIVE: To evaluate the effects of 3 months of twice daily intranasal oxytocin (dose range 16‐40 IU/day), compared to placebo, on behaviour and hyperphagia in children with PWS. DESIGN: Randomized, double‐blind, placebo‐controlled, crossover study in the Dutch PWS Reference Center. PATIENTS: Twenty‐six children with PWS aged 3‐11 years. MAIN OUTCOME MEASURES: (Change in) behaviour and hyperphagia measured by Oxytocin Questionnaire and Dykens hyperphagia questionnaire. RESULTS: In the total group, no significant effects of oxytocin on social behaviour or hyperphagia were found. However, in boys, the Oxytocin Questionnaire scores improved significantly during oxytocin treatment, compared to a deterioration during placebo (4.5 (−0.8 to 15.3) vs. −4.0 (−11.3 to 0.8), P = .025). The Dykens hyperphagia questionnaire scores remained similar during oxytocin treatment, while there was a deterioration during placebo (0.0 (−0.8 to 4.3) vs. −3.5 (−6.0 to 0.0), P = .046). Patients with a deletion had significant improvements in both questionnaire scores during oxytocin treatment, but deteriorations during placebo. Oxytocin treatment was well tolerated, and there were no serious adverse events. CONCLUSIONS: Intranasal oxytocin treatment has positive effects on social and eating behaviour in 3‐11 years aged boys with PWS and in children with a deletion without safety concerns. Intranasal oxytocin in children with PWS might be considered, but individual effects should be carefully evaluated and treatment discontinued if no effects are found. John Wiley and Sons Inc. 2020-12-21 2021-05 /pmc/articles/PMC8246775/ /pubmed/33296519 http://dx.doi.org/10.1111/cen.14387 Text en © 2020 The Authors. Clinical Endocrinology published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ORIGINAL ARTICLES
Damen, Layla
Grootjen, Lionne N.
Juriaans, Alicia F.
Donze, Stephany H.
Huisman, T. Martin
Visser, Jenny A.
Delhanty, Patric J.D.
Hokken‐Koelega, Anita C.S.
Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title_full Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title_fullStr Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title_full_unstemmed Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title_short Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
title_sort oxytocin in young children with prader‐willi syndrome: results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246775/
https://www.ncbi.nlm.nih.gov/pubmed/33296519
http://dx.doi.org/10.1111/cen.14387
work_keys_str_mv AT damenlayla oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT grootjenlionnen oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT juriaansaliciaf oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT donzestephanyh oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT huismantmartin oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT visserjennya oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT delhantypatricjd oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin
AT hokkenkoelegaanitacs oxytocininyoungchildrenwithpraderwillisyndromeresultsofarandomizeddoubleblindplacebocontrolledcrossovertrialinvestigating3monthsofoxytocin