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Developmental trajectories of executive functions in 22q11.2 deletion syndrome
BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder associated with a specific cognitive profile. Higher-order cognitive skills like executive functions (EF) are reported as a relative weakness in this population. The present study aimed to delineate the developmental trajectorie...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807556/ https://www.ncbi.nlm.nih.gov/pubmed/27018204 http://dx.doi.org/10.1186/s11689-016-9141-1 |
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author | Maeder, Johanna Schneider, Maude Bostelmann, Mathilde Debbané, Martin Glaser, Bronwyn Menghetti, Sarah Schaer, Marie Eliez, Stephan |
author_facet | Maeder, Johanna Schneider, Maude Bostelmann, Mathilde Debbané, Martin Glaser, Bronwyn Menghetti, Sarah Schaer, Marie Eliez, Stephan |
author_sort | Maeder, Johanna |
collection | PubMed |
description | BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder associated with a specific cognitive profile. Higher-order cognitive skills like executive functions (EF) are reported as a relative weakness in this population. The present study aimed to delineate the developmental trajectories of multiple EF domains in a longitudinal sample using a broader age range than previous studies. Given the high incidence of psychotic symptoms in 22q11.2DS, we also compared the development of EF in participants with/without comorbid psychotic symptoms. Given the importance of EF in daily life, the third aim of the study was to characterize the link between EF and adaptive functioning. METHODS: The sample consisted of 95 individuals with 22q11.2DS and 100 typically developing controls aged 6–26 years. A large proportion of the sample (55.38 %) had multiple time points available. Between-group differences in the developmental trajectories of three subdomains of EF (verbal fluency, working memory, and inhibition) were examined using mixed models regression analyses. Analyses were repeated comparing only the 22q11.2DS group based on the presence/absence of psychotic symptoms to investigate the influence of executive dysfunction on the emergence of psychotic symptoms. Hierarchical stepwise regression analyses were also conducted to investigate the predictive value of EF on adaptive functioning. RESULTS: We observed lower performance on EF domains, as well as atypical development of working memory and verbal fluency. Participants who presented with negative symptoms exhibited different developmental trajectories of inhibition and working memory. Adaptive functioning level was not significantly predicted by EF scores. CONCLUSIONS: The present study highlighted domain-specific atypical trajectories of EF in individuals with 22q11.DS and explored the link with psychotic symptoms. However, no relation between EF and adaptive functioning was observed. |
format | Online Article Text |
id | pubmed-4807556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48075562016-03-25 Developmental trajectories of executive functions in 22q11.2 deletion syndrome Maeder, Johanna Schneider, Maude Bostelmann, Mathilde Debbané, Martin Glaser, Bronwyn Menghetti, Sarah Schaer, Marie Eliez, Stephan J Neurodev Disord Research BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a genetic disorder associated with a specific cognitive profile. Higher-order cognitive skills like executive functions (EF) are reported as a relative weakness in this population. The present study aimed to delineate the developmental trajectories of multiple EF domains in a longitudinal sample using a broader age range than previous studies. Given the high incidence of psychotic symptoms in 22q11.2DS, we also compared the development of EF in participants with/without comorbid psychotic symptoms. Given the importance of EF in daily life, the third aim of the study was to characterize the link between EF and adaptive functioning. METHODS: The sample consisted of 95 individuals with 22q11.2DS and 100 typically developing controls aged 6–26 years. A large proportion of the sample (55.38 %) had multiple time points available. Between-group differences in the developmental trajectories of three subdomains of EF (verbal fluency, working memory, and inhibition) were examined using mixed models regression analyses. Analyses were repeated comparing only the 22q11.2DS group based on the presence/absence of psychotic symptoms to investigate the influence of executive dysfunction on the emergence of psychotic symptoms. Hierarchical stepwise regression analyses were also conducted to investigate the predictive value of EF on adaptive functioning. RESULTS: We observed lower performance on EF domains, as well as atypical development of working memory and verbal fluency. Participants who presented with negative symptoms exhibited different developmental trajectories of inhibition and working memory. Adaptive functioning level was not significantly predicted by EF scores. CONCLUSIONS: The present study highlighted domain-specific atypical trajectories of EF in individuals with 22q11.DS and explored the link with psychotic symptoms. However, no relation between EF and adaptive functioning was observed. BioMed Central 2016-03-25 /pmc/articles/PMC4807556/ /pubmed/27018204 http://dx.doi.org/10.1186/s11689-016-9141-1 Text en © Maeder et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Maeder, Johanna Schneider, Maude Bostelmann, Mathilde Debbané, Martin Glaser, Bronwyn Menghetti, Sarah Schaer, Marie Eliez, Stephan Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title | Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title_full | Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title_fullStr | Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title_full_unstemmed | Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title_short | Developmental trajectories of executive functions in 22q11.2 deletion syndrome |
title_sort | developmental trajectories of executive functions in 22q11.2 deletion syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807556/ https://www.ncbi.nlm.nih.gov/pubmed/27018204 http://dx.doi.org/10.1186/s11689-016-9141-1 |
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