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Psychopathology and cognition in children with 22q11.2 deletion syndrome
Background Children with 22q11.2 deletion syndrome (22q11.2DS) have been reported to have high rates of cognitive and psychiatric problems. Aims To establish the nature and prevalence of psychiatric disorder and neurocognitive impairment in children with 22q11.2DS and test whether risk of psychopath...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal College of Psychiatrists
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877833/ https://www.ncbi.nlm.nih.gov/pubmed/24115343 http://dx.doi.org/10.1192/bjp.bp.113.132324 |
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author | Niarchou, Maria Zammit, Stanley van Goozen, Stephanie H. M. Thapar, Anita Tierling, Hayley M. Owen, Michael J. van den Bree, Marianne B. M. |
author_facet | Niarchou, Maria Zammit, Stanley van Goozen, Stephanie H. M. Thapar, Anita Tierling, Hayley M. Owen, Michael J. van den Bree, Marianne B. M. |
author_sort | Niarchou, Maria |
collection | PubMed |
description | Background Children with 22q11.2 deletion syndrome (22q11.2DS) have been reported to have high rates of cognitive and psychiatric problems. Aims To establish the nature and prevalence of psychiatric disorder and neurocognitive impairment in children with 22q11.2DS and test whether risk of psychopathology is mediated by the children’s intellectual impairment. Method Neurocognition and psychopathology were assessed in 80 children with 22q11.2DS (mean age 10.2 years, s.d. = 2.1) and 39 sibling controls (mean age 10.9 years, s.d. = 2.0). Results More than half (54%) of children with 22q11.2DS met diagnostic criteria for one or more DSM-IV-TR psychiatric disorder. These children had lower IQ (mean 76.8, s.d. = 13.0) than controls (mean 108.6, s.d. = 15.2) (P<0.001) and showed a range of neurocognitive impairments. Increased risk of psychopathology was not mediated by intellectual impairment. Conclusions 22q11.2DS is not related to a specific psychiatric phenotype in children. Moreover, the deletion has largely independent effects on IQ and risk of psychopathology, indicating that psychopathology in 22q11.2DS is not a non-specific consequence of generalised cognitive impairment. |
format | Online Article Text |
id | pubmed-3877833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Royal College of Psychiatrists |
record_format | MEDLINE/PubMed |
spelling | pubmed-38778332014-01-06 Psychopathology and cognition in children with 22q11.2 deletion syndrome Niarchou, Maria Zammit, Stanley van Goozen, Stephanie H. M. Thapar, Anita Tierling, Hayley M. Owen, Michael J. van den Bree, Marianne B. M. Br J Psychiatry Papers Background Children with 22q11.2 deletion syndrome (22q11.2DS) have been reported to have high rates of cognitive and psychiatric problems. Aims To establish the nature and prevalence of psychiatric disorder and neurocognitive impairment in children with 22q11.2DS and test whether risk of psychopathology is mediated by the children’s intellectual impairment. Method Neurocognition and psychopathology were assessed in 80 children with 22q11.2DS (mean age 10.2 years, s.d. = 2.1) and 39 sibling controls (mean age 10.9 years, s.d. = 2.0). Results More than half (54%) of children with 22q11.2DS met diagnostic criteria for one or more DSM-IV-TR psychiatric disorder. These children had lower IQ (mean 76.8, s.d. = 13.0) than controls (mean 108.6, s.d. = 15.2) (P<0.001) and showed a range of neurocognitive impairments. Increased risk of psychopathology was not mediated by intellectual impairment. Conclusions 22q11.2DS is not related to a specific psychiatric phenotype in children. Moreover, the deletion has largely independent effects on IQ and risk of psychopathology, indicating that psychopathology in 22q11.2DS is not a non-specific consequence of generalised cognitive impairment. Royal College of Psychiatrists 2014-01 /pmc/articles/PMC3877833/ /pubmed/24115343 http://dx.doi.org/10.1192/bjp.bp.113.132324 Text en Royal College of Psychiatrists Royal College of Psychiatrists, This paper accords with the Wellcome Trust Open Access policy and is governed by the licence available at http://www.rcpsych.ac.uk/pdf/Wellcome%20Trust%20licence.pdf |
spellingShingle | Papers Niarchou, Maria Zammit, Stanley van Goozen, Stephanie H. M. Thapar, Anita Tierling, Hayley M. Owen, Michael J. van den Bree, Marianne B. M. Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title | Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title_full | Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title_fullStr | Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title_full_unstemmed | Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title_short | Psychopathology and cognition in children with 22q11.2 deletion syndrome |
title_sort | psychopathology and cognition in children with 22q11.2 deletion syndrome |
topic | Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877833/ https://www.ncbi.nlm.nih.gov/pubmed/24115343 http://dx.doi.org/10.1192/bjp.bp.113.132324 |
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