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Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome

BACKGROUND: Neuropsychiatric disorders are common in 22q11.2 Deletion Syndrome (22q11DS) with about 25% of affected individuals developing schizophrenia spectrum disorders by young adulthood. Longitudinal evaluation of psychosis spectrum features and neurocognition can establish developmental trajec...

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Autores principales: Gur, Raquel E., McDonald-McGinn, Donna M., Moore, Tyler M., Gallagher, R. Sean, McClellan, Emily, White, Lauren, Ruparel, Kosha, Hillman, Noah, Crowley, T. Blaine, McGinn, Daniel E., Zackai, Elaine, Emanuel, Beverly S., Calkins, Monica E., Roalf, David R., Gur, Ruben C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600823/
https://www.ncbi.nlm.nih.gov/pubmed/36987693
http://dx.doi.org/10.1017/S0033291723000259
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author Gur, Raquel E.
McDonald-McGinn, Donna M.
Moore, Tyler M.
Gallagher, R. Sean
McClellan, Emily
White, Lauren
Ruparel, Kosha
Hillman, Noah
Crowley, T. Blaine
McGinn, Daniel E.
Zackai, Elaine
Emanuel, Beverly S.
Calkins, Monica E.
Roalf, David R.
Gur, Ruben C.
author_facet Gur, Raquel E.
McDonald-McGinn, Donna M.
Moore, Tyler M.
Gallagher, R. Sean
McClellan, Emily
White, Lauren
Ruparel, Kosha
Hillman, Noah
Crowley, T. Blaine
McGinn, Daniel E.
Zackai, Elaine
Emanuel, Beverly S.
Calkins, Monica E.
Roalf, David R.
Gur, Ruben C.
author_sort Gur, Raquel E.
collection PubMed
description BACKGROUND: Neuropsychiatric disorders are common in 22q11.2 Deletion Syndrome (22q11DS) with about 25% of affected individuals developing schizophrenia spectrum disorders by young adulthood. Longitudinal evaluation of psychosis spectrum features and neurocognition can establish developmental trajectories and impact on functional outcome. METHODS: 157 youth with 22q11DS were assessed longitudinally for psychopathology focusing on psychosis spectrum symptoms, neurocognitive performance and global functioning. We contrasted the pattern of positive and negative psychosis spectrum symptoms and neurocognitive performance differentiating those with more prominent Psychosis Spectrum symptoms (PS+) to those without prominent psychosis symptoms (PS−). RESULTS: We identified differences in the trajectories of psychosis symptoms and neurocognitive performance between the groups. The PS+ group showed age associated increase in symptom severity, especially negative symptoms and general nonspecific symptoms. Correspondingly, their level of functioning was worse and deteriorated more steeply than the PS− group. Neurocognitive performance was generally comparable in PS+ and PS− groups and demonstrated a similar age-related trajectory. However, worsening executive functioning distinguished the PS+ group from PS− counterparts. Notably, of the three executive function measures examined, only working memory showed a significant difference between the groups in rate of change. Finally, structural equation modeling showed that neurocognitive decline drove the clinical change. CONCLUSIONS: Youth with 22q11DS and more prominent psychosis features show worsening of symptoms and functional decline driven by neurocognitive decline, most related to executive functions and specifically working memory. The results underscore the importance of working memory in the developmental progression of psychosis.
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spelling pubmed-106008232023-10-27 Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome Gur, Raquel E. McDonald-McGinn, Donna M. Moore, Tyler M. Gallagher, R. Sean McClellan, Emily White, Lauren Ruparel, Kosha Hillman, Noah Crowley, T. Blaine McGinn, Daniel E. Zackai, Elaine Emanuel, Beverly S. Calkins, Monica E. Roalf, David R. Gur, Ruben C. Psychol Med Original Article BACKGROUND: Neuropsychiatric disorders are common in 22q11.2 Deletion Syndrome (22q11DS) with about 25% of affected individuals developing schizophrenia spectrum disorders by young adulthood. Longitudinal evaluation of psychosis spectrum features and neurocognition can establish developmental trajectories and impact on functional outcome. METHODS: 157 youth with 22q11DS were assessed longitudinally for psychopathology focusing on psychosis spectrum symptoms, neurocognitive performance and global functioning. We contrasted the pattern of positive and negative psychosis spectrum symptoms and neurocognitive performance differentiating those with more prominent Psychosis Spectrum symptoms (PS+) to those without prominent psychosis symptoms (PS−). RESULTS: We identified differences in the trajectories of psychosis symptoms and neurocognitive performance between the groups. The PS+ group showed age associated increase in symptom severity, especially negative symptoms and general nonspecific symptoms. Correspondingly, their level of functioning was worse and deteriorated more steeply than the PS− group. Neurocognitive performance was generally comparable in PS+ and PS− groups and demonstrated a similar age-related trajectory. However, worsening executive functioning distinguished the PS+ group from PS− counterparts. Notably, of the three executive function measures examined, only working memory showed a significant difference between the groups in rate of change. Finally, structural equation modeling showed that neurocognitive decline drove the clinical change. CONCLUSIONS: Youth with 22q11DS and more prominent psychosis features show worsening of symptoms and functional decline driven by neurocognitive decline, most related to executive functions and specifically working memory. The results underscore the importance of working memory in the developmental progression of psychosis. Cambridge University Press 2023-10 2023-03-29 /pmc/articles/PMC10600823/ /pubmed/36987693 http://dx.doi.org/10.1017/S0033291723000259 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
Gur, Raquel E.
McDonald-McGinn, Donna M.
Moore, Tyler M.
Gallagher, R. Sean
McClellan, Emily
White, Lauren
Ruparel, Kosha
Hillman, Noah
Crowley, T. Blaine
McGinn, Daniel E.
Zackai, Elaine
Emanuel, Beverly S.
Calkins, Monica E.
Roalf, David R.
Gur, Ruben C.
Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title_full Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title_fullStr Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title_full_unstemmed Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title_short Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
title_sort psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600823/
https://www.ncbi.nlm.nih.gov/pubmed/36987693
http://dx.doi.org/10.1017/S0033291723000259
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