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Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study

Schizophrenia, a debilitating disorder with typical manifestation of clinical symptoms in early adulthood, is characterized by cognitive impairments in executive processes such as in working memory (WM). However, there is a rare case of individuals with early-onset schizophrenia (EOS) starting befor...

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Autores principales: Ioakeimidis, Vasileios, Haenschel, Corinna, Fett, Anne-Kathrin, Kyriakopoulos, Marinos, Dima, Danai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372770/
https://www.ncbi.nlm.nih.gov/pubmed/35967473
http://dx.doi.org/10.1016/j.scog.2022.100268
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author Ioakeimidis, Vasileios
Haenschel, Corinna
Fett, Anne-Kathrin
Kyriakopoulos, Marinos
Dima, Danai
author_facet Ioakeimidis, Vasileios
Haenschel, Corinna
Fett, Anne-Kathrin
Kyriakopoulos, Marinos
Dima, Danai
author_sort Ioakeimidis, Vasileios
collection PubMed
description Schizophrenia, a debilitating disorder with typical manifestation of clinical symptoms in early adulthood, is characterized by cognitive impairments in executive processes such as in working memory (WM). However, there is a rare case of individuals with early-onset schizophrenia (EOS) starting before their 18th birthday, while WM and its neural substrates are still undergoing maturation. Using the WM n-back task with functional magnetic resonance imaging, we assessed the functional neurodevelopment of WM in adolescents with EOS and age- and gender-matched typically developing controls. Participants underwent neuroimaging in the same scanner twice, once at age 17 and at 21 (mean interscan interval = 4.3 years). General linear model analysis was performed to explore WM neurodevelopmental changes within and between groups. Psychopathological scores were entered in multiple regressions to detect brain regions whose longitudinal functional change was predicted by baseline symptoms in EOS. WM neurodevelopment was characterized by widespread functional reductions in frontotemporal and cingulate brain areas in patients and controls. No between-group differences were found in the trajectory of WM change. Baseline symptom scores predicted functional neurodevelopmental changes in frontal, cingulate, parietal, occipital, and cerebellar areas. The adolescent brain undergoes developmental processes such as synaptic pruning, which may underlie the refinement WM of network. Prefrontal and parietooccipital activity reduction is affected by clinical presentation of symptoms. Using longitudinal neuroimaging methods in a rare diagnostic sample of patients with EOS may help the advancement of neurodevelopmental biomarkers intended as pharmacological targets to tackle WM impairment.
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spelling pubmed-93727702022-08-13 Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study Ioakeimidis, Vasileios Haenschel, Corinna Fett, Anne-Kathrin Kyriakopoulos, Marinos Dima, Danai Schizophr Res Cogn Research Paper Schizophrenia, a debilitating disorder with typical manifestation of clinical symptoms in early adulthood, is characterized by cognitive impairments in executive processes such as in working memory (WM). However, there is a rare case of individuals with early-onset schizophrenia (EOS) starting before their 18th birthday, while WM and its neural substrates are still undergoing maturation. Using the WM n-back task with functional magnetic resonance imaging, we assessed the functional neurodevelopment of WM in adolescents with EOS and age- and gender-matched typically developing controls. Participants underwent neuroimaging in the same scanner twice, once at age 17 and at 21 (mean interscan interval = 4.3 years). General linear model analysis was performed to explore WM neurodevelopmental changes within and between groups. Psychopathological scores were entered in multiple regressions to detect brain regions whose longitudinal functional change was predicted by baseline symptoms in EOS. WM neurodevelopment was characterized by widespread functional reductions in frontotemporal and cingulate brain areas in patients and controls. No between-group differences were found in the trajectory of WM change. Baseline symptom scores predicted functional neurodevelopmental changes in frontal, cingulate, parietal, occipital, and cerebellar areas. The adolescent brain undergoes developmental processes such as synaptic pruning, which may underlie the refinement WM of network. Prefrontal and parietooccipital activity reduction is affected by clinical presentation of symptoms. Using longitudinal neuroimaging methods in a rare diagnostic sample of patients with EOS may help the advancement of neurodevelopmental biomarkers intended as pharmacological targets to tackle WM impairment. Elsevier 2022-08-08 /pmc/articles/PMC9372770/ /pubmed/35967473 http://dx.doi.org/10.1016/j.scog.2022.100268 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Ioakeimidis, Vasileios
Haenschel, Corinna
Fett, Anne-Kathrin
Kyriakopoulos, Marinos
Dima, Danai
Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title_full Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title_fullStr Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title_full_unstemmed Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title_short Functional neurodevelopment of working memory in early-onset schizophrenia: A longitudinal FMRI study
title_sort functional neurodevelopment of working memory in early-onset schizophrenia: a longitudinal fmri study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372770/
https://www.ncbi.nlm.nih.gov/pubmed/35967473
http://dx.doi.org/10.1016/j.scog.2022.100268
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