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Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents.
Bullying victimization is associated with a doubled risk of attempting suicide in adulthood. Two longitudinal brain morphometry studies identified the fusiform gyrus and putamen as vulnerable to bullying. No study identified how neural alterations may mediate the effect of bullying on cognition. We...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163612/ https://www.ncbi.nlm.nih.gov/pubmed/37119589 http://dx.doi.org/10.1016/j.dcn.2023.101247 |
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author | Menken, Miriam S. Rodriguez Rivera, Pedro J Isaiah, Amal Ernst, Thomas Cloak, Christine C. Chang, Linda |
author_facet | Menken, Miriam S. Rodriguez Rivera, Pedro J Isaiah, Amal Ernst, Thomas Cloak, Christine C. Chang, Linda |
author_sort | Menken, Miriam S. |
collection | PubMed |
description | Bullying victimization is associated with a doubled risk of attempting suicide in adulthood. Two longitudinal brain morphometry studies identified the fusiform gyrus and putamen as vulnerable to bullying. No study identified how neural alterations may mediate the effect of bullying on cognition. We assessed participants with caregiver-reported bullying (N = 323) and matched non-bullied controls (N = 322) from the Adolescent Brain Cognitive Development Study dataset to identify changes in brain morphometry associated with ongoing bullying victimization over two years and determine whether such alterations mediated the effect of bullying on cognition. Bullied children (38.7% girls, 47.7% racial minorities, 9.88 ± 0.62 years at baseline) had poorer cognitive performance (P < 0.05), larger right hippocampus (P = 0.036), left entorhinal cortex, left superior parietal cortex, and right fusiform gyrus volumes (all P < 0.05), as well as larger surface areas in multiple other frontal, parietal, and occipital cortices. Thinner cortices were also found in the left hemisphere, particularly in the left temporal lobe, and right frontal region (all P < 0.05). Importantly, larger surface area in the fusiform cortices partially suppressed (12–16%), and thinner precentral cortices partially mitigated, (7%) the effect of bullying on cognition (P < 0.05). These findings highlight the negative impact of prolonged bullying victimization on brain morphometry and cognition. |
format | Online Article Text |
id | pubmed-10163612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101636122023-05-07 Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. Menken, Miriam S. Rodriguez Rivera, Pedro J Isaiah, Amal Ernst, Thomas Cloak, Christine C. Chang, Linda Dev Cogn Neurosci Original Research Bullying victimization is associated with a doubled risk of attempting suicide in adulthood. Two longitudinal brain morphometry studies identified the fusiform gyrus and putamen as vulnerable to bullying. No study identified how neural alterations may mediate the effect of bullying on cognition. We assessed participants with caregiver-reported bullying (N = 323) and matched non-bullied controls (N = 322) from the Adolescent Brain Cognitive Development Study dataset to identify changes in brain morphometry associated with ongoing bullying victimization over two years and determine whether such alterations mediated the effect of bullying on cognition. Bullied children (38.7% girls, 47.7% racial minorities, 9.88 ± 0.62 years at baseline) had poorer cognitive performance (P < 0.05), larger right hippocampus (P = 0.036), left entorhinal cortex, left superior parietal cortex, and right fusiform gyrus volumes (all P < 0.05), as well as larger surface areas in multiple other frontal, parietal, and occipital cortices. Thinner cortices were also found in the left hemisphere, particularly in the left temporal lobe, and right frontal region (all P < 0.05). Importantly, larger surface area in the fusiform cortices partially suppressed (12–16%), and thinner precentral cortices partially mitigated, (7%) the effect of bullying on cognition (P < 0.05). These findings highlight the negative impact of prolonged bullying victimization on brain morphometry and cognition. Elsevier 2023-04-25 /pmc/articles/PMC10163612/ /pubmed/37119589 http://dx.doi.org/10.1016/j.dcn.2023.101247 Text en © 2023 Published by Elsevier Ltd. 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 | Original Research Menken, Miriam S. Rodriguez Rivera, Pedro J Isaiah, Amal Ernst, Thomas Cloak, Christine C. Chang, Linda Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title | Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title_full | Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title_fullStr | Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title_full_unstemmed | Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title_short | Longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
title_sort | longitudinal alterations in brain morphometry mediated the effects of bullying victimization on cognitive development in preadolescents. |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163612/ https://www.ncbi.nlm.nih.gov/pubmed/37119589 http://dx.doi.org/10.1016/j.dcn.2023.101247 |
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