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Age-related brain deviations and aggression
BACKGROUND: Disruptive behavior disorders (DBD) are heterogeneous at the clinical and the biological level. Therefore, the aims were to dissect the heterogeneous neurodevelopmental deviations of the affective brain circuitry and provide an integration of these differences across modalities. METHODS:...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325848/ https://www.ncbi.nlm.nih.gov/pubmed/35450543 http://dx.doi.org/10.1017/S003329172200068X |
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author | Holz, Nathalie E. Floris, Dorothea L. Llera, Alberto Aggensteiner, Pascal M. Kia, Seyed Mostafa Wolfers, Thomas Baumeister, Sarah Böttinger, Boris Glennon, Jeffrey C. Hoekstra, Pieter J. Dietrich, Andrea Saam, Melanie C. Schulze, Ulrike M. E. Lythgoe, David J. Williams, Steve C. R. Santosh, Paramala Rosa-Justicia, Mireia Bargallo, Nuria Castro-Fornieles, Josefina Arango, Celso Penzol, Maria J. Walitza, Susanne Meyer-Lindenberg, Andreas Zwiers, Marcel Franke, Barbara Buitelaar, Jan Naaijen, Jilly Brandeis, Daniel Beckmann, Christian Banaschewski, Tobias Marquand, Andre F. |
author_facet | Holz, Nathalie E. Floris, Dorothea L. Llera, Alberto Aggensteiner, Pascal M. Kia, Seyed Mostafa Wolfers, Thomas Baumeister, Sarah Böttinger, Boris Glennon, Jeffrey C. Hoekstra, Pieter J. Dietrich, Andrea Saam, Melanie C. Schulze, Ulrike M. E. Lythgoe, David J. Williams, Steve C. R. Santosh, Paramala Rosa-Justicia, Mireia Bargallo, Nuria Castro-Fornieles, Josefina Arango, Celso Penzol, Maria J. Walitza, Susanne Meyer-Lindenberg, Andreas Zwiers, Marcel Franke, Barbara Buitelaar, Jan Naaijen, Jilly Brandeis, Daniel Beckmann, Christian Banaschewski, Tobias Marquand, Andre F. |
author_sort | Holz, Nathalie E. |
collection | PubMed |
description | BACKGROUND: Disruptive behavior disorders (DBD) are heterogeneous at the clinical and the biological level. Therefore, the aims were to dissect the heterogeneous neurodevelopmental deviations of the affective brain circuitry and provide an integration of these differences across modalities. METHODS: We combined two novel approaches. First, normative modeling to map deviations from the typical age-related pattern at the level of the individual of (i) activity during emotion matching and (ii) of anatomical images derived from DBD cases (n = 77) and controls (n = 52) aged 8–18 years from the EU-funded Aggressotype and MATRICS consortia. Second, linked independent component analysis to integrate subject-specific deviations from both modalities. RESULTS: While cases exhibited on average a higher activity than would be expected for their age during face processing in regions such as the amygdala when compared to controls these positive deviations were widespread at the individual level. A multimodal integration of all functional and anatomical deviations explained 23% of the variance in the clinical DBD phenotype. Most notably, the top marker, encompassing the default mode network (DMN) and subcortical regions such as the amygdala and the striatum, was related to aggression across the whole sample. CONCLUSIONS: Overall increased age-related deviations in the amygdala in DBD suggest a maturational delay, which has to be further validated in future studies. Further, the integration of individual deviation patterns from multiple imaging modalities allowed to dissect some of the heterogeneity of DBD and identified the DMN, the striatum and the amygdala as neural signatures that were associated with aggression. |
format | Online Article Text |
id | pubmed-10325848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103258482023-07-07 Age-related brain deviations and aggression Holz, Nathalie E. Floris, Dorothea L. Llera, Alberto Aggensteiner, Pascal M. Kia, Seyed Mostafa Wolfers, Thomas Baumeister, Sarah Böttinger, Boris Glennon, Jeffrey C. Hoekstra, Pieter J. Dietrich, Andrea Saam, Melanie C. Schulze, Ulrike M. E. Lythgoe, David J. Williams, Steve C. R. Santosh, Paramala Rosa-Justicia, Mireia Bargallo, Nuria Castro-Fornieles, Josefina Arango, Celso Penzol, Maria J. Walitza, Susanne Meyer-Lindenberg, Andreas Zwiers, Marcel Franke, Barbara Buitelaar, Jan Naaijen, Jilly Brandeis, Daniel Beckmann, Christian Banaschewski, Tobias Marquand, Andre F. Psychol Med Original Article BACKGROUND: Disruptive behavior disorders (DBD) are heterogeneous at the clinical and the biological level. Therefore, the aims were to dissect the heterogeneous neurodevelopmental deviations of the affective brain circuitry and provide an integration of these differences across modalities. METHODS: We combined two novel approaches. First, normative modeling to map deviations from the typical age-related pattern at the level of the individual of (i) activity during emotion matching and (ii) of anatomical images derived from DBD cases (n = 77) and controls (n = 52) aged 8–18 years from the EU-funded Aggressotype and MATRICS consortia. Second, linked independent component analysis to integrate subject-specific deviations from both modalities. RESULTS: While cases exhibited on average a higher activity than would be expected for their age during face processing in regions such as the amygdala when compared to controls these positive deviations were widespread at the individual level. A multimodal integration of all functional and anatomical deviations explained 23% of the variance in the clinical DBD phenotype. Most notably, the top marker, encompassing the default mode network (DMN) and subcortical regions such as the amygdala and the striatum, was related to aggression across the whole sample. CONCLUSIONS: Overall increased age-related deviations in the amygdala in DBD suggest a maturational delay, which has to be further validated in future studies. Further, the integration of individual deviation patterns from multiple imaging modalities allowed to dissect some of the heterogeneity of DBD and identified the DMN, the striatum and the amygdala as neural signatures that were associated with aggression. Cambridge University Press 2023-07 2022-04-22 /pmc/articles/PMC10325848/ /pubmed/35450543 http://dx.doi.org/10.1017/S003329172200068X Text en © Central Institute of Mental Health 2022 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 Holz, Nathalie E. Floris, Dorothea L. Llera, Alberto Aggensteiner, Pascal M. Kia, Seyed Mostafa Wolfers, Thomas Baumeister, Sarah Böttinger, Boris Glennon, Jeffrey C. Hoekstra, Pieter J. Dietrich, Andrea Saam, Melanie C. Schulze, Ulrike M. E. Lythgoe, David J. Williams, Steve C. R. Santosh, Paramala Rosa-Justicia, Mireia Bargallo, Nuria Castro-Fornieles, Josefina Arango, Celso Penzol, Maria J. Walitza, Susanne Meyer-Lindenberg, Andreas Zwiers, Marcel Franke, Barbara Buitelaar, Jan Naaijen, Jilly Brandeis, Daniel Beckmann, Christian Banaschewski, Tobias Marquand, Andre F. Age-related brain deviations and aggression |
title | Age-related brain deviations and aggression |
title_full | Age-related brain deviations and aggression |
title_fullStr | Age-related brain deviations and aggression |
title_full_unstemmed | Age-related brain deviations and aggression |
title_short | Age-related brain deviations and aggression |
title_sort | age-related brain deviations and aggression |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325848/ https://www.ncbi.nlm.nih.gov/pubmed/35450543 http://dx.doi.org/10.1017/S003329172200068X |
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