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dc.date.accessioned2023-02-04T17:47:28Z
dc.date.available2023-02-04T17:47:28Z
dc.date.created2022-10-19T10:44:10Z
dc.date.issued2022
dc.identifier.citationHolz, 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. Psychological Medicine. 2022
dc.identifier.urihttp://hdl.handle.net/10852/99661
dc.description.abstractBackground 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.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAge-related brain deviations and aggression
dc.title.alternativeENEngelskEnglishAge-related brain deviations and aggression
dc.typeJournal article
dc.creator.authorHolz, Nathalie E.
dc.creator.authorFloris, Dorothea L.
dc.creator.authorLlera, Alberto
dc.creator.authorAggensteiner, Pascal M.
dc.creator.authorKia, Seyed Mostafa
dc.creator.authorWolfers, Thomas
dc.creator.authorBaumeister, Sarah
dc.creator.authorBöttinger, Boris
dc.creator.authorGlennon, Jeffrey C.
dc.creator.authorHoekstra, Pieter J.
dc.creator.authorDietrich, Andrea
dc.creator.authorSaam, Melanie C.
dc.creator.authorSchulze, Ulrike M. E.
dc.creator.authorLythgoe, David J.
dc.creator.authorWilliams, Steve C. R.
dc.creator.authorSantosh, Paramala
dc.creator.authorRosa-Justicia, Mireia
dc.creator.authorBargallo, Nuria
dc.creator.authorCastro-Fornieles, Josefina
dc.creator.authorArango, Celso
dc.creator.authorPenzol, Maria J.
dc.creator.authorWalitza, Susanne
dc.creator.authorMeyer-Lindenberg, Andreas
dc.creator.authorZwiers, Marcel
dc.creator.authorFranke, Barbara
dc.creator.authorBuitelaar, Jan
dc.creator.authorNaaijen, Jilly
dc.creator.authorBrandeis, Daniel
dc.creator.authorBeckmann, Christian
dc.creator.authorBanaschewski, Tobias
dc.creator.authorMarquand, Andre F.
cristin.unitcode185,53,10,70
cristin.unitnameNORMENT part UiO
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2062661
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Psychological Medicine&rft.volume=&rft.spage=&rft.date=2022
dc.identifier.jtitlePsychological Medicine
dc.identifier.startpage1
dc.identifier.endpage10
dc.identifier.pagecount10
dc.identifier.doihttps://doi.org/10.1017/S003329172200068X
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0033-2917
dc.type.versionPublishedVersion


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