TY - JOUR
T1 - Age-related brain deviations and aggression
AU - Holz, Nathalie E.
AU - Floris, Dorothea L.
AU - Llera, Alberto
AU - Aggensteiner, Pascal M.
AU - Kia, Seyed Mostafa
AU - Wolfers, Thomas
AU - Baumeister, Sarah
AU - Boettinger, Boris
AU - Glennon, Jeffrey C.
AU - Hoekstra, Pieter J.
AU - Dietrich, Andrea
AU - Saam, Melanie C.
AU - Schulze, Ulrike M. E.
AU - Lythgoe, David J.
AU - Williams, Steve C. R.
AU - Santosh, Paramala
AU - Rosa-Justicia, Mireia
AU - Bargallo, Nuria
AU - Castro-Fornieles, Josefina
AU - Arango, Celso
AU - Penzol, Maria J.
AU - Walitza, Susanne
AU - Meyer-Lindenberg, Andreas
AU - Zwiers, Marcel
AU - Franke, Barbara
AU - Buitelaar, Jan
AU - Naaijen, Jilly
AU - Brandeis, Daniel
AU - Beckmann, Christian
AU - Banaschewski, Tobias
AU - Marquand, Andre F.
PY - 2022/4/22
Y1 - 2022/4/22
N2 - 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.
AB - 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.
KW - Aggression
KW - disruptive behavior disorders
KW - emotion processing
KW - fMRI
KW - normative modeling
KW - CALLOUS-UNEMOTIONAL TRAITS
KW - INDEPENDENT COMPONENT ANALYSIS
KW - OPPOSITIONAL DEFIANT DISORDER
KW - CONDUCT DISORDER
KW - PROACTIVE AGGRESSION
KW - METAANALYSIS
KW - CHILDREN
KW - RELIABILITY
KW - VALIDITY
KW - YOUTHS
U2 - 10.1017/S003329172200068X
DO - 10.1017/S003329172200068X
M3 - Article
C2 - 35450543
SN - 0033-2917
JO - Psychological Medicine
JF - Psychological Medicine
ER -