<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Perlstein S</submitter><funding>NIDA NIH HHS</funding><pagination>477-488</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11293992</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>133(6)</volume><pubmed_abstract>Childhood externalizing psychopathology is heterogeneous. Symptom variability in conduct disorder (CD), oppositional defiant disorder (ODD), attention-deficit/hyperactivity disorder (ADHD), and callous-unemotional (CU) traits designate different subgroups of children with externalizing problems who have specific treatment needs. However, CD, ODD, ADHD, and CU traits are highly comorbid. Studies need to generate insights into shared versus unique risk mechanisms, including through the use of functional magnetic resonance imaging (fMRI). In this study, we tested whether symptoms of CD, ODD, ADHD, and CU traits were best represented within a bifactor framework, simultaneously modeling shared (i.e., general externalizing problems) and unique (i.e., symptom-specific) variance, or through a four-correlated factor or second-order factor model. Participants (&lt;i>N&lt;/i> = 11,878, age, &lt;i>M&lt;/i> = 9 years) were from the Adolescent Brain and Cognitive Development Study. We used questionnaire and functional magnetic resonance imaging data (emotional N-back task) from the baseline assessment. A bifactor model specifying a general externalizing and specific CD, ODD, ADHD, and CU traits factors demonstrated the best fit. The four-correlated and second-order factor models both fit the data well and were retained for analyses. Across models, reduced right amygdala activity to fearful faces was associated with more general externalizing problems and reduced dorsolateral prefrontal cortex activity to fearful faces was associated with higher CU traits. ADHD scores were related to greater right nucleus accumbens activation to fearful and happy faces. Results give insights into risk mechanisms underlying comorbidity and heterogeneity within externalizing psychopathology. (PsycInfo Database Record (c) 2024 APA, all rights reserved).</pubmed_abstract><journal>Journal of psychopathology and clinical science</journal><pubmed_title>Unique versus shared neural correlates of externalizing psychopathology in late childhood.</pubmed_title><pmcid>PMC11293992</pmcid><funding_grant_id>U01 DA051037</funding_grant_id><funding_grant_id>U01 DA041117</funding_grant_id><funding_grant_id>U24 DA041123</funding_grant_id><funding_grant_id>U01 DA041106</funding_grant_id><funding_grant_id>U01 DA041028</funding_grant_id><funding_grant_id>U24 DA041147</funding_grant_id><funding_grant_id>U01 DA041089</funding_grant_id><funding_grant_id>U01 DA041022</funding_grant_id><funding_grant_id>U01 DA041120</funding_grant_id><funding_grant_id>U01 DA041174</funding_grant_id><funding_grant_id>U01 DA041148</funding_grant_id><funding_grant_id>U01 DA041048</funding_grant_id><funding_grant_id>U01 DA041025</funding_grant_id><funding_grant_id>U01 DA041134</funding_grant_id><funding_grant_id>U01 DA041156</funding_grant_id><funding_grant_id>U01 DA051039</funding_grant_id><funding_grant_id>U01 DA051016</funding_grant_id><funding_grant_id>U01 DA051038</funding_grant_id><funding_grant_id>U01 DA051018</funding_grant_id><funding_grant_id>U01 DA050988</funding_grant_id><funding_grant_id>U01 DA050987</funding_grant_id><funding_grant_id>U01 DA041093</funding_grant_id><funding_grant_id>U01 DA050989</funding_grant_id><pubmed_authors>Gur RE</pubmed_authors><pubmed_authors>Perlstein S</pubmed_authors><pubmed_authors>Waller R</pubmed_authors><pubmed_authors>Byrd AL</pubmed_authors><pubmed_authors>Barzilay R</pubmed_authors><pubmed_authors>Laird AR</pubmed_authors><pubmed_authors>Hawes SW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unique versus shared neural correlates of externalizing psychopathology in late childhood.</name><description>Childhood externalizing psychopathology is heterogeneous. Symptom variability in conduct disorder (CD), oppositional defiant disorder (ODD), attention-deficit/hyperactivity disorder (ADHD), and callous-unemotional (CU) traits designate different subgroups of children with externalizing problems who have specific treatment needs. However, CD, ODD, ADHD, and CU traits are highly comorbid. Studies need to generate insights into shared versus unique risk mechanisms, including through the use of functional magnetic resonance imaging (fMRI). In this study, we tested whether symptoms of CD, ODD, ADHD, and CU traits were best represented within a bifactor framework, simultaneously modeling shared (i.e., general externalizing problems) and unique (i.e., symptom-specific) variance, or through a four-correlated factor or second-order factor model. Participants (&lt;i>N&lt;/i> = 11,878, age, &lt;i>M&lt;/i> = 9 years) were from the Adolescent Brain and Cognitive Development Study. We used questionnaire and functional magnetic resonance imaging data (emotional N-back task) from the baseline assessment. A bifactor model specifying a general externalizing and specific CD, ODD, ADHD, and CU traits factors demonstrated the best fit. The four-correlated and second-order factor models both fit the data well and were retained for analyses. Across models, reduced right amygdala activity to fearful faces was associated with more general externalizing problems and reduced dorsolateral prefrontal cortex activity to fearful faces was associated with higher CU traits. ADHD scores were related to greater right nucleus accumbens activation to fearful and happy faces. Results give insights into risk mechanisms underlying comorbidity and heterogeneity within externalizing psychopathology. (PsycInfo Database Record (c) 2024 APA, all rights reserved).</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-03-17T15:32:14.729Z</modification><creation>2025-08-16T03:06:55.71Z</creation></dates><accession>S-EPMC11293992</accession><cross_references><pubmed>38869879</pubmed><doi>10.1037/abn0000923</doi></cross_references></HashMap>