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Psychopathology in children: The transdiagnostic contribution of affiliative capacity and inhibitory control

Published online by Cambridge University Press:  09 June 2022

Isabella M. Palumbo*
Affiliation:
Department of Psychology, Georgia State University, Atlanta, GA, USA
Christopher J. Patrick
Affiliation:
Department of Psychology, Florida State University, Tallahassee, FL, USA
Robert D. Latzman
Affiliation:
Takeda Pharmaceuticals, Tokyo, Japan
*
Corresponding author: Isabella M. Palumbo, email: ipalumbo1@gsu.edu
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Abstract

Recent initiatives have focused on integrating transdiagnostic biobehavioral processes or dispositions with dimensional models of psychopathology. Toward this goal, biobehavioral traits of affiliative capacity (AFF) and inhibitory control (INH) hold particular promise as they demonstrate transdiagnostic stability and predictive validity across developmental stages and differing measurement modalities. The current study employed data from different modes of measurement in a sample of 1830 children aged 5–10 years to test for associations of AFF and INH, individually and interactively, with broad dimensions of psychopathology. Low AFF, assessed via parent-report, evidenced predictive relations with distress- and externalizing-related problems. INH as assessed by cognitive-task performance did not relate itself to either psychopathology dimension, but it moderated the effects observed for low AFF, such that high INH protected against distress symptoms in low-AFF participants, whereas low INH amplified distress and externalizing symptoms in low-AFF participants. Results are discussed in the context of the interface of general trait transdiagnostic risk factors with quantitatively derived dimensional models of psychopathology.

Information

Type
Regular Article
Copyright
© The Author(s), 2022. Published by Cambridge University Press
Figure 0

Figure 1. Confirmatory factor analysis of K-SADS psychopathology lifetime symptom counts (RMSEA = .037, CFI = .876, TLI = .825, SRMR = .039, Chi-squared = 92.836, p < .001); K-SADS = Kiddie Schedule Affective Disorders and Schizophrenia. N = 1360.

Figure 1

Figure 2. Exploratory factor analysis of affiliative capacity (RMSEA = .075, CFI = .901, TLI = .877, SRMR = .051, Chi-squared = 578.562, p < .001); ICU = Inventory of Callous Unemotional Traits, CBCL = Child Behavior Checklist, SDQ = Strengths and Difficulties Questionnaire. * indicates reverse-keyed items. N = 1430.

Figure 2

Figure 3. Confirmatory factor analysis of neurocognitive task-based indicators (df = 0; model just-identified); SAIT = Sustained Attention and Impulsivity Task. N = 794.

Figure 3

Figure 4. Main effect of low affiliative capacity and inhibitory control on factors of psychopathology; N = 1671.

Figure 4

Figure 5. Simple slopes plot of interaction between HBN meanness (low affiliative capacity) and inhibitory control in the prediction of distress.

Figure 5

Figure 6. Simple slopes plot of interaction between meanness (low affiliative capacity) and inhibitory control in the prediction of externalizing. Note. Region of significance: lower bound = −0.40, upper bound = 0.91; N = 311; 19%. Region of significance: lower bound = −0.09, upper bound = 0.37; N = 525, 31%.

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