Clarifying Relations Between ADHD and Functional Impairment in Adulthood: Utilization of Network and Machine Learning Approaches
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Psychology
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Using network analysis and random forest regression, this study identified attention-deficit/hyperactivity disorder (ADHD) symptoms most important for indicating impairment in various functional domains. Participants comprised a nationally representative sample of 1249 adults in the United States. Bridge symptoms were identified as those demonstrating unique relations with impairment domains that, in total, were stronger than those involving other symptoms. Results suggested three inattentive (i.e., ) and one hyperactive () bridge symptoms. Random forest regression results supported bridge symptoms as most important (compared to other symptoms) for predicting global and specific impairment domains. Hyperactive/impulsive symptoms appeared more strongly related to impairment in women, whereas and appeared more related to impairment in men. Clarification of bridge symptoms may help identify core characteristics of ADHD in adulthood and specify screening and intervention targets to reduce risk for related impairment.
Komijani S, Ghosal D, Singh M, Schweitzer J, Mukherjee P Front Psychiatry. 2025; 15:1467486.
PMID: 40013023 PMC: 11861207. DOI: 10.3389/fpsyt.2024.1467486.
van der Pal Z, Geurts H, Haslbeck J, van Keeken A, Bruijn A, Douw L Eur Child Adolesc Psychiatry. 2024; .
PMID: 39527154 DOI: 10.1007/s00787-024-02610-8.
Impulsivity as key bridge symptoms in cross-sectional and longitudinal networks of ADHD and ODD.
Bansal P, Goh P, Southward M, Sizemore Y, Martel M J Child Psychol Psychiatry. 2023; 65(1):52-63.
PMID: 37474723 PMC: 10799176. DOI: 10.1111/jcpp.13863.
Cao M, Martin E, Li X Transl Psychiatry. 2023; 13(1):236.
PMID: 37391419 PMC: 10313824. DOI: 10.1038/s41398-023-02536-w.
Networks of Neuropsychological Functions in the Clinical Evaluation of Adult ADHD.
Guo N, Fuermaier A, Koerts J, Tucha O, Scherbaum N, Muller B Assessment. 2022; 30(6):1719-1736.
PMID: 36031877 PMC: 10363951. DOI: 10.1177/10731911221118673.