Investigating the neurodevelopmental correlates of early adolescent-onset emotional problems.

ALSPAC Attention deficit hyperactivity disorder Autism Spectrum disorder Emotional disorders Neurodevelopmental conditions

Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
10 Aug 2024
Historique:
received: 15 03 2024
revised: 04 06 2024
accepted: 09 08 2024
medline: 13 8 2024
pubmed: 13 8 2024
entrez: 12 8 2024
Statut: aheadofprint

Résumé

Emotional problems (EPs) increase sharply after mid-adolescence. Earlier EPs are associated with poorer long-term outcomes, and their underlying mechanisms may differ to later-onset EPs. Given an established relationship between ADHD, autism, and later depression, we aimed to examine associations between neurodevelopmental conditions and correlates and early adolescent-onset EPs. Adolescents in two UK population cohorts, Avon Longitudinal Study of Parents and Children (ALSPAC) and Millennium Cohort Study (MCS), were included. Individuals scoring >6 on the Strengths and Difficulties Questionnaire (SDQ) emotional problems subscale between ages 11-14 were defined as having early adolescent-onset EP, whilst those scoring >6 for the first time at 16-25 were defined as having later-onset EP. We tested associations between early adolescent-onset EP (total cases = 887, controls = 19,582) and ICD-10/DSM-5 neurodevelopmental conditions and known correlates, including: sex, birth complications, low cognitive ability, special educational needs (SEND), and epilepsy. Analyses were conducted separately in ALSPAC and MCS then meta-analysed. In the meta-analysis of both cohorts, early adolescent-onset EPs were associated with female sex and greater likelihood of low cognitive ability, SEND, autism, ADHD, and reading difficulties. Compared to later-onset EP, early adolescent-onset EPs were associated with male sex, low cognitive ability, SEND, epilepsy, ASD, ADHD, and reading difficulties. A clinical definition of depression/anxiety was available only in ALSPAC, instead we primarily defined EP via questionnaires, which capture a broader phenotype. Individuals with early adolescent-onset EP are likely to have a co-occurring neurodevelopmental condition. Clinicians should consider assessing for neurodevelopmental conditions in young adolescents with EPs.

Sections du résumé

BACKGROUND BACKGROUND
Emotional problems (EPs) increase sharply after mid-adolescence. Earlier EPs are associated with poorer long-term outcomes, and their underlying mechanisms may differ to later-onset EPs. Given an established relationship between ADHD, autism, and later depression, we aimed to examine associations between neurodevelopmental conditions and correlates and early adolescent-onset EPs.
METHODS METHODS
Adolescents in two UK population cohorts, Avon Longitudinal Study of Parents and Children (ALSPAC) and Millennium Cohort Study (MCS), were included. Individuals scoring >6 on the Strengths and Difficulties Questionnaire (SDQ) emotional problems subscale between ages 11-14 were defined as having early adolescent-onset EP, whilst those scoring >6 for the first time at 16-25 were defined as having later-onset EP. We tested associations between early adolescent-onset EP (total cases = 887, controls = 19,582) and ICD-10/DSM-5 neurodevelopmental conditions and known correlates, including: sex, birth complications, low cognitive ability, special educational needs (SEND), and epilepsy. Analyses were conducted separately in ALSPAC and MCS then meta-analysed.
RESULTS RESULTS
In the meta-analysis of both cohorts, early adolescent-onset EPs were associated with female sex and greater likelihood of low cognitive ability, SEND, autism, ADHD, and reading difficulties. Compared to later-onset EP, early adolescent-onset EPs were associated with male sex, low cognitive ability, SEND, epilepsy, ASD, ADHD, and reading difficulties.
LIMITATIONS CONCLUSIONS
A clinical definition of depression/anxiety was available only in ALSPAC, instead we primarily defined EP via questionnaires, which capture a broader phenotype.
CONCLUSIONS CONCLUSIONS
Individuals with early adolescent-onset EP are likely to have a co-occurring neurodevelopmental condition. Clinicians should consider assessing for neurodevelopmental conditions in young adolescents with EPs.

Identifiants

pubmed: 39134151
pii: S0165-0327(24)01223-0
doi: 10.1016/j.jad.2024.08.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors report no conflicts of interest or disclosures.

Auteurs

Charlotte A Dennison (CA)

Wolfson Centre for Young People's Mental Health, Cardiff University, UK; Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.

Amy Shakeshaft (A)

Wolfson Centre for Young People's Mental Health, Cardiff University, UK; Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.

Olga Eyre (O)

Wolfson Centre for Young People's Mental Health, Cardiff University, UK; Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.

Kate Tilling (K)

MRC Integrative Epidemiology Unit, Bristol University, UK.

Frances Rice (F)

Wolfson Centre for Young People's Mental Health, Cardiff University, UK; Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK.

Anita Thapar (A)

Wolfson Centre for Young People's Mental Health, Cardiff University, UK; Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK. Electronic address: thapar@cardiff.ac.uk.

Classifications MeSH