The neurodevelopmental nature of attention-deficit hyperactivity disorder in adults.


Journal

The British journal of psychiatry : the journal of mental science
ISSN: 1472-1465
Titre abrégé: Br J Psychiatry
Pays: England
ID NLM: 0342367

Informations de publication

Date de publication:
01 2021
Historique:
pubmed: 3 12 2020
medline: 5 6 2021
entrez: 2 12 2020
Statut: ppublish

Résumé

Population studies have suggested that most adults with attention-deficit hyperactivity disorder (ADHD) did not have the disorder in childhood, challenging the neurodevelopmental conceptualisation of ADHD. Arbitrary definitions of age at onset and lack of defined trajectories were accounted for the findings. The objective of this study was to assess the proportion of individuals presenting with either a neurodevelopmental trajectory or late-onset disorder, and to assess risk factors associated with them. Data of 4676 individuals from the 1993 Pelotas birth cohort at 11, 15, 18 and 22 years of age were used. Polythetic and latent class mixed model analyses were performed to define ADHD trajectories from childhood to adulthood, and characterise the neurodevelopmental or late-onset courses. Regression models were applied to assess factors associated with different trajectories. Classical polythetic analyses showed that 67% of those with ADHD at 22 years of age had a neurodevelopmental course of the disorder. Latent class mixed model analysis indicated that 78% of adults with ADHD had a trajectory of persistent symptoms, more common in males. The remaining adults with ADHD had an ascending symptom trajectory that occurred after puberty, with late-onset ADHD associated with female gender and higher IQ. Both polythetic and latent trajectories analyses provided empirical evidence supporting that the large majority of adults with ADHD had a neurodevelopmental disorder.

Sections du résumé

BACKGROUND
Population studies have suggested that most adults with attention-deficit hyperactivity disorder (ADHD) did not have the disorder in childhood, challenging the neurodevelopmental conceptualisation of ADHD. Arbitrary definitions of age at onset and lack of defined trajectories were accounted for the findings.
AIMS
The objective of this study was to assess the proportion of individuals presenting with either a neurodevelopmental trajectory or late-onset disorder, and to assess risk factors associated with them.
METHOD
Data of 4676 individuals from the 1993 Pelotas birth cohort at 11, 15, 18 and 22 years of age were used. Polythetic and latent class mixed model analyses were performed to define ADHD trajectories from childhood to adulthood, and characterise the neurodevelopmental or late-onset courses. Regression models were applied to assess factors associated with different trajectories.
RESULTS
Classical polythetic analyses showed that 67% of those with ADHD at 22 years of age had a neurodevelopmental course of the disorder. Latent class mixed model analysis indicated that 78% of adults with ADHD had a trajectory of persistent symptoms, more common in males. The remaining adults with ADHD had an ascending symptom trajectory that occurred after puberty, with late-onset ADHD associated with female gender and higher IQ.
CONCLUSIONS
Both polythetic and latent trajectories analyses provided empirical evidence supporting that the large majority of adults with ADHD had a neurodevelopmental disorder.

Identifiants

pubmed: 33263274
doi: 10.1192/bjp.2020.200
pii: S0007125020002007
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

43-50

Subventions

Organisme : Wellcome Trust
ID : 086974/Z/08/Z
Pays : United Kingdom

Auteurs

Vitor Breda (V)

ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre; and Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Brazil.

Luis Augusto Rohde (LA)

Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul; and National Institute of Developmental Psychiatry for Children and Adolescents, Brazil.

Ana Maria Baptista Menezes (AMB)

Postgraduate Program in Epidemiology, Universidade Federal de Pelotas, Brazil.

Luciana Anselmi (L)

Postgraduate Program in Epidemiology, Universidade Federal de Pelotas, Brazil.

Arthur Caye (A)

Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Brazil.

Diego Luiz Rovaris (DL)

Department of Physiology and Biophysics, Instituto de Ciências Biomédicas, Universidade de São Paulo, Brazil.

Eduardo Schneider Vitola (ES)

ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre; and Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Brazil.

Claiton Henrique Dotto Bau (CHD)

ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre; and Department of Genetics, Universidade Federal do Rio Grande do Sul, Brazil.

Eugenio Horacio Grevet (EH)

ADHD Outpatient Program, Hospital de Clínicas de Porto Alegre; and Department of Psychiatry, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Brazil.

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Classifications MeSH