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Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study

BACKGROUND: Multiple risk behaviours (MRBs), typically beginning in adolescence, are associated with increased risk of adverse health and social outcomes. The association between autism and MRBs is little understood. METHODS: Data were from the Avon Longitudinal Study of Parents and Children, an UK-...

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Autores principales: Ly, Amanda, Heron, Jon, Rai, Dheeraj, Wright, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317793/
https://www.ncbi.nlm.nih.gov/pubmed/35481795
http://dx.doi.org/10.1017/S0033291722000940
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author Ly, Amanda
Heron, Jon
Rai, Dheeraj
Wright, Caroline
author_facet Ly, Amanda
Heron, Jon
Rai, Dheeraj
Wright, Caroline
author_sort Ly, Amanda
collection PubMed
description BACKGROUND: Multiple risk behaviours (MRBs), typically beginning in adolescence, are associated with increased risk of adverse health and social outcomes. The association between autism and MRBs is little understood. METHODS: Data were from the Avon Longitudinal Study of Parents and Children, an UK-based longitudinal, birth cohort study. Exposures were diagnosed autism and four autistic traits: social communication difficulties, pragmatic language, repetitive behaviours and reduced sociability. Outcomes were participation in up to 14 risk behaviours, including alcohol consumption, smoking, risky sexual behaviours and physical inactivity. Outcome data were collected at ages approximately 12, 14, 16 and 18. RESULTS: Up to 4300 participants were included in latent basis growth curve analyses with adjustment for confounders. Social communication difficulties were associated with an above average level of MRBs engagement at ~12 years (mean difference β 0.26; 95% CI 0.13–0.40), and above average rate of engagement from ages ~12–18 (β 0.08; 95% CI 0.02–0.13). Repetitive behaviours were associated with above average levels of engagement in MRBs at ~12 years (β 0.24; 95% CI 0.09–0.38). Contrastingly, reduced sociability was associated with a reduced rate of engagement in MRBs from ages ~12–18 (β −0.06; 95% CI −0.11 to −0.02). In sex-specific analyses, persisting differences in MRB engagement patterns from ages ~12–18 were observed in males with social communication difficulties and females with reduced sociability temperament. CONCLUSIONS: Having elevated levels of some autistic traits appear to have differentiated effects on MRB engagement patterns. These findings could reflect difficulties fitting in and/or coping mechanisms relating to difficulties with fitting in.
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spelling pubmed-103177932023-07-05 Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study Ly, Amanda Heron, Jon Rai, Dheeraj Wright, Caroline Psychol Med Original Article BACKGROUND: Multiple risk behaviours (MRBs), typically beginning in adolescence, are associated with increased risk of adverse health and social outcomes. The association between autism and MRBs is little understood. METHODS: Data were from the Avon Longitudinal Study of Parents and Children, an UK-based longitudinal, birth cohort study. Exposures were diagnosed autism and four autistic traits: social communication difficulties, pragmatic language, repetitive behaviours and reduced sociability. Outcomes were participation in up to 14 risk behaviours, including alcohol consumption, smoking, risky sexual behaviours and physical inactivity. Outcome data were collected at ages approximately 12, 14, 16 and 18. RESULTS: Up to 4300 participants were included in latent basis growth curve analyses with adjustment for confounders. Social communication difficulties were associated with an above average level of MRBs engagement at ~12 years (mean difference β 0.26; 95% CI 0.13–0.40), and above average rate of engagement from ages ~12–18 (β 0.08; 95% CI 0.02–0.13). Repetitive behaviours were associated with above average levels of engagement in MRBs at ~12 years (β 0.24; 95% CI 0.09–0.38). Contrastingly, reduced sociability was associated with a reduced rate of engagement in MRBs from ages ~12–18 (β −0.06; 95% CI −0.11 to −0.02). In sex-specific analyses, persisting differences in MRB engagement patterns from ages ~12–18 were observed in males with social communication difficulties and females with reduced sociability temperament. CONCLUSIONS: Having elevated levels of some autistic traits appear to have differentiated effects on MRB engagement patterns. These findings could reflect difficulties fitting in and/or coping mechanisms relating to difficulties with fitting in. Cambridge University Press 2023-07 2022-04-28 /pmc/articles/PMC10317793/ /pubmed/35481795 http://dx.doi.org/10.1017/S0033291722000940 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
Ly, Amanda
Heron, Jon
Rai, Dheeraj
Wright, Caroline
Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title_full Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title_fullStr Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title_full_unstemmed Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title_short Autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
title_sort autism, autistic traits and multiple risk behaviours in adolescence: a longitudinal birth cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317793/
https://www.ncbi.nlm.nih.gov/pubmed/35481795
http://dx.doi.org/10.1017/S0033291722000940
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