A polygenic score for age-at-first-birth predicts disinhibition.


Journal

Journal of child psychology and psychiatry, and allied disciplines
ISSN: 1469-7610
Titre abrégé: J Child Psychol Psychiatry
Pays: England
ID NLM: 0375361

Informations de publication

Date de publication:
12 2020
Historique:
accepted: 03 02 2020
pubmed: 29 3 2020
medline: 30 9 2021
entrez: 29 3 2020
Statut: ppublish

Résumé

A recent genome-wide association study identified molecular-genetic associations with age-at-first-birth. However, the meaning of these genetic discoveries is unclear. Drawing on evidence linking early pregnancy with disinhibitory behavior, we tested the hypothesis that genetic discoveries for age-at-first-birth predict disinhibition. We included participants with genotype data from the two-decade-long Environmental Risk (E-Risk) Study (N = 1,999) and the four-decade-long Dunedin Study (N = 918). We calculated a genome-wide polygenic score for age-at-first-birth and tested whether it was associated with a range of disinhibitory outcomes across the life course, including low childhood self-control; risk for externalizing psychopathology; officially recorded criminal offending; substance dependence; informant reports of disinhibitory problems; and number of lifetime sexual partners. We further tested whether associations were attributable to accelerated pubertal maturation. In both cohorts, the age-at-first-birth polygenic score predicted low childhood self-control, externalizing psychopathology, officially recorded criminal offending, substance dependence, and number of sexual partners. Associations were modest, but robust across replication. Childhood disinhibition partly mediated associations between the polygenic score and reproductive behaviors. In contrast, associations were not attributable to accelerated pubertal timing. Genomic discoveries for age-at-first-birth are about more than reproductive biology: They provide insight into the disinhibitory traits and behaviors that accompany early parenthood. Age-at-first-birth is a useful proxy phenotype for researchers interested in disinhibition. Further, interventions that improve self-regulation abilities may benefit young parents and their children.

Sections du résumé

BACKGROUND
A recent genome-wide association study identified molecular-genetic associations with age-at-first-birth. However, the meaning of these genetic discoveries is unclear. Drawing on evidence linking early pregnancy with disinhibitory behavior, we tested the hypothesis that genetic discoveries for age-at-first-birth predict disinhibition.
METHODS
We included participants with genotype data from the two-decade-long Environmental Risk (E-Risk) Study (N = 1,999) and the four-decade-long Dunedin Study (N = 918). We calculated a genome-wide polygenic score for age-at-first-birth and tested whether it was associated with a range of disinhibitory outcomes across the life course, including low childhood self-control; risk for externalizing psychopathology; officially recorded criminal offending; substance dependence; informant reports of disinhibitory problems; and number of lifetime sexual partners. We further tested whether associations were attributable to accelerated pubertal maturation.
RESULTS
In both cohorts, the age-at-first-birth polygenic score predicted low childhood self-control, externalizing psychopathology, officially recorded criminal offending, substance dependence, and number of sexual partners. Associations were modest, but robust across replication. Childhood disinhibition partly mediated associations between the polygenic score and reproductive behaviors. In contrast, associations were not attributable to accelerated pubertal timing.
CONCLUSIONS
Genomic discoveries for age-at-first-birth are about more than reproductive biology: They provide insight into the disinhibitory traits and behaviors that accompany early parenthood. Age-at-first-birth is a useful proxy phenotype for researchers interested in disinhibition. Further, interventions that improve self-regulation abilities may benefit young parents and their children.

Identifiants

pubmed: 32220142
doi: 10.1111/jcpp.13224
pmc: PMC7529719
mid: NIHMS1589250
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Twin Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1349-1359

Subventions

Organisme : NICHD NIH HHS
ID : P2C HD065563
Pays : United States
Organisme : Medical Research Council
ID : P005918
Pays : United Kingdom
Organisme : NICHD NIH HHS
ID : R01 HD077482
Pays : United States
Organisme : NICHD NIH HHS
ID : HD007376
Pays : United States
Organisme : NICHD NIH HHS
ID : T32 HD007376
Pays : United States
Organisme : NICHD NIH HHS
ID : HD077482
Pays : United States
Organisme : Medical Research Council
ID : G1002190
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : AG032282
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG032282
Pays : United States

Informations de copyright

© 2020 The Authors. Journal of Child Psychology and Psychiatry published by John Wiley & Sons Ltd on behalf of Association for Child and Adolescent Mental Health.

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Auteurs

Leah S Richmond-Rakerd (LS)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
Frank Porter Graham Child Development Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Terrie E Moffitt (TE)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Center for Genomic and Computational Biology, Duke University, Durham, NC, USA.
Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK.

Louise Arseneault (L)

Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK.

Daniel W Belsky (DW)

Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA.

Jennie Connor (J)

Department of Preventive and Social Medicine, University of Otago, Dunedin, New Zealand.

David L Corcoran (DL)

Center for Genomic and Computational Biology, Duke University, Durham, NC, USA.

HonaLee Harrington (H)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

Renate M Houts (RM)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

Richie Poulton (R)

Dunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.

Joey A Prinz (JA)

Center for Genomic and Computational Biology, Duke University, Durham, NC, USA.

Sandhya Ramrakha (S)

Dunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.

Karen Sugden (K)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

Jasmin Wertz (J)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

Benjamin S Williams (BS)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.

Avshalom Caspi (A)

Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC, USA.
Center for Genomic and Computational Biology, Duke University, Durham, NC, USA.
Institute of Psychiatry, Psychology, and Neuroscience, King's College London, London, UK.

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