Life-Course Persistent Antisocial Behavior and Accelerated Biological Aging in a Longitudinal Birth Cohort.

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dc.contributor.author Langevin, Stephanie
dc.contributor.author Caspi, Ashalom
dc.contributor.author Barnes, JC
dc.contributor.author Brennan, Grace
dc.contributor.author Poulton, Richie
dc.contributor.author Purdy, Suzanne C
dc.contributor.author Ramrakha, Sandhya
dc.contributor.author Tanksley, Peter T
dc.contributor.author Thorne, Peter R
dc.contributor.author Wilson, Graham
dc.contributor.author Moffitt, Terrie E
dc.coverage.spatial Switzerland
dc.date.accessioned 2023-01-24T03:18:31Z
dc.date.available 2023-01-24T03:18:31Z
dc.date.issued 2022-11
dc.identifier.citation (2022). International Journal of Environmental Research and Public Health, 19(21), 14402-.
dc.identifier.issn 1661-7827
dc.identifier.uri https://hdl.handle.net/2292/62545
dc.description.abstract Prior research shows that individuals who have exhibited antisocial behavior are in poorer health than their same-aged peers. A major driver of poor health is aging itself, yet research has not investigated relationships between offending trajectories and biological aging. We tested the hypothesis that individuals following a life-course persistent (LCP) antisocial trajectory show accelerated aging in midlife. Trajectories of antisocial behavior from age 7 to 26 years were studied in the Dunedin Multidisciplinary Health and Development Study, a population-representative birth cohort (N = 1037). Signs of aging were assessed at age 45 years using previously validated measures including biomarkers, clinical tests, and self-reports. First, we tested whether the association between antisocial behavior trajectories and midlife signs of faster aging represented a decline from initial childhood health. We then tested whether decline was attributable to tobacco smoking, antipsychotic medication use, debilitating illnesses in adulthood, adverse exposures in childhood (maltreatment, socioeconomic disadvantage) and adulthood (incarceration), and to childhood self-control difficulties. Study members with a history of antisocial behavior had a significantly faster pace of biological aging by midlife, and this was most evident among individuals following the LCP trajectory (β, 0.22, 95%CI, 0.14, 0.28, <i>p</i> ≤ 0.001). This amounted to 4.3 extra years of biological aging between ages 25-45 years for Study members following the LCP trajectory compared to low-antisocial trajectory individuals. LCP offenders also experienced more midlife difficulties with hearing (β, -0.14, 95%CI, -0.21, -0.08, <i>p</i> ≤ 0.001), balance (β, -0.13, 95%CI, -0.18, -0.06, <i>p</i> ≤ 0.001), gait speed (β, -0.18, 95%CI, -0.24, -0.10, <i>p</i> ≤ 0.001), and cognitive functioning (β, -0.25, 95%CI, -0.31, -0.18, <i>p</i> ≤ 0.001). Associations represented a decline from childhood health. Associations persisted after controlling individually for tobacco smoking, antipsychotic medication use, midlife illnesses, maltreatment, socioeconomic status, incarceration, and childhood self-control difficulties. However, the cumulative effect of these lifestyle characteristics together explained why LCP offenders have a faster Pace of Aging than their peers. While older adults typically age-out of crime, LCP offenders will likely age-into the healthcare system earlier than their chronologically same-aged peers. Preventing young people from offending is likely to have substantial benefits for health, and people engaging in a LCP trajectory of antisocial behaviors might be the most in need of health promotion programs. We offer prevention and intervention strategies to reduce the financial burden of offenders on healthcare systems and improve their wellbeing.
dc.format.medium Electronic
dc.language eng
dc.publisher MDPI
dc.relation.ispartofseries International journal of environmental research and public health
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Humans
dc.subject Antipsychotic Agents
dc.subject Longitudinal Studies
dc.subject Antisocial Personality Disorder
dc.subject Aging
dc.subject Adolescent
dc.subject Adult
dc.subject Aged
dc.subject Middle Aged
dc.subject Birth Cohort
dc.subject accelerated aging
dc.subject antisocial trajectories
dc.subject biological aging
dc.subject crime
dc.subject Clinical Trials and Supportive Activities
dc.subject Pediatric
dc.subject Clinical Research
dc.subject Prevention
dc.subject Behavioral and Social Science
dc.subject Violence Research
dc.subject Youth Violence
dc.subject Mental Health
dc.subject Brain Disorders
dc.subject 2.3 Psychological, social and economic factors
dc.subject 2 Aetiology
dc.subject 3 Good Health and Well Being
dc.title Life-Course Persistent Antisocial Behavior and Accelerated Biological Aging in a Longitudinal Birth Cohort.
dc.type Journal Article
dc.identifier.doi 10.3390/ijerph192114402
pubs.issue 21
pubs.begin-page 14402
pubs.volume 19
dc.date.updated 2022-12-03T04:52:19Z
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 36361282 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/36361282
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Journal Article
pubs.elements-id 927623
pubs.org-id Science
pubs.org-id Psychology
dc.identifier.eissn 1660-4601
dc.identifier.pii ijerph192114402
pubs.record-created-at-source-date 2022-12-03
pubs.online-publication-date 2022-11-03


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