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Association of childhood blood lead levels with criminal offending
Department of Psychology and Neuroscience, Duke University, Durham, United States; Demography Unit, Stockholm University, Stockholm, Sweden.ORCID iD: 0000-0002-4513-1501
Department of Psychology and Neuroscience, Duke University, Durham, United States; Computational Biology, Duke University, Durham, United States; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, England; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, United States.
Sir John Walsh Research Institute, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.
Department of Psychology and Neuroscience, Duke University, Durham, United States.
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2018 (English)In: JAMA pediatrics, ISSN 2168-6203, E-ISSN 2168-6211, Vol. 172, no 2, p. 166-173Article in journal (Refereed) Published
Abstract [en]

Importance:  Lead is a neurotoxin with well-documented effects on health. Research suggests that lead may be associated with criminal behavior. This association is difficult to disentangle from low socioeconomic status, a factor in both lead exposure and criminal offending.

Objective:  To test the hypothesis that a higher childhood blood lead level (BLL) is associated with greater risk of criminal conviction, recidivism (repeat conviction), conviction for violent offenses, and variety of self-reported criminal offending in a setting where BLL was not associated with low socioeconomic status.

Design, Setting, and Participants:  A total of 553 individuals participated in a prospective study based on a population-representative cohort born between April 1, 1972, and March 31, 1973, from New Zealand; the Dunedin Multidisciplinary Health and Development Study observed participants to age 38 years (December 2012). Statistical analysis was performed from November 10, 2016, to September 5, 2017.

Exposures:  Blood lead level measured at age 11 years.

Main Outcomes and Measures:  Official criminal conviction cumulative to age 38 years (data collected in 2013), single conviction or recidivism, conviction for nonviolent or violent crime, and self-reported variety of crime types at ages 15, 18, 21, 26, 32, and 38 years.

Results: Participants included 553 individuals (255 female and 298 male participants) who had their blood tested for lead at age 11 years. The mean (SD) BLL at age 11 years was 11.01 (4.62) μg/dL. A total of 154 participants (27.8%) had a criminal conviction, 86 (15.6%) had recidivated, and 53 (9.6%) had a violent offense conviction. Variety scores for self-reported offending ranged from 0 to 10 offense types at each assessment; higher numbers indicated greater crime involvement. Self-reported offending followed the well-established age-crime curve (ie, the mean [SD] variety of self-reported offending increased from 1.99 [2.82] at age 15 years to its peak of 4.24 [3.15] at age 18 years and 4.22 [3.02] at age 21 years and declined thereafter to 1.10 [1.59] at age 38 years). Blood lead level was a poor discriminator between no conviction and conviction (area under the curve, 0.58). Overall, associations between BLL and conviction outcomes were weak. The estimated effect of BLL was lower for recidivism than for single convictions and lower for violent offending than for nonviolent offending. Sex-adjusted associations between BLL reached statistical significance for only 1 of the 6 self-reported offending outcomes at age 15 years (r = 0.10; 95% CI, 0.01-0.18; P = .02).

Conclusions and Relevance:  This study overcomes past limitations of studies of BLL and crime by studying the association in a place and time where the correlation was not confounded by childhood socioeconomic status. Findings failed to support a dose-response association between BLL and consequential criminal offending.

Place, publisher, year, edition, pages
American Medical Association (AMA), 2018. Vol. 172, no 2, p. 166-173
National Category
Public Health, Global Health and Social Medicine
Identifiers
URN: urn:nbn:se:oru:diva-113777DOI: 10.1001/jamapediatrics.2017.4005ISI: 000424150700019PubMedID: 29279896Scopus ID: 2-s2.0-85041672901OAI: oai:DiVA.org:oru-113777DiVA, id: diva2:1859977
Funder
EU, FP7, Seventh Framework Programme
Note

The Dunedin Multidisciplinary Health and Development Research Unit is supported by the New Zealand Health Research Council and the New Zealand Ministry of Business, Innovation, and Employment. This research was supported by grants R01AG032282, R01AG049789, and R01AG048895 from the US National Institute on Aging; grants MR/K00381X and MR/P005918/1 from the UK Medical Research Council; grant ES/M010309/1 from the Economic and Social Research Council; and the Jacobs Foundation and the Avielle Foundation. Dr Beckley is supported by grant 2015-01189 from the Seventh Framework Programme.

Available from: 2024-05-23 Created: 2024-05-23 Last updated: 2025-02-20Bibliographically approved

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