Evidence map›Paper›PMID 32478847›Full record

Observational studyJAMA network open2020

Association of Neighborhood Disadvantage in Childhood With DNA Methylation in Young Adulthood.

Aaron Reuben, Karen Sugden, Louise Arseneault, David L Corcoran, Andrea Danese, Helen L Fisher, Terrie E Moffitt, Joanne B Newbury, Candice Odgers, Joey Prinz and 4 more

Open access · goldAbstract readObservational StudyTwin Study
In one paragraph

Observational study in JAMA network open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
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  13. Autistic traits in childhood and post-traumatic stress disorder as young adults: a cohort study.Journal of child psychology and psychiatry, and allied disciplines · 2025
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  19. Targeting hardship: poverty as a modifiable risk factor in childhood leukemia and lymphoma treatment.Hematology. American Society of Hematology. Education Program · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Aaron ReubenDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Karen SugdenDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Louise ArseneaultSocial, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
David L CorcoranCenter for Genomic and Computational Biology, Duke University, Durham, North Carolina.
Andrea DaneseSocial, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Helen L FisherSocial, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Terrie E MoffittDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Joanne B NewburySocial, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.
Candice OdgersSanford School of Public Policy, Duke University, Durham, North Carolina.
Joey PrinzCenter for Genomic and Computational Biology, Duke University, Durham, North Carolina.
Line J H RasmussenDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Ben WilliamsDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Jonathan MillUniversity of Exeter Medical School, University of Exeter, Exeter, United Kingdom.
Avshalom CaspiDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Duke University · USKing's College London · GBHvidovre Hospital · DKUniversity of Exeter · GB

Funding

Science CoreP2CHD065563 · NICHD · DUKE UNIVERSITY · PI Giovanna M Merli · 2015 to 2026
$5.7M
Evaluating neurodegenerative risk in middle-aged adults exposed to lead as childrenF31ES029358 · NIEHS · DUKE UNIVERSITY · PI REUBEN, AARON · 2018 to 2020
$113k
Chief Scientist OfficeCIHRMedical Research Council G1002190NICHD NIH HHS P2C HD065563NIEHS NIH HHS F31 ES029358
6 · The paper itself

Abstract

Importance: DNA methylation has been proposed as an epigenetic mechanism by which the childhood neighborhood environment may have implications for the genome that compromise adult health. Objective: To ascertain whether childhood neighborhood socioeconomic disadvantage is associated with differences in DNA methylation by age 18 years. Design, Setting, and Participants: This longitudinal cohort study analyzed data from the Environmental Risk (E-Risk) Longitudinal Twin Study, a nationally representative birth cohort of children born between 1994 and 1995 in England and Wales and followed up from age 5 to 18 years. Data analysis was performed from March 15, 2019, to June 30, 2019. Exposures: High-resolution neighborhood data (indexing deprivation, dilapidation, disconnection, and dangerousness) collected across childhood. Main Outcomes and Measures: DNA methylation in whole blood was drawn at age 18 years. Associations between neighborhood socioeconomic disadvantage and methylation were tested using 3 prespecified approaches: (1) testing probes annotated to candidate genes involved in biological responses to growing up in socioeconomically disadvantaged neighborhoods and investigated in previous epigenetic research (stress reactivity-related and inflammation-related genes), (2) polyepigenetic scores indexing differential methylation in phenotypes associated with growing up in disadvantaged neighborhoods (obesity, inflammation, and smoking), and (3) a theory-free epigenome-wide association study. Results: A total of 1619 participants (806 female individuals [50%]) had complete neighborhood and DNA methylation data. Children raised in socioeconomically disadvantaged neighborhoods exhibited differential DNA methylation in genes involved in inflammation (β = 0.12; 95% CI, 0.06-0.19; P < .001) and smoking (β = 0.18; 95% CI, 0.11-0.25; P < .001) but not obesity (β = 0.05; 95% CI, -0.01 to 0.11; P = .12). An epigenome-wide association study identified multiple CpG sites at an arraywide significance level of P < 1.16 × 10-7 in genes involved in the metabolism of hydrocarbons. Associations between neighborhood disadvantage and methylation were small but robust to family-level socioeconomic factors and to individual-level tobacco smoking. Conclusions and Relevance: Children raised in more socioeconomically disadvantaged neighborhoods appeared to enter young adulthood epigenetically distinct from their less disadvantaged peers. This finding suggests that epigenetic regulation may be a mechanism by which the childhood neighborhood environment alters adult health.

Indexed as

AdolescentAir PollutantsChildChild, PreschoolDNADNA MethylationEnglandEpigenesis, GeneticFemaleHumansInflammationLongitudinal StudiesMaleObesityOutcome Assessment, Health CarePhenotypeAir PollutantsDNA

Identifiers

PMID32478847
PMCPMC7265095
OpenAlexW3030138306

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.