Evidence map›Paper›PMID 31200609›Full record

ArticleEpigenetics2019

Exposure to polybrominated biphenyl and stochastic epigenetic mutations: application of a novel epigenetic approach to environmental exposure in the Michigan polybrominated biphenyl registry.

Sarah W Curtis, Dawayland O Cobb, Varun Kilaru, Metrecia L Terrell, M Elizabeth Marder, Dana Boyd Barr, Carmen J Marsit, Michele Marcus, Karen N Conneely, Alicia K Smith

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Sarah W Curtisa Genetics and Molecular Biology Program, Laney Graduate School, Emory University School of Medicine , Atlanta , GA , USA.ORCID 0000-0002-9131-9601
Dawayland O Cobbb Department of Gynecology and Obstetrics, Emory University School of Medicine , Atlanta , GA , USA.
Varun Kilarub Department of Gynecology and Obstetrics, Emory University School of Medicine , Atlanta , GA , USA.
Metrecia L Terrellc Department of Epidemiology, Emory University Rollins School of Public Health , Atlanta , GA , USA.ORCID 0000-0001-9406-2226
M Elizabeth Marderd Department of Environmental Health, Emory University Rollins School of Public Health , Atlanta , GA , USA.
Dana Boyd Barrd Department of Environmental Health, Emory University Rollins School of Public Health , Atlanta , GA , USA.
Carmen J Marsitd Department of Environmental Health, Emory University Rollins School of Public Health , Atlanta , GA , USA.
Michele Marcuse Departments of Epidemiology, Environmental Health, Emory University Rollins School of Public Health, and Department of Pediatrics Emory University School of Medicine , Atlanta , GA , USA.
Karen N Conneelyf Department of Human Genetics, Emory University School of Medicine , Atlanta , GA , USA.
Alicia K Smithg Departments of Gynecology and Obstetrics & Psychiatry and Behavioral Science, Emory University School of Medicine , Atlanta , GA , USA.ORCID 0000-0002-8537-5156
Emory University · US

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
Pilot Project ProgramP30ES019776 · NIEHS · EMORY UNIVERSITY · PI William Michael Caudle · 2013 to 2026
$22.6M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008490 · NIGMS · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 1993 to 2022
$8.0M
MI PBB Cohort 30 years later: Endocrine Disruption?R01ES012014 · NIEHS · EMORY UNIVERSITY · PI MARCUS, MICHELE · 2002 to 2014
$5.8M
Collaborative Research and Action: Empowering an Exposed CommunityR01ES025775 · NIEHS · EMORY UNIVERSITY · PI MARCUS, MICHELE · 2016 to 2022
$3.9M
The Michigan PBB Cohort: A unique, highly exposed community followed for 50 years and three generationsR24ES028528 · NIEHS · EMORY UNIVERSITY · PI MICHELE MARCUS, Melanie Alice PEARSON · 2018 to 2026
$2.2M
Genetic Biomarkers of Polybrominated Biphenyl (PBB)R01ES024790 · NIEHS · EMORY UNIVERSITY · PI CONNEELY, KAREN, SMITH, ALICIA K · 2015 to 2018
$1.7M
The Michigan PBB Cohort: A unique, highly exposed community followed for 50 years and three generationsU24ES028528 · NIEHS · EMORY UNIVERSITY · PI MARCUS, MICHELE, PEARSON, MELANIE ALICE · 2024 to 2025
$758k
NCATS NIH HHS UL1 TR002378NIEHS NIH HHS P30 ES019776NIEHS NIH HHS R01 ES012014NIEHS NIH HHS R01 ES024790NIEHS NIH HHS R01 ES025775NIEHS NIH HHS R24 ES028528NIEHS NIH HHS U24 ES028528NIGMS NIH HHS T32 GM008490
6 · The paper itself

Abstract

Endocrine-disrupting compounds are associated with altered epigenetic regulation and adverse health outcomes, although inconsistent results suggest that people have varied responses to the same exposure. Interpersonal variation in response to environmental exposures is not identified using standard, population-based methods. However, methods that capture an individual's response, such as analyzing stochastic epigenetic mutations (SEMs), may capture currently missed effects of environmental exposure. To test whether polybrominated biphenyl (PBB) was associated with SEMs, DNA methylation was measured using Illumina's MethylationEPIC array in PBB-exposed individuals, and SEMs were identified. Association was tested using a linear regression with robust sandwich variance estimators, controlling for age, sex, lipids, and cell types. The number of SEMs was variable (range: 119-18,309), and positively associated with age (p = 1.23e-17), but not with sex (p = 0.97). PBBs and SEMs were only positively associated in people who were older when they were exposed (p = 0.02 vs. p = 0.91). Many subjects had SEMs enriched in biological pathways, particularly in pathways involved with xenobiotic metabolism and endocrine function. Higher number of SEMs was also associated with higher age acceleration (intrinsic: p = 1.70e-3; extrinsic: p = 3.59e-11), indicating that SEMs may be associated with age-related health problems. Finding an association between environmental contaminants and higher SEMs may provide insight into individual differences in response to environmental contaminants, as well as into the biological mechanism behind SEM formation. Furthermore, these results suggest that people may be particularly vulnerable to epigenetic dysregulation from environmental exposures as they age.

Indexed as

MutationAdultAgedAge FactorsCohort StudiesDNA MethylationEnvironmental ExposureEpigenesis, GeneticFemaleGenome-Wide Association StudyHumansLinear ModelsMaleMichiganMiddle AgedPolybrominated BiphenylsPolybrominated Biphenylsbrominated flame retardantDNA methylationEndocrine-disrupting compoundenvironmental healthepigeneticsepimutationsinterpersonal variationPBBpolybrominated biphenylSEM

Identifiers

PMID31200609
PMCPMC6691996
OpenAlexW2950752221

What OpenQuestion holds

Textmetadata
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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.