Evidence map›Paper›PMID 31739726›Full record

ArticleEpigenetics2020

Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome.

Kumaraswamy Naidu Chitrala, Dena G Hernandez, Michael A Nalls, Nicolle A Mode, Alan B Zonderman, Ngozi Ezike, Michele K Evans

Open access · greenAbstract read
In one paragraph

Article in Epigenetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

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  20. A biosocial return to race? A cautionary view for the postgenomic era.American journal of human biology : the official journal of the Human Biology Council · 2022
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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

7 authors at 1 institution in 1 country.

Kumaraswamy Naidu ChitralaLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Dena G HernandezLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-0188-9927
Michael A NallsLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Nicolle A ModeLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.ORCID 0000-0002-8193-0554
Alan B ZondermanLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Ngozi EzikeLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Michele K EvansLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.ORCID 0000-0002-8546-2831
National Institutes of Health · US

Funding

The Underlying Biology of Health DisparitiesZIAAG000519 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2009 to 2025
$15.7M
Effects of race and socioeconomic status on the epigenetic aging clockZIAAG000988 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2017 to 2025
$2.7M
PERIPHERAL NEUROPATHY, SENSORIMOTOR FUNCTIONS &BALANCEK23AG000989 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RICHARDSON, JAMES K · 2000 to 2004
$711k
NIA NIH HHS K23 AG000989
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a cluster of cardiometabolic risk factors for all-cause mortality, cardiovascular disease, and cancer. Identifying epigenetic alterations associated with MetS in African Americans (AAs) and Whites may provide insight into genes that influence its differential health outcomes. We examined DNA methylation (DNAm) and performed an epigenome-wide association study (EWAS) of MetS among AAs and Whites with and without MetS. We assessed age, race and poverty status associated DNAm among AAs (n = 225) and White (n = 233) adults using NCEP-ATP III guidelines. Genome-wide DNAm measurement was assessed using Illumina Infinium Methylation EPIC BeadChip. Differentially methylated positions (DMPs) and differentially methylated regions (DMRs) were identified using

Indexed as

DNA MethylationAdultBlack or African AmericanCarrier ProteinsFemaleGlutathione TransferaseHumansIntracellular Signaling Peptides and ProteinsMaleMetabolic SyndromeMetalloendopeptidasesMiddle AgedRepressor ProteinsStearoyl-CoA DesaturaseTranscriptomeWhite PeopleCarrier Proteinsglutathione S-transferase T1Glutathione TransferaseIntracellular Signaling Peptides and ProteinsMetalloendopeptidasesmitochondrial intermediate peptidasePPP1R13L protein, humanRepressor ProteinsSCD1 protein, humanStearoyl-CoA DesaturaseTXNIP protein, humanAfrican Americansepigenomic wide association studyhealth disparitiesMetabolic syndromemethylationrace

Identifiers

PMID31739726
PMCPMC7188395
OpenAlexW2990464639

What OpenQuestion holds

Textmetadata
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.