Evidence map›Paper›PMID 25541553›Full record

ArticleInternational journal of epidemiology2015

Adiposity is associated with DNA methylation profile in adipose tissue.

Golareh Agha, E Andres Houseman, Karl T Kelsey, Charles B Eaton, Stephen L Buka, Eric B Loucks

Open access · bronzeAbstract read
In one paragraph

Article in International journal of epidemiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
17.7field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

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  9. Fasting influences aquaporin expression, water transport and adipocyte metabolism in the peritoneal membrane.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2023
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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

6 authors at 2 institutions in 1 country.

Golareh AghaDepartment of Environmental Health, Harvard School of Public Health, Boston, MA, USA, gagha@hsph.harvard.edu.
E Andres HousemanCollege of Public Health and Human Sciences, Oregon State University, Corvallis, OR, USA.
Karl T KelseyDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA, Department of Pathology and Laboratory Medicine and.
Charles B EatonDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA, Department of Family Medicine, Alpert Medical School of Brown University, Providence, RI, USA.
Stephen L BukaDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
Eric B LoucksDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
Brown University · USOregon State University · US

Funding

Spatial Analysis CoreR24HD041020 · NICHD · BROWN UNIVERSITY · PI LOGAN, JOHN R · 2001 to 2016
$7.4M
The New England Family Study: Fifty Year Post-Perinatal Follow-Up for Life CourseRC2AG036666 · NIA · BROWN UNIVERSITY · PI BUKA, STEPHEN L, EATON, CHARLES B · 2009 to 2010
$1.7M
Identifying Targets for Reducing Obesity Caused by Early Life DisadvantageR01AG048825 · NIA · BROWN UNIVERSITY · PI GILMAN, STEPHEN E, LOUCKS, ERIC · 2014 to 2015
$576k
NIA NIH HHS 1R01AG048825NIA NIH HHS 1RC2AG036666NIA NIH HHS R01 AG048825NIA NIH HHS RC2 AG036666NICHD NIH HHS R24 HD041020
6 · The paper itself

Abstract

backgroundAdiposity is a risk factor for type 2 diabetes and cardiovascular disease, suggesting an important role for adipose tissue in the development of these conditions. The epigenetic underpinnings of adiposity are not well understood, and studies of DNA methylation in relation to adiposity have rarely focused on target adipose tissue. Objectives were to evaluate whether genome-wide DNA methylation profiles in subcutaneous adipose tissue and peripheral blood leukocytes are associated with measures of adiposity, including central fat mass, body fat distribution and body mass index.

methodsParticipants were 106 men and women (mean age 47 years) from the New England Family Study. DNA methylation was evaluated using the Infinium HumanMethylation450K BeadChip. Adiposity phenotypes included dual-energy X-ray absorptiometry-assessed android fat mass, android:gynoid fat ratio and trunk:limb fat ratio, as well as body mass index.

resultsAdipose tissue genome-wide DNA methylation profiles were associated with all four adiposity phenotypes, after adjusting for race, sex and current smoking (omnibus p-values <0.001). After further adjustment for adipose cell-mixture effects, associations with android fat mass, android:gynoid fat ratio, and trunk:limb fat ratio remained. In gene-specific analyses, adiposity phenotypes were associated with adipose tissue DNA methylation in several genes that are biologically relevant to the development of adiposity, such as AOC3, LIPE, SOD3, AQP7 and CETP. Blood DNA methylation profiles were not associated with adiposity, before or after adjustment for blood leukocyte cell mixture effects.

conclusionFindings show that DNA methylation patterns in adipose tissue are associated with adiposity.

Indexed as

DNA MethylationAbsorptiometry, PhotonAdipose TissueAdiposityAdultBody Mass IndexFemaleGenome-Wide Association StudyHumansMaleMiddle AgedNew EnglandRisk Factorsadipose tissueAdiposityDNA methylationepigenetics

Identifiers

PMID25541553
PMCPMC4588857
OpenAlexW2124572258

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.