Evidence map›Paper›PMID 26110043›Full record

ArticleClinical epigenetics2015

Insulin resistance is associated with epigenetic and genetic regulation of mitochondrial DNA in obese humans.

Louise D Zheng, Leah E Linarelli, Longhua Liu, Sarah S Wall, Mark H Greenawald, Richard W Seidel, Paul A Estabrooks, Fabio A Almeida, Zhiyong Cheng

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 2 syntheses or guidelines pooled it, 125 citations in OpenAlex.

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  16. 1,2-Dicinnamoyl-Nutrients · 2024
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6 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

Louise D ZhengDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Leah E LinarelliDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Longhua LiuDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Sarah S WallDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Mark H GreenawaldDepartment of Family and Community Medicine, Carilion Clinic, Roanoke, Virginia, USA.
Richard W SeidelDepartment of Psychiatry, Carilion Clinic, Roanoke, Virginia, USA.
Paul A EstabrooksDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA ; Department of Family and Community Medicine, Carilion Clinic, Roanoke, Virginia, USA.
Fabio A AlmeidaDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Zhiyong ChengDepartment of Human Nutrition, Foods and Exercise, Fralin Translational Obesity Research Center, College of Agriculture and Life Science, Virginia Tech, Blacksburg, Virginia USA.
Virginia Tech · USCarilion Clinic · US

Funding

The Reach and Effectiveness of Technology-Enhanced Diabetes Prevention ProgramsR18DK091811 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI ALMEIDA, FABIO ARAUJO · 2012 to 2016
$3.2M
NIDDK NIH HHS R18 DK091811
6 · The paper itself

Abstract

backgroundMitochondrial alterations have been observed in subjects with metabolic disorders such as obesity and diabetes. Studies on animal models and cell cultures suggest aberrant glucose and lipid levels, and impaired insulin signaling might lead to mitochondrial changes. However, the molecular mechanism underlying mitochondrial aberrance remains largely unexplored in human subjects.

resultsHere we show that the mitochondrial DNA copy number (mtDNAn) was significantly reduced (6.9-fold lower, p < 0.001) in the leukocytes from obese humans (BMI >30). The reduction of mtDNAn was strongly associated with insulin resistance (HOMA-IR: -0.703, p < 0.05; fasting insulin level: -0.015, p < 0.05); by contrast, the correlation between fasting glucose or lipid levels and mtDNAn was not significant. Epigenetic study of the displacement loop (D-loop) region of mitochondrial genome, which controls the replication and transcription of the mitochondrial DNA as well as organization of the mitochondrial nucleoid, revealed a dramatic increase of DNA methylation in obese (5.2-fold higher vs. lean subjects, p < 0.05) and insulin-resistant (4.6-fold higher vs. insulin-sensitive subjects, p < 0.05) individuals.

conclusionsThe reduction of mtDNAn in obese human subjects is associated with insulin resistance and may arise from increased D-loop methylation, suggesting an insulin signaling-epigenetic-genetic axis in mitochondrial regulation.

Indexed as

D-loopDNA methylationEpigeneticGeneticInsulin resistanceMetabolismMitochondrial regulationObesity

Identifiers

PMID26110043
PMCPMC4479353
OpenAlexW1799046027

What OpenQuestion holds

Textmetadata
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.