Evidence map›Paper›PMID 23369247›Full record

ArticleBMC medical genomics2013

Integrated lipidomics and transcriptomic analysis of peripheral blood reveals significantly enriched pathways in type 2 diabetes mellitus.

Chen Zhao, Jinghe Mao, Junmei Ai, Ming Shenwu, Tieliu Shi, Daqing Zhang, Xiaonan Wang, Yunliang Wang, Youping Deng

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

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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

35 citing papers in PubMed, 55 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

9 authors at 5 institutions in 2 countries.

Chen ZhaoWuhan University of Science and Technology, Wuhan, Hubei 430081, PR China.
Jinghe Mao
Junmei Ai
Ming Shenwu
Tieliu Shi
Daqing Zhang
Xiaonan Wang
Yunliang Wang
Youping Deng
Wuhan University of Science and Technology · CNTougaloo College · USEast China Normal University · CNRush University Medical Center · USSoochow University · CN

Funding

Using Mass Spectroscopy to Characterize Transcription Proteins and F2-IsoprostaneP20MD002725 · NIMHD · TOUGALOO COLLEGE · PI MAO, JINGHE · 2007 to 2011
$3.9M
NIMHD NIH HHS P20MD002725
6 · The paper itself

Abstract

backgroundInsulin resistance is a key element in the pathogenesis of type 2 diabetes mellitus. Plasma free fatty acids were assumed to mediate the insulin resistance, while the relationship between lipid and glucose disposal remains to be demonstrated across liver, skeletal muscle and blood.

methodsWe profiled both lipidomics and gene expression of 144 total peripheral blood samples, 84 from patients with T2D and 60 from healthy controls. Then, factor and partial least squares models were used to perform a combined analysis of lipidomics and gene expression profiles to uncover the bioprocesses that are associated with lipidomic profiles in type 2 diabetes.

resultsAccording to factor analysis of the lipidomic profile, several species of lipids were found to be correlated with different phenotypes, including diabetes-related C23:2CE, C23:3CE, C23:4CE, ePE36:4, ePE36:5, ePE36:6; race-related (African-American) PI36:1; and sex-related PE34:1 and LPC18:2. The major variance of gene expression profile was not caused by known factors and no significant difference can be directly derived from differential gene expression profile. However, the combination of lipidomic and gene expression analyses allows us to reveal the correlation between the altered lipid profile with significantly enriched pathways, such as one carbon pool by folate, arachidonic acid metabolism, insulin signaling pathway, amino sugar and nucleotide sugar metabolism, propanoate metabolism, and starch and sucrose metabolism. The genes in these pathways showed a good capability to classify diabetes samples.

conclusionCombined analysis of gene expression and lipidomic profiling reveals type 2 diabetes-associated lipid species and enriched biological pathways in peripheral blood, while gene expression profile does not show direct correlation. Our findings provide a new clue to better understand the mechanism of disordered lipid metabolism in association with type 2 diabetes.

Indexed as

Gene Expression ProfilingAdultAgedCluster AnalysisDiabetes Mellitus, Type 2FemaleHumansInsulinInsulin ResistanceLipid MetabolismMaleMiddle AgedOligonucleotide Array Sequence AnalysisPhenotypeSex FactorsSignal TransductionInsulin

Identifiers

PMID23369247
PMCPMC3552685
OpenAlexW1584878576

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.