Evidence map›Paper›PMID 39497634›Full record

ArticleObesity (Silver Spring, Md.)2024

In silico and functional analysis identifies key gene networks and novel gene candidates in obesity-linked human visceral fat.

Lijin Wang, Pratap Veerabrahma Seshachalam, Ruiming Chua, Hongwen Zhou, Sun Lei, Sujoy Ghosh

Abstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Lijin WangCentre for Computational Biology, Duke-NUS Medical School, Singapore.
Pratap Veerabrahma SeshachalamProgram in Clinical and Translational Liver Cancer Research, National Cancer Centre, Singapore.
Ruiming ChuaProgram in Cardiovascular and Metabolic Disorders, Duke-NUS Medical School, Singapore.
Hongwen ZhouFirst Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Sun LeiProgram in Cardiovascular and Metabolic Disorders, Duke-NUS Medical School, Singapore.
Sujoy GhoshCentre for Computational Biology, Duke-NUS Medical School, Singapore.ORCID https://orcid.org/0000-0002-7601-165X

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
Molecular Basis of Exercise-induced Changes in HDL FunctionR01HL146462 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI SARZYNSKI, MARK ANDREW · 2019 to 2023
$3.6M
Duke-NUS Medical School KBrFA/2022/0060NHLBI NIH HHS R01 HL146462NHLBI NIH HHS R01HL146462-01NIDDK NIH HHS P30 DK072476NIDDK NIH HHS P30DK072476NIGMS NIH HHS 2U54GM104940NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

objectiveVisceral adiposity is associated with increased proinflammatory activity, insulin resistance, diabetes risk, and mortality rate. Numerous individual genes have been associated with obesity, but studies investigating gene regulatory networks in human visceral obesity have been lacking.

methodsWe analyzed gene regulatory networks in human visceral adipose tissue (VAT) from 48 and 11 Chinese patients with and without obesity, respectively, using gene coexpression and gene regulatory network construction from RNA-sequencing data. We also conducted RNA interference-based functional tests on selected genes for effects on adipocyte differentiation.

resultsA scale-free gene coexpression network was constructed from 360 differentially expressed genes between VAT samples from patients with and without obesity (absolute log fold change > 1, false discovery rate [FDR] < 0.05), with edge probability > 0.8. Gene regulatory network analysis identified candidate transcription factors associated with differentially expressed genes. A total of 15 subnetworks (communities) displayed altered connectivity patterns between obesity and nonobesity networks. Genes in proinflammatory pathways showed increased network connectivity in VAT samples with obesity, whereas the oxidative phosphorylation pathway displayed reduced connectivity (enrichment FDR < 0.05). Functional screening via RNA interference identified genes such as SOX30, SIRPB1, and OSBPL3 as potential network-derived candidates influencing adipocyte differentiation.

conclusionsThis approach highlights the network architecture in human obesity, identifies novel candidate genes, and generates new hypotheses regarding network-assisted gene regulation in VAT.

Indexed as

Gene Regulatory NetworksIntra-Abdominal FatAdipocytesAdultComputer SimulationFemaleHumansMaleMiddle AgedObesityObesity, AbdominalRNA InterferenceTranscription FactorsTranscription Factors

Identifiers

PMID39497634
PMCPMC11548800

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.