Evidence map›Paper›PMID 41109913›Full record

ArticleInternational journal of obesity (2005)2026

Genetic regulation of exosome biogenesis pathway in human adipose and muscle tissue and association with obesity and insulin resistance.

Swapan K Das, Gagan Deep, Mary E Comeau, Carl D Langefeld

Abstract read
In one paragraph

Article in International journal of obesity (2005), 2026. 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

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Swapan K DasDepartment of Internal Medicine, Section on Endocrinology and Metabolism, Wake Forest University Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA. sdas@wakehealth.edu.ORCID 0000-0002-2197-8855
Gagan DeepAtrium Health Wake Forest Baptist Comprehensive Cancer Center, Wake Forest University Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Mary E ComeauDepartment of Biostatistics and Data Science, Wake Forest University Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Carl D LangefeldCenter for Precision Medicine, Wake Forest University Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.ORCID 0000-0002-4266-6949

Funding

Wake Forest University School of Medicine Alzheimer's Disease Research CenterP30AG072947 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUZANNE CRAFT · 2021 to 2026
$24.3M
Mapping Diabetes Susceptibility by Expression Traits in African AmericansR01DK090111 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DAS, SWAPAN KUMAR · 2011 to 2015
$2.5M
Identifying Genetic Drivers of Expression Networks Causing Insulin ResistanceR01DK118243 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DAS, SWAPAN KUMAR · 2018 to 2020
$1.1M
NIA NIH HHS P30 AG072947NIDDK NIH HHS R01 DK090111NIDDK NIH HHS R01 DK118243
6 · The paper itself

Abstract

backgroundAnimal studies provide evidence of a link between exosome profile, obesity and insulin resistance (IR). Although it is known that exosomes mediate cell-cell communication via their macromolecular cargo, the genetic factors regulating exosomes in humans are largely unknown.

methodsLeveraging genome-wide expression and genotype data from the African American Genetics of expression and Metabolism (AAGMEx) cohort, we focused on 262 genes in "Exosome pathway", curated by us, to examine the relationship of the expression of these genes with IR and obesity and tested the role of single nucleotide polymorphisms (SNPs) in determining the variability in the expression of these genes in adipose and muscle tissue. Publicly available gene expression data on European ancestry individuals, genome-wide association studies (GWAS), and bioinformatic approaches were used to validate the role of obesity-associated genetic variants in regulating exosome pathway genes.

resultsTranscript levels of 96 and 15 exosome pathway genes were associated with gluco-metabolic traits (BMI and insulin sensitivity) in adipose and muscle tissue, respectively. Data also suggest transancestral replication of association. The cis-expression quantitative trait (cis-eQTL) analysis of exosome pathway genes identified 45 and 65 cis-eGenes in adipose and muscle tissue, respectively. Expression of a subset of 26 cis-eGenes in adipose was also associated with gluco-metabolic traits. Based on combined SNP-to-gene-linking analysis 35 and 82 adipose expressed exosomal genes (e.g. AHNAK, RAP2A) were identified as target genes for gluco-metabolic trait-associated SNPs in GWAS catalogue and UKBB GWAS datasets, respectively.

conclusionsThe expression of exosome pathway genes in adipose and muscle tissue are associated with obesity and IR, and expression of a subset of these genes are determined by SNPs. Furthermore, analysis of target genes of GWAS identified gluco-metabolic trait-associated SNPs suggests that a subset of these SNPs is potentially involved in causing obesity and related gluco-metabolic diseases, likely by modulating exosome biogenesis.

Indexed as

Adipose TissueExosomesInsulin ResistanceMuscle, SkeletalObesityAdultBlack or African AmericanFemaleGene Expression RegulationGenome-Wide Association StudyHumansMalePolymorphism, Single NucleotideWhite

Identifiers

PMID41109913
PMCPMC13293148

What Socratic holds

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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 Socratic graph.