Publication:
Type 2 diabetes is associated with decreased PGC1α expression in epicardial adipose tissue of patients with coronary artery disease.

dc.contributor.authorMoreno-Santos, Inmaculada
dc.contributor.authorPérez-Belmonte, Luis Miguel
dc.contributor.authorMacías-González, Manuel
dc.contributor.authorMataró, María José
dc.contributor.authorCastellano, Daniel
dc.contributor.authorLópez-Garrido, Miguel
dc.contributor.authorPorras-Martín, Carlos
dc.contributor.authorSánchez-Fernández, Pedro L
dc.contributor.authorGómez-Doblas, Juan José
dc.contributor.authorCardona, Fernando
dc.contributor.authorde Teresa-Galván, Eduardo
dc.contributor.authorJiménez-Navarro, Manuel
dc.date.accessioned2023-01-25T08:35:39Z
dc.date.available2023-01-25T08:35:39Z
dc.date.issued2016-08-19
dc.description.abstractAlthough recent studies indicate that epicardial adipose tissue expresses brown fat-like genes, such as PGC1α, UCP1 and PRDM16, the association of these genes with type 2 diabetes mellitus (DM2) in coronary artery disease (CAD) remains unknown. PGC1α, UCP1, and PRDM16 mRNAs expression levels were measured by real-time PCR in epicardial and thoracic subcutaneous adipose tissue from 44 CAD patients (22 with DM2 [CAD-DM2] and 22 without DM2 [CAD-NDM2]) and 23 non-CAD patients (NCAD). The CAD-DM2 patients had significantly lower PGC1α and UCP1 expression in epicardial adipose tissue than the CAD-NDM2 and NCAD patients. However, PGC1α and UCP1 mRNA trended upward in subcutaneous adipose tissue from CAD-DM2 patients. At multiple regression analysis, age, body mass index, left ventricular ejection fraction, UCP1 expression of epicardial adipose tissue and diabetes came out to be independent predictors of PGC1α levels. Epicardial adipose tissue PGC1α expression was dependent on the number of injured coronary arteries and logistic regression analysis showed that PGC1α expression in epicardial adipose tissue could exert a protective effect against coronary lesions. DM2 is associated with decreased expression of PGC1α and UCP1 mRNA in epicardial adipose tissue of patients with CAD, likely reflecting a loss of brown-like fat features. Decreased expression of PGC1α in human epicardial adipose tissue is associated with higher prevalence of coronary lesions.
dc.identifier.doi10.1186/s12967-016-0999-1
dc.identifier.essn1479-5876
dc.identifier.pmcPMC4992233
dc.identifier.pmid27542888
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992233/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1186/s12967-016-0999-1
dc.identifier.urihttp://hdl.handle.net/10668/10373
dc.issue.number1
dc.journal.titleJournal of translational medicine
dc.journal.titleabbreviationJ Transl Med
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Virgen de la Victoria
dc.page.number243
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCoronary artery disease
dc.subjectEpicardial adipose tissue
dc.subjectPeroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α)
dc.subjectType 2 diabetes mellitus
dc.subject.meshAdipose Tissue
dc.subject.meshCoronary Artery Disease
dc.subject.meshDNA-Binding Proteins
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshFemale
dc.subject.meshGene Expression Regulation
dc.subject.meshHumans
dc.subject.meshLogistic Models
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPericardium
dc.subject.meshPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
dc.subject.meshRNA, Messenger
dc.subject.meshSubcutaneous Fat
dc.subject.meshThermogenesis
dc.subject.meshTranscription Factors
dc.subject.meshUncoupling Protein 1
dc.titleType 2 diabetes is associated with decreased PGC1α expression in epicardial adipose tissue of patients with coronary artery disease.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number14
dspace.entity.typePublication

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