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dc.contributor.authorMardinoglu A
dc.contributor.authorGogg S
dc.contributor.authorLotta LA
dc.contributor.authorStancáková A
dc.contributor.authorNerstedt A
dc.contributor.authorBoren J
dc.contributor.authorBlüher M
dc.contributor.authorFerrannini E
dc.contributor.authorLangenberg C
dc.contributor.authorWareham NJ
dc.contributor.authorLaakso M
dc.contributor.authorSmith U
dc.date.accessioned2018-02-12T09:38:54Z
dc.date.available2018-02-12T09:38:54Z
dc.date.issued2018
dc.identifier.urihttps://erepo.uef.fi/handle/123456789/6084
dc.description.abstractBranched-chain amino acids (BCAAs) metabolite, 3-Hydroxyisobutyric acid (3-HIB) has been identified as a secreted mediator of endothelial cell fatty acid transport and insulin resistance (IR) using animal models. To identify if 3-HIB is a marker of human IR and future risk of developing Type 2 diabetes (T2D), we measured plasma levels of 3-HIB and associated metabolites in around 10,000 extensively phenotyped individuals. The levels of 3-HIB were increased in obesity but not robustly associated with degree of IR after adjusting for BMI. Nevertheless, also after adjusting for obesity and plasma BCAA, 3-HIB levels were associated with future risk of incident T2D. We also examined the effect of 3-HIB on fatty acid uptake in human cells and found that both HUVEC and human cardiac endothelial cells respond to 3-HIB whereas human adipose tissue-derived endothelial cells do not respond to 3-HIB. In conclusion, we found that increased plasma level of 3-HIB is a marker of future risk of T2D and 3-HIB may be important for the regulation of metabolic flexibility in heart and muscles.en
dc.language.isoENen
dc.publisherElsevier BVen
dc.relation.ispartofseriesEBioMedicineen
dc.relation.urihttp://dx.doi.org/10.1016/j.ebiom.2017.12.008en
dc.rightsCC BY 4.0
dc.subject3-Hydroxyisobutyric acid (3-HIB)en
dc.subjectBranched-chain amino acids (BCAAs)en
dc.subjectT2Den
dc.subjectInsulin resistanceen
dc.subjectInsulin secretionen
dc.titleElevated Plasma Levels of 3-Hydroxyisobutyric Acid Are Associated With Incident Type 2 Diabetesen
dc.description.versionpublished versionen
dc.contributor.departmentSchool of Medicine / Clinical Medicineen
uef.solecris.id52405978en
dc.type.publicationinfo:eu-repo/semantics/articleen
dc.relation.doi10.1016/j.ebiom.2017.12.008en
dc.description.reviewstatuspeerRevieweden
dc.format.pagerange151-155en
dc.relation.issn2352-3964en
dc.relation.volume27en
dc.rights.accesslevelopenAccessen
dc.type.okmA1en
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
uef.solecris.openaccessOpen access -julkaisukanavassa ilmestynyt julkaisu
dc.rights.copyright© Authors
dc.type.displayTypearticleen
dc.type.displayTypeartikkelifi
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/


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