Publication:
Serotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146.

cris.virtualsource.author-orcide8356e7e-2af5-42ba-86d8-cfad17b9f99d
datacite.rightsopen.access
dc.contributor.authorLeiherer, Andreas
dc.contributor.authorMuendlein, Axel
dc.contributor.authorSaely, Christoph H
dc.contributor.authorFraunberger, Peter
dc.contributor.authorDrexel, Heinz
dc.date.accessioned2024-10-28T17:39:36Z
dc.date.available2024-10-28T17:39:36Z
dc.date.issued2019-09-06
dc.description.abstractThe transcription factor 7-like 2 (TCF7L2) polymorphism rs7903146 is known to be tightly associated with an elevated risk for type 2 diabetes, whereas the molecular mechanisms remain elusive. We evaluated the metabolic profile of a total of 394 patients' serum samples with respect to their rs7903146 genotype using targeted metabolomics in a discovery (n = 154) and a validation (n = 240) study. We have identified serotonin as the top metabolite being increased in carriers of the risk allele. Serotonin was significantly associated with the rs7903146 genotype after full adjustment including type 2 diabetes and further top ranked metabolites. Given the role of peripheral serotonin in metabolic homeostasis and type 2 diabetes, this finding provides a first hint that the well-known impact of the TCF7L2 polymorphism on type 2 diabetes risk may involve a serotonin-dependent pathway.
dc.description.sponsorshipUniversitätsklinik für Angiologie
dc.identifier.doi10.7892/boris.135233
dc.identifier.pmid31492908
dc.identifier.publisherDOI10.1038/s41598-019-49347-y
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/183422
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofScientific reports
dc.relation.issn2045-2322
dc.relation.organizationDCD5A442C44DE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleSerotonin is elevated in risk-genotype carriers of TCF7L2 - rs7903146.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage12863
oaire.citation.volume9
oairecerif.author.affiliationUniversitätsklinik für Angiologie
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unibe.date.licenseChanged2019-11-20 09:27:12
unibe.description.ispublishedpub
unibe.eprints.legacyId135233
unibe.refereedtrue
unibe.subtype.articlejournal

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