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dc.contributor.authorStienen, Susan
dc.contributor.authorFerreira, João Pedro
dc.contributor.authorKobayashi, Masatake
dc.contributor.authorPreud'homme, Gregoire
dc.contributor.authorDobre, Daniela
dc.contributor.authorMachu, Jean-Loup
dc.contributor.authorDuarte, Kevin
dc.contributor.authorBresso, Emmanuel
dc.contributor.authorDevignes, Marie-Domique
dc.contributor.authorLopez-Andres, Natalia
dc.contributor.authorGirerd, Nicolas
dc.contributor.authorAakhus, Svend
dc.contributor.authorAmbrosio, Giuseppe
dc.contributor.authorBrunner-La Rocca, Hans-Peter
dc.contributor.authorFontes-Carvalho, Ricardo
dc.contributor.authorFraser, Alan G.
dc.contributor.authorde Keulenaer, Gilles
dc.contributor.authorMarino, Paolo
dc.contributor.authorMcDonald, Kenneth
dc.contributor.authorMebazaa, Alexandre
dc.contributor.authorPapp, Zoltan
dc.contributor.authorRaddino, Riccardo
dc.contributor.authorTschöpe, Carsten
dc.contributor.authorPaulus, Walter J.
dc.contributor.authorZannad, Faiez
dc.contributor.authorRossignol, Patrick
dc.date.accessioned2022-12-08T10:06:48Z
dc.date.available2022-12-08T10:06:48Z
dc.date.created2021-01-14T21:17:59Z
dc.date.issued2020
dc.identifier.issn2042-6410
dc.identifier.urihttps://hdl.handle.net/11250/3036705
dc.description.abstractBackground Many patients with heart failure with preserved ejection fraction (HFpEF) are women. Exploring mechanisms underlying the sex differences may improve our understanding of the pathophysiology of HFpEF. Studies focusing on sex differences in circulating proteins in HFpEF patients are scarce. Methods A total of 415 proteins were analyzed in 392 HFpEF patients included in The Metabolic Road to Diastolic Heart Failure: Diastolic Heart Failure study (MEDIA-DHF). Sex differences in these proteins were assessed using adjusted logistic regression analyses. The associations between candidate proteins and cardiovascular (CV) death or CV hospitalization (with sex interaction) were assessed using Cox regression models. Results We found 9 proteins to be differentially expressed between female and male patients. Women expressed more LPL and PLIN1, which are markers of lipid metabolism; more LHB, IGFBP3, and IL1RL2 as markers of transcriptional regulation; and more Ep-CAM as marker of hemostasis. Women expressed less MMP-3, which is a marker associated with extracellular matrix organization; less NRP1, which is associated with developmental processes; and less ACE2, which is related to metabolism. Sex was not associated with the study outcomes (adj. HR 1.48, 95% CI 0.83–2.63), p = 0.18. Conclusion In chronic HFpEF, assessing sex differences in a wide range of circulating proteins led to the identification of 9 proteins that were differentially expressed between female and male patients. These findings may help further investigations into potential pathophysiological processes contributing to HFpEF.en_US
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSex differences in circulating proteins in heart failure with preserved ejection fractionen_US
dc.title.alternativeSex differences in circulating proteins in heart failure with preserved ejection fractionen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume11en_US
dc.source.journalBiology of Sex Differencesen_US
dc.source.issue47en_US
dc.identifier.doi10.1186/s13293-020-00322-7
dc.identifier.cristin1871653
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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