Publication:
Telomere Length as Cardiovascular Aging Biomarker: JACC Review Topic of the Week

dc.contributor.authorDe Meyer, Tim
dc.contributor.authorNawrot, Tim
dc.contributor.authorBekaert, Sofie
dc.contributor.authorDe Buyzere, Marc L
dc.contributor.authorRietzschel, Ernst R
dc.contributor.authorAndres, Vicente
dc.contributor.funderMinisterio de Economía, Industria y Competitividad (España)
dc.contributor.funderFundación ProCNIC
dc.date.accessioned2020-04-21T14:52:50Z
dc.date.available2020-04-21T14:52:50Z
dc.date.issued2018-08
dc.description.abstractTelomeres shorten with age, the major risk factor for atherosclerotic cardiovascular disease (aCVD). The observation of shorter telomeres in aCVD patients thus suggested that critical telomere shortening may contribute to premature biological aging and aCVD. Therefore, telomere length often is suggested as a causal aCVD risk factor, a proposal supported by recent Mendelian randomization studies; however, epidemiological research has shown disappointingly low effect sizes. It therefore remains uncertain whether telomere shortening is a cause of aCVD or merely a consequence. The authors argue that elucidating the mechanistic foundation of these findings is essential for any possible translation of telomere biology to the clinic. Here, they critically evaluate evidence for causality in animal models and human studies, and review popular hypotheses and discuss their clinical implications. The authors identify 4 key questions that any successful mechanistic theory should address, and they discuss how atherosclerosis-associated local telomere attrition may provide the answers.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipFunding provided by the Spanish Ministerio de Economia, Industria y Competitividad and the Pro-CNIC Foundation, and a Severo Ochoa Center of Excellence (award SEV-2015-0505) in support of CNIC. The authors have reported that they have no relationships relevant to the contents of this paper to disclose.es_ES
dc.format.number7es_ES
dc.format.page805-813es_ES
dc.format.volume72es_ES
dc.identifier.citationJ Am Coll Cardiol. 2018; 72(7):805-813es_ES
dc.identifier.doi10.1016/j.jacc.2018.06.014es_ES
dc.identifier.e-issn1558-3597es_ES
dc.identifier.issn0735-1097es_ES
dc.identifier.journalJournal of the American College of Cardiologyes_ES
dc.identifier.pubmedID30092957es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/9670
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SEV-2015-0505es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.jacc.2018.06.014es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Fisiopatología Cardiovascular Molecular y Genéticaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectatherosclerosises_ES
dc.subjectbiological aginges_ES
dc.subjectepidemiologyes_ES
dc.subjecttelomerasees_ES
dc.subject.meshAginges_ES
dc.subject.meshAnimalses_ES
dc.subject.meshAtherosclerosises_ES
dc.subject.meshBiomarkerses_ES
dc.subject.meshCardiovascular Diseaseses_ES
dc.subject.meshCardiovascular Systemes_ES
dc.subject.meshHumanses_ES
dc.subject.meshTelomerees_ES
dc.subject.meshTelomere Shorteninges_ES
dc.titleTelomere Length as Cardiovascular Aging Biomarker: JACC Review Topic of the Weekes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication3bb85851-071a-490a-976b-c234983847a7
relation.isAuthorOfPublication.latestForDiscovery3bb85851-071a-490a-976b-c234983847a7

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