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dc.contributor.authorPello, Ana María
dc.contributor.authorCristóbal, Carmen
dc.contributor.authorTarín, Nieves
dc.contributor.authorHuelmos, Ana
dc.contributor.authorAceña Navarro, Álvaro 
dc.contributor.authorCarda, Rocío
dc.contributor.authorGonzález-Casaus, María Luisa
dc.contributor.authorAlonso, Joaquín
dc.contributor.authorLorenzo González, Óscar 
dc.contributor.authorBlanco-Colio, Luis
dc.contributor.authorMartín Ventura, José Luis 
dc.contributor.authorFranco Peláez, Juan Antonio
dc.contributor.authorMahillo, Ignacio
dc.contributor.authorFarré, Jerónimo
dc.contributor.authorLópez-Bescós, Lorenzo
dc.contributor.authorEgido, Jesús
dc.contributor.authorTuñón Fernández, José Luis 
dc.contributor.otherUAM. Departamento de Medicinaes_ES
dc.contributor.otherInstituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD)es_ES
dc.date.accessioned2016-05-30T13:37:37Z
dc.date.available2016-05-30T13:37:37Z
dc.date.issued2016-01-01
dc.identifier.citationJournal of Cardiology 66.1 (2015): 22-7es_ES
dc.identifier.issn0914-5087es_ES
dc.identifier.issn1876-4738 (on line)es_ES
dc.identifier.urihttp://hdl.handle.net/10486/671134
dc.description.abstractBACKGROUND Patients with coronary heart disease (CHD) without classical cardiovascular risk factors (CRF) are uncommon, and their profile has not been thoroughly studied. In CHD patients, we have assessed the differences in several biomarkers between those with and without CRF. METHODS We studied 704 patients with CHD, analyzing plasma levels of biomarkers related to inflammation, thrombosis, renal damage, and heart failure: hs-CRP (high-sensitivity C-reactive protein), MCP-1 (monocyte chemoattractant protein-1), galectin-3, NT-pro-BNP (N-terminal fragment of brain natriuretic peptide), calcidiol (vitamin D metabolite), fibroblast growth factor-23 (FGF-23), parathormone, and phosphate. RESULTS Twenty patients (2.8%) exhibited no CRFs. Clinical variables were well balanced in both groups, with the logical exceptions of no use of antidiabetic drugs, lower triglyceride and glucose, and higher high-density lipoprotein cholesterol in no-CRF patients. No-CRF patients showed lower hs-CRP (2.574±3.120 vs 4.554±9.786 mg/L; P=0.018), MCP-1 (114.75±36.29 vs 143.56±65.37 pg/ml; P=0.003) and FGF-23 (79.28±40.22 vs 105.17±156.61 RU/ml; P=0.024) and higher calcidiol (23.66±9.12 vs 19.49±8.18 ng/ml; P=0.025) levels. At follow-up, 10.0% vs 11.0% patients experienced acute ischemic event, heart failure, or death in the non-CRF and CRF groups, respectively (P=0.815, log-rank test). The limited number of non-CRF patients may have influenced this finding. A Cox regression analysis in the whole population showed that high calcidiol, and low MCP-1 and FGF-23 plasma levels are associated to a better prognosis. CONCLUSIONS CHD patients without CRFs show a favorable biomarker profile in terms of inflammation and mineral metabolism. Further studies are needed to investigate whether this difference translates into a better prognosis.es_ES
dc.description.sponsorshipThis work was supported by grants from Fondo de Investigaciones Sanitarias (PI05/0451, PI05/1497, PI05/52475, PI05/1043, PS09/01405, and PI10/00072); Spanish Society of Cardiology; Spanish Heart Foundation; Spanish Society of Arteriosclerosis; RECAVA (RD06/0014/0035); Fundación Lilly; Instituto de Salud Carlos III FEDER (FJD Biobank: RD09/0076/00101); and AbbVie Laboratorieses_ES
dc.format.extent16 pag.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isospaes_ES
dc.publisherElsevier Inces_ES
dc.publisherJapanese College of Cardiologyes_ES
dc.relation.ispartofJournal of Cardiologyes_ES
dc.rights© 2014 Japanese College of Cardiologyes_ES
dc.subject.otherAtherosclerosises_ES
dc.subject.otherBiomarkerses_ES
dc.subject.otherCardiovascular risk factorses_ES
dc.subject.otherFibroblast growth factor-23es_ES
dc.subject.otherMonocyte chemoattractant protein-1es_ES
dc.titleDifferential profile in inflammatory and mineral metabolism biomarkers in patients with ischemic heart disease without classical coronary risk factorses_ES
dc.typearticlees_ES
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.jjcc.2014.11.006es_ES
dc.identifier.doi10.1016/j.jjcc.2014.11.006es_ES
dc.identifier.publicationfirstpage22es_ES
dc.identifier.publicationissue1es_ES
dc.identifier.publicationlastpage27es_ES
dc.identifier.publicationvolume66es_ES
dc.type.versioninfo:eu-repo/semantics/draftes_ES
dc.rights.accessRightsopenAccesses_ES
dc.authorUAMAceña Navarro, Álvaro (279732)
dc.authorUAMTuñón Fernández, José Luis (258858)
dc.facultadUAMFacultad de Medicina
dc.institutoUAMInstituto de Investigación Sanitaria Fundación Jiménez Díaz (ISS-FJD)


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