Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/69820
DC FieldValueLanguage
dc.contributor.authorPerez-Calahorra, Sofíaen_US
dc.contributor.authorLaclaustra, Martínen_US
dc.contributor.authorMarco-Benedí, Victoriaen_US
dc.contributor.authorLamiquiz-Moneo, Itziaren_US
dc.contributor.authorPedro-Botet, Juanen_US
dc.contributor.authorPlana, Núriaen_US
dc.contributor.authorSánchez Hernández, Rosa Maríaen_US
dc.contributor.authorAmor, Antonio J.en_US
dc.contributor.authorAlmagro, Fátimaen_US
dc.contributor.authorFuentes, Franciscoen_US
dc.contributor.authorSuarez-Tembra, Manuelen_US
dc.contributor.authorCiveira, Fernandoen_US
dc.date.accessioned2020-02-05T12:50:21Z-
dc.date.available2020-02-05T12:50:21Z-
dc.date.issued2019en_US
dc.identifier.issn0021-9150en_US
dc.identifier.otherScopus-
dc.identifier.urihttp://hdl.handle.net/10553/69820-
dc.description.abstractBackground and aims: The impact on heterozygous familial hypercholesterolemia (HeFH)health led by high-intensity lipid-lowering therapy (HILLT)is unknown, and the question remains if there is still an unacceptably high residual risk to justify treatment with new lipid-lowering drugs. Methods: This observational, retrospective, multicenter, national study in Spain, whose information was obtained from a national dyslipemia registry, was designed to establish the current prevalence of cardiovascular disease (CVD)in HeFH and to define the impact of HILLT on CVD in this population. Odds were estimated using several logistic regression models with progressive adjustment. Results: 1958 HeFH, mean age 49.3 ± 14.3 years, were included in the analysis. At inclusion in the registry, 295 patients (15.1%)had suffered CVD and 164 (55.6%)had suffered the first event before the onset lipid-lowering treatment. Exposition to treatment associated more than ten times lower odds for CVD than in subjects naïve to treatment (OR 0.085, 95% CI 0.063–0.114, p < 0.001). A first CVD event after a mean treatment period of 9.1 ± 7.2 years occurred in 131 out of 1615 (8.1%)HeFH subjects, and 115 (87.8%)of them were on HILLT. Conclusions: Current prevalence of CVD among HeFH is one third of that reported before the statins era. Early initiation and prolonged lipid-lowering treatment was associated with a reduction in CVD. New cases of CVD, in spite of HILLT, appeared mostly among patients accumulating risk factors and probably they may be considered for further lipid-lowering drugs.en_US
dc.languageengen_US
dc.relation.ispartofAtherosclerosisen_US
dc.sourceAtherosclerosis [ISSN 0021-9150], v. 284, p. 245-252en_US
dc.subject32 Ciencias médicasen_US
dc.subject.otherCardiovascular Diseaseen_US
dc.subject.otherFamilial Hypercholesterolemiaen_US
dc.subject.otherLipid-Loweringen_US
dc.subject.otherStatinsen_US
dc.titleEffect of lipid-lowering treatment in cardiovascular disease prevalence in familial hypercholesterolemiaen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.atherosclerosis.2019.02.003
dc.identifier.scopus85062153668-
dc.identifier.isi000466155400037
dc.contributor.authorscopusid49864143900-
dc.contributor.authorscopusid10046356900-
dc.contributor.authorscopusid57189493797-
dc.contributor.authorscopusid56042148300-
dc.contributor.authorscopusid7004796457-
dc.contributor.authorscopusid22980898600-
dc.contributor.authorscopusid57203232814-
dc.contributor.authorscopusid54419413900-
dc.contributor.authorscopusid6507683958-
dc.contributor.authorscopusid55650129500-
dc.contributor.authorscopusid6507919181-
dc.contributor.authorscopusid35517335700-
dc.description.lastpage252-
dc.description.firstpage245-
dc.relation.volume284-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid1403031
dc.contributor.daisngid576146
dc.contributor.daisngid2491184
dc.contributor.daisngid1724129
dc.contributor.daisngid228640
dc.contributor.daisngid335717
dc.contributor.daisngid3549698
dc.contributor.daisngid1754006
dc.contributor.daisngid2898107
dc.contributor.daisngid32138999
dc.contributor.daisngid5324185
dc.contributor.daisngid89578
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Perez-Calahorra, S
dc.contributor.wosstandardWOS:Laclaustra, M
dc.contributor.wosstandardWOS:Marco-Benedi, V
dc.contributor.wosstandardWOS:Lamiquiz-Moneo, I
dc.contributor.wosstandardWOS:Pedro-Botet, J
dc.contributor.wosstandardWOS:Plana, N
dc.contributor.wosstandardWOS:Sanchez-Hernandez, RM
dc.contributor.wosstandardWOS:Amor, AJ
dc.contributor.wosstandardWOS:Almagro, F
dc.contributor.wosstandardWOS:Fuentes, F
dc.contributor.wosstandardWOS:Suarez-Tembra, M
dc.contributor.wosstandardWOS:Civeira, F
dc.date.coverdateMayo 2019
dc.identifier.ulpgces
dc.description.sjr1,515
dc.description.jcr3,919
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0003-4991-7445-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameSanchez Hernández, Rosa María-
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