Favorable effects of ezetimibe alone or in association with simvastatin on the removal from plasma of chylomicrons in coronary heart disease subjects

dc.contributor.authorMANGILI, OTAVIO C.
dc.contributor.authorGAGLIARDI, ANA C.M.
dc.contributor.authorMANGILI, LEONARDO C.
dc.contributor.authorMESQUITA, CARLOS H.
dc.contributor.authorCESAR, LUIZ A.M.
dc.contributor.authorTANAKA, AKIRA
dc.contributor.authorSCHAEFER, ERNST J.
dc.contributor.authorMARANHAO, RAUL C.
dc.contributor.authorSANTOS, RAUL D.
dc.coverageInternacionalpt_BR
dc.date.accessioned2014-08-15T11:31:27Z
dc.date.available2014-08-15T11:31:27Z
dc.date.issued2014pt_BR
dc.description.abstractObjective: Reductions on the clearance from plasma of chylomicrons are associated with atherosclerosis. Statins improve the removal from plasma of chylomicrons in a dose dependent manner. There is controversy whether ezetimibe modifies the plasma clearance of chylomicrons. Effects of ezetimibe alone or in combination with simvastatin were compared with low and high dose of the latter, upon the kinetics of a chylomicron-like emulsion in coronary heart disease (CHD) patients. Methods: 25 CHD patients were randomized for treatment with ezetimibe 10 mg (group 1) or simvastatin 20 mg (group 2) with progression to ezetimibe þ simvastatin 10/20 mg or simvastatin 80 mg, respectively. Kinetic studies were performed at baseline and after each treatment period of 6 weeks. The fractional catabolic rates (FCR) of the emulsion labeled with 14C-CE and 3 H-TG, that represent respectively chylomicron remnant and triglyceride removal, were calculated. Comparisons were made by ANOVA. Results: The 14CE-FCR in group 1 were 0.005 0.004, 0.011 0.008 and 0.018 0.005 min1 and in group 2 were 0.004 0.003, 0.011 0.008 and 0.019 0.007 min1 respectively at baseline, after 6 and 12 weeks (p < 0.05 vs. baseline, and 6 vs. 12 weeks). The 3 H-TG-FCR in group 1 were 0.017 0.011, 0.024 0.011 and 0.042 0.013 min1 and in group 2 were 0.016 0.009, 0.022 0.009 and 0.037 0.012 min1 at baseline, after 6 and 12 weeks (p < 0.05 vs. baseline, and 6 vs. 12 weeks). There were no differences between groups in time. Conclusion: Both treatments increased similarly the removal from plasma of chylomicron and remnants in CHD patients.
dc.format.extent319-325pt_BR
dc.identifier.citationMANGILI, OTAVIO C.; GAGLIARDI, ANA C.M.; MANGILI, LEONARDO C.; MESQUITA, CARLOS H.; CESAR, LUIZ A.M.; TANAKA, AKIRA; SCHAEFER, ERNST J.; MARANHAO, RAUL C.; SANTOS, RAUL D. Favorable effects of ezetimibe alone or in association with simvastatin on the removal from plasma of chylomicrons in coronary heart disease subjects. <b>Atherosclerosis</b>, v. 233, n. 1, p. 319-325, 2014. DOI: <a href="https://dx.doi.org/10.1016/j.atherosclerosis.2013.12.008">10.1016/j.atherosclerosis.2013.12.008</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/8944.
dc.identifier.doi10.1016/j.atherosclerosis.2013.12.008
dc.identifier.fasciculo1pt_BR
dc.identifier.issn0021-9150pt_BR
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/8944
dc.identifier.vol233pt_BR
dc.relation.ispartofAtherosclerosispt_BR
dc.rightsopenAccess
dc.subjectcardiovascular diseases
dc.subjectcoronaries
dc.subjectcholesterol
dc.subjectdrugs
dc.subjectblood plasma
dc.subjectchylomicrons
dc.subjecttriglycerides
dc.subjectlipoproteins
dc.subjectemulsions
dc.subjectphoton emission
dc.titleFavorable effects of ezetimibe alone or in association with simvastatin on the removal from plasma of chylomicrons in coronary heart disease subjectspt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorCARLOS HENRIQUE DE MESQUITA
ipen.codigoautor1149
ipen.contributor.ipenauthorCARLOS HENRIQUE DE MESQUITA
ipen.date.recebimento14-08pt_BR
ipen.identifier.fi3.994pt_BR
ipen.identifier.ipendoc20106pt_BR
ipen.identifier.iwosWoSpt_BR
ipen.identifier.ods3
ipen.range.fi3.000 - 4.499
ipen.type.genreArtigo
relation.isAuthorOfPublication20d22e5e-a0d1-4286-b4d9-20e5ac53cb51
relation.isAuthorOfPublication.latestForDiscovery20d22e5e-a0d1-4286-b4d9-20e5ac53cb51
sigepi.autor.atividadeMESQUITA, CARLOS H.:1149:240:N

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