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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68050
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dc.contributor.authorMalavazi, I.-
dc.contributor.authorAbrão, E. P.-
dc.contributor.authorMikawa, A. Y.-
dc.contributor.authorLandgraf, V. O.-
dc.contributor.authorCosta, P. I.-
dc.date.accessioned2014-05-27T11:21:14Z-
dc.date.accessioned2016-10-25T18:20:17Z-
dc.date.available2014-05-27T11:21:14Z-
dc.date.available2016-10-25T18:20:17Z-
dc.date.issued2004-12-01-
dc.identifier.citationRevista de Ciencias Farmaceuticas, v. 25, n. 2, p. 69-78, 2004.-
dc.identifier.issn0101-3793-
dc.identifier.urihttp://hdl.handle.net/11449/68050-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68050-
dc.description.abstractThe HIV-infected individuals have been identified as a peculiar group whose propensity to the development of abnormalities in lipids metabolism supports the hypothesis that AIDS itself can be considered as an independent risk factor for the occlusive diseases development. The AIDS progression, as well as the therapy against HIV has been capable to show an array of metabolic disturbances that HIV-infected patients are prone to. These metabolic alterations affect the fate of plasmatic lipids and homocysteine as a result of three factor mainly: (i) the viral infection per se which triggers the development of hypertriglyceridemia and hipocholesterolemia; (ii) multiple vitamins and micronutrients deficiencies, that favors an onset of hyperhomocysteinemia; (iii) the state-of-the-art therapy for HIV infection, which is accompanied to idiosyncratic effects encompassing the lipid metabolism. In this context, a variety of risk factors to atherosclerosis can be identified in the HIV-infected individual. Of note, it must be considered that once life expectancy of these patients has been expanded due to the effective therapy, on the other hand they can accelerate atherosclerotic disease or its pathological appearance in the same extent.en
dc.format.extent69-78-
dc.language.isopor-
dc.sourceScopus-
dc.subjectAntiretroviral-
dc.subjectApolipoproteins-
dc.subjectHAART-
dc.subjectHIV-
dc.subjectHomocysteine-
dc.subjectLipoproteins-
dc.subjectantiretrovirus agent-
dc.subjectcytochrome P450 3A-
dc.subjectdidanosine-
dc.subjecthigh density lipoprotein-
dc.subjecthomocysteine-
dc.subjectlipid-
dc.subjectlow density lipoprotein-
dc.subjectperoxisome proliferator activated receptor gamma-
dc.subjectretinoid X receptor-
dc.subjectRNA directed DNA polymerase inhibitor-
dc.subjectvery low density lipoprotein-
dc.subjectzalcitabine-
dc.subjectzidovudine-
dc.subjectacquired immune deficiency syndrome-
dc.subjectatherosclerosis-
dc.subjectcoronary artery disease-
dc.subjectdisease course-
dc.subjecthighly active antiretroviral therapy-
dc.subjecthuman-
dc.subjectHuman immunodeficiency virus-
dc.subjectHuman immunodeficiency virus infection-
dc.subjecthyperhomocysteinemia-
dc.subjecthypertriglyceridemia-
dc.subjecthypocholesterolemia-
dc.subjectlife expectancy-
dc.subjectlipid metabolism-
dc.subjectmetabolic disorder-
dc.subjectnonhuman-
dc.subjectpathology-
dc.subjectreview-
dc.subjectvirus infection-
dc.subjectvitamin deficiency-
dc.titleDoença arterial coronariana: Um novo paradigma na AIDSpt
dc.title.alternativeCoronary artery disease: A new paradigm in AIDSen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationPrograma de Pós-Graduação em Biotecnologia Instituto de Química de Araraquara UNESP-
dc.description.affiliationPrograma de Pós-Graduação em Análises Clínicas Faculdade de Ciências Farmacêuticas de Araraquara UNESP-
dc.description.affiliationUnespPrograma de Pós-Graduação em Biotecnologia Instituto de Química de Araraquara UNESP-
dc.description.affiliationUnespPrograma de Pós-Graduação em Análises Clínicas Faculdade de Ciências Farmacêuticas de Araraquara UNESP-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofRevista de Ciencias Farmaceuticas-
dc.identifier.scopus2-s2.0-27444438021-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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