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Long-Term and Concentration-Dependent Beneficial Effect of Efavirenz on HDL-Cholesterol in HIV-Infected Patients

dc.contributor.authorPereira, SA
dc.contributor.authorBranco, T
dc.contributor.authorCôrte-Real, R
dc.contributor.authorGermano, I
dc.contributor.authorLampreia, F
dc.contributor.authorCaixas, U
dc.contributor.authorMonteiro, E
dc.date.accessioned2014-04-08T11:52:21Z
dc.date.available2014-04-08T11:52:21Z
dc.date.issued2006
dc.description.abstractAIMS: To investigate the long-term effects of efavirenz on cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein (LDL-C) and triglycerides (TG). METHODS: Thirty-four HIV-infected patients who commenced efavirenz therapy were monitored for 36 months. RESULTS: In patients with baseline HDL-C<40 mg.dL-1 an increase in HDL-C from 31+/-1 mg.dL-1 to 44+/-2 mg.dL-1 (95% confidence interval 5.9, 21.9, P<0.01) was observed and remained throughout the follow-up period. Median efavirenz plasma concentration was 1.98 mg.L-1 and a direct correlation between percentage of HDL-C variation or TC/HDL-C ratio and efavirenz plasma concentrations was found. CONCLUSIONS: There is evidence of a long-term and concentration-dependent beneficial effect of efavirenz on HDL-C in HIV-infected patients.por
dc.identifier.citationBr J Clin Pharmacol. 2006 May;61(5):601-4por
dc.identifier.urihttp://hdl.handle.net/10400.17/1777
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherWileypor
dc.subjectCHLC MEDpor
dc.subjectBenzoxazinaspor
dc.subjectColesterolpor
dc.subjectColesterol HDLpor
dc.subjectRelação Dose-Resposta a Medicamentopor
dc.subjectEstudos de Follow-Uppor
dc.subjectGlicoproteínaspor
dc.subjectInfecção por HIVpor
dc.subjectHIV-1por
dc.subjectOxazinaspor
dc.subjectEstudos Prospectivospor
dc.subjectInibidores de Transcriptase Reversapor
dc.subjectFactores de Tempopor
dc.subjectResultado de Tratamentopor
dc.titleLong-Term and Concentration-Dependent Beneficial Effect of Efavirenz on HDL-Cholesterol in HIV-Infected Patientspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage604por
oaire.citation.startPage601por
oaire.citation.titleBritish Journal of Clinical Pharmacologypor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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