Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1590/S1413-86702006000300001 |
Texto Completo: | http://dx.doi.org/10.1590/S1413-86702006000300001 http://hdl.handle.net/11449/68900 |
Resumo: | The use of highly active antiretroviral therapy (HAART) in HIV-infected patients has been associated with the development of risk factors for cardiovascular diseases (CD) including dyslipidemia and insulin resistance, hypertriglyceridemia being the most frequent metabolic disturbance in these patients. Fibrates are indicated when hypertriglyceridemia is accentuated and persists for over six months. We evaluated the efficacy and safety of bezafibrate for the treatment of hypertriglyceridemia in HIV-infected individuals on HAART. All patients received 400mg/day of bezafibrate and were evaluated three times: Mo (pre-treatment), M1 (one month after treatment), and M2 (six months after treatment). Fifteen adult individuals, eight males and seven females with mean age = 41.2 ± 7.97 years and triglyceride serum levels ≥400mg/dL were included in the study. Smoking, alcohol ingestion and sedentarism rates were 50%, 6.66% and 60%, respectively. Family history of CD, hypertension and diabetes mellitus was reported in 33.3%, 40% and 46.7% of the cases, respectively, while dyslipidemia was reported by only 13.3%. More than half of the patients were using a protease inhibitor plus a nucleotide analog transcriptase inhibitor. Eutrophy and tendency toward overweight were observed at all three study time points. There were significant reductions in triglyceride serum levels from Mo to M1 and from Mo to M2. No significant changes were observed in the serum levels of creatine phosphokinase, hepatic enzymes, CD4 +, CD8 + and viral load. Therefore, bezafibrate seems to be safe and effective for the reduction of hypertriglyceridemia in HIV-infected patients on HAART. © 2006 by The Brazilian Journal of Infectious Diseases and Contexto Publishing. All rights reserved. |
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Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapyBezafibrateHAARTHIVHypertriglyceridemiaantiretrovirus agentbezafibrateCD4 antigenCD8 antigencedura retardcreatine kinaseliver enzymeproteinase inhibitorRNA directed DNA polymerase inhibitortriacylglyceroladultalcohol consumptioncardiovascular diseaseclinical articlecontrolled studycreatine kinase blood leveldiabetes mellitusdrug dose regimendrug efficacydrug safetydyslipidemiafamily historyfemalefollow uphighly active antiretroviral therapyhumanHuman immunodeficiency virus 1Human immunodeficiency virus infected patientHuman immunodeficiency virus infectionhypertensionhypertriglyceridemiamalenonhumanobesitysittingsmokingtriacylglycerol blood levelvirus loadAdultAntilipemic AgentsAntiretroviral Therapy, Highly ActiveCD4-CD8 RatioFemaleHIV InfectionsHumansMaleTreatment OutcomeViral LoadThe use of highly active antiretroviral therapy (HAART) in HIV-infected patients has been associated with the development of risk factors for cardiovascular diseases (CD) including dyslipidemia and insulin resistance, hypertriglyceridemia being the most frequent metabolic disturbance in these patients. Fibrates are indicated when hypertriglyceridemia is accentuated and persists for over six months. We evaluated the efficacy and safety of bezafibrate for the treatment of hypertriglyceridemia in HIV-infected individuals on HAART. All patients received 400mg/day of bezafibrate and were evaluated three times: Mo (pre-treatment), M1 (one month after treatment), and M2 (six months after treatment). Fifteen adult individuals, eight males and seven females with mean age = 41.2 ± 7.97 years and triglyceride serum levels ≥400mg/dL were included in the study. Smoking, alcohol ingestion and sedentarism rates were 50%, 6.66% and 60%, respectively. Family history of CD, hypertension and diabetes mellitus was reported in 33.3%, 40% and 46.7% of the cases, respectively, while dyslipidemia was reported by only 13.3%. More than half of the patients were using a protease inhibitor plus a nucleotide analog transcriptase inhibitor. Eutrophy and tendency toward overweight were observed at all three study time points. There were significant reductions in triglyceride serum levels from Mo to M1 and from Mo to M2. No significant changes were observed in the serum levels of creatine phosphokinase, hepatic enzymes, CD4 +, CD8 + and viral load. Therefore, bezafibrate seems to be safe and effective for the reduction of hypertriglyceridemia in HIV-infected patients on HAART. © 2006 by The Brazilian Journal of Infectious Diseases and Contexto Publishing. All rights reserved.Tropical Diseases Department Faculty of Medicine of Botucatu State University of São Paulo - UNESP, Distrito de Rubiao Junior s/no, 18618-000 Botucatu, SPTropical Diseases Department Faculty of Medicine of Botucatu State University of São Paulo - UNESP, Distrito de Rubiao Junior s/no, 18618-000 Botucatu, SPUniversidade Estadual Paulista (Unesp)Geraix, Juliana [UNESP]de Souza, Micheli Evangelista [UNESP]Delatim, Francieli Cristina [UNESP]Pereira, Paulo Câmara Marques [UNESP]2014-05-27T11:21:52Z2014-05-27T11:21:52Z2006-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article159-164application/pdfhttp://dx.doi.org/10.1590/S1413-86702006000300001Brazilian Journal of Infectious Diseases, v. 10, n. 3, p. 159-164, 2006.1413-8670http://hdl.handle.net/11449/6890010.1590/S1413-86702006000300001S1413-867020060003000012-s2.0-337490792042-s2.0-33749079204.pdf13653204274182040000-0001-5771-8943Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrazilian Journal of Infectious Diseases2.0830,817info:eu-repo/semantics/openAccess2024-08-15T15:22:25Zoai:repositorio.unesp.br:11449/68900Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-15T15:22:25Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
title |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
spellingShingle |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy Geraix, Juliana [UNESP] Bezafibrate HAART HIV Hypertriglyceridemia antiretrovirus agent bezafibrate CD4 antigen CD8 antigen cedura retard creatine kinase liver enzyme proteinase inhibitor RNA directed DNA polymerase inhibitor triacylglycerol adult alcohol consumption cardiovascular disease clinical article controlled study creatine kinase blood level diabetes mellitus drug dose regimen drug efficacy drug safety dyslipidemia family history female follow up highly active antiretroviral therapy human Human immunodeficiency virus 1 Human immunodeficiency virus infected patient Human immunodeficiency virus infection hypertension hypertriglyceridemia male nonhuman obesity sitting smoking triacylglycerol blood level virus load Adult Antilipemic Agents Antiretroviral Therapy, Highly Active CD4-CD8 Ratio Female HIV Infections Humans Male Treatment Outcome Viral Load Geraix, Juliana [UNESP] Bezafibrate HAART HIV Hypertriglyceridemia antiretrovirus agent bezafibrate CD4 antigen CD8 antigen cedura retard creatine kinase liver enzyme proteinase inhibitor RNA directed DNA polymerase inhibitor triacylglycerol adult alcohol consumption cardiovascular disease clinical article controlled study creatine kinase blood level diabetes mellitus drug dose regimen drug efficacy drug safety dyslipidemia family history female follow up highly active antiretroviral therapy human Human immunodeficiency virus 1 Human immunodeficiency virus infected patient Human immunodeficiency virus infection hypertension hypertriglyceridemia male nonhuman obesity sitting smoking triacylglycerol blood level virus load Adult Antilipemic Agents Antiretroviral Therapy, Highly Active CD4-CD8 Ratio Female HIV Infections Humans Male Treatment Outcome Viral Load |
title_short |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
title_full |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
title_fullStr |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
title_full_unstemmed |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
title_sort |
Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy |
author |
Geraix, Juliana [UNESP] |
author_facet |
Geraix, Juliana [UNESP] Geraix, Juliana [UNESP] de Souza, Micheli Evangelista [UNESP] Delatim, Francieli Cristina [UNESP] Pereira, Paulo Câmara Marques [UNESP] de Souza, Micheli Evangelista [UNESP] Delatim, Francieli Cristina [UNESP] Pereira, Paulo Câmara Marques [UNESP] |
author_role |
author |
author2 |
de Souza, Micheli Evangelista [UNESP] Delatim, Francieli Cristina [UNESP] Pereira, Paulo Câmara Marques [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Geraix, Juliana [UNESP] de Souza, Micheli Evangelista [UNESP] Delatim, Francieli Cristina [UNESP] Pereira, Paulo Câmara Marques [UNESP] |
dc.subject.por.fl_str_mv |
Bezafibrate HAART HIV Hypertriglyceridemia antiretrovirus agent bezafibrate CD4 antigen CD8 antigen cedura retard creatine kinase liver enzyme proteinase inhibitor RNA directed DNA polymerase inhibitor triacylglycerol adult alcohol consumption cardiovascular disease clinical article controlled study creatine kinase blood level diabetes mellitus drug dose regimen drug efficacy drug safety dyslipidemia family history female follow up highly active antiretroviral therapy human Human immunodeficiency virus 1 Human immunodeficiency virus infected patient Human immunodeficiency virus infection hypertension hypertriglyceridemia male nonhuman obesity sitting smoking triacylglycerol blood level virus load Adult Antilipemic Agents Antiretroviral Therapy, Highly Active CD4-CD8 Ratio Female HIV Infections Humans Male Treatment Outcome Viral Load |
topic |
Bezafibrate HAART HIV Hypertriglyceridemia antiretrovirus agent bezafibrate CD4 antigen CD8 antigen cedura retard creatine kinase liver enzyme proteinase inhibitor RNA directed DNA polymerase inhibitor triacylglycerol adult alcohol consumption cardiovascular disease clinical article controlled study creatine kinase blood level diabetes mellitus drug dose regimen drug efficacy drug safety dyslipidemia family history female follow up highly active antiretroviral therapy human Human immunodeficiency virus 1 Human immunodeficiency virus infected patient Human immunodeficiency virus infection hypertension hypertriglyceridemia male nonhuman obesity sitting smoking triacylglycerol blood level virus load Adult Antilipemic Agents Antiretroviral Therapy, Highly Active CD4-CD8 Ratio Female HIV Infections Humans Male Treatment Outcome Viral Load |
description |
The use of highly active antiretroviral therapy (HAART) in HIV-infected patients has been associated with the development of risk factors for cardiovascular diseases (CD) including dyslipidemia and insulin resistance, hypertriglyceridemia being the most frequent metabolic disturbance in these patients. Fibrates are indicated when hypertriglyceridemia is accentuated and persists for over six months. We evaluated the efficacy and safety of bezafibrate for the treatment of hypertriglyceridemia in HIV-infected individuals on HAART. All patients received 400mg/day of bezafibrate and were evaluated three times: Mo (pre-treatment), M1 (one month after treatment), and M2 (six months after treatment). Fifteen adult individuals, eight males and seven females with mean age = 41.2 ± 7.97 years and triglyceride serum levels ≥400mg/dL were included in the study. Smoking, alcohol ingestion and sedentarism rates were 50%, 6.66% and 60%, respectively. Family history of CD, hypertension and diabetes mellitus was reported in 33.3%, 40% and 46.7% of the cases, respectively, while dyslipidemia was reported by only 13.3%. More than half of the patients were using a protease inhibitor plus a nucleotide analog transcriptase inhibitor. Eutrophy and tendency toward overweight were observed at all three study time points. There were significant reductions in triglyceride serum levels from Mo to M1 and from Mo to M2. No significant changes were observed in the serum levels of creatine phosphokinase, hepatic enzymes, CD4 +, CD8 + and viral load. Therefore, bezafibrate seems to be safe and effective for the reduction of hypertriglyceridemia in HIV-infected patients on HAART. © 2006 by The Brazilian Journal of Infectious Diseases and Contexto Publishing. All rights reserved. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-06-01 2014-05-27T11:21:52Z 2014-05-27T11:21:52Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S1413-86702006000300001 Brazilian Journal of Infectious Diseases, v. 10, n. 3, p. 159-164, 2006. 1413-8670 http://hdl.handle.net/11449/68900 10.1590/S1413-86702006000300001 S1413-86702006000300001 2-s2.0-33749079204 2-s2.0-33749079204.pdf 1365320427418204 0000-0001-5771-8943 |
url |
http://dx.doi.org/10.1590/S1413-86702006000300001 http://hdl.handle.net/11449/68900 |
identifier_str_mv |
Brazilian Journal of Infectious Diseases, v. 10, n. 3, p. 159-164, 2006. 1413-8670 10.1590/S1413-86702006000300001 S1413-86702006000300001 2-s2.0-33749079204 2-s2.0-33749079204.pdf 1365320427418204 0000-0001-5771-8943 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Infectious Diseases 2.083 0,817 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
159-164 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1822182455787913216 |
dc.identifier.doi.none.fl_str_mv |
10.1590/S1413-86702006000300001 |