Bezafibrate for the treatment of hypertriglyceridemia in HIV1-infected patients on highly active antiretroviral therapy

Detalhes bibliográficos
Autor(a) principal: Geraix, Juliana [UNESP]
Data de Publicação: 2006
Outros Autores: de Souza, Micheli Evangelista [UNESP], Delatim, Francieli Cristina [UNESP], Pereira, Paulo Câmara Marques [UNESP]
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.
id UNSP_ddbca80360fe27fb96dd72627953743e
oai_identifier_str oai:repositorio.unesp.br:11449/68900
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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