Increase of lipids during HCV treatment: Virus action or medication?

Detalhes bibliográficos
Autor(a) principal: De Andrade, Vanessa Gutierrez [UNESP]
Data de Publicação: 2018
Outros Autores: Yamashiro, Fabio da Silva [UNESP], Oliveira, Cassio Vieira [UNESP], Kurozawa, Leticia Lastória [UNESP], Moreira, Alecsandro [UNESP], Silva, Giovanni Faria [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/s0004-2803.201800000-33
http://hdl.handle.net/11449/176665
Resumo: Background - The interaction between serum lipids and C virus infection is well known, as are serum lipid levels in the Peg-IFN/RBV-based treatment. However, with direct action antivirals (DAAs) this behavior is still unclear. Objective - To compare serum lipids levels between patients treated with Peg-IFN/RBV and DAAs and to evaluate lipids in sustained virological response (SVR) with DAAs. Methods - Retro prospective study comparing the behavior of total cholesterol (TC), low-density lipoprotein (LDL) and triglycerides (TG) serum levels during treatment with DAAs (G-DAAs) and a control historic group Peg-IFN/RBV (G-PR). Coorte, prospective study, to study the behavior of lipids in the SVR with DAAs. Data were collected at the beginning of treatment (baseline: t-base) and at week 12 of treatment (t-12) for G-DAAs and at week 24 (t-24) for G-PR, groups. In the cohort evaluation, the samples at t-base and at week 12 after the end of treatment (t-SVR). Delta lipids: difference between lipids in t-12/t-24 minus t-base for comparison between G-PR and G-AADs groups and t-SVR minus t-base for lipid analysis in SVR. Analysis with Kruskal Wallis and Wilcoxon tests to compare the delta lipids of the groups. The P value was 0.05. Results - In the assessment between G-PR and G-DAAs groups, we included 63 and 121 patients, respectively. The groups did not differ one from the other (BMI, sex, genotype, fibrosis, total cholesterol, LDL, and TG) except by age (50.38 ± 10.44 vs 56 ± 9.69, P=0.0006). We observed a decrease in levels of TC and LDL and an increase in TG, in G-PR, and in G-DAAs the opposite (Δ TC -13.9 ± 34.5 vs 4.12 ± 34.3 P=0.0005, Δ LDL -7.16 ± 32 vs 10.13 ± 29.92, P=0.003, Δ TG 4.51 ± 53.7 vs -8.24 ± 49.93, P=0.0025). In the coorte analysis, we included 102 patients, 70% men and 56% F4, 95 of them reached SVR. We observed an increase of TC and LDL and a decrease of TG in both groups (SVR and non SVR), with no statistical difference (Δ TC P=0.68; Δ LDL P=0.69; Δ TG P=0.43). We did not find significant difference in delta evaluation by genotype 1 and 3 (Δ TC +29.7 ± 40.2 vs +13.4 ± 30.3, P=0.06; Δ LDL +21.4 ± 28.6 vs +16.6 ± 31.3, P=0.41; Δ TG -3.6 ± 60.6 vs -0.7 ± 40, P=0.91). Conclusion - Serum lipids level differed during treatment with Peg-IFN and DAAs. Treatment with DAAs was associated with an increase of TC and LDL and a decrease of TG, independently of SVR.
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spelling Increase of lipids during HCV treatment: Virus action or medication?Aumento dos lipídes durante tratamento para VHC: Ação do vírus ou da medicação?Antiviral agentsHepatitis CInterferon-alphaLipid metabolismTherapeutic useVirological analysisBackground - The interaction between serum lipids and C virus infection is well known, as are serum lipid levels in the Peg-IFN/RBV-based treatment. However, with direct action antivirals (DAAs) this behavior is still unclear. Objective - To compare serum lipids levels between patients treated with Peg-IFN/RBV and DAAs and to evaluate lipids in sustained virological response (SVR) with DAAs. Methods - Retro prospective study comparing the behavior of total cholesterol (TC), low-density lipoprotein (LDL) and triglycerides (TG) serum levels during treatment with DAAs (G-DAAs) and a control historic group Peg-IFN/RBV (G-PR). Coorte, prospective study, to study the behavior of lipids in the SVR with DAAs. Data were collected at the beginning of treatment (baseline: t-base) and at week 12 of treatment (t-12) for G-DAAs and at week 24 (t-24) for G-PR, groups. In the cohort evaluation, the samples at t-base and at week 12 after the end of treatment (t-SVR). Delta lipids: difference between lipids in t-12/t-24 minus t-base for comparison between G-PR and G-AADs groups and t-SVR minus t-base for lipid analysis in SVR. Analysis with Kruskal Wallis and Wilcoxon tests to compare the delta lipids of the groups. The P value was 0.05. Results - In the assessment between G-PR and G-DAAs groups, we included 63 and 121 patients, respectively. The groups did not differ one from the other (BMI, sex, genotype, fibrosis, total cholesterol, LDL, and TG) except by age (50.38 ± 10.44 vs 56 ± 9.69, P=0.0006). We observed a decrease in levels of TC and LDL and an increase in TG, in G-PR, and in G-DAAs the opposite (Δ TC -13.9 ± 34.5 vs 4.12 ± 34.3 P=0.0005, Δ LDL -7.16 ± 32 vs 10.13 ± 29.92, P=0.003, Δ TG 4.51 ± 53.7 vs -8.24 ± 49.93, P=0.0025). In the coorte analysis, we included 102 patients, 70% men and 56% F4, 95 of them reached SVR. We observed an increase of TC and LDL and a decrease of TG in both groups (SVR and non SVR), with no statistical difference (Δ TC P=0.68; Δ LDL P=0.69; Δ TG P=0.43). We did not find significant difference in delta evaluation by genotype 1 and 3 (Δ TC +29.7 ± 40.2 vs +13.4 ± 30.3, P=0.06; Δ LDL +21.4 ± 28.6 vs +16.6 ± 31.3, P=0.41; Δ TG -3.6 ± 60.6 vs -0.7 ± 40, P=0.91). Conclusion - Serum lipids level differed during treatment with Peg-IFN and DAAs. Treatment with DAAs was associated with an increase of TC and LDL and a decrease of TG, independently of SVR.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Universidade Estadual Paulista ‘Júlio de Mesquita Filho’ (UNESP) Campus Botucatu Faculdade de Medicina Departamento de Clínica MédicaUniversidade Estadual Paulista ‘Júlio de Mesquita Filho’ (UNESP) Campus Botucatu Faculdade de Medicina Departamento de Clínica MédicaUniversidade Estadual Paulista (Unesp)De Andrade, Vanessa Gutierrez [UNESP]Yamashiro, Fabio da Silva [UNESP]Oliveira, Cassio Vieira [UNESP]Kurozawa, Leticia Lastória [UNESP]Moreira, Alecsandro [UNESP]Silva, Giovanni Faria [UNESP]2018-12-11T17:21:59Z2018-12-11T17:21:59Z2018-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article184-187application/pdfhttp://dx.doi.org/10.1590/s0004-2803.201800000-33Arquivos de Gastroenterologia, v. 55, n. 2, p. 184-187, 2018.1678-42190004-2803http://hdl.handle.net/11449/17666510.1590/s0004-2803.201800000-33S0004-280320180002001842-s2.0-85050874724S0004-28032018000200184.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengArquivos de Gastroenterologia0,396info:eu-repo/semantics/openAccess2024-08-14T17:23:09Zoai:repositorio.unesp.br:11449/176665Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:23:09Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Increase of lipids during HCV treatment: Virus action or medication?
Aumento dos lipídes durante tratamento para VHC: Ação do vírus ou da medicação?
title Increase of lipids during HCV treatment: Virus action or medication?
spellingShingle Increase of lipids during HCV treatment: Virus action or medication?
De Andrade, Vanessa Gutierrez [UNESP]
Antiviral agents
Hepatitis C
Interferon-alpha
Lipid metabolism
Therapeutic use
Virological analysis
title_short Increase of lipids during HCV treatment: Virus action or medication?
title_full Increase of lipids during HCV treatment: Virus action or medication?
title_fullStr Increase of lipids during HCV treatment: Virus action or medication?
title_full_unstemmed Increase of lipids during HCV treatment: Virus action or medication?
title_sort Increase of lipids during HCV treatment: Virus action or medication?
author De Andrade, Vanessa Gutierrez [UNESP]
author_facet De Andrade, Vanessa Gutierrez [UNESP]
Yamashiro, Fabio da Silva [UNESP]
Oliveira, Cassio Vieira [UNESP]
Kurozawa, Leticia Lastória [UNESP]
Moreira, Alecsandro [UNESP]
Silva, Giovanni Faria [UNESP]
author_role author
author2 Yamashiro, Fabio da Silva [UNESP]
Oliveira, Cassio Vieira [UNESP]
Kurozawa, Leticia Lastória [UNESP]
Moreira, Alecsandro [UNESP]
Silva, Giovanni Faria [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv De Andrade, Vanessa Gutierrez [UNESP]
Yamashiro, Fabio da Silva [UNESP]
Oliveira, Cassio Vieira [UNESP]
Kurozawa, Leticia Lastória [UNESP]
Moreira, Alecsandro [UNESP]
Silva, Giovanni Faria [UNESP]
dc.subject.por.fl_str_mv Antiviral agents
Hepatitis C
Interferon-alpha
Lipid metabolism
Therapeutic use
Virological analysis
topic Antiviral agents
Hepatitis C
Interferon-alpha
Lipid metabolism
Therapeutic use
Virological analysis
description Background - The interaction between serum lipids and C virus infection is well known, as are serum lipid levels in the Peg-IFN/RBV-based treatment. However, with direct action antivirals (DAAs) this behavior is still unclear. Objective - To compare serum lipids levels between patients treated with Peg-IFN/RBV and DAAs and to evaluate lipids in sustained virological response (SVR) with DAAs. Methods - Retro prospective study comparing the behavior of total cholesterol (TC), low-density lipoprotein (LDL) and triglycerides (TG) serum levels during treatment with DAAs (G-DAAs) and a control historic group Peg-IFN/RBV (G-PR). Coorte, prospective study, to study the behavior of lipids in the SVR with DAAs. Data were collected at the beginning of treatment (baseline: t-base) and at week 12 of treatment (t-12) for G-DAAs and at week 24 (t-24) for G-PR, groups. In the cohort evaluation, the samples at t-base and at week 12 after the end of treatment (t-SVR). Delta lipids: difference between lipids in t-12/t-24 minus t-base for comparison between G-PR and G-AADs groups and t-SVR minus t-base for lipid analysis in SVR. Analysis with Kruskal Wallis and Wilcoxon tests to compare the delta lipids of the groups. The P value was 0.05. Results - In the assessment between G-PR and G-DAAs groups, we included 63 and 121 patients, respectively. The groups did not differ one from the other (BMI, sex, genotype, fibrosis, total cholesterol, LDL, and TG) except by age (50.38 ± 10.44 vs 56 ± 9.69, P=0.0006). We observed a decrease in levels of TC and LDL and an increase in TG, in G-PR, and in G-DAAs the opposite (Δ TC -13.9 ± 34.5 vs 4.12 ± 34.3 P=0.0005, Δ LDL -7.16 ± 32 vs 10.13 ± 29.92, P=0.003, Δ TG 4.51 ± 53.7 vs -8.24 ± 49.93, P=0.0025). In the coorte analysis, we included 102 patients, 70% men and 56% F4, 95 of them reached SVR. We observed an increase of TC and LDL and a decrease of TG in both groups (SVR and non SVR), with no statistical difference (Δ TC P=0.68; Δ LDL P=0.69; Δ TG P=0.43). We did not find significant difference in delta evaluation by genotype 1 and 3 (Δ TC +29.7 ± 40.2 vs +13.4 ± 30.3, P=0.06; Δ LDL +21.4 ± 28.6 vs +16.6 ± 31.3, P=0.41; Δ TG -3.6 ± 60.6 vs -0.7 ± 40, P=0.91). Conclusion - Serum lipids level differed during treatment with Peg-IFN and DAAs. Treatment with DAAs was associated with an increase of TC and LDL and a decrease of TG, independently of SVR.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:21:59Z
2018-12-11T17:21:59Z
2018-04-01
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/s0004-2803.201800000-33
Arquivos de Gastroenterologia, v. 55, n. 2, p. 184-187, 2018.
1678-4219
0004-2803
http://hdl.handle.net/11449/176665
10.1590/s0004-2803.201800000-33
S0004-28032018000200184
2-s2.0-85050874724
S0004-28032018000200184.pdf
url http://dx.doi.org/10.1590/s0004-2803.201800000-33
http://hdl.handle.net/11449/176665
identifier_str_mv Arquivos de Gastroenterologia, v. 55, n. 2, p. 184-187, 2018.
1678-4219
0004-2803
10.1590/s0004-2803.201800000-33
S0004-28032018000200184
2-s2.0-85050874724
S0004-28032018000200184.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Arquivos de Gastroenterologia
0,396
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 184-187
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
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