Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients

Detalhes bibliográficos
Autor(a) principal: Camargo, Eduardo Guimaraes
Data de Publicação: 2012
Outros Autores: Weinert, Leticia Schwerz, Soares, Ariana Aguiar, Ferreira, Mariana Nunes, Araujo, Gustavo Neves, Silveiro, Sandra Pinho
Tipo de documento: Artigo
Idioma: por
Título da fonte: Clinical and Biomedical Research
Texto Completo: https://seer.ufrgs.br/index.php/hcpa/article/view/24313
Resumo: BACKGROUND: Low-grade inflammation has been implicated in the pathogenesis of diabetic nephropathy, and anti-inflammatory drugs could be potentially useful as a therapeutic tool. The aim of this study was to analyze the effect of low-dose aspirin (300 mg/d) on urinary albumin excretion (UAE) and glomerular filtration rate (GFR) levels of microalbuminuric type 2 DM patients.METHODS: In this randomized, double-blind, crossover, placebo-controlled study, 18 microalbuminuric (UAE=30-300 mg/24 h) type 2 DM patients received aspirin (300 mg/d) or identical placebo for 8 weeks, with a 6-week washout period. The patients were aged 56±9 years, had a diabetes duration of 16±7.5 years; 11 (61%) were female, and they were all using enalapril 10 mg bid. GFR was measured by 51Cr-EDTA single-injection method and UAE by immunoturbidimetry. The sample-size calculation showed that 17 patients were needed to detect a 30% change in UAE (α= 0.05 and β= 0.20).RESULTS: After 8 weeks of treatment, there were no significant differences between placebo and aspirin, respectively, regarding UAE [57.7 (8.9-420.0) vs. 63 (8.2-272.0) mg/24 h; P=0.45] and GFR (108±34 vs. 111±47 ml/min/1.73 m2; P=0.90). C-reactive protein levels [2.72 (0.34-10.3) vs. 2.03 (0.25-10.3) μg/l; P=0.21] were comparable after placebo and aspirin, respectively. There were no period (P=0.41) or carry-over effects (P=0.49).CONCLUSION: Low-dose aspirin did not affect GFR and UAE levels of microalbuminuric type 2 DM. It seems that the putative low-grade inflammation of diabetic nephropathy does not respond to these low doses of the drug.
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spelling Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patientsaspirindiabetic nephropathyGFRglomerular filtration ratemicroalbuminuriaBACKGROUND: Low-grade inflammation has been implicated in the pathogenesis of diabetic nephropathy, and anti-inflammatory drugs could be potentially useful as a therapeutic tool. The aim of this study was to analyze the effect of low-dose aspirin (300 mg/d) on urinary albumin excretion (UAE) and glomerular filtration rate (GFR) levels of microalbuminuric type 2 DM patients.METHODS: In this randomized, double-blind, crossover, placebo-controlled study, 18 microalbuminuric (UAE=30-300 mg/24 h) type 2 DM patients received aspirin (300 mg/d) or identical placebo for 8 weeks, with a 6-week washout period. The patients were aged 56±9 years, had a diabetes duration of 16±7.5 years; 11 (61%) were female, and they were all using enalapril 10 mg bid. GFR was measured by 51Cr-EDTA single-injection method and UAE by immunoturbidimetry. The sample-size calculation showed that 17 patients were needed to detect a 30% change in UAE (α= 0.05 and β= 0.20).RESULTS: After 8 weeks of treatment, there were no significant differences between placebo and aspirin, respectively, regarding UAE [57.7 (8.9-420.0) vs. 63 (8.2-272.0) mg/24 h; P=0.45] and GFR (108±34 vs. 111±47 ml/min/1.73 m2; P=0.90). C-reactive protein levels [2.72 (0.34-10.3) vs. 2.03 (0.25-10.3) μg/l; P=0.21] were comparable after placebo and aspirin, respectively. There were no period (P=0.41) or carry-over effects (P=0.49).CONCLUSION: Low-dose aspirin did not affect GFR and UAE levels of microalbuminuric type 2 DM. It seems that the putative low-grade inflammation of diabetic nephropathy does not respond to these low doses of the drug.HCPA/FAMED/UFRGS2012-01-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer-reviewed ArticleAvaliado por Paresapplication/pdfhttps://seer.ufrgs.br/index.php/hcpa/article/view/24313Clinical & Biomedical Research; Vol. 31 No. 4 (2011): Revista HCPAClinical and Biomedical Research; v. 31 n. 4 (2011): Revista HCPA2357-9730reponame:Clinical and Biomedical Researchinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSporhttps://seer.ufrgs.br/index.php/hcpa/article/view/24313/14954Camargo, Eduardo GuimaraesWeinert, Leticia SchwerzSoares, Ariana AguiarFerreira, Mariana NunesAraujo, Gustavo NevesSilveiro, Sandra Pinhoinfo:eu-repo/semantics/openAccess2020-01-16T18:23:19Zoai:seer.ufrgs.br:article/24313Revistahttps://www.seer.ufrgs.br/index.php/hcpaPUBhttps://seer.ufrgs.br/index.php/hcpa/oai||cbr@hcpa.edu.br2357-97302357-9730opendoar:2020-01-16T18:23:19Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.none.fl_str_mv Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
title Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
spellingShingle Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
Camargo, Eduardo Guimaraes
aspirin
diabetic nephropathy
GFR
glomerular filtration rate
microalbuminuria
title_short Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
title_full Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
title_fullStr Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
title_full_unstemmed Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
title_sort Low-dose aspirin does not affect the renal function of microalbuminuric type 2 Diabetic patients
author Camargo, Eduardo Guimaraes
author_facet Camargo, Eduardo Guimaraes
Weinert, Leticia Schwerz
Soares, Ariana Aguiar
Ferreira, Mariana Nunes
Araujo, Gustavo Neves
Silveiro, Sandra Pinho
author_role author
author2 Weinert, Leticia Schwerz
Soares, Ariana Aguiar
Ferreira, Mariana Nunes
Araujo, Gustavo Neves
Silveiro, Sandra Pinho
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Camargo, Eduardo Guimaraes
Weinert, Leticia Schwerz
Soares, Ariana Aguiar
Ferreira, Mariana Nunes
Araujo, Gustavo Neves
Silveiro, Sandra Pinho
dc.subject.por.fl_str_mv aspirin
diabetic nephropathy
GFR
glomerular filtration rate
microalbuminuria
topic aspirin
diabetic nephropathy
GFR
glomerular filtration rate
microalbuminuria
description BACKGROUND: Low-grade inflammation has been implicated in the pathogenesis of diabetic nephropathy, and anti-inflammatory drugs could be potentially useful as a therapeutic tool. The aim of this study was to analyze the effect of low-dose aspirin (300 mg/d) on urinary albumin excretion (UAE) and glomerular filtration rate (GFR) levels of microalbuminuric type 2 DM patients.METHODS: In this randomized, double-blind, crossover, placebo-controlled study, 18 microalbuminuric (UAE=30-300 mg/24 h) type 2 DM patients received aspirin (300 mg/d) or identical placebo for 8 weeks, with a 6-week washout period. The patients were aged 56±9 years, had a diabetes duration of 16±7.5 years; 11 (61%) were female, and they were all using enalapril 10 mg bid. GFR was measured by 51Cr-EDTA single-injection method and UAE by immunoturbidimetry. The sample-size calculation showed that 17 patients were needed to detect a 30% change in UAE (α= 0.05 and β= 0.20).RESULTS: After 8 weeks of treatment, there were no significant differences between placebo and aspirin, respectively, regarding UAE [57.7 (8.9-420.0) vs. 63 (8.2-272.0) mg/24 h; P=0.45] and GFR (108±34 vs. 111±47 ml/min/1.73 m2; P=0.90). C-reactive protein levels [2.72 (0.34-10.3) vs. 2.03 (0.25-10.3) μg/l; P=0.21] were comparable after placebo and aspirin, respectively. There were no period (P=0.41) or carry-over effects (P=0.49).CONCLUSION: Low-dose aspirin did not affect GFR and UAE levels of microalbuminuric type 2 DM. It seems that the putative low-grade inflammation of diabetic nephropathy does not respond to these low doses of the drug.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-27
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Avaliado por Pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/24313
url https://seer.ufrgs.br/index.php/hcpa/article/view/24313
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/24313/14954
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv HCPA/FAMED/UFRGS
publisher.none.fl_str_mv HCPA/FAMED/UFRGS
dc.source.none.fl_str_mv Clinical & Biomedical Research; Vol. 31 No. 4 (2011): Revista HCPA
Clinical and Biomedical Research; v. 31 n. 4 (2011): Revista HCPA
2357-9730
reponame:Clinical and Biomedical Research
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Clinical and Biomedical Research
collection Clinical and Biomedical Research
repository.name.fl_str_mv Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv ||cbr@hcpa.edu.br
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