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Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers

BACKGROUND: Dyslipidemia and type 2 diabetes are two of the most significant risk factors for the development of cardiovascular disease. Measurement of lipoprotein subclasses provides important information about derangements in lipid metabolism and helps refine cardiovascular risk assessment. Exenat...

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Autores principales: Chiquette, Elaine, Toth, Peter P, Ramirez, Gilbert, Cobble, Michael, Chilton, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500143/
https://www.ncbi.nlm.nih.gov/pubmed/23166441
http://dx.doi.org/10.2147/VHRM.S37969
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author Chiquette, Elaine
Toth, Peter P
Ramirez, Gilbert
Cobble, Michael
Chilton, Robert
author_facet Chiquette, Elaine
Toth, Peter P
Ramirez, Gilbert
Cobble, Michael
Chilton, Robert
author_sort Chiquette, Elaine
collection PubMed
description BACKGROUND: Dyslipidemia and type 2 diabetes are two of the most significant risk factors for the development of cardiovascular disease. Measurement of lipoprotein subclasses provides important information about derangements in lipid metabolism and helps refine cardiovascular risk assessment. Exenatide, a glucagon-like peptide 1 receptor agonist, improved glycemic control, obesity, hypertension, and dyslipidemia in patients with type 2 diabetes in clinical trials. METHODS: In the DURATION-1 trial, patients with type 2 diabetes were treated with exenatide once weekly or twice daily for 30 weeks. This post hoc analysis evaluated the impact of exenatide on lipoprotein subclasses in 211 DURATION-1 patients using vertical auto profile methodology and the Statistical Package for the Social Sciences general linear model adjusted for glycosylated hemoglobin (HbA(1c)) and weight. RESULTS: Baseline lipids and high sensitivity C-reactive protein were normal overall based on the standard lipid panel. Once-weekly exenatide reduced apolipoprotein B and the apolipoprotein B to apolipoprotein A1 ratio (P < 0.05), independent of glycemic improvement and weight loss. A significant shift in lipoprotein pattern away from small, dense low-density lipoprotein-4 cholesterol was also observed (P < 0.05). Exenatide once weekly increased high-density lipoprotein-2 cholesterol, even after adjustment for changes in HbA(1c) and weight (P < 0.05). Triglycerides, very low-density lipoprotein cholesterol, and high sensitivity C-reactive protein were reduced with both the once-weekly and twice-daily exenatide regimens (P < 0.05). CONCLUSION: In this post hoc analysis, exenatide significantly improved a number of cardiovascular risk markers. Continuous exenatide exposure with exenatide once weekly elicited a greater response than did immediate-release exenatide twice daily, generally independent of glycemic improvement and weight loss. Thus, in addition to improving glycemic control, exenatide induced favorable changes in lipid and lipoprotein metabolism and decreased systemic inflammation.
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spelling pubmed-35001432012-11-19 Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers Chiquette, Elaine Toth, Peter P Ramirez, Gilbert Cobble, Michael Chilton, Robert Vasc Health Risk Manag Original Research BACKGROUND: Dyslipidemia and type 2 diabetes are two of the most significant risk factors for the development of cardiovascular disease. Measurement of lipoprotein subclasses provides important information about derangements in lipid metabolism and helps refine cardiovascular risk assessment. Exenatide, a glucagon-like peptide 1 receptor agonist, improved glycemic control, obesity, hypertension, and dyslipidemia in patients with type 2 diabetes in clinical trials. METHODS: In the DURATION-1 trial, patients with type 2 diabetes were treated with exenatide once weekly or twice daily for 30 weeks. This post hoc analysis evaluated the impact of exenatide on lipoprotein subclasses in 211 DURATION-1 patients using vertical auto profile methodology and the Statistical Package for the Social Sciences general linear model adjusted for glycosylated hemoglobin (HbA(1c)) and weight. RESULTS: Baseline lipids and high sensitivity C-reactive protein were normal overall based on the standard lipid panel. Once-weekly exenatide reduced apolipoprotein B and the apolipoprotein B to apolipoprotein A1 ratio (P < 0.05), independent of glycemic improvement and weight loss. A significant shift in lipoprotein pattern away from small, dense low-density lipoprotein-4 cholesterol was also observed (P < 0.05). Exenatide once weekly increased high-density lipoprotein-2 cholesterol, even after adjustment for changes in HbA(1c) and weight (P < 0.05). Triglycerides, very low-density lipoprotein cholesterol, and high sensitivity C-reactive protein were reduced with both the once-weekly and twice-daily exenatide regimens (P < 0.05). CONCLUSION: In this post hoc analysis, exenatide significantly improved a number of cardiovascular risk markers. Continuous exenatide exposure with exenatide once weekly elicited a greater response than did immediate-release exenatide twice daily, generally independent of glycemic improvement and weight loss. Thus, in addition to improving glycemic control, exenatide induced favorable changes in lipid and lipoprotein metabolism and decreased systemic inflammation. Dove Medical Press 2012 2012-11-12 /pmc/articles/PMC3500143/ /pubmed/23166441 http://dx.doi.org/10.2147/VHRM.S37969 Text en © 2012 Chiquette et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Chiquette, Elaine
Toth, Peter P
Ramirez, Gilbert
Cobble, Michael
Chilton, Robert
Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title_full Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title_fullStr Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title_full_unstemmed Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title_short Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
title_sort treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500143/
https://www.ncbi.nlm.nih.gov/pubmed/23166441
http://dx.doi.org/10.2147/VHRM.S37969
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