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Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans

BACKGROUND: GLP-1 is an incretine hormone which gets secreted from intestinal L-cells in response to nutritional stimuli leading to pancreatic insulin secretion and suppression of glucagon release. GLP-1 further inhibits gastric motility and reduces appetite which in conjunction improves postprandia...

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Autores principales: Piotrowski, Katja, Becker, Melanie, Zugwurst, Julia, Biller-Friedmann, Ingeborg, Spoettl, Gerald, Greif, Martin, Leber, Alexander W, Becker, Alexander, Laubender, Rüdiger P, Lebherz, Corinna, Goeke, Burkhard, Marx, Nikolaus, Parhofer, Klaus G, Lehrke, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765863/
https://www.ncbi.nlm.nih.gov/pubmed/23953602
http://dx.doi.org/10.1186/1475-2840-12-117
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author Piotrowski, Katja
Becker, Melanie
Zugwurst, Julia
Biller-Friedmann, Ingeborg
Spoettl, Gerald
Greif, Martin
Leber, Alexander W
Becker, Alexander
Laubender, Rüdiger P
Lebherz, Corinna
Goeke, Burkhard
Marx, Nikolaus
Parhofer, Klaus G
Lehrke, Michael
author_facet Piotrowski, Katja
Becker, Melanie
Zugwurst, Julia
Biller-Friedmann, Ingeborg
Spoettl, Gerald
Greif, Martin
Leber, Alexander W
Becker, Alexander
Laubender, Rüdiger P
Lebherz, Corinna
Goeke, Burkhard
Marx, Nikolaus
Parhofer, Klaus G
Lehrke, Michael
author_sort Piotrowski, Katja
collection PubMed
description BACKGROUND: GLP-1 is an incretine hormone which gets secreted from intestinal L-cells in response to nutritional stimuli leading to pancreatic insulin secretion and suppression of glucagon release. GLP-1 further inhibits gastric motility and reduces appetite which in conjunction improves postprandial glucose metabolism. Additional vasoprotective effects have been described for GLP-1 in experimental models. Despite these vasoprotective actions, associations between endogenous levels of GLP-1 and cardiovascular disease have yet not been investigated in humans which was the aim of the present study. METHODS: GLP-1 serum levels were assessed in a cohort of 303 patients receiving coronary CT-angiography due to typical or atypical chest pain. RESULTS: GLP-1 was found to be positively associated with total coronary plaque burden in a fully adjusted model containing age, sex, BMI, hypertension, diabetes mellitus, smoking, triglycerides, LDL-C (low density lipoprotein cholesterol), hsCRP (high-sensitive C-reactive protein), and eGFR (estimated glomerular filtration rate) (OR: 2.53 (95% CI: 1.12 – 6.08; p = 0.03). CONCLUSION: Circulating GLP-1 was found to be positivity associated with coronary atherosclerosis in humans. The clinical relevance of this observation needs further investigations.
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spelling pubmed-37658632013-09-08 Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans Piotrowski, Katja Becker, Melanie Zugwurst, Julia Biller-Friedmann, Ingeborg Spoettl, Gerald Greif, Martin Leber, Alexander W Becker, Alexander Laubender, Rüdiger P Lebherz, Corinna Goeke, Burkhard Marx, Nikolaus Parhofer, Klaus G Lehrke, Michael Cardiovasc Diabetol Original Investigation BACKGROUND: GLP-1 is an incretine hormone which gets secreted from intestinal L-cells in response to nutritional stimuli leading to pancreatic insulin secretion and suppression of glucagon release. GLP-1 further inhibits gastric motility and reduces appetite which in conjunction improves postprandial glucose metabolism. Additional vasoprotective effects have been described for GLP-1 in experimental models. Despite these vasoprotective actions, associations between endogenous levels of GLP-1 and cardiovascular disease have yet not been investigated in humans which was the aim of the present study. METHODS: GLP-1 serum levels were assessed in a cohort of 303 patients receiving coronary CT-angiography due to typical or atypical chest pain. RESULTS: GLP-1 was found to be positively associated with total coronary plaque burden in a fully adjusted model containing age, sex, BMI, hypertension, diabetes mellitus, smoking, triglycerides, LDL-C (low density lipoprotein cholesterol), hsCRP (high-sensitive C-reactive protein), and eGFR (estimated glomerular filtration rate) (OR: 2.53 (95% CI: 1.12 – 6.08; p = 0.03). CONCLUSION: Circulating GLP-1 was found to be positivity associated with coronary atherosclerosis in humans. The clinical relevance of this observation needs further investigations. BioMed Central 2013-08-16 /pmc/articles/PMC3765863/ /pubmed/23953602 http://dx.doi.org/10.1186/1475-2840-12-117 Text en Copyright © 2013 Piotrowski et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Piotrowski, Katja
Becker, Melanie
Zugwurst, Julia
Biller-Friedmann, Ingeborg
Spoettl, Gerald
Greif, Martin
Leber, Alexander W
Becker, Alexander
Laubender, Rüdiger P
Lebherz, Corinna
Goeke, Burkhard
Marx, Nikolaus
Parhofer, Klaus G
Lehrke, Michael
Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title_full Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title_fullStr Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title_full_unstemmed Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title_short Circulating concentrations of GLP-1 are associated with coronary atherosclerosis in humans
title_sort circulating concentrations of glp-1 are associated with coronary atherosclerosis in humans
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765863/
https://www.ncbi.nlm.nih.gov/pubmed/23953602
http://dx.doi.org/10.1186/1475-2840-12-117
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