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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-3765863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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