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Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study

BACKGROUND: To investigate the association between fasting serum insulin and glucose levels with atherosclerotic plaque composition in the carotid artery. Impaired insulin and glucose levels are implicated in the etiology of cardiovascular disease; however, their influence on the formation and compo...

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Autores principales: Mujaj, Blerim, Bos, Daniel, Kavousi, Maryam, van der Lugt, Aad, Staessen, Jan A, Franco, Oscar H, Vernooij, Meike W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087499/
https://www.ncbi.nlm.nih.gov/pubmed/31958313
http://dx.doi.org/10.1530/EJE-19-0620
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author Mujaj, Blerim
Bos, Daniel
Kavousi, Maryam
van der Lugt, Aad
Staessen, Jan A
Franco, Oscar H
Vernooij, Meike W
author_facet Mujaj, Blerim
Bos, Daniel
Kavousi, Maryam
van der Lugt, Aad
Staessen, Jan A
Franco, Oscar H
Vernooij, Meike W
author_sort Mujaj, Blerim
collection PubMed
description BACKGROUND: To investigate the association between fasting serum insulin and glucose levels with atherosclerotic plaque composition in the carotid artery. Impaired insulin and glucose levels are implicated in the etiology of cardiovascular disease; however, their influence on the formation and composition of atherosclerotic plaque remains unclear. METHODS: In 1740 participants (mean age 72.9 years, 46% women, 14.4% diabetes mellitus) from the population-based Rotterdam Study, we performed carotid MRI to evaluate the presence of calcification, lipid core, and intraplaque hemorrhage in carotid atherosclerosis. All participants also underwent blood sampling to obtain information on serum insulin and glucose levels. Using logistic regression models, we assessed the association of serum insulin and glucose levels (per s.d. and in tertiles) with the different plaque components, while adjusting for sex, age, intima-media thickness, and cardiovascular risk factors. RESULTS: Serum insulin levels were associated with the presence of intraplaque hemorrhage (adjusted odds ratio (OR): 1.42 (95% CI: 1.12–1.7)) We found no association with the presence of calcification or lipid core. Sensitivity analyses restricted to individuals without diabetes mellitus yielded similar results. No associations were found between serum glucose levels and any of the plaque components. CONCLUSIONS: Serum insulin levels are associated with the presence of vulnerable components of carotid plaque, specifically with intraplaque hemorrhage. These findings suggest a complex role for serum insulin in the pathophysiology of carotid atherosclerosis and in plaque vulnerability.
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spelling pubmed-70874992020-03-26 Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study Mujaj, Blerim Bos, Daniel Kavousi, Maryam van der Lugt, Aad Staessen, Jan A Franco, Oscar H Vernooij, Meike W Eur J Endocrinol Clinical Study BACKGROUND: To investigate the association between fasting serum insulin and glucose levels with atherosclerotic plaque composition in the carotid artery. Impaired insulin and glucose levels are implicated in the etiology of cardiovascular disease; however, their influence on the formation and composition of atherosclerotic plaque remains unclear. METHODS: In 1740 participants (mean age 72.9 years, 46% women, 14.4% diabetes mellitus) from the population-based Rotterdam Study, we performed carotid MRI to evaluate the presence of calcification, lipid core, and intraplaque hemorrhage in carotid atherosclerosis. All participants also underwent blood sampling to obtain information on serum insulin and glucose levels. Using logistic regression models, we assessed the association of serum insulin and glucose levels (per s.d. and in tertiles) with the different plaque components, while adjusting for sex, age, intima-media thickness, and cardiovascular risk factors. RESULTS: Serum insulin levels were associated with the presence of intraplaque hemorrhage (adjusted odds ratio (OR): 1.42 (95% CI: 1.12–1.7)) We found no association with the presence of calcification or lipid core. Sensitivity analyses restricted to individuals without diabetes mellitus yielded similar results. No associations were found between serum glucose levels and any of the plaque components. CONCLUSIONS: Serum insulin levels are associated with the presence of vulnerable components of carotid plaque, specifically with intraplaque hemorrhage. These findings suggest a complex role for serum insulin in the pathophysiology of carotid atherosclerosis and in plaque vulnerability. Bioscientifica Ltd 2020-01-20 /pmc/articles/PMC7087499/ /pubmed/31958313 http://dx.doi.org/10.1530/EJE-19-0620 Text en © 2020 The authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Study
Mujaj, Blerim
Bos, Daniel
Kavousi, Maryam
van der Lugt, Aad
Staessen, Jan A
Franco, Oscar H
Vernooij, Meike W
Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title_full Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title_fullStr Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title_full_unstemmed Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title_short Serum insulin levels are associated with vulnerable plaque components in the carotid artery: the Rotterdam Study
title_sort serum insulin levels are associated with vulnerable plaque components in the carotid artery: the rotterdam study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087499/
https://www.ncbi.nlm.nih.gov/pubmed/31958313
http://dx.doi.org/10.1530/EJE-19-0620
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