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Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study

OBJECTIVE—The purpose of this study was to analyze the interrelationship among oxidation, myocardial infarction (MI), and type 2 diabetes in a population-based case-control study of MI. RESEARCH DESIGN AND METHODS—Participants were 1,709 individuals from western New York: 257 women and men with inci...

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Autores principales: Stranges, Saverio, Dorn, Joan M., Donahue, Richard P., Browne, Richard W., Freudenheim, Jo L., Hovey, Kathleen M., Trevisan, Maurizio
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518360/
https://www.ncbi.nlm.nih.gov/pubmed/18535189
http://dx.doi.org/10.2337/dc08-0558
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author Stranges, Saverio
Dorn, Joan M.
Donahue, Richard P.
Browne, Richard W.
Freudenheim, Jo L.
Hovey, Kathleen M.
Trevisan, Maurizio
author_facet Stranges, Saverio
Dorn, Joan M.
Donahue, Richard P.
Browne, Richard W.
Freudenheim, Jo L.
Hovey, Kathleen M.
Trevisan, Maurizio
author_sort Stranges, Saverio
collection PubMed
description OBJECTIVE—The purpose of this study was to analyze the interrelationship among oxidation, myocardial infarction (MI), and type 2 diabetes in a population-based case-control study of MI. RESEARCH DESIGN AND METHODS—Participants were 1,709 individuals from western New York: 257 women and men with incident MI and 1,452 healthy control subjects (aged 35–70 years). Lipid peroxidation was measured by plasma levels of thiobarbituric acid reactive substances (TBARS). History of type 2 diabetes was determined by self-reported history of medical diagnosis. RESULTS—In multivariate analyses, there was no significant difference in TBARS levels between case and control subjects in both sexes. In subgroup analyses by diabetes status, diabetic subjects, regardless of MI status, exhibited significantly higher TBARS values than nondiabetic subjects. For diabetic women, TBARS values were 1.84 and 1.83 nmol/ml for case and control subjects, respectively. Values for nondiabetic women were 1.29 and 1.31 nmol/ml, respectively. In diabetic men, values were 1.65 and 1.97 nmol/ml for case and control subjects, respectively. Values for nondiabetic men were 1.36 and 1.36 nmol/ml, respectively. CONCLUSIONS—Whereas type 2 diabetes may be an important correlate of lipid peroxidation, clinical coronary heart disease may not.
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spelling pubmed-25183602009-09-01 Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study Stranges, Saverio Dorn, Joan M. Donahue, Richard P. Browne, Richard W. Freudenheim, Jo L. Hovey, Kathleen M. Trevisan, Maurizio Diabetes Care Pathophysiology/Complications OBJECTIVE—The purpose of this study was to analyze the interrelationship among oxidation, myocardial infarction (MI), and type 2 diabetes in a population-based case-control study of MI. RESEARCH DESIGN AND METHODS—Participants were 1,709 individuals from western New York: 257 women and men with incident MI and 1,452 healthy control subjects (aged 35–70 years). Lipid peroxidation was measured by plasma levels of thiobarbituric acid reactive substances (TBARS). History of type 2 diabetes was determined by self-reported history of medical diagnosis. RESULTS—In multivariate analyses, there was no significant difference in TBARS levels between case and control subjects in both sexes. In subgroup analyses by diabetes status, diabetic subjects, regardless of MI status, exhibited significantly higher TBARS values than nondiabetic subjects. For diabetic women, TBARS values were 1.84 and 1.83 nmol/ml for case and control subjects, respectively. Values for nondiabetic women were 1.29 and 1.31 nmol/ml, respectively. In diabetic men, values were 1.65 and 1.97 nmol/ml for case and control subjects, respectively. Values for nondiabetic men were 1.36 and 1.36 nmol/ml, respectively. CONCLUSIONS—Whereas type 2 diabetes may be an important correlate of lipid peroxidation, clinical coronary heart disease may not. American Diabetes Association 2008-09 /pmc/articles/PMC2518360/ /pubmed/18535189 http://dx.doi.org/10.2337/dc08-0558 Text en Copyright © 2008, DIABETES CARE Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Pathophysiology/Complications
Stranges, Saverio
Dorn, Joan M.
Donahue, Richard P.
Browne, Richard W.
Freudenheim, Jo L.
Hovey, Kathleen M.
Trevisan, Maurizio
Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title_full Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title_fullStr Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title_full_unstemmed Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title_short Oxidation, Type 2 Diabetes, and Coronary Heart Disease: A Complex Interaction: Findings from a population-based study
title_sort oxidation, type 2 diabetes, and coronary heart disease: a complex interaction: findings from a population-based study
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518360/
https://www.ncbi.nlm.nih.gov/pubmed/18535189
http://dx.doi.org/10.2337/dc08-0558
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