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Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study
OBJECTIVE: Although cumulative evidence suggests that increased oxidative stress may lead to insulin resistance in vivo or in vitro, community-based studies are scarce. This study examined the longitudinal relationships of oxidative stress biomarkers with the development of insulin resistance and wh...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699736/ https://www.ncbi.nlm.nih.gov/pubmed/19389821 http://dx.doi.org/10.2337/dc09-0259 |
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author | Park, Kyong Gross, Myron Lee, Duk-Hee Holvoet, Paul Himes, John H. Shikany, James M. Jacobs, David R. |
author_facet | Park, Kyong Gross, Myron Lee, Duk-Hee Holvoet, Paul Himes, John H. Shikany, James M. Jacobs, David R. |
author_sort | Park, Kyong |
collection | PubMed |
description | OBJECTIVE: Although cumulative evidence suggests that increased oxidative stress may lead to insulin resistance in vivo or in vitro, community-based studies are scarce. This study examined the longitudinal relationships of oxidative stress biomarkers with the development of insulin resistance and whether these relationships were independent of obesity in nondiabetic young adults. RESEARCH DESIGN AND METHODS: Biomarkers of oxidative stress (F(2)-isoprostanes [F(2)Isop] and oxidized LDL [oxLDL]), insulin resistance (the homeostasis model assessment of insulin resistance [HOMA-IR]), and various fatness measures (BMI, waist circumference, and estimated percent fat) were obtained in a population-based observational study (Coronary Artery Risk Development in Young Adults) and its ancillary study (Young Adult Longitudinal Trends in Antioxidants) during 2000–2006. RESULTS: There were substantial increases in estimated mean HOMA-IR over time. OxLDL and F(2)Isop showed little association with each other. Mean evolving HOMA-IR increased with increasing levels of oxidative stress markers (P < 0.001 for oxLDL and P = 0.06 for F(2)Isop), measured in 2000–2001. After additional adjustment for adiposity, a positive association between oxLDL and HOMA-IR was strongly evident, whereas the association between F(2)Isop and HOMA-IR was not. CONCLUSIONS: We observed positive associations between each of two oxidative stress markers and insulin resistance. The association with oxidized LDL was independent of obesity, but that with F(2)Isop was not. |
format | Text |
id | pubmed-2699736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-26997362010-07-01 Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study Park, Kyong Gross, Myron Lee, Duk-Hee Holvoet, Paul Himes, John H. Shikany, James M. Jacobs, David R. Diabetes Care Original Research OBJECTIVE: Although cumulative evidence suggests that increased oxidative stress may lead to insulin resistance in vivo or in vitro, community-based studies are scarce. This study examined the longitudinal relationships of oxidative stress biomarkers with the development of insulin resistance and whether these relationships were independent of obesity in nondiabetic young adults. RESEARCH DESIGN AND METHODS: Biomarkers of oxidative stress (F(2)-isoprostanes [F(2)Isop] and oxidized LDL [oxLDL]), insulin resistance (the homeostasis model assessment of insulin resistance [HOMA-IR]), and various fatness measures (BMI, waist circumference, and estimated percent fat) were obtained in a population-based observational study (Coronary Artery Risk Development in Young Adults) and its ancillary study (Young Adult Longitudinal Trends in Antioxidants) during 2000–2006. RESULTS: There were substantial increases in estimated mean HOMA-IR over time. OxLDL and F(2)Isop showed little association with each other. Mean evolving HOMA-IR increased with increasing levels of oxidative stress markers (P < 0.001 for oxLDL and P = 0.06 for F(2)Isop), measured in 2000–2001. After additional adjustment for adiposity, a positive association between oxLDL and HOMA-IR was strongly evident, whereas the association between F(2)Isop and HOMA-IR was not. CONCLUSIONS: We observed positive associations between each of two oxidative stress markers and insulin resistance. The association with oxidized LDL was independent of obesity, but that with F(2)Isop was not. American Diabetes Association 2009-07 2009-04-23 /pmc/articles/PMC2699736/ /pubmed/19389821 http://dx.doi.org/10.2337/dc09-0259 Text en © 2009 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/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/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details. |
spellingShingle | Original Research Park, Kyong Gross, Myron Lee, Duk-Hee Holvoet, Paul Himes, John H. Shikany, James M. Jacobs, David R. Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title | Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title_full | Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title_fullStr | Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title_full_unstemmed | Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title_short | Oxidative Stress and Insulin Resistance: The Coronary Artery Risk Development in Young Adults study |
title_sort | oxidative stress and insulin resistance: the coronary artery risk development in young adults study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699736/ https://www.ncbi.nlm.nih.gov/pubmed/19389821 http://dx.doi.org/10.2337/dc09-0259 |
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