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Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease
OBJECTIVE: Insulin resistance (IR) is the key feature of the metabolic syndrome (MetS); its association with peripheral arterial disease (PAD) is unclear. We hypothesized that IR is associated with both the MetS and sonographically proven PAD. METHODS: IR was determined by the Homeostasis Model Asse...
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/PMC3720189/ https://www.ncbi.nlm.nih.gov/pubmed/23866050 http://dx.doi.org/10.1186/1475-2840-12-106 |
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author | Vonbank, Alexander Saely, Christoph H Rein, Philipp Drexel, Heinz |
author_facet | Vonbank, Alexander Saely, Christoph H Rein, Philipp Drexel, Heinz |
author_sort | Vonbank, Alexander |
collection | PubMed |
description | OBJECTIVE: Insulin resistance (IR) is the key feature of the metabolic syndrome (MetS); its association with peripheral arterial disease (PAD) is unclear. We hypothesized that IR is associated with both the MetS and sonographically proven PAD. METHODS: IR was determined by the Homeostasis Model Assessment (HOMA) index in 214 patients with sonographically proven PAD as well as in 197 controls, who did not have a history of PAD and in whom coronary artery disease was ruled out angiographically; the MetS was defined according to NCEP-ATPIII criteria. RESULTS: HOMA IR scores were significantly higher in MetS patients than in subjects without the MetS (5.9 ± 6.2 vs. 2.9 ± 3.9; p <0.001). However, HOMA IR did not differ significantly between patients with PAD and controls (4.2 ± 5.4 vs. 3.3 ± 4.3; p = 0.124). When both, the presence of MetS and of PAD were considered, HOMA IR was significantly higher in patients with the MetS both among those with PAD (6.1 ± 5.7 vs. 3.6 ± 5.2; p<0.001) and among controls (5.8 ± 6.8 vs. 2.3 ± 1.8; p <0.001), whereas it did not differ significantly between patients with PAD and controls among patients with the MetS (5.8 ± 6.8 vs. 6.1 ± 5.7; p = 0.587) nor among those without the MetS (2.3 ± 1.8 vs. 3.6 ± 5.2; p = 0.165). Similar results were obtained with the International Diabetes Federation definition of the MetS. CONCLUSION: IR is significantly associated with the MetS but not with sonographically proven PAD. |
format | Online Article Text |
id | pubmed-3720189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37201892013-07-24 Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease Vonbank, Alexander Saely, Christoph H Rein, Philipp Drexel, Heinz Cardiovasc Diabetol Original Investigation OBJECTIVE: Insulin resistance (IR) is the key feature of the metabolic syndrome (MetS); its association with peripheral arterial disease (PAD) is unclear. We hypothesized that IR is associated with both the MetS and sonographically proven PAD. METHODS: IR was determined by the Homeostasis Model Assessment (HOMA) index in 214 patients with sonographically proven PAD as well as in 197 controls, who did not have a history of PAD and in whom coronary artery disease was ruled out angiographically; the MetS was defined according to NCEP-ATPIII criteria. RESULTS: HOMA IR scores were significantly higher in MetS patients than in subjects without the MetS (5.9 ± 6.2 vs. 2.9 ± 3.9; p <0.001). However, HOMA IR did not differ significantly between patients with PAD and controls (4.2 ± 5.4 vs. 3.3 ± 4.3; p = 0.124). When both, the presence of MetS and of PAD were considered, HOMA IR was significantly higher in patients with the MetS both among those with PAD (6.1 ± 5.7 vs. 3.6 ± 5.2; p<0.001) and among controls (5.8 ± 6.8 vs. 2.3 ± 1.8; p <0.001), whereas it did not differ significantly between patients with PAD and controls among patients with the MetS (5.8 ± 6.8 vs. 6.1 ± 5.7; p = 0.587) nor among those without the MetS (2.3 ± 1.8 vs. 3.6 ± 5.2; p = 0.165). Similar results were obtained with the International Diabetes Federation definition of the MetS. CONCLUSION: IR is significantly associated with the MetS but not with sonographically proven PAD. BioMed Central 2013-07-17 /pmc/articles/PMC3720189/ /pubmed/23866050 http://dx.doi.org/10.1186/1475-2840-12-106 Text en Copyright © 2013 Vonbank 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 Vonbank, Alexander Saely, Christoph H Rein, Philipp Drexel, Heinz Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title | Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title_full | Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title_fullStr | Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title_full_unstemmed | Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title_short | Insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
title_sort | insulin resistance is significantly associated with the metabolic syndrome, but not with sonographically proven peripheral arterial disease |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720189/ https://www.ncbi.nlm.nih.gov/pubmed/23866050 http://dx.doi.org/10.1186/1475-2840-12-106 |
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