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Diabetes and Vascular Disease in Different Arterial Territories

OBJECTIVE: The aim of this study was to investigate the relationship between diabetes and different phenotypes of peripheral vascular disease (lower extremity peripheral artery disease [PAD], carotid artery stenosis [CAS], and abdominal aortic aneurysm [AAA]). RESEARCH DESIGN AND METHODS: Prevalence...

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Autores principales: Shah, Binita, Rockman, Caron B., Guo, Yu, Chesner, Jaclyn, Schwartzbard, Arthur Z., Weintraub, Howard S., Adelman, Mark A., Riles, Thomas S., Berger, Jeffrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030086/
https://www.ncbi.nlm.nih.gov/pubmed/24705616
http://dx.doi.org/10.2337/dc13-2432
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author Shah, Binita
Rockman, Caron B.
Guo, Yu
Chesner, Jaclyn
Schwartzbard, Arthur Z.
Weintraub, Howard S.
Adelman, Mark A.
Riles, Thomas S.
Berger, Jeffrey S.
author_facet Shah, Binita
Rockman, Caron B.
Guo, Yu
Chesner, Jaclyn
Schwartzbard, Arthur Z.
Weintraub, Howard S.
Adelman, Mark A.
Riles, Thomas S.
Berger, Jeffrey S.
author_sort Shah, Binita
collection PubMed
description OBJECTIVE: The aim of this study was to investigate the relationship between diabetes and different phenotypes of peripheral vascular disease (lower extremity peripheral artery disease [PAD], carotid artery stenosis [CAS], and abdominal aortic aneurysm [AAA]). RESEARCH DESIGN AND METHODS: Prevalence of vascular disease was evaluated in 3,696,778 participants of the Life Line Screening survey between 2003 and 2008. PAD was defined as ankle-brachial pressure index <0.90 or prior revascularization, CAS as ≥50% stenosis or prior revascularization, and AAA as infrarenal aortic diameter ≥3 cm or prior repair. Odds ratios (ORs) and 95% CIs were assessed using logistic regression modeling. RESULTS: Diabetes mellitus was present in 10.8% of participants (n = 399,884). Prevalence of PAD, CAS, and AAA was significantly higher (P < 0.0001) in participants with compared with those without diabetes. After multivariate adjustment for baseline demographics and clinical risk factors, a significant interaction existed between diabetes and vascular disease phenotype (P < 0.0001). Diabetes was associated with increased odds of PAD (OR 1.42 [95% CI 1.41–1.4]; P < 0.0001) and CAS (1.45 [1.43–1.47]; P < 0.0001) but decreased odds of AAA (0.86 [0.84–0.88]; P < 0.0001). The strength of association increased with increasing severity of disease in each vascular phenotype, and this association persisted in the population with asymptomatic vascular disease. CONCLUSIONS: In a large population-based study, the association between diabetes and vascular disease differed according to vascular phenotype. Future studies exploring the mechanism for these vascular-specific differences are needed.
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spelling pubmed-40300862015-06-01 Diabetes and Vascular Disease in Different Arterial Territories Shah, Binita Rockman, Caron B. Guo, Yu Chesner, Jaclyn Schwartzbard, Arthur Z. Weintraub, Howard S. Adelman, Mark A. Riles, Thomas S. Berger, Jeffrey S. Diabetes Care Epidemiology/Health Services Research OBJECTIVE: The aim of this study was to investigate the relationship between diabetes and different phenotypes of peripheral vascular disease (lower extremity peripheral artery disease [PAD], carotid artery stenosis [CAS], and abdominal aortic aneurysm [AAA]). RESEARCH DESIGN AND METHODS: Prevalence of vascular disease was evaluated in 3,696,778 participants of the Life Line Screening survey between 2003 and 2008. PAD was defined as ankle-brachial pressure index <0.90 or prior revascularization, CAS as ≥50% stenosis or prior revascularization, and AAA as infrarenal aortic diameter ≥3 cm or prior repair. Odds ratios (ORs) and 95% CIs were assessed using logistic regression modeling. RESULTS: Diabetes mellitus was present in 10.8% of participants (n = 399,884). Prevalence of PAD, CAS, and AAA was significantly higher (P < 0.0001) in participants with compared with those without diabetes. After multivariate adjustment for baseline demographics and clinical risk factors, a significant interaction existed between diabetes and vascular disease phenotype (P < 0.0001). Diabetes was associated with increased odds of PAD (OR 1.42 [95% CI 1.41–1.4]; P < 0.0001) and CAS (1.45 [1.43–1.47]; P < 0.0001) but decreased odds of AAA (0.86 [0.84–0.88]; P < 0.0001). The strength of association increased with increasing severity of disease in each vascular phenotype, and this association persisted in the population with asymptomatic vascular disease. CONCLUSIONS: In a large population-based study, the association between diabetes and vascular disease differed according to vascular phenotype. Future studies exploring the mechanism for these vascular-specific differences are needed. American Diabetes Association 2014-06 2014-05-10 /pmc/articles/PMC4030086/ /pubmed/24705616 http://dx.doi.org/10.2337/dc13-2432 Text en © 2014 by the American Diabetes Association. 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 Epidemiology/Health Services Research
Shah, Binita
Rockman, Caron B.
Guo, Yu
Chesner, Jaclyn
Schwartzbard, Arthur Z.
Weintraub, Howard S.
Adelman, Mark A.
Riles, Thomas S.
Berger, Jeffrey S.
Diabetes and Vascular Disease in Different Arterial Territories
title Diabetes and Vascular Disease in Different Arterial Territories
title_full Diabetes and Vascular Disease in Different Arterial Territories
title_fullStr Diabetes and Vascular Disease in Different Arterial Territories
title_full_unstemmed Diabetes and Vascular Disease in Different Arterial Territories
title_short Diabetes and Vascular Disease in Different Arterial Territories
title_sort diabetes and vascular disease in different arterial territories
topic Epidemiology/Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030086/
https://www.ncbi.nlm.nih.gov/pubmed/24705616
http://dx.doi.org/10.2337/dc13-2432
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