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Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study

BACKGROUND: Hyperglycemia leading to increased oxidative stress is implicated in the increased risk for the development of macrovascular and microvascular complications in patients with type 1 diabetes mellitus. METHODS AND RESULTS: A random subcohort of 349 participants was selected from the DCCT/E...

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Autores principales: Tang, W.H. Wilson, McGee, Paula, Lachin, John M., Li, Daniel Y., Hoogwerf, Byron, Hazen, Stanley L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015340/
http://dx.doi.org/10.1161/JAHA.117.008368
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author Tang, W.H. Wilson
McGee, Paula
Lachin, John M.
Li, Daniel Y.
Hoogwerf, Byron
Hazen, Stanley L.
author_facet Tang, W.H. Wilson
McGee, Paula
Lachin, John M.
Li, Daniel Y.
Hoogwerf, Byron
Hazen, Stanley L.
author_sort Tang, W.H. Wilson
collection PubMed
description BACKGROUND: Hyperglycemia leading to increased oxidative stress is implicated in the increased risk for the development of macrovascular and microvascular complications in patients with type 1 diabetes mellitus. METHODS AND RESULTS: A random subcohort of 349 participants was selected from the DCCT/EDIC (Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications) cohort. This included 320 controls and 29 cardiovascular disease cases that were augmented with 98 additional known cases to yield a case cohort of 447 participants (320 controls, 127 cases). Biosamples from DCCT baseline, year 1, and closeout of DCCT, and 1 to 2 years post‐DCCT (EDIC years 1 and 2) were measured for markers of oxidative stress, including plasma myeloperoxidase, paraoxonase activity, urinary F(2α) isoprostanes, and its metabolite, 2,3 dinor‐8 iso prostaglandin F(2α). Following adjustment for glycated hemoblobin and weighting the observations inversely proportional to the sampling selection probabilities, higher paraoxonase activity, reflective of antioxidant activity, and 2,3 dinor‐8 iso prostaglandin F(2α), an oxidative marker, were significantly associated with lower risk of cardiovascular disease (−4.5% risk for 10% higher paraoxonase, P<0.003; −5.3% risk for 10% higher 2,3 dinor‐8 iso prostaglandin F(2α), P=0.0092). In contrast, the oxidative markers myeloperoxidase and F(2α) isoprostanes were not significantly associated with cardiovascular disease after adjustment for glycated hemoblobin. There were no significant differences between DCCT intensive and conventional treatment groups in the change in all biomarkers across time segments. CONCLUSIONS: Heightened antioxidant activity (rather than diminished oxidative stress markers) is associated with lower cardiovascular disease risk in type 1 diabetes mellitus, but these biomarkers did not change over time with intensification of glycemic control. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT00360815 and NCT00360893.
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spelling pubmed-60153402018-07-05 Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study Tang, W.H. Wilson McGee, Paula Lachin, John M. Li, Daniel Y. Hoogwerf, Byron Hazen, Stanley L. J Am Heart Assoc Original Research BACKGROUND: Hyperglycemia leading to increased oxidative stress is implicated in the increased risk for the development of macrovascular and microvascular complications in patients with type 1 diabetes mellitus. METHODS AND RESULTS: A random subcohort of 349 participants was selected from the DCCT/EDIC (Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications) cohort. This included 320 controls and 29 cardiovascular disease cases that were augmented with 98 additional known cases to yield a case cohort of 447 participants (320 controls, 127 cases). Biosamples from DCCT baseline, year 1, and closeout of DCCT, and 1 to 2 years post‐DCCT (EDIC years 1 and 2) were measured for markers of oxidative stress, including plasma myeloperoxidase, paraoxonase activity, urinary F(2α) isoprostanes, and its metabolite, 2,3 dinor‐8 iso prostaglandin F(2α). Following adjustment for glycated hemoblobin and weighting the observations inversely proportional to the sampling selection probabilities, higher paraoxonase activity, reflective of antioxidant activity, and 2,3 dinor‐8 iso prostaglandin F(2α), an oxidative marker, were significantly associated with lower risk of cardiovascular disease (−4.5% risk for 10% higher paraoxonase, P<0.003; −5.3% risk for 10% higher 2,3 dinor‐8 iso prostaglandin F(2α), P=0.0092). In contrast, the oxidative markers myeloperoxidase and F(2α) isoprostanes were not significantly associated with cardiovascular disease after adjustment for glycated hemoblobin. There were no significant differences between DCCT intensive and conventional treatment groups in the change in all biomarkers across time segments. CONCLUSIONS: Heightened antioxidant activity (rather than diminished oxidative stress markers) is associated with lower cardiovascular disease risk in type 1 diabetes mellitus, but these biomarkers did not change over time with intensification of glycemic control. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifiers: NCT00360815 and NCT00360893. John Wiley and Sons Inc. 2018-05-09 /pmc/articles/PMC6015340/ http://dx.doi.org/10.1161/JAHA.117.008368 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Tang, W.H. Wilson
McGee, Paula
Lachin, John M.
Li, Daniel Y.
Hoogwerf, Byron
Hazen, Stanley L.
Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title_full Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title_fullStr Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title_full_unstemmed Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title_short Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
title_sort oxidative stress and cardiovascular risk in type 1 diabetes mellitus: insights from the dcct/edic study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015340/
http://dx.doi.org/10.1161/JAHA.117.008368
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