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Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
OBJECTIVE—We investigated stroke mortality in individuals in different categories of glycemia and compared hazard ratios (HRs) corresponding to a 1-SD increase in 2-h plasma glucose and fasting plasma glucose (FPG) criteria. RESEARCH DESIGN AND METHODS—We examined data from 2-h 75-g oral glucose tol...
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/PMC2628706/ https://www.ncbi.nlm.nih.gov/pubmed/19017775 http://dx.doi.org/10.2337/dc08-1411 |
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author | Hyvärinen, Marjukka Qiao, Qing Tuomilehto, Jaakko Laatikainen, Tiina Heine, Robert J. Stehouwer, Coen D.A. Alberti, K. George M.M. Pyörälä, Kalevi Zethelius, Björn Stegmayr, Birgitta |
author_facet | Hyvärinen, Marjukka Qiao, Qing Tuomilehto, Jaakko Laatikainen, Tiina Heine, Robert J. Stehouwer, Coen D.A. Alberti, K. George M.M. Pyörälä, Kalevi Zethelius, Björn Stegmayr, Birgitta |
author_sort | Hyvärinen, Marjukka |
collection | PubMed |
description | OBJECTIVE—We investigated stroke mortality in individuals in different categories of glycemia and compared hazard ratios (HRs) corresponding to a 1-SD increase in 2-h plasma glucose and fasting plasma glucose (FPG) criteria. RESEARCH DESIGN AND METHODS—We examined data from 2-h 75-g oral glucose tolerance tests taken from 13 European cohorts comprising 11,844 (55%) men and 9,862 (45%) women who were followed up for a median of 10.5 years. A multivariate adjusted Cox proportional hazards model was used to estimate HRs for stroke mortality. RESULTS—In men and women without a prior history of diabetes, multivariate adjusted HRs for stroke mortality corresponding to a 1-SD increase in FPG were 1.02 (95% CI 0.83–1.25) and 1.52 (1.22–1.88) and those in 2-h plasma glucose 1.21 (1.06–1.38) and 1.31 (1.06–1.61), respectively. Addition of 2-h plasma glucose to the model with FPG significantly improved prediction of stroke mortality in men (χ(2) = 10.12; P = 0.001) but not in women (χ(2) = 0.01; P = 0.94), whereas addition of FPG to 2-h plasma glucose improved stroke mortality in women (χ(2) = 4.08; P = 0.04) but not in men (χ(2) = 3.29; P = 0.07). CONCLUSIONS—Diabetes defined by either FPG or 2-h plasma glucose increases the risk of stroke mortality. In individuals without a history of diabetes, elevated 2-h postchallenge glucose is a better predictor than elevated fasting glucose in men, whereas the latter is better than the former in women. |
format | Text |
id | pubmed-2628706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-26287062010-02-01 Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria Hyvärinen, Marjukka Qiao, Qing Tuomilehto, Jaakko Laatikainen, Tiina Heine, Robert J. Stehouwer, Coen D.A. Alberti, K. George M.M. Pyörälä, Kalevi Zethelius, Björn Stegmayr, Birgitta Diabetes Care Cardiovascular and Metabolic Risk OBJECTIVE—We investigated stroke mortality in individuals in different categories of glycemia and compared hazard ratios (HRs) corresponding to a 1-SD increase in 2-h plasma glucose and fasting plasma glucose (FPG) criteria. RESEARCH DESIGN AND METHODS—We examined data from 2-h 75-g oral glucose tolerance tests taken from 13 European cohorts comprising 11,844 (55%) men and 9,862 (45%) women who were followed up for a median of 10.5 years. A multivariate adjusted Cox proportional hazards model was used to estimate HRs for stroke mortality. RESULTS—In men and women without a prior history of diabetes, multivariate adjusted HRs for stroke mortality corresponding to a 1-SD increase in FPG were 1.02 (95% CI 0.83–1.25) and 1.52 (1.22–1.88) and those in 2-h plasma glucose 1.21 (1.06–1.38) and 1.31 (1.06–1.61), respectively. Addition of 2-h plasma glucose to the model with FPG significantly improved prediction of stroke mortality in men (χ(2) = 10.12; P = 0.001) but not in women (χ(2) = 0.01; P = 0.94), whereas addition of FPG to 2-h plasma glucose improved stroke mortality in women (χ(2) = 4.08; P = 0.04) but not in men (χ(2) = 3.29; P = 0.07). CONCLUSIONS—Diabetes defined by either FPG or 2-h plasma glucose increases the risk of stroke mortality. In individuals without a history of diabetes, elevated 2-h postchallenge glucose is a better predictor than elevated fasting glucose in men, whereas the latter is better than the former in women. American Diabetes Association 2009-02 /pmc/articles/PMC2628706/ /pubmed/19017775 http://dx.doi.org/10.2337/dc08-1411 Text en Copyright © 2009, 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/ for details. |
spellingShingle | Cardiovascular and Metabolic Risk Hyvärinen, Marjukka Qiao, Qing Tuomilehto, Jaakko Laatikainen, Tiina Heine, Robert J. Stehouwer, Coen D.A. Alberti, K. George M.M. Pyörälä, Kalevi Zethelius, Björn Stegmayr, Birgitta Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria |
title | Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
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title_full | Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
|
title_fullStr | Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
|
title_full_unstemmed | Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
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title_short | Hyperglycemia and Stroke Mortality: Comparison between fasting and 2-h glucose criteria
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title_sort | hyperglycemia and stroke mortality: comparison between fasting and 2-h glucose criteria |
topic | Cardiovascular and Metabolic Risk |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628706/ https://www.ncbi.nlm.nih.gov/pubmed/19017775 http://dx.doi.org/10.2337/dc08-1411 |
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