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Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes
BACKGROUND: Metabolic abnormalities, such as impaired fasting glucose (IFG), are dynamic phenomena; however, it is unclear whether the timing of IFG exposure and cumulative exposure to IFG are related to cardiovascular disease (CVD) and mortality risk. METHODS: Data were extracted from a nationwide...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Endocrine Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566122/ https://www.ncbi.nlm.nih.gov/pubmed/34674499 http://dx.doi.org/10.3803/EnM.2021.1218 |
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author | Lee, Seung-Hwan Han, Kyungdo Kwon, Hyuk-Sang Kim, Mee Kyoung |
author_facet | Lee, Seung-Hwan Han, Kyungdo Kwon, Hyuk-Sang Kim, Mee Kyoung |
author_sort | Lee, Seung-Hwan |
collection | PubMed |
description | BACKGROUND: Metabolic abnormalities, such as impaired fasting glucose (IFG), are dynamic phenomena; however, it is unclear whether the timing of IFG exposure and cumulative exposure to IFG are related to cardiovascular disease (CVD) and mortality risk. METHODS: Data were extracted from a nationwide population-based cohort in South Korea for adults (n=2,206,679) who were free of diabetes and had 4 years of consecutive health examination data. Fasting blood glucose levels of 100 to 125 mg/dL were defined as IFG, and the number of IFG diagnoses for each adult in the 4-year period was tabulated as the IFG exposure score (range, 0 to 4). Adults with persistent IFG for the 4-year period received a score of 4. RESULTS: The median follow-up was 8.2 years. There were 24,820 deaths, 13,502 cases of stroke, and 13,057 cases of myocardial infarction (MI). IFG exposure scores of 1, 2, 3, and 4 were associated with all-cause mortality (multivariable-adjusted hazard ratio [aHR], 1.11; 95% confidence interval [CI], 1.08 to 1.15; aHR, 1.16; 95% CI, 1.12 to 1.20; aHR, 1.20; 95% CI, 1.15 to 1.25; aHR, 1.18; 95% CI, 1.11 to 1.25, respectively) compared with an IFG exposure score of 0. Adjusting for hypertension and dyslipidemia attenuated the slightly increased risk of MI or stroke associated with high IFG exposure scores, but significant associations for all-cause mortality remained. CONCLUSION: The intensity of IFG exposure was associated with an elevated risk of all-cause mortality, independent of cardiovascular risk factors. The association between IFG exposure and CVD risk was largely mediated by the coexistence of dyslipidemia and hypertension. |
format | Online Article Text |
id | pubmed-8566122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85661222021-11-18 Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes Lee, Seung-Hwan Han, Kyungdo Kwon, Hyuk-Sang Kim, Mee Kyoung Endocrinol Metab (Seoul) Original Article BACKGROUND: Metabolic abnormalities, such as impaired fasting glucose (IFG), are dynamic phenomena; however, it is unclear whether the timing of IFG exposure and cumulative exposure to IFG are related to cardiovascular disease (CVD) and mortality risk. METHODS: Data were extracted from a nationwide population-based cohort in South Korea for adults (n=2,206,679) who were free of diabetes and had 4 years of consecutive health examination data. Fasting blood glucose levels of 100 to 125 mg/dL were defined as IFG, and the number of IFG diagnoses for each adult in the 4-year period was tabulated as the IFG exposure score (range, 0 to 4). Adults with persistent IFG for the 4-year period received a score of 4. RESULTS: The median follow-up was 8.2 years. There were 24,820 deaths, 13,502 cases of stroke, and 13,057 cases of myocardial infarction (MI). IFG exposure scores of 1, 2, 3, and 4 were associated with all-cause mortality (multivariable-adjusted hazard ratio [aHR], 1.11; 95% confidence interval [CI], 1.08 to 1.15; aHR, 1.16; 95% CI, 1.12 to 1.20; aHR, 1.20; 95% CI, 1.15 to 1.25; aHR, 1.18; 95% CI, 1.11 to 1.25, respectively) compared with an IFG exposure score of 0. Adjusting for hypertension and dyslipidemia attenuated the slightly increased risk of MI or stroke associated with high IFG exposure scores, but significant associations for all-cause mortality remained. CONCLUSION: The intensity of IFG exposure was associated with an elevated risk of all-cause mortality, independent of cardiovascular risk factors. The association between IFG exposure and CVD risk was largely mediated by the coexistence of dyslipidemia and hypertension. Korean Endocrine Society 2021-10 2021-10-21 /pmc/articles/PMC8566122/ /pubmed/34674499 http://dx.doi.org/10.3803/EnM.2021.1218 Text en Copyright © 2021 Korean Endocrine Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Seung-Hwan Han, Kyungdo Kwon, Hyuk-Sang Kim, Mee Kyoung Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title | Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title_full | Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title_fullStr | Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title_full_unstemmed | Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title_short | Frequency of Exposure to Impaired Fasting Glucose and Risk of Mortality and Cardiovascular Outcomes |
title_sort | frequency of exposure to impaired fasting glucose and risk of mortality and cardiovascular outcomes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566122/ https://www.ncbi.nlm.nih.gov/pubmed/34674499 http://dx.doi.org/10.3803/EnM.2021.1218 |
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