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Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes

CONTEXT: The interaction of glycated hemoglobin A1c (HbA1c) and glycemic variability in relation to diabetes-related outcomes remains unknown. OBJECTIVE: To evaluate the relationship between HbA1c and all-cause mortality across varying degrees of glycemic variability in patients with type 2 diabetes...

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Autores principales: Lu, Jingyi, Wang, Chunfang, Cai, Jinghao, Shen, Yun, Chen, Lei, Zhang, Lei, Lu, Wei, Zhu, Wei, Hu, Gang, Xia, Tian, Zhou, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530707/
https://www.ncbi.nlm.nih.gov/pubmed/34279663
http://dx.doi.org/10.1210/clinem/dgab532
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author Lu, Jingyi
Wang, Chunfang
Cai, Jinghao
Shen, Yun
Chen, Lei
Zhang, Lei
Lu, Wei
Zhu, Wei
Hu, Gang
Xia, Tian
Zhou, Jian
author_facet Lu, Jingyi
Wang, Chunfang
Cai, Jinghao
Shen, Yun
Chen, Lei
Zhang, Lei
Lu, Wei
Zhu, Wei
Hu, Gang
Xia, Tian
Zhou, Jian
author_sort Lu, Jingyi
collection PubMed
description CONTEXT: The interaction of glycated hemoglobin A1c (HbA1c) and glycemic variability in relation to diabetes-related outcomes remains unknown. OBJECTIVE: To evaluate the relationship between HbA1c and all-cause mortality across varying degrees of glycemic variability in patients with type 2 diabetes. DESIGN, SETTING, AND PATIENTS: This was a prospective study conducted in a single referral center. Data of 6090 hospitalized patients with type 2 diabetes was analyzed. Glucose coefficient of variation [coefficient of variation (CV)] was obtained as the measure of glycemic variability by using continuous glucose monitoring for 3 days. Cox proportional hazards regression models were used to estimate hazard ratios and 95% CIs for all-cause mortality. RESULTS: During a median follow-up of 6.8 years, 815 patients died. In patients with the lowest and middle tertiles of glucose CV, HbA1c ≥ 8.0% was associated with 136% (95% CI 1.46-3.81) and 92% (95% CI 1.22-3.03) higher risks of all-cause mortality, respectively, as compared with HbA1c 6.0%-6.9%, after adjusting for confounders. However, a null association of HbA1c with mortality was found in patients with the highest tertile of glucose CV. CONCLUSIONS: HbA1c may not be a robust marker of all-cause mortality in patients with high degree of glycemic variability. New metrics of glycemic control may be needed in these individuals to achieve better diabetes management.
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spelling pubmed-85307072021-10-25 Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes Lu, Jingyi Wang, Chunfang Cai, Jinghao Shen, Yun Chen, Lei Zhang, Lei Lu, Wei Zhu, Wei Hu, Gang Xia, Tian Zhou, Jian J Clin Endocrinol Metab Clinical Research Article CONTEXT: The interaction of glycated hemoglobin A1c (HbA1c) and glycemic variability in relation to diabetes-related outcomes remains unknown. OBJECTIVE: To evaluate the relationship between HbA1c and all-cause mortality across varying degrees of glycemic variability in patients with type 2 diabetes. DESIGN, SETTING, AND PATIENTS: This was a prospective study conducted in a single referral center. Data of 6090 hospitalized patients with type 2 diabetes was analyzed. Glucose coefficient of variation [coefficient of variation (CV)] was obtained as the measure of glycemic variability by using continuous glucose monitoring for 3 days. Cox proportional hazards regression models were used to estimate hazard ratios and 95% CIs for all-cause mortality. RESULTS: During a median follow-up of 6.8 years, 815 patients died. In patients with the lowest and middle tertiles of glucose CV, HbA1c ≥ 8.0% was associated with 136% (95% CI 1.46-3.81) and 92% (95% CI 1.22-3.03) higher risks of all-cause mortality, respectively, as compared with HbA1c 6.0%-6.9%, after adjusting for confounders. However, a null association of HbA1c with mortality was found in patients with the highest tertile of glucose CV. CONCLUSIONS: HbA1c may not be a robust marker of all-cause mortality in patients with high degree of glycemic variability. New metrics of glycemic control may be needed in these individuals to achieve better diabetes management. Oxford University Press 2021-07-19 /pmc/articles/PMC8530707/ /pubmed/34279663 http://dx.doi.org/10.1210/clinem/dgab532 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Lu, Jingyi
Wang, Chunfang
Cai, Jinghao
Shen, Yun
Chen, Lei
Zhang, Lei
Lu, Wei
Zhu, Wei
Hu, Gang
Xia, Tian
Zhou, Jian
Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title_full Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title_fullStr Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title_full_unstemmed Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title_short Association of HbA1c With All-cause Mortality Across Varying Degrees of Glycemic Variability in Type 2 Diabetes
title_sort association of hba1c with all-cause mortality across varying degrees of glycemic variability in type 2 diabetes
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530707/
https://www.ncbi.nlm.nih.gov/pubmed/34279663
http://dx.doi.org/10.1210/clinem/dgab532
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