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Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes
BACKGROUND: Diabetes has been reported to be associated with carotid artery plaque (CAP). However, it remains unclear whether hemoglobin A1c (HbA1c) level, a marker for long-term glycemic status, is associated with altered CAP risk in individuals with fasting blood glucose (FBG) concentrations below...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857319/ https://www.ncbi.nlm.nih.gov/pubmed/31727070 http://dx.doi.org/10.1186/s12933-019-0963-5 |
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author | Xu, Renying Zhang, Ting Wan, Yanping Fan, Zhuping Gao, Xiang |
author_facet | Xu, Renying Zhang, Ting Wan, Yanping Fan, Zhuping Gao, Xiang |
author_sort | Xu, Renying |
collection | PubMed |
description | BACKGROUND: Diabetes has been reported to be associated with carotid artery plaque (CAP). However, it remains unclear whether hemoglobin A1c (HbA1c) level, a marker for long-term glycemic status, is associated with altered CAP risk in individuals with fasting blood glucose (FBG) concentrations below the current cutoff for diabetes. METHODS: Included were 16,863 Chinese adults (aged 18 years or more; 9855 men and 7008 women) with fasting blood glucose < 7.0 mmol/L at baseline (2013). Both HbA1c level and CAP (assessed via ultrasound B-mode imaging) were annually assessed during 2014–2018. All the participants were further classified into three groups based on baseline HbA1c level: ≤ 5.6%, 5.7–6.4%, and ≥ 6.5%. We used Cox proportional-hazards model to evaluate the association between HbA1c level and incident CAP, adjusting for a series of potential confounders. RESULTS: During 5 years of follow up, 3942 incident CAP cases were identified. Individuals with higher baseline HbA1c had higher future risk of CAP (p-trend < 0.001). In the full-adjusted model, each percent increase of HbA1c was associated with a 56% (HR = 1.56, 95% CI 1.37, 1.78) higher risk of CAP. Excluding participants with chronic inflammation, as assessed by high-sensitivity C-reactive protein and white blood cell, and those with FBG ≥ 5.6 mmol/L at baseline generated similar results. CONCLUSIONS: Elevated HbA1c level was associated with high risk of developing CAP in Chinese adults without FBG defined diabetes. |
format | Online Article Text |
id | pubmed-6857319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68573192019-12-05 Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes Xu, Renying Zhang, Ting Wan, Yanping Fan, Zhuping Gao, Xiang Cardiovasc Diabetol Original Investigation BACKGROUND: Diabetes has been reported to be associated with carotid artery plaque (CAP). However, it remains unclear whether hemoglobin A1c (HbA1c) level, a marker for long-term glycemic status, is associated with altered CAP risk in individuals with fasting blood glucose (FBG) concentrations below the current cutoff for diabetes. METHODS: Included were 16,863 Chinese adults (aged 18 years or more; 9855 men and 7008 women) with fasting blood glucose < 7.0 mmol/L at baseline (2013). Both HbA1c level and CAP (assessed via ultrasound B-mode imaging) were annually assessed during 2014–2018. All the participants were further classified into three groups based on baseline HbA1c level: ≤ 5.6%, 5.7–6.4%, and ≥ 6.5%. We used Cox proportional-hazards model to evaluate the association between HbA1c level and incident CAP, adjusting for a series of potential confounders. RESULTS: During 5 years of follow up, 3942 incident CAP cases were identified. Individuals with higher baseline HbA1c had higher future risk of CAP (p-trend < 0.001). In the full-adjusted model, each percent increase of HbA1c was associated with a 56% (HR = 1.56, 95% CI 1.37, 1.78) higher risk of CAP. Excluding participants with chronic inflammation, as assessed by high-sensitivity C-reactive protein and white blood cell, and those with FBG ≥ 5.6 mmol/L at baseline generated similar results. CONCLUSIONS: Elevated HbA1c level was associated with high risk of developing CAP in Chinese adults without FBG defined diabetes. BioMed Central 2019-11-14 /pmc/articles/PMC6857319/ /pubmed/31727070 http://dx.doi.org/10.1186/s12933-019-0963-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Investigation Xu, Renying Zhang, Ting Wan, Yanping Fan, Zhuping Gao, Xiang Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title | Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title_full | Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title_fullStr | Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title_full_unstemmed | Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title_short | Prospective study of hemoglobin A1c and incident carotid artery plaque in Chinese adults without diabetes |
title_sort | prospective study of hemoglobin a1c and incident carotid artery plaque in chinese adults without diabetes |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857319/ https://www.ncbi.nlm.nih.gov/pubmed/31727070 http://dx.doi.org/10.1186/s12933-019-0963-5 |
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