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High hemoglobin glycation index is associated with increased systemic arterial stiffness independent of hyperglycemia in real-world Japanese population: A cross-sectional study
AIMS: To investigate the association of metabolic parameters including hemoglobin glycation index (HGI, observed HbA1c – predicted HbA1c) with systemic arterial stiffness assessed by cardio-ankle vascular index (CAVI). SUBJECTS: We analyzed the cross-sectional data from 22,696 subjects (mean age 48....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919210/ https://www.ncbi.nlm.nih.gov/pubmed/32985267 http://dx.doi.org/10.1177/1479164120958625 |
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author | Nagayama, Daiji Watanabe, Yasuhiro Yamaguchi, Takashi Saiki, Atsuhito Shirai, Kohji Tatsuno, Ichiro |
author_facet | Nagayama, Daiji Watanabe, Yasuhiro Yamaguchi, Takashi Saiki, Atsuhito Shirai, Kohji Tatsuno, Ichiro |
author_sort | Nagayama, Daiji |
collection | PubMed |
description | AIMS: To investigate the association of metabolic parameters including hemoglobin glycation index (HGI, observed HbA1c – predicted HbA1c) with systemic arterial stiffness assessed by cardio-ankle vascular index (CAVI). SUBJECTS: We analyzed the cross-sectional data from 22,696 subjects (mean age 48.0 years, mean FPG 88 mg/dL, mean HbA1c 5.5%) with or without past history of metabolic disorders including diabetes. RESULTS: Men had higher body mass index (BMI), CAVI, blood pressure (BP), FPG, HbA1c, total cholesterol and triglyceride; and lower age, HGI and HDL-cholesterol. After stratifying subjects into HGI quartiles, the highest quartile (Q4) group showed higher age, female ratio, and frequencies of obesity, hypertension, diabetes, and dyslipidemia. Furthermore, bivariate logistic regression model revealed that the Q4 of HGI was a significant predictor of high CAVI (⩾9.0) independent of the presence of diabetes. CONCLUSION: High HGI is associated with systemic arterial stiffening independent of hyperglycemia. This index is therefore expected to be not only a predictor of hypoglycemia, but also a therapeutic guide for atherosclerosis. |
format | Online Article Text |
id | pubmed-7919210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79192102021-03-02 High hemoglobin glycation index is associated with increased systemic arterial stiffness independent of hyperglycemia in real-world Japanese population: A cross-sectional study Nagayama, Daiji Watanabe, Yasuhiro Yamaguchi, Takashi Saiki, Atsuhito Shirai, Kohji Tatsuno, Ichiro Diab Vasc Dis Res Original Article AIMS: To investigate the association of metabolic parameters including hemoglobin glycation index (HGI, observed HbA1c – predicted HbA1c) with systemic arterial stiffness assessed by cardio-ankle vascular index (CAVI). SUBJECTS: We analyzed the cross-sectional data from 22,696 subjects (mean age 48.0 years, mean FPG 88 mg/dL, mean HbA1c 5.5%) with or without past history of metabolic disorders including diabetes. RESULTS: Men had higher body mass index (BMI), CAVI, blood pressure (BP), FPG, HbA1c, total cholesterol and triglyceride; and lower age, HGI and HDL-cholesterol. After stratifying subjects into HGI quartiles, the highest quartile (Q4) group showed higher age, female ratio, and frequencies of obesity, hypertension, diabetes, and dyslipidemia. Furthermore, bivariate logistic regression model revealed that the Q4 of HGI was a significant predictor of high CAVI (⩾9.0) independent of the presence of diabetes. CONCLUSION: High HGI is associated with systemic arterial stiffening independent of hyperglycemia. This index is therefore expected to be not only a predictor of hypoglycemia, but also a therapeutic guide for atherosclerosis. SAGE Publications 2020-09-26 /pmc/articles/PMC7919210/ /pubmed/32985267 http://dx.doi.org/10.1177/1479164120958625 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Nagayama, Daiji Watanabe, Yasuhiro Yamaguchi, Takashi Saiki, Atsuhito Shirai, Kohji Tatsuno, Ichiro High hemoglobin glycation index is associated with increased systemic arterial stiffness independent of hyperglycemia in real-world Japanese population: A cross-sectional study |
title | High hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world Japanese
population: A cross-sectional study |
title_full | High hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world Japanese
population: A cross-sectional study |
title_fullStr | High hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world Japanese
population: A cross-sectional study |
title_full_unstemmed | High hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world Japanese
population: A cross-sectional study |
title_short | High hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world Japanese
population: A cross-sectional study |
title_sort | high hemoglobin glycation index is associated with increased systemic
arterial stiffness independent of hyperglycemia in real-world japanese
population: a cross-sectional study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919210/ https://www.ncbi.nlm.nih.gov/pubmed/32985267 http://dx.doi.org/10.1177/1479164120958625 |
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