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Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values

To define the features of glycemic variations in drug naïve type 2 diabetic (T2D) patients with different HbA(1c) values using continuous glucose monitoring (CGM), a total of 195 drug naïve T2D patients were admitted. The subjects were divided into the following groups: lower HbA(1c) values (≤8%), m...

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Autores principales: Li, Feng-fei, Liu, Bing-li, Yan, Reng-na, Zhu, Hong-hong, Zhou, Pei-hua, Li, Hui-qin, Su, Xiao-fei, Wu, Jin-dan, Zhang, Dan-feng, Ye, Lei, Ma, Jian-hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431480/
https://www.ncbi.nlm.nih.gov/pubmed/28484269
http://dx.doi.org/10.1038/s41598-017-01719-y
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author Li, Feng-fei
Liu, Bing-li
Yan, Reng-na
Zhu, Hong-hong
Zhou, Pei-hua
Li, Hui-qin
Su, Xiao-fei
Wu, Jin-dan
Zhang, Dan-feng
Ye, Lei
Ma, Jian-hua
author_facet Li, Feng-fei
Liu, Bing-li
Yan, Reng-na
Zhu, Hong-hong
Zhou, Pei-hua
Li, Hui-qin
Su, Xiao-fei
Wu, Jin-dan
Zhang, Dan-feng
Ye, Lei
Ma, Jian-hua
author_sort Li, Feng-fei
collection PubMed
description To define the features of glycemic variations in drug naïve type 2 diabetic (T2D) patients with different HbA(1c) values using continuous glucose monitoring (CGM), a total of 195 drug naïve T2D patients were admitted. The subjects were divided into the following groups: lower HbA(1c) values (≤8%), moderate HbA(1c) values (>8% and ≤10%), and higher HbA(1c) values (>10%). The patients underwent oral glucose tolerance tests and were then subjected to 3-day CGM. The primary endpoint was the differences in the 24-hr mean amplitude of glycemic excursions (MAGE) in patients with different HbA(1c) values. Patients with higher HbA(1c) values had larger MAGEs than those in the moderate and lower groups (7.44 ± 3.00 vs. 6.30 ± 2.38, P < 0.05, 7.44 ± 3.00 vs. 5.20 ± 2.35, P < 0.01, respectively). The 24-hr mean glucose concentrations increased incrementally in the patients with lower, moderate and higher HbA(1c) values. Moreover, the patients with higher HbA(1c) values exhibited higher peak glucose concentrations and prolongation in the time to peak glucose. Patients with higher HbA(1c) values had larger MAGE compared with those with lower and moderate HbA(1c) values. Our data indicated patients with higher HbA(1c) values should receive special therapy aimed at reducing the larger glycemic variations.
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spelling pubmed-54314802017-05-16 Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values Li, Feng-fei Liu, Bing-li Yan, Reng-na Zhu, Hong-hong Zhou, Pei-hua Li, Hui-qin Su, Xiao-fei Wu, Jin-dan Zhang, Dan-feng Ye, Lei Ma, Jian-hua Sci Rep Article To define the features of glycemic variations in drug naïve type 2 diabetic (T2D) patients with different HbA(1c) values using continuous glucose monitoring (CGM), a total of 195 drug naïve T2D patients were admitted. The subjects were divided into the following groups: lower HbA(1c) values (≤8%), moderate HbA(1c) values (>8% and ≤10%), and higher HbA(1c) values (>10%). The patients underwent oral glucose tolerance tests and were then subjected to 3-day CGM. The primary endpoint was the differences in the 24-hr mean amplitude of glycemic excursions (MAGE) in patients with different HbA(1c) values. Patients with higher HbA(1c) values had larger MAGEs than those in the moderate and lower groups (7.44 ± 3.00 vs. 6.30 ± 2.38, P < 0.05, 7.44 ± 3.00 vs. 5.20 ± 2.35, P < 0.01, respectively). The 24-hr mean glucose concentrations increased incrementally in the patients with lower, moderate and higher HbA(1c) values. Moreover, the patients with higher HbA(1c) values exhibited higher peak glucose concentrations and prolongation in the time to peak glucose. Patients with higher HbA(1c) values had larger MAGE compared with those with lower and moderate HbA(1c) values. Our data indicated patients with higher HbA(1c) values should receive special therapy aimed at reducing the larger glycemic variations. Nature Publishing Group UK 2017-05-08 /pmc/articles/PMC5431480/ /pubmed/28484269 http://dx.doi.org/10.1038/s41598-017-01719-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Feng-fei
Liu, Bing-li
Yan, Reng-na
Zhu, Hong-hong
Zhou, Pei-hua
Li, Hui-qin
Su, Xiao-fei
Wu, Jin-dan
Zhang, Dan-feng
Ye, Lei
Ma, Jian-hua
Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title_full Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title_fullStr Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title_full_unstemmed Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title_short Features of glycemic variations in drug naïve type 2 diabetic patients with different HbA(1c) values
title_sort features of glycemic variations in drug naïve type 2 diabetic patients with different hba(1c) values
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431480/
https://www.ncbi.nlm.nih.gov/pubmed/28484269
http://dx.doi.org/10.1038/s41598-017-01719-y
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