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Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring

PURPOSE: To observe the glycemic variation (GV) in uncontrolled Graves’ disease (GD) patients with normal glucose metabolism measured by continuous glucose monitoring (CGM). METHODS: This was a single-center, open-label, observational study. From January 2017 to October 2017, 20 GD patients with nor...

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Autores principales: Gao, Gu, Li, Feng-fei, Hu, Yun, Yan, Reng-na, Liu, Bing-li, Liu, Xiao-mei, Su, Xiao-fei, Ma, Jian-hua, Hu, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531392/
https://www.ncbi.nlm.nih.gov/pubmed/30515677
http://dx.doi.org/10.1007/s12020-018-1820-0
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author Gao, Gu
Li, Feng-fei
Hu, Yun
Yan, Reng-na
Liu, Bing-li
Liu, Xiao-mei
Su, Xiao-fei
Ma, Jian-hua
Hu, Gang
author_facet Gao, Gu
Li, Feng-fei
Hu, Yun
Yan, Reng-na
Liu, Bing-li
Liu, Xiao-mei
Su, Xiao-fei
Ma, Jian-hua
Hu, Gang
author_sort Gao, Gu
collection PubMed
description PURPOSE: To observe the glycemic variation (GV) in uncontrolled Graves’ disease (GD) patients with normal glucose metabolism measured by continuous glucose monitoring (CGM). METHODS: This was a single-center, open-label, observational study. From January 2017 to October 2017, 20 GD patients with normal glucose metabolism and 24 healthy control subjects were recruited. Serum samples were obtained at 0, 30, and 120 min after oral glucose loading for glucose, insulin, and C-peptide level measurements. Fasting plasma fasting free triiodothyronine (FT3), free thyroxin (FT4), and thyroid stimulating hormone concentrations were also detected. All participants were subjected to a 3-day CGM after baseline data were collected. The primary endpoint was the difference in the mean amplitude of the glycemic excursions between the two groups. RESULTS: Compared with the healthy subjects, the GD patients had higher mean amplitude of glycemic excursions (MAGE) (P < 0.01). Multiple linear stepwise regression analysis showed that FT4 level was an independent factor for the MAGE. Interestingly, the GD patients had a significant prolongation in the time to peak glucose, especially after breakfast (P < 0.01), and the elevation in the incremental area under the curve of glucose after breakfast till 4 hours later. CONCLUSIONS: Uncontrolled GD patients with normal glucose metabolism had a greater GV, and the FT4 level may contributed to the increased GV.
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spelling pubmed-65313922019-06-07 Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring Gao, Gu Li, Feng-fei Hu, Yun Yan, Reng-na Liu, Bing-li Liu, Xiao-mei Su, Xiao-fei Ma, Jian-hua Hu, Gang Endocrine Original Article PURPOSE: To observe the glycemic variation (GV) in uncontrolled Graves’ disease (GD) patients with normal glucose metabolism measured by continuous glucose monitoring (CGM). METHODS: This was a single-center, open-label, observational study. From January 2017 to October 2017, 20 GD patients with normal glucose metabolism and 24 healthy control subjects were recruited. Serum samples were obtained at 0, 30, and 120 min after oral glucose loading for glucose, insulin, and C-peptide level measurements. Fasting plasma fasting free triiodothyronine (FT3), free thyroxin (FT4), and thyroid stimulating hormone concentrations were also detected. All participants were subjected to a 3-day CGM after baseline data were collected. The primary endpoint was the difference in the mean amplitude of the glycemic excursions between the two groups. RESULTS: Compared with the healthy subjects, the GD patients had higher mean amplitude of glycemic excursions (MAGE) (P < 0.01). Multiple linear stepwise regression analysis showed that FT4 level was an independent factor for the MAGE. Interestingly, the GD patients had a significant prolongation in the time to peak glucose, especially after breakfast (P < 0.01), and the elevation in the incremental area under the curve of glucose after breakfast till 4 hours later. CONCLUSIONS: Uncontrolled GD patients with normal glucose metabolism had a greater GV, and the FT4 level may contributed to the increased GV. Springer US 2018-12-04 2019 /pmc/articles/PMC6531392/ /pubmed/30515677 http://dx.doi.org/10.1007/s12020-018-1820-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, 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.
spellingShingle Original Article
Gao, Gu
Li, Feng-fei
Hu, Yun
Yan, Reng-na
Liu, Bing-li
Liu, Xiao-mei
Su, Xiao-fei
Ma, Jian-hua
Hu, Gang
Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title_full Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title_fullStr Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title_full_unstemmed Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title_short Glycemic variation in uncontrolled Graves’ disease patients with normal glucose metabolism: Assessment by continuous glucose monitoring
title_sort glycemic variation in uncontrolled graves’ disease patients with normal glucose metabolism: assessment by continuous glucose monitoring
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531392/
https://www.ncbi.nlm.nih.gov/pubmed/30515677
http://dx.doi.org/10.1007/s12020-018-1820-0
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