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The impact of fasting plasma glucose variability on osteoporotic fractures

PURPOSE: To investigate the impact of FPG variability on osteoporotic fractures in the entire community population. METHODS: All participants were from the Kailuan Study. Participants completed three consecutive surveys from 2006–2007, 2008–2009, and 2010–2011. We excluded individuals with an osteop...

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Autores principales: Liu, Ri, Gao, Lishu, Guo, Lu, Xu, Wenqi, Wu, Shouling, Tian, Dehu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348823/
https://www.ncbi.nlm.nih.gov/pubmed/37455924
http://dx.doi.org/10.3389/fendo.2023.1187682
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author Liu, Ri
Gao, Lishu
Guo, Lu
Xu, Wenqi
Wu, Shouling
Tian, Dehu
author_facet Liu, Ri
Gao, Lishu
Guo, Lu
Xu, Wenqi
Wu, Shouling
Tian, Dehu
author_sort Liu, Ri
collection PubMed
description PURPOSE: To investigate the impact of FPG variability on osteoporotic fractures in the entire community population. METHODS: All participants were from the Kailuan Study. Participants completed three consecutive surveys from 2006–2007, 2008–2009, and 2010–2011. We excluded individuals with an osteoporotic fracture in or prior to the index year and those without complete FPG records at the first 3 examinations. All participants were followed from the date of the 3rd examination to the first occurrence of an endpoint event or December 31, 2021. According to the SD of FPG levels, the included subjects were divided into three groups. A Cox proportional hazards model was performed to further analyze the effect of different FPG-SD groups on the risk of osteoporotic fractures. RESULTS: Ultimately, the study population included 57295 participants. During a median follow-up time of 11.00 years, we documented 772 new osteoporotic fracture cases. When evaluating the FPG-SD level as a categorical variable, the HRs for osteoporotic fractures were 1.07 (95% CI: 0.89-1.29) for T2 and 1.32 (95% CI: 1.10–1.60) for T3 when compared with T1. We found that increased FPG variability was associated with a greater risk of osteoporotic fractures in people with diabetes than in those without diabetes (47% vs. 32%) CONCLUSION: Increased FPG variability was an independent predictor of incident osteoporotic fracture, especially in individuals older than 50 years old, nonobese individuals, diabetes patients, and individuals with positive FPG-SD variability.
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spelling pubmed-103488232023-07-15 The impact of fasting plasma glucose variability on osteoporotic fractures Liu, Ri Gao, Lishu Guo, Lu Xu, Wenqi Wu, Shouling Tian, Dehu Front Endocrinol (Lausanne) Endocrinology PURPOSE: To investigate the impact of FPG variability on osteoporotic fractures in the entire community population. METHODS: All participants were from the Kailuan Study. Participants completed three consecutive surveys from 2006–2007, 2008–2009, and 2010–2011. We excluded individuals with an osteoporotic fracture in or prior to the index year and those without complete FPG records at the first 3 examinations. All participants were followed from the date of the 3rd examination to the first occurrence of an endpoint event or December 31, 2021. According to the SD of FPG levels, the included subjects were divided into three groups. A Cox proportional hazards model was performed to further analyze the effect of different FPG-SD groups on the risk of osteoporotic fractures. RESULTS: Ultimately, the study population included 57295 participants. During a median follow-up time of 11.00 years, we documented 772 new osteoporotic fracture cases. When evaluating the FPG-SD level as a categorical variable, the HRs for osteoporotic fractures were 1.07 (95% CI: 0.89-1.29) for T2 and 1.32 (95% CI: 1.10–1.60) for T3 when compared with T1. We found that increased FPG variability was associated with a greater risk of osteoporotic fractures in people with diabetes than in those without diabetes (47% vs. 32%) CONCLUSION: Increased FPG variability was an independent predictor of incident osteoporotic fracture, especially in individuals older than 50 years old, nonobese individuals, diabetes patients, and individuals with positive FPG-SD variability. Frontiers Media S.A. 2023-06-30 /pmc/articles/PMC10348823/ /pubmed/37455924 http://dx.doi.org/10.3389/fendo.2023.1187682 Text en Copyright © 2023 Liu, Gao, Guo, Xu, Wu and Tian https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Liu, Ri
Gao, Lishu
Guo, Lu
Xu, Wenqi
Wu, Shouling
Tian, Dehu
The impact of fasting plasma glucose variability on osteoporotic fractures
title The impact of fasting plasma glucose variability on osteoporotic fractures
title_full The impact of fasting plasma glucose variability on osteoporotic fractures
title_fullStr The impact of fasting plasma glucose variability on osteoporotic fractures
title_full_unstemmed The impact of fasting plasma glucose variability on osteoporotic fractures
title_short The impact of fasting plasma glucose variability on osteoporotic fractures
title_sort impact of fasting plasma glucose variability on osteoporotic fractures
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348823/
https://www.ncbi.nlm.nih.gov/pubmed/37455924
http://dx.doi.org/10.3389/fendo.2023.1187682
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