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Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study

Given the fact that diabetes remains a leading cause of end-stage kidney disease (ESKD), multi-aspect approaches anticipating the risk for ESKD and timely correction are crucial. We investigated whether fasting glucose variability (FGV) could anticipate the development of ESKD and identify the popul...

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Autores principales: Lee, Da Young, Kim, Jaeyoung, Park, Sanghyun, Park, So Young, Yu, Ji Hee, Seo, Ji A., Kim, Nam Hoon, Yoo, Hye Jin, Kim, Sin Gon, Choi, Kyung Mook, Baik, Sei Hyun, Han, Kyungdo, Kim, Nan Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705330/
https://www.ncbi.nlm.nih.gov/pubmed/34945244
http://dx.doi.org/10.3390/jcm10245948
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author Lee, Da Young
Kim, Jaeyoung
Park, Sanghyun
Park, So Young
Yu, Ji Hee
Seo, Ji A.
Kim, Nam Hoon
Yoo, Hye Jin
Kim, Sin Gon
Choi, Kyung Mook
Baik, Sei Hyun
Han, Kyungdo
Kim, Nan Hee
author_facet Lee, Da Young
Kim, Jaeyoung
Park, Sanghyun
Park, So Young
Yu, Ji Hee
Seo, Ji A.
Kim, Nam Hoon
Yoo, Hye Jin
Kim, Sin Gon
Choi, Kyung Mook
Baik, Sei Hyun
Han, Kyungdo
Kim, Nan Hee
author_sort Lee, Da Young
collection PubMed
description Given the fact that diabetes remains a leading cause of end-stage kidney disease (ESKD), multi-aspect approaches anticipating the risk for ESKD and timely correction are crucial. We investigated whether fasting glucose variability (FGV) could anticipate the development of ESKD and identify the population prone to the harmful effects of GV. We included 777,192 Koreans with diabetes who had undergone health examinations more than three times in 2005–2010. We evaluated the risk of the first diagnosis of ESKD until 2017, according to the quartile of variability independent of the mean (VIM) of FG using multivariate-adjusted Cox proportional hazards analyses. During the 8-year follow-up, a total of 7290 incidents of ESKD were found. Subjects in the FG VIM quartile 4 had a 27% higher risk for ESKD compared to quartile 1, with adjustment for cardiovascular risk factors and the characteristics of diabetes. This effect was more distinct in patients aged < 65 years; those with a long duration of diabetes; the presence of hypertension or dyslipidemia; and prescribed angiotensin-converting enzyme inhibitors, metformin, sulfonylurea, α-glucosidase inhibitors, and insulin. In contrast, the relationship between baseline FG status and ESKD risk showed a U-shaped association. FGV is an independent risk factor for kidney failure regardless of FG.
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spelling pubmed-87053302021-12-25 Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study Lee, Da Young Kim, Jaeyoung Park, Sanghyun Park, So Young Yu, Ji Hee Seo, Ji A. Kim, Nam Hoon Yoo, Hye Jin Kim, Sin Gon Choi, Kyung Mook Baik, Sei Hyun Han, Kyungdo Kim, Nan Hee J Clin Med Article Given the fact that diabetes remains a leading cause of end-stage kidney disease (ESKD), multi-aspect approaches anticipating the risk for ESKD and timely correction are crucial. We investigated whether fasting glucose variability (FGV) could anticipate the development of ESKD and identify the population prone to the harmful effects of GV. We included 777,192 Koreans with diabetes who had undergone health examinations more than three times in 2005–2010. We evaluated the risk of the first diagnosis of ESKD until 2017, according to the quartile of variability independent of the mean (VIM) of FG using multivariate-adjusted Cox proportional hazards analyses. During the 8-year follow-up, a total of 7290 incidents of ESKD were found. Subjects in the FG VIM quartile 4 had a 27% higher risk for ESKD compared to quartile 1, with adjustment for cardiovascular risk factors and the characteristics of diabetes. This effect was more distinct in patients aged < 65 years; those with a long duration of diabetes; the presence of hypertension or dyslipidemia; and prescribed angiotensin-converting enzyme inhibitors, metformin, sulfonylurea, α-glucosidase inhibitors, and insulin. In contrast, the relationship between baseline FG status and ESKD risk showed a U-shaped association. FGV is an independent risk factor for kidney failure regardless of FG. MDPI 2021-12-18 /pmc/articles/PMC8705330/ /pubmed/34945244 http://dx.doi.org/10.3390/jcm10245948 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Da Young
Kim, Jaeyoung
Park, Sanghyun
Park, So Young
Yu, Ji Hee
Seo, Ji A.
Kim, Nam Hoon
Yoo, Hye Jin
Kim, Sin Gon
Choi, Kyung Mook
Baik, Sei Hyun
Han, Kyungdo
Kim, Nan Hee
Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title_full Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title_fullStr Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title_full_unstemmed Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title_short Fasting Glucose Variability as a Risk Indicator for End-Stage Kidney Disease in Patients with Diabetes: A Nationwide Population-Based Study
title_sort fasting glucose variability as a risk indicator for end-stage kidney disease in patients with diabetes: a nationwide population-based study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705330/
https://www.ncbi.nlm.nih.gov/pubmed/34945244
http://dx.doi.org/10.3390/jcm10245948
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