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Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018

BACKGROUND: Obesity is associated with an increased risk of developing type 2 diabetes mellitus (T2DM) and end‐stage renal disease (ESRD). This study aimed to examine the effect of waist circumference (WC) on the risk for ESRD based on glycaemic status in a Korean population‐based sample. METHODS: T...

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Autores principales: Cho, Yun Kyung, Huh, Ji Hye, Moon, Shinje, Kim, Yoon Jung, Kim, Yang‐Hyun, Han, Kyung‐do, Kang, Jun Goo, Lee, Seong Jin, Ihm, Sung‐Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891961/
https://www.ncbi.nlm.nih.gov/pubmed/36564188
http://dx.doi.org/10.1002/jcsm.13164
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author Cho, Yun Kyung
Huh, Ji Hye
Moon, Shinje
Kim, Yoon Jung
Kim, Yang‐Hyun
Han, Kyung‐do
Kang, Jun Goo
Lee, Seong Jin
Ihm, Sung‐Hee
author_facet Cho, Yun Kyung
Huh, Ji Hye
Moon, Shinje
Kim, Yoon Jung
Kim, Yang‐Hyun
Han, Kyung‐do
Kang, Jun Goo
Lee, Seong Jin
Ihm, Sung‐Hee
author_sort Cho, Yun Kyung
collection PubMed
description BACKGROUND: Obesity is associated with an increased risk of developing type 2 diabetes mellitus (T2DM) and end‐stage renal disease (ESRD). This study aimed to examine the effect of waist circumference (WC) on the risk for ESRD based on glycaemic status in a Korean population‐based sample. METHODS: This cohort study with a 9.2‐year follow‐up period used a population‐based National Health Insurance Service health checkup database with approximately 10 585 852 participants who were followed up from 2009 to the time of ESRD diagnosis. WC was categorized into seven levels in 5‐cm increments, with Level 4 as the reference group. Glycaemic status was categorized into the following groups: normal fasting glucose (NFG), impaired fasting glucose (IFG), newly diagnosed T2DM, T2DM treated with ≤2 oral hypoglycaemic agents (OHAs) and diabetes treated with ≥3 OHAs or insulin. We calculated hazard ratios (HRs) and 95% confidence intervals (CIs) for ESRD according to WC values and glycaemic status of the participants. RESULTS: The study finally included 10 177 245 patients with a mean age of 47.1 (13.8) years. The study population included 5 604 446 men (55.1%) and 4 572 799 women (45.9%). In total, 8.3% (n = 877 143) of the study population had diabetes. During the mean follow‐up of 9.2 (1.0) years (93 554 951 person‐years of follow‐up), 23 031 individuals were newly diagnosed with ESRD. The ESRD risk increased in parallel with an increase in WC in participants without T2DM, that is, the NFG and IFG groups (adjusted HRs [95% CIs] of WC Levels 4, 5 and 6: 1.17 [1.09–1.26], 1.37 [1.25–1.51] and 1.84 [1.63–2.07] in the NFG group and 1.06 [0.97–1.16], 1.23 [1.10–1.38] and 1.80 [1.57–2.06] in the IFG group, respectively). In patients with T2DM, the risk for ESRD was significantly increased in those with a low WC (adjusted HRs [95% CIs] of WC Level 1: 2.23 [1.77–2.80], 3.18 [2.70–3.74] and 10.31 [9.18–11.59] in patients with newly diagnosed diabetes, patients on ≤2 OHAs and those on ≥3 OHAs or insulin, respectively). The association between WC and ESRD thus showed a J‐shaped pattern in patients with newly diagnosed T2DM and a U‐shaped pattern in those on ≤2 OHAs and on ≥3 OHAs or insulin. CONCLUSIONS: Central obesity substantially increases the risk of developing ESRD regardless of glycaemic status. The harmful effects of low WC only become significant with the progression of T2DM.
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spelling pubmed-98919612023-02-02 Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018 Cho, Yun Kyung Huh, Ji Hye Moon, Shinje Kim, Yoon Jung Kim, Yang‐Hyun Han, Kyung‐do Kang, Jun Goo Lee, Seong Jin Ihm, Sung‐Hee J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Obesity is associated with an increased risk of developing type 2 diabetes mellitus (T2DM) and end‐stage renal disease (ESRD). This study aimed to examine the effect of waist circumference (WC) on the risk for ESRD based on glycaemic status in a Korean population‐based sample. METHODS: This cohort study with a 9.2‐year follow‐up period used a population‐based National Health Insurance Service health checkup database with approximately 10 585 852 participants who were followed up from 2009 to the time of ESRD diagnosis. WC was categorized into seven levels in 5‐cm increments, with Level 4 as the reference group. Glycaemic status was categorized into the following groups: normal fasting glucose (NFG), impaired fasting glucose (IFG), newly diagnosed T2DM, T2DM treated with ≤2 oral hypoglycaemic agents (OHAs) and diabetes treated with ≥3 OHAs or insulin. We calculated hazard ratios (HRs) and 95% confidence intervals (CIs) for ESRD according to WC values and glycaemic status of the participants. RESULTS: The study finally included 10 177 245 patients with a mean age of 47.1 (13.8) years. The study population included 5 604 446 men (55.1%) and 4 572 799 women (45.9%). In total, 8.3% (n = 877 143) of the study population had diabetes. During the mean follow‐up of 9.2 (1.0) years (93 554 951 person‐years of follow‐up), 23 031 individuals were newly diagnosed with ESRD. The ESRD risk increased in parallel with an increase in WC in participants without T2DM, that is, the NFG and IFG groups (adjusted HRs [95% CIs] of WC Levels 4, 5 and 6: 1.17 [1.09–1.26], 1.37 [1.25–1.51] and 1.84 [1.63–2.07] in the NFG group and 1.06 [0.97–1.16], 1.23 [1.10–1.38] and 1.80 [1.57–2.06] in the IFG group, respectively). In patients with T2DM, the risk for ESRD was significantly increased in those with a low WC (adjusted HRs [95% CIs] of WC Level 1: 2.23 [1.77–2.80], 3.18 [2.70–3.74] and 10.31 [9.18–11.59] in patients with newly diagnosed diabetes, patients on ≤2 OHAs and those on ≥3 OHAs or insulin, respectively). The association between WC and ESRD thus showed a J‐shaped pattern in patients with newly diagnosed T2DM and a U‐shaped pattern in those on ≤2 OHAs and on ≥3 OHAs or insulin. CONCLUSIONS: Central obesity substantially increases the risk of developing ESRD regardless of glycaemic status. The harmful effects of low WC only become significant with the progression of T2DM. John Wiley and Sons Inc. 2022-12-23 /pmc/articles/PMC9891961/ /pubmed/36564188 http://dx.doi.org/10.1002/jcsm.13164 Text en © 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Cho, Yun Kyung
Huh, Ji Hye
Moon, Shinje
Kim, Yoon Jung
Kim, Yang‐Hyun
Han, Kyung‐do
Kang, Jun Goo
Lee, Seong Jin
Ihm, Sung‐Hee
Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title_full Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title_fullStr Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title_full_unstemmed Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title_short Waist circumference and end‐stage renal disease based on glycaemic status: National Health Insurance Service data 2009–2018
title_sort waist circumference and end‐stage renal disease based on glycaemic status: national health insurance service data 2009–2018
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891961/
https://www.ncbi.nlm.nih.gov/pubmed/36564188
http://dx.doi.org/10.1002/jcsm.13164
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