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Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population
BACKGROUND: Diabetic kidney disease (DKD) is associated with an elevated risk of fractures. However, little is known about the association between proteinuric or non-proteinuric DKD and the risk of hip fracture. Thus, we investigated the incidence of hip fractures among Korean adults with type 2 dia...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Endocrine Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901970/ https://www.ncbi.nlm.nih.gov/pubmed/35255607 http://dx.doi.org/10.3803/EnM.2021.1315 |
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author | Lee, Seung Eun Yoo, Juhwan Kim, Kyoung-Ah Han, Kyungdo Choi, Han Seok |
author_facet | Lee, Seung Eun Yoo, Juhwan Kim, Kyoung-Ah Han, Kyungdo Choi, Han Seok |
author_sort | Lee, Seung Eun |
collection | PubMed |
description | BACKGROUND: Diabetic kidney disease (DKD) is associated with an elevated risk of fractures. However, little is known about the association between proteinuric or non-proteinuric DKD and the risk of hip fracture. Thus, we investigated the incidence of hip fractures among Korean adults with type 2 diabetes mellitus (T2DM) stratified by DKD phenotype. METHODS: In this retrospective cohort study using the Korean National Health Insurance Service database, patients with T2DM who received at least one general health checkup between 2009 and 2012 were followed until the date of hip fracture, death, or December 31, 2018. We classified the DKD phenotype by proteinuria and estimated glomerular filtration rate (eGFR), as follows: no DKD (PU(−)GFR(−)), proteinuric DKD with normal eGFR (PU(+)GFR(−)), non-proteinuric DKD with reduced eGFR (PU(−)GFR(+)), and proteinuric DKD with reduced eGFR (PU(+)GFR(+)) RESULTS: The cumulative incidence of hip fractures was highest in the PU(+)GFR(+) group, followed by the PU(−)GFR(+) group and the PU(+)GFR(−) group. After adjustment for confounding factors, the hazard ratio (HR) for hip fracture was still highest in the PU(+)GFR(+) group. However, the PU(+)GFR(−) group had a higher HR for hip fracture than the PU(−)GFR(+) group (PU(+)GFR(+): HR, 1.69; 95% confidence interval [CI], 1.57 to 1.81; PU(+)GFR(−): HR, 1.37; 95% CI, 1.30 to 1.46; PU(−)GFR(+): HR, 1.20; 95% CI, 1.16 to 1.24 using the PU(−)GFR(−) group as the reference category). CONCLUSION: The present study demonstrated that DKD was significantly associated with a higher risk of hip fracture, with proteinuria as a major determinant. |
format | Online Article Text |
id | pubmed-8901970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89019702022-03-14 Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population Lee, Seung Eun Yoo, Juhwan Kim, Kyoung-Ah Han, Kyungdo Choi, Han Seok Endocrinol Metab (Seoul) Original Article BACKGROUND: Diabetic kidney disease (DKD) is associated with an elevated risk of fractures. However, little is known about the association between proteinuric or non-proteinuric DKD and the risk of hip fracture. Thus, we investigated the incidence of hip fractures among Korean adults with type 2 diabetes mellitus (T2DM) stratified by DKD phenotype. METHODS: In this retrospective cohort study using the Korean National Health Insurance Service database, patients with T2DM who received at least one general health checkup between 2009 and 2012 were followed until the date of hip fracture, death, or December 31, 2018. We classified the DKD phenotype by proteinuria and estimated glomerular filtration rate (eGFR), as follows: no DKD (PU(−)GFR(−)), proteinuric DKD with normal eGFR (PU(+)GFR(−)), non-proteinuric DKD with reduced eGFR (PU(−)GFR(+)), and proteinuric DKD with reduced eGFR (PU(+)GFR(+)) RESULTS: The cumulative incidence of hip fractures was highest in the PU(+)GFR(+) group, followed by the PU(−)GFR(+) group and the PU(+)GFR(−) group. After adjustment for confounding factors, the hazard ratio (HR) for hip fracture was still highest in the PU(+)GFR(+) group. However, the PU(+)GFR(−) group had a higher HR for hip fracture than the PU(−)GFR(+) group (PU(+)GFR(+): HR, 1.69; 95% confidence interval [CI], 1.57 to 1.81; PU(+)GFR(−): HR, 1.37; 95% CI, 1.30 to 1.46; PU(−)GFR(+): HR, 1.20; 95% CI, 1.16 to 1.24 using the PU(−)GFR(−) group as the reference category). CONCLUSION: The present study demonstrated that DKD was significantly associated with a higher risk of hip fracture, with proteinuria as a major determinant. Korean Endocrine Society 2022-02 2022-02-28 /pmc/articles/PMC8901970/ /pubmed/35255607 http://dx.doi.org/10.3803/EnM.2021.1315 Text en Copyright © 2022 Korean Endocrine Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Seung Eun Yoo, Juhwan Kim, Kyoung-Ah Han, Kyungdo Choi, Han Seok Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title | Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title_full | Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title_fullStr | Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title_full_unstemmed | Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title_short | Hip Fracture Risk According to Diabetic Kidney Disease Phenotype in a Korean Population |
title_sort | hip fracture risk according to diabetic kidney disease phenotype in a korean population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901970/ https://www.ncbi.nlm.nih.gov/pubmed/35255607 http://dx.doi.org/10.3803/EnM.2021.1315 |
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