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Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients

INTRODUCTION: Bone mineral density (BMD) measured with dual-energy X-ray absorptiometry (DXA) can be used to predict fractures, but its clinical utility has not been fully established in chronic kidney disease (CKD) patients. Magnesium is an essential trace element. Although magnesium is associated...

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Autores principales: Hori, Mayuko, Yasuda, Kaoru, Takahashi, Hiroshi, Yamazaki, Chikao, Morozumi, Kunio, Maruyama, Shoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136656/
https://www.ncbi.nlm.nih.gov/pubmed/34014999
http://dx.doi.org/10.1371/journal.pone.0251912
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author Hori, Mayuko
Yasuda, Kaoru
Takahashi, Hiroshi
Yamazaki, Chikao
Morozumi, Kunio
Maruyama, Shoichi
author_facet Hori, Mayuko
Yasuda, Kaoru
Takahashi, Hiroshi
Yamazaki, Chikao
Morozumi, Kunio
Maruyama, Shoichi
author_sort Hori, Mayuko
collection PubMed
description INTRODUCTION: Bone mineral density (BMD) measured with dual-energy X-ray absorptiometry (DXA) can be used to predict fractures, but its clinical utility has not been fully established in chronic kidney disease (CKD) patients. Magnesium is an essential trace element. Although magnesium is associated with the risk of fractures in non-CKD populations, the relationship is unknown in CKD patients. METHODS: BMD and serum magnesium levels were measured in 358 stable outpatients undergoing maintenance hemodialysis therapy. The primary outcome was fragility fracture. Patients were divided into groups according to the median level of magnesium and the normal threshold value of lumbar spine BMD. RESULTS: During the median follow-up period of 36 months, 36 (10.0%) fractures occurred. The cumulative incidence rates of fractures were 17.6% and 5.2% [adjusted hazard ratio (aHR) 2.31, 95% confidence interval (CI) 1.03–5.17, P = 0.030] in the lower (<2.6 mg/dL) and higher (≥2.6 mg/dL) magnesium (Mg) groups, respectively, and 21.2% and 7.3% (aHR 2.59, 95% CI 1.09–6.16, P = 0.027) in the low- and high-BMD groups, respectively. The lower-Mg and low-BMD group had a 9.21-fold higher risk of fractures (95% CI; 2.35–47.00; P = 0.0010) than the higher-Mg and high-BMD group. Furthermore, adding both magnesium levels and lumbar spine BMD levels to the established risk factors significantly improved the prediction of fractures (C-index: 0.784 to 0.830, p = 0.041). DISCUSSION/CONCLUSIONS: The combination of serum magnesium and lumbar spine BMD can be used for fracture risk stratification and synergistically improves the prediction of fractures in CKD patients.
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spelling pubmed-81366562021-06-02 Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients Hori, Mayuko Yasuda, Kaoru Takahashi, Hiroshi Yamazaki, Chikao Morozumi, Kunio Maruyama, Shoichi PLoS One Research Article INTRODUCTION: Bone mineral density (BMD) measured with dual-energy X-ray absorptiometry (DXA) can be used to predict fractures, but its clinical utility has not been fully established in chronic kidney disease (CKD) patients. Magnesium is an essential trace element. Although magnesium is associated with the risk of fractures in non-CKD populations, the relationship is unknown in CKD patients. METHODS: BMD and serum magnesium levels were measured in 358 stable outpatients undergoing maintenance hemodialysis therapy. The primary outcome was fragility fracture. Patients were divided into groups according to the median level of magnesium and the normal threshold value of lumbar spine BMD. RESULTS: During the median follow-up period of 36 months, 36 (10.0%) fractures occurred. The cumulative incidence rates of fractures were 17.6% and 5.2% [adjusted hazard ratio (aHR) 2.31, 95% confidence interval (CI) 1.03–5.17, P = 0.030] in the lower (<2.6 mg/dL) and higher (≥2.6 mg/dL) magnesium (Mg) groups, respectively, and 21.2% and 7.3% (aHR 2.59, 95% CI 1.09–6.16, P = 0.027) in the low- and high-BMD groups, respectively. The lower-Mg and low-BMD group had a 9.21-fold higher risk of fractures (95% CI; 2.35–47.00; P = 0.0010) than the higher-Mg and high-BMD group. Furthermore, adding both magnesium levels and lumbar spine BMD levels to the established risk factors significantly improved the prediction of fractures (C-index: 0.784 to 0.830, p = 0.041). DISCUSSION/CONCLUSIONS: The combination of serum magnesium and lumbar spine BMD can be used for fracture risk stratification and synergistically improves the prediction of fractures in CKD patients. Public Library of Science 2021-05-20 /pmc/articles/PMC8136656/ /pubmed/34014999 http://dx.doi.org/10.1371/journal.pone.0251912 Text en © 2021 Hori et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hori, Mayuko
Yasuda, Kaoru
Takahashi, Hiroshi
Yamazaki, Chikao
Morozumi, Kunio
Maruyama, Shoichi
Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title_full Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title_fullStr Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title_full_unstemmed Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title_short Impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
title_sort impact of serum magnesium and bone mineral density on systemic fractures in chronic hemodialysis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136656/
https://www.ncbi.nlm.nih.gov/pubmed/34014999
http://dx.doi.org/10.1371/journal.pone.0251912
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