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Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease

BACKGROUND: Vascular calcification (VC) is a major component of mineral bone disorders in patients with end-stage renal disease (ESRD). Bone metabolism is affected by various factors, including sex hormones. This study investigated whether there was a sex-specific relationship between VC and inciden...

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Autores principales: Nam,, Yun Jung, Hwang,, So Yeon, Kim,, Da Won, Kim,, Dongryul, Shin,, Seok Joon, Yoon, Hye Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Nephrology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530357/
https://www.ncbi.nlm.nih.gov/pubmed/32522894
http://dx.doi.org/10.23876/j.krcp.20.013
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author Nam,, Yun Jung
Hwang,, So Yeon
Kim,, Da Won
Kim,, Dongryul
Shin,, Seok Joon
Yoon, Hye Eun
author_facet Nam,, Yun Jung
Hwang,, So Yeon
Kim,, Da Won
Kim,, Dongryul
Shin,, Seok Joon
Yoon, Hye Eun
author_sort Nam,, Yun Jung
collection PubMed
description BACKGROUND: Vascular calcification (VC) is a major component of mineral bone disorders in patients with end-stage renal disease (ESRD). Bone metabolism is affected by various factors, including sex hormones. This study investigated whether there was a sex-specific relationship between VC and incident fracture in patients with ESRD. METHODS: This was a retrospective cohort study of dialysis patients from a single center. VC was assessed by the aortic calcification index (ACI) using abdominal computed tomography. Patients were grouped by sex and stratified into low or high ACI groups, according to the median ACI value. The association between ACI and incident fracture was analyzed. RESULTS: Data from 593 patients (male n = 328, median ACI, 14.57; female n = 265, median ACI, 19.44) were included. During a median follow-up of 36.7 months, 71 patients (12.0%) developed fractures. The fracture-free survival rate was significantly lower in the high ACI group versus the low ACI group, both in males (P = 0.021) and females (P = 0.001). In males, multivariate analysis showed that the high ACI group and ACI per se were not significant risks for fracture. However, in females, both the high ACI group (adjusted hazard ratio, 2.720; P = 0.003) and ACI per se (adjusted hazard ratio, 1.768; P = 0.035) were independently associated with fracture after adjustment for confounding variables. CONCLUSION: VC was independently associated with incident fracture in female patients with ESRD. There may be a sex-specific relationship between VC and fracture in patients with ESRD.
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spelling pubmed-75303572020-10-08 Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease Nam,, Yun Jung Hwang,, So Yeon Kim,, Da Won Kim,, Dongryul Shin,, Seok Joon Yoon, Hye Eun Kidney Res Clin Pract Original Article BACKGROUND: Vascular calcification (VC) is a major component of mineral bone disorders in patients with end-stage renal disease (ESRD). Bone metabolism is affected by various factors, including sex hormones. This study investigated whether there was a sex-specific relationship between VC and incident fracture in patients with ESRD. METHODS: This was a retrospective cohort study of dialysis patients from a single center. VC was assessed by the aortic calcification index (ACI) using abdominal computed tomography. Patients were grouped by sex and stratified into low or high ACI groups, according to the median ACI value. The association between ACI and incident fracture was analyzed. RESULTS: Data from 593 patients (male n = 328, median ACI, 14.57; female n = 265, median ACI, 19.44) were included. During a median follow-up of 36.7 months, 71 patients (12.0%) developed fractures. The fracture-free survival rate was significantly lower in the high ACI group versus the low ACI group, both in males (P = 0.021) and females (P = 0.001). In males, multivariate analysis showed that the high ACI group and ACI per se were not significant risks for fracture. However, in females, both the high ACI group (adjusted hazard ratio, 2.720; P = 0.003) and ACI per se (adjusted hazard ratio, 1.768; P = 0.035) were independently associated with fracture after adjustment for confounding variables. CONCLUSION: VC was independently associated with incident fracture in female patients with ESRD. There may be a sex-specific relationship between VC and fracture in patients with ESRD. Korean Society of Nephrology 2020-09-30 2020-09-30 /pmc/articles/PMC7530357/ /pubmed/32522894 http://dx.doi.org/10.23876/j.krcp.20.013 Text en Copyright © 2020 by The Korean Society of Nephrology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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
Nam,, Yun Jung
Hwang,, So Yeon
Kim,, Da Won
Kim,, Dongryul
Shin,, Seok Joon
Yoon, Hye Eun
Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title_full Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title_fullStr Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title_full_unstemmed Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title_short Sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
title_sort sex-specific relationship between vascular calcification and incident fracture in patients with end-stage renal disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530357/
https://www.ncbi.nlm.nih.gov/pubmed/32522894
http://dx.doi.org/10.23876/j.krcp.20.013
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