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Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease

INTRODUCTION: Chronic kidney disease—mineral and bone disorders (CKD-MBD) is characterised by generalised vascular calcification (VC) and impaired bone health. We aimed to investigate the relationship between VC and bone mineral density (BMD) in CKD patients. METHODS: We performed a cross-sectional...

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Autores principales: Uhlinova, Jana, Kuudeberg, Anne, Metsküla, Kaja, Lember, Margus, Rosenberg, Mai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533531/
https://www.ncbi.nlm.nih.gov/pubmed/36199013
http://dx.doi.org/10.1186/s12882-022-02955-9
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author Uhlinova, Jana
Kuudeberg, Anne
Metsküla, Kaja
Lember, Margus
Rosenberg, Mai
author_facet Uhlinova, Jana
Kuudeberg, Anne
Metsküla, Kaja
Lember, Margus
Rosenberg, Mai
author_sort Uhlinova, Jana
collection PubMed
description INTRODUCTION: Chronic kidney disease—mineral and bone disorders (CKD-MBD) is characterised by generalised vascular calcification (VC) and impaired bone health. We aimed to investigate the relationship between VC and bone mineral density (BMD) in CKD patients. METHODS: We performed a cross-sectional study of patients with different stages of CKD. For assessment of VC of abdominal aorta lateral lumbar X-rays (Kauppila score), the ankle-brachial index (ABI) and echocardiography were used. Total body densitometry provided BMD. RESULTS: Ninety patients (41% male, median age 64 years (range 29–87)) were included, of whom 41.1% had a Kauppila score > 1. Evidence of peripheral VC as measured by ABI was detected in 23.3% of cases. Lesions of the heart valves were found in 46.7% of patients. There was a significant association between high ABI and lesions of the heart valves. In the multivariate regression model to analyse the independent determinants of abdominal aorta calcification (AAC) and ABI, the BMD of the femoral neck was identified as significant for both (p = 0.001, p = 0.001). The total spine BMD was found to be significant for AAC (p = 0.001), and the BMD of spine L1-L4 and the ribs were found to be significant for ABI (p = 0.01, p = 0.002 respectively). In factorial regression analysis, where BMD was independent determinant, valvular calcification was significant for BMD of femur, femoral neck and total BMD. Age and tALP were inversely correlated with the BMD of femur and femoral neck. CONCLUSIONS: Our work highlighted clinically important relationships between VC and bone mineral density (BMD) in CKD patients. We detected inverse relationships between AAC, high ABI and BMD. Secondly, BMD at certain bone sites (femur, femoral neck) and total BMD were associated with important lesions of heart valves. Thirdly, a significant association between a high ABI and lesions of the heart valves. We believe that the results of our study will help in the planning of future research and in current clinical practice for the early diagnosis, further monitoring and management of CKD-MBD. Additionally, these results may have treatment implications on use of different CKD-MBD medications.
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spelling pubmed-95335312022-10-06 Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease Uhlinova, Jana Kuudeberg, Anne Metsküla, Kaja Lember, Margus Rosenberg, Mai BMC Nephrol Research INTRODUCTION: Chronic kidney disease—mineral and bone disorders (CKD-MBD) is characterised by generalised vascular calcification (VC) and impaired bone health. We aimed to investigate the relationship between VC and bone mineral density (BMD) in CKD patients. METHODS: We performed a cross-sectional study of patients with different stages of CKD. For assessment of VC of abdominal aorta lateral lumbar X-rays (Kauppila score), the ankle-brachial index (ABI) and echocardiography were used. Total body densitometry provided BMD. RESULTS: Ninety patients (41% male, median age 64 years (range 29–87)) were included, of whom 41.1% had a Kauppila score > 1. Evidence of peripheral VC as measured by ABI was detected in 23.3% of cases. Lesions of the heart valves were found in 46.7% of patients. There was a significant association between high ABI and lesions of the heart valves. In the multivariate regression model to analyse the independent determinants of abdominal aorta calcification (AAC) and ABI, the BMD of the femoral neck was identified as significant for both (p = 0.001, p = 0.001). The total spine BMD was found to be significant for AAC (p = 0.001), and the BMD of spine L1-L4 and the ribs were found to be significant for ABI (p = 0.01, p = 0.002 respectively). In factorial regression analysis, where BMD was independent determinant, valvular calcification was significant for BMD of femur, femoral neck and total BMD. Age and tALP were inversely correlated with the BMD of femur and femoral neck. CONCLUSIONS: Our work highlighted clinically important relationships between VC and bone mineral density (BMD) in CKD patients. We detected inverse relationships between AAC, high ABI and BMD. Secondly, BMD at certain bone sites (femur, femoral neck) and total BMD were associated with important lesions of heart valves. Thirdly, a significant association between a high ABI and lesions of the heart valves. We believe that the results of our study will help in the planning of future research and in current clinical practice for the early diagnosis, further monitoring and management of CKD-MBD. Additionally, these results may have treatment implications on use of different CKD-MBD medications. BioMed Central 2022-10-05 /pmc/articles/PMC9533531/ /pubmed/36199013 http://dx.doi.org/10.1186/s12882-022-02955-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Uhlinova, Jana
Kuudeberg, Anne
Metsküla, Kaja
Lember, Margus
Rosenberg, Mai
Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title_full Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title_fullStr Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title_full_unstemmed Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title_short Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
title_sort significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533531/
https://www.ncbi.nlm.nih.gov/pubmed/36199013
http://dx.doi.org/10.1186/s12882-022-02955-9
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