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Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study

BACKGROUND: Patients with chronic kidney disease (CKD) reportedly have a high prevalence of aortic valve calcification (AVC). In population-based studies, AVC is considered a manifestation of systemic atherosclerosis. The association of AVC with atherosclerotic lesions has not been fully investigate...

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Autores principales: Arita, Yui, Nakayama, Masaru, Matsukuma, Yuta, Yoshitomi, Ryota, Seki, Makiko, Fukui, Akiko, Tsuda, Susumu, Sonoda, Yuri, Imazu, Rina, Arakawa, Kimika, Tominaga, Mitsuhiro, Nakano, Toshiaki, Tsuruya, Kazuhiko, Kitazono, Takanari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260754/
https://www.ncbi.nlm.nih.gov/pubmed/32471374
http://dx.doi.org/10.1186/s12882-020-01864-z
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author Arita, Yui
Nakayama, Masaru
Matsukuma, Yuta
Yoshitomi, Ryota
Seki, Makiko
Fukui, Akiko
Tsuda, Susumu
Sonoda, Yuri
Imazu, Rina
Arakawa, Kimika
Tominaga, Mitsuhiro
Nakano, Toshiaki
Tsuruya, Kazuhiko
Kitazono, Takanari
author_facet Arita, Yui
Nakayama, Masaru
Matsukuma, Yuta
Yoshitomi, Ryota
Seki, Makiko
Fukui, Akiko
Tsuda, Susumu
Sonoda, Yuri
Imazu, Rina
Arakawa, Kimika
Tominaga, Mitsuhiro
Nakano, Toshiaki
Tsuruya, Kazuhiko
Kitazono, Takanari
author_sort Arita, Yui
collection PubMed
description BACKGROUND: Patients with chronic kidney disease (CKD) reportedly have a high prevalence of aortic valve calcification (AVC). In population-based studies, AVC is considered a manifestation of systemic atherosclerosis. The association of AVC with atherosclerotic lesions has not been fully investigated in predialysis patients. The present study was performed to determine whether carotid artery lesions and peripheral artery disease (PAD) are associated with AVC in patients with CKD not on dialysis. METHODS: In total, 749 patients were included in this cross-sectional study. AVC was evaluated using echocardiography. Carotid artery lesions including carotid artery plaque (CAP) and PAD were simultaneously examined in each patient. A logistic regression analysis was applied to determine the factors associated with AVC. RESULTS: AVC, CAP, and PAD were found in 201, 583, and 123 patients, respectively. In the multivariable analyses adjusted for covariates including the estimated glomerular filtration rate and makers of mineral metabolism (serum calcium, serum phosphorus, parathyroid hormone, 1,25-dihydroxyvitamin D, and fibroblast growth factor 23), AVC was significantly associated with the presence of CAP [odds ratio (OR), 3.37; 95% confidence interval (CI), 1.43–7.95], the presence of PAD (OR, 1.76; 95% CI, 1.10–2.81), the CAP score (per 1.0-point increase) (OR, 1.06; 95% CI, 1.02–1.11), and the ankle-brachial blood pressure index (per 0.1-point increase) (OR, 0.83; 95% CI, 0.72–0.95). CONCLUSIONS: AVC was associated with atherosclerotic lesions independent of kidney function and mineral metabolism. We consider that this association between AVC and atherosclerosis might reflect the burden of shared atherosclerotic risk factors.
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spelling pubmed-72607542020-06-07 Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study Arita, Yui Nakayama, Masaru Matsukuma, Yuta Yoshitomi, Ryota Seki, Makiko Fukui, Akiko Tsuda, Susumu Sonoda, Yuri Imazu, Rina Arakawa, Kimika Tominaga, Mitsuhiro Nakano, Toshiaki Tsuruya, Kazuhiko Kitazono, Takanari BMC Nephrol Research Article BACKGROUND: Patients with chronic kidney disease (CKD) reportedly have a high prevalence of aortic valve calcification (AVC). In population-based studies, AVC is considered a manifestation of systemic atherosclerosis. The association of AVC with atherosclerotic lesions has not been fully investigated in predialysis patients. The present study was performed to determine whether carotid artery lesions and peripheral artery disease (PAD) are associated with AVC in patients with CKD not on dialysis. METHODS: In total, 749 patients were included in this cross-sectional study. AVC was evaluated using echocardiography. Carotid artery lesions including carotid artery plaque (CAP) and PAD were simultaneously examined in each patient. A logistic regression analysis was applied to determine the factors associated with AVC. RESULTS: AVC, CAP, and PAD were found in 201, 583, and 123 patients, respectively. In the multivariable analyses adjusted for covariates including the estimated glomerular filtration rate and makers of mineral metabolism (serum calcium, serum phosphorus, parathyroid hormone, 1,25-dihydroxyvitamin D, and fibroblast growth factor 23), AVC was significantly associated with the presence of CAP [odds ratio (OR), 3.37; 95% confidence interval (CI), 1.43–7.95], the presence of PAD (OR, 1.76; 95% CI, 1.10–2.81), the CAP score (per 1.0-point increase) (OR, 1.06; 95% CI, 1.02–1.11), and the ankle-brachial blood pressure index (per 0.1-point increase) (OR, 0.83; 95% CI, 0.72–0.95). CONCLUSIONS: AVC was associated with atherosclerotic lesions independent of kidney function and mineral metabolism. We consider that this association between AVC and atherosclerosis might reflect the burden of shared atherosclerotic risk factors. BioMed Central 2020-05-29 /pmc/articles/PMC7260754/ /pubmed/32471374 http://dx.doi.org/10.1186/s12882-020-01864-z Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Arita, Yui
Nakayama, Masaru
Matsukuma, Yuta
Yoshitomi, Ryota
Seki, Makiko
Fukui, Akiko
Tsuda, Susumu
Sonoda, Yuri
Imazu, Rina
Arakawa, Kimika
Tominaga, Mitsuhiro
Nakano, Toshiaki
Tsuruya, Kazuhiko
Kitazono, Takanari
Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title_full Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title_fullStr Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title_full_unstemmed Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title_short Association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
title_sort association of aortic valve calcification with carotid artery lesions and peripheral artery disease in patients with chronic kidney disease: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260754/
https://www.ncbi.nlm.nih.gov/pubmed/32471374
http://dx.doi.org/10.1186/s12882-020-01864-z
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