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Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis

Vascular calcification (VC) is an important promoter of cardiovascular disease (CVD) in patients undergoing peritoneal dialysis (PD). Several indices can be used to evaluate VC, including the abdominal aortic calcification index (AACI) and carotid artery intima–media thickness (IMT); however, simple...

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Autores principales: Yang, Ning, Yang, Wei, Cui, Wenting, Zhou, Dan, Du, Xiangning, Li, Longkai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269073/
https://www.ncbi.nlm.nih.gov/pubmed/32406320
http://dx.doi.org/10.1080/0886022X.2020.1762646
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author Yang, Ning
Yang, Wei
Cui, Wenting
Zhou, Dan
Du, Xiangning
Li, Longkai
author_facet Yang, Ning
Yang, Wei
Cui, Wenting
Zhou, Dan
Du, Xiangning
Li, Longkai
author_sort Yang, Ning
collection PubMed
description Vascular calcification (VC) is an important promoter of cardiovascular disease (CVD) in patients undergoing peritoneal dialysis (PD). Several indices can be used to evaluate VC, including the abdominal aortic calcification index (AACI) and carotid artery intima–media thickness (IMT); however, simpler and lesser expensive predictors, such as the radial augmentation index (RAI), should be investigated. A total of 101 patients undergoing PD were recruited to measure RAI, AACI, and carotid artery IMT and perform echocardiography. Fifty healthy controls (HCs) were recruited to undergo RAI measurement. RAI in patients undergoing PD was significantly higher than the RAI in HCs (86.25%±8.39% vs. 76.05%±9.81%, p < 0.05). Patients undergoing PD and who suffer with diabetic mellitus, hypertension, and CVD had more severe VC than those without the abovementioned diseases. In patients with PD, RAI was positively correlated with AACI (r = 0.671, p < 0.05) and carotid artery IMT (r = 0.596, p < 0.05). RAI was positively correlated with left ventricular end-diastolic dimensions (LVDd; r = 0.678, p < 0.05), left ventricular mass index (r = 0.595, p < 0.05), and negatively correlated with early-diastolic mitral inflow velocity/late-diastolic mitral inflow velocity (r = −0.342, p < 0.05) and left ventricular ejection fraction (r= −0.497, p < 0.05). Multiple linear regression analysis showed that RAI was associated with AACI, LVDd, age, and serum phosphate (p < 0.05). RAI might be an effective predictor of VC and cardiac structural/functional abnormalities in patients undergoing PD.
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spelling pubmed-72690732020-06-11 Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis Yang, Ning Yang, Wei Cui, Wenting Zhou, Dan Du, Xiangning Li, Longkai Ren Fail Clinical Study Vascular calcification (VC) is an important promoter of cardiovascular disease (CVD) in patients undergoing peritoneal dialysis (PD). Several indices can be used to evaluate VC, including the abdominal aortic calcification index (AACI) and carotid artery intima–media thickness (IMT); however, simpler and lesser expensive predictors, such as the radial augmentation index (RAI), should be investigated. A total of 101 patients undergoing PD were recruited to measure RAI, AACI, and carotid artery IMT and perform echocardiography. Fifty healthy controls (HCs) were recruited to undergo RAI measurement. RAI in patients undergoing PD was significantly higher than the RAI in HCs (86.25%±8.39% vs. 76.05%±9.81%, p < 0.05). Patients undergoing PD and who suffer with diabetic mellitus, hypertension, and CVD had more severe VC than those without the abovementioned diseases. In patients with PD, RAI was positively correlated with AACI (r = 0.671, p < 0.05) and carotid artery IMT (r = 0.596, p < 0.05). RAI was positively correlated with left ventricular end-diastolic dimensions (LVDd; r = 0.678, p < 0.05), left ventricular mass index (r = 0.595, p < 0.05), and negatively correlated with early-diastolic mitral inflow velocity/late-diastolic mitral inflow velocity (r = −0.342, p < 0.05) and left ventricular ejection fraction (r= −0.497, p < 0.05). Multiple linear regression analysis showed that RAI was associated with AACI, LVDd, age, and serum phosphate (p < 0.05). RAI might be an effective predictor of VC and cardiac structural/functional abnormalities in patients undergoing PD. Taylor & Francis 2020-05-14 /pmc/articles/PMC7269073/ /pubmed/32406320 http://dx.doi.org/10.1080/0886022X.2020.1762646 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (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 Clinical Study
Yang, Ning
Yang, Wei
Cui, Wenting
Zhou, Dan
Du, Xiangning
Li, Longkai
Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title_full Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title_fullStr Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title_full_unstemmed Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title_short Radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
title_sort radial augmentation index may be an effective predictor of vascular calcification in patients on peritoneal dialysis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269073/
https://www.ncbi.nlm.nih.gov/pubmed/32406320
http://dx.doi.org/10.1080/0886022X.2020.1762646
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