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Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes

BACKGROUND: It is unclear whether faster progression of atherosclerosis explains the higher risk of cardiovascular events in CKD. The objectives of this study were to 1. Characterize the associations of CKD with presence and morphology of atherosclerotic plaques on carotid magnetic resonance imaging...

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Autores principales: Beddhu, Srinivasan, Boucher, Robert E., Sun, Jie, Balu, Niranjan, Chonchol, Michel, Navaneethan, Sankar, Chertow, Glenn M., Townsend, Raymond, Haley, William, Cheung, Alfred K., Conroy, Molly B., Raj, Dominic S., Xu, Dongxiang, George, Thomas, Yunis, Reem, Wei, Guo, Canton, Gador, Bates, Jeffrey, Chen, Jing, Papademetriou, Vasilios, Punzi, Henry, Wiggers, Alan, Wright, Jackson T., Greene, Tom, Yuan, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905597/
https://www.ncbi.nlm.nih.gov/pubmed/33627066
http://dx.doi.org/10.1186/s12882-021-02260-x
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author Beddhu, Srinivasan
Boucher, Robert E.
Sun, Jie
Balu, Niranjan
Chonchol, Michel
Navaneethan, Sankar
Chertow, Glenn M.
Townsend, Raymond
Haley, William
Cheung, Alfred K.
Conroy, Molly B.
Raj, Dominic S.
Xu, Dongxiang
George, Thomas
Yunis, Reem
Wei, Guo
Canton, Gador
Bates, Jeffrey
Chen, Jing
Papademetriou, Vasilios
Punzi, Henry
Wiggers, Alan
Wright, Jackson T.
Greene, Tom
Yuan, Chun
author_facet Beddhu, Srinivasan
Boucher, Robert E.
Sun, Jie
Balu, Niranjan
Chonchol, Michel
Navaneethan, Sankar
Chertow, Glenn M.
Townsend, Raymond
Haley, William
Cheung, Alfred K.
Conroy, Molly B.
Raj, Dominic S.
Xu, Dongxiang
George, Thomas
Yunis, Reem
Wei, Guo
Canton, Gador
Bates, Jeffrey
Chen, Jing
Papademetriou, Vasilios
Punzi, Henry
Wiggers, Alan
Wright, Jackson T.
Greene, Tom
Yuan, Chun
author_sort Beddhu, Srinivasan
collection PubMed
description BACKGROUND: It is unclear whether faster progression of atherosclerosis explains the higher risk of cardiovascular events in CKD. The objectives of this study were to 1. Characterize the associations of CKD with presence and morphology of atherosclerotic plaques on carotid magnetic resonance imaging (MRI) and 2. Examine the associations of baseline CKD and carotid atherosclerotic plaques with subsequent cardiovascular events. METHODS: In a subgroup (N = 465) of Systolic Blood Pressure Intervention Trial. (SPRINT) participants, we measured carotid plaque presence and morphology at baseline and after 30-months with MRI. We examined the associations of CKD (baseline eGFR < 60 ml/min/1.73m(2)) with progression of carotid plaques and the SPRINT cardiovascular endpoint. RESULTS: One hundred and ninety six (42%) participants had CKD. Baseline eGFR in the non-CKD and CKD subgroups were 77 ± 14 and 49 ± 8 ml/min/1.73 m(2), respectively. Lipid rich necrotic-core plaque was present in 137 (29.5%) participants. In 323 participants with both baseline and follow-up MRI measurements of maximum wall thickness, CKD was not associated with progression of maximum wall thickness (OR 0.62, 95% CI 0.36 to 1.07, p = 0.082). In 96 participants with necrotic core plaque at baseline and with a valid follow-up MRI, CKD was associated with lower odds of progression of necrotic core plaque (OR 0.41, 95% CI 0.17 to 0.95, p = 0.039). There were 28 cardiovascular events over 1764 person-years of follow-up. In separate Cox models, necrotic core plaque (HR 2.59, 95% CI 1.15 to 5.85) but not plaque defined by maximum wall thickness or presence of a plaque component (HR 1.79, 95% CI 0.73 to 4.43) was associated with cardiovascular events. Independent of necrotic core plaque, CKD (HR 3.35, 95% CI 1.40 to 7.99) was associated with cardiovascular events. CONCLUSIONS: Presence of necrotic core in carotid plaque rather than the presence of plaque per se was associated with increased risk of cardiovascular events. We did not find CKD to be associated with faster progression of necrotic core plaques, although both were independently associated with cardiovascular events. Thus, CKD may contribute to cardiovascular disease principally via mechanisms other than atherosclerosis such as arterial media calcification or stiffening. TRIAL REGISTRATION: NCT01475747, registered on November 21, 2011. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02260-x.
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spelling pubmed-79055972021-02-25 Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes Beddhu, Srinivasan Boucher, Robert E. Sun, Jie Balu, Niranjan Chonchol, Michel Navaneethan, Sankar Chertow, Glenn M. Townsend, Raymond Haley, William Cheung, Alfred K. Conroy, Molly B. Raj, Dominic S. Xu, Dongxiang George, Thomas Yunis, Reem Wei, Guo Canton, Gador Bates, Jeffrey Chen, Jing Papademetriou, Vasilios Punzi, Henry Wiggers, Alan Wright, Jackson T. Greene, Tom Yuan, Chun BMC Nephrol Research Article BACKGROUND: It is unclear whether faster progression of atherosclerosis explains the higher risk of cardiovascular events in CKD. The objectives of this study were to 1. Characterize the associations of CKD with presence and morphology of atherosclerotic plaques on carotid magnetic resonance imaging (MRI) and 2. Examine the associations of baseline CKD and carotid atherosclerotic plaques with subsequent cardiovascular events. METHODS: In a subgroup (N = 465) of Systolic Blood Pressure Intervention Trial. (SPRINT) participants, we measured carotid plaque presence and morphology at baseline and after 30-months with MRI. We examined the associations of CKD (baseline eGFR < 60 ml/min/1.73m(2)) with progression of carotid plaques and the SPRINT cardiovascular endpoint. RESULTS: One hundred and ninety six (42%) participants had CKD. Baseline eGFR in the non-CKD and CKD subgroups were 77 ± 14 and 49 ± 8 ml/min/1.73 m(2), respectively. Lipid rich necrotic-core plaque was present in 137 (29.5%) participants. In 323 participants with both baseline and follow-up MRI measurements of maximum wall thickness, CKD was not associated with progression of maximum wall thickness (OR 0.62, 95% CI 0.36 to 1.07, p = 0.082). In 96 participants with necrotic core plaque at baseline and with a valid follow-up MRI, CKD was associated with lower odds of progression of necrotic core plaque (OR 0.41, 95% CI 0.17 to 0.95, p = 0.039). There were 28 cardiovascular events over 1764 person-years of follow-up. In separate Cox models, necrotic core plaque (HR 2.59, 95% CI 1.15 to 5.85) but not plaque defined by maximum wall thickness or presence of a plaque component (HR 1.79, 95% CI 0.73 to 4.43) was associated with cardiovascular events. Independent of necrotic core plaque, CKD (HR 3.35, 95% CI 1.40 to 7.99) was associated with cardiovascular events. CONCLUSIONS: Presence of necrotic core in carotid plaque rather than the presence of plaque per se was associated with increased risk of cardiovascular events. We did not find CKD to be associated with faster progression of necrotic core plaques, although both were independently associated with cardiovascular events. Thus, CKD may contribute to cardiovascular disease principally via mechanisms other than atherosclerosis such as arterial media calcification or stiffening. TRIAL REGISTRATION: NCT01475747, registered on November 21, 2011. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02260-x. BioMed Central 2021-02-24 /pmc/articles/PMC7905597/ /pubmed/33627066 http://dx.doi.org/10.1186/s12882-021-02260-x Text en © The Author(s) 2021 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
Beddhu, Srinivasan
Boucher, Robert E.
Sun, Jie
Balu, Niranjan
Chonchol, Michel
Navaneethan, Sankar
Chertow, Glenn M.
Townsend, Raymond
Haley, William
Cheung, Alfred K.
Conroy, Molly B.
Raj, Dominic S.
Xu, Dongxiang
George, Thomas
Yunis, Reem
Wei, Guo
Canton, Gador
Bates, Jeffrey
Chen, Jing
Papademetriou, Vasilios
Punzi, Henry
Wiggers, Alan
Wright, Jackson T.
Greene, Tom
Yuan, Chun
Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title_full Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title_fullStr Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title_full_unstemmed Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title_short Chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
title_sort chronic kidney disease, atherosclerotic plaque characteristics on carotid magnetic resonance imaging, and cardiovascular outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905597/
https://www.ncbi.nlm.nih.gov/pubmed/33627066
http://dx.doi.org/10.1186/s12882-021-02260-x
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