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Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification

BACKGROUND: Rheumatic diseases are related to both abnormal bone turnover and atherogenesis, but a mechanistic link was missing. METHODS AND RESULTS: We investigated the effect of cumulative rheumatic inflammation (CRI) on risk of coronary calcification in a retrospective cohort of 145 rheumatoid ar...

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Autores principales: Chan, Yap‐Hang, Ngai, Michael Cheong, Chen, Yan, Wu, Mei‐Zhen, Yu, Yu‐Juan, Zhen, Zhe, Lai, Kevin, Cheung, Tommy, Ho, Lai‐Ming, Chung, Ho‐Yin, Lau, Chak‐Sing, Tse, Hung‐Fat, Yiu, Kai‐Hang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585350/
https://www.ncbi.nlm.nih.gov/pubmed/31130038
http://dx.doi.org/10.1161/JAHA.118.011540
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author Chan, Yap‐Hang
Ngai, Michael Cheong
Chen, Yan
Wu, Mei‐Zhen
Yu, Yu‐Juan
Zhen, Zhe
Lai, Kevin
Cheung, Tommy
Ho, Lai‐Ming
Chung, Ho‐Yin
Lau, Chak‐Sing
Tse, Hung‐Fat
Yiu, Kai‐Hang
author_facet Chan, Yap‐Hang
Ngai, Michael Cheong
Chen, Yan
Wu, Mei‐Zhen
Yu, Yu‐Juan
Zhen, Zhe
Lai, Kevin
Cheung, Tommy
Ho, Lai‐Ming
Chung, Ho‐Yin
Lau, Chak‐Sing
Tse, Hung‐Fat
Yiu, Kai‐Hang
author_sort Chan, Yap‐Hang
collection PubMed
description BACKGROUND: Rheumatic diseases are related to both abnormal bone turnover and atherogenesis, but a mechanistic link was missing. METHODS AND RESULTS: We investigated the effect of cumulative rheumatic inflammation (CRI) on risk of coronary calcification in a retrospective cohort of 145 rheumatoid arthritis patients. A time‐adjusted aggregate CRI score was derived by conglomerating all quarterly biomarker encounters of serum C‐reactive protein over 60 months immediately preceding computed tomography coronary angiography. Flow cytometry was performed to measure the osteocalcin‐positive (OCN (+)) CD34(+) KDR (+) and OCN (+) CD34(+) circulating endothelial progenitor cells (EPCs). Conventional early circulating EPCs CD34(+) CD133(+) KDR (+) was determined. Coronary calcification was defined as any Agatston score >0. 50% of patients (n=72/145) had coronary calcification. CRI score was associated with presence of coronary calcification (P=0.004) (multivariable‐adjusted: highest versus lowest quartile: odds ratio=5.6 [95% CI 1.1–28.9], P=0.041). Receiver operating characteristics curve revealed divergent behavior of OCN‐expressing circulating EPCs (OCN (+) CD34(+) EPCs: area under the curve=0.60, P=0.034; OCN (+) CD34(+) KDR (+) EPCs: area under the curve=0.59, P=0.053, positive predictors) versus conventional early EPCs (CD34(+) CD133(+) KDR (+): area under the curve=0.60, P=0.034, negative predictor) for coronary calcification, which persisted after multivariable adjustments (OCN (+) CD34(+) KDR (+) [>75th percentile]: odds ratio=7.2 [95% CI 1.8–27.9], P=0.005; OCN (+) CD34(+) EPCs [>75th percentile]: odds ratio=6.0 [95% CI 1.5–23.3], P=0.010; CD34(+) CD133(+) KDR (+) [>75th percentile: odds ratio=0.3 [95% CI 0.1–1.0], P=0.053). Intriguingly, the CRI score was associated with increased OCN (+) CD34(+) EPCs (highest versus lowest quartile: B=+25.6 [95% CI 0.8–50.5] [×10(3)/mL peripheral blood], P=0.043), but reduced CD34(+) CD133(+) KDR (+) EPCs (highest versus lowest quartile: B=−16.2 [95% CI −31.5 to −0.9], P=0.038). CONCLUSIONS: Preceding 60 months of CRI is associated with increased risk of coronary calcification and altered OCN expression in circulating EPCs.
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spelling pubmed-65853502019-06-27 Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification Chan, Yap‐Hang Ngai, Michael Cheong Chen, Yan Wu, Mei‐Zhen Yu, Yu‐Juan Zhen, Zhe Lai, Kevin Cheung, Tommy Ho, Lai‐Ming Chung, Ho‐Yin Lau, Chak‐Sing Tse, Hung‐Fat Yiu, Kai‐Hang J Am Heart Assoc Original Research BACKGROUND: Rheumatic diseases are related to both abnormal bone turnover and atherogenesis, but a mechanistic link was missing. METHODS AND RESULTS: We investigated the effect of cumulative rheumatic inflammation (CRI) on risk of coronary calcification in a retrospective cohort of 145 rheumatoid arthritis patients. A time‐adjusted aggregate CRI score was derived by conglomerating all quarterly biomarker encounters of serum C‐reactive protein over 60 months immediately preceding computed tomography coronary angiography. Flow cytometry was performed to measure the osteocalcin‐positive (OCN (+)) CD34(+) KDR (+) and OCN (+) CD34(+) circulating endothelial progenitor cells (EPCs). Conventional early circulating EPCs CD34(+) CD133(+) KDR (+) was determined. Coronary calcification was defined as any Agatston score >0. 50% of patients (n=72/145) had coronary calcification. CRI score was associated with presence of coronary calcification (P=0.004) (multivariable‐adjusted: highest versus lowest quartile: odds ratio=5.6 [95% CI 1.1–28.9], P=0.041). Receiver operating characteristics curve revealed divergent behavior of OCN‐expressing circulating EPCs (OCN (+) CD34(+) EPCs: area under the curve=0.60, P=0.034; OCN (+) CD34(+) KDR (+) EPCs: area under the curve=0.59, P=0.053, positive predictors) versus conventional early EPCs (CD34(+) CD133(+) KDR (+): area under the curve=0.60, P=0.034, negative predictor) for coronary calcification, which persisted after multivariable adjustments (OCN (+) CD34(+) KDR (+) [>75th percentile]: odds ratio=7.2 [95% CI 1.8–27.9], P=0.005; OCN (+) CD34(+) EPCs [>75th percentile]: odds ratio=6.0 [95% CI 1.5–23.3], P=0.010; CD34(+) CD133(+) KDR (+) [>75th percentile: odds ratio=0.3 [95% CI 0.1–1.0], P=0.053). Intriguingly, the CRI score was associated with increased OCN (+) CD34(+) EPCs (highest versus lowest quartile: B=+25.6 [95% CI 0.8–50.5] [×10(3)/mL peripheral blood], P=0.043), but reduced CD34(+) CD133(+) KDR (+) EPCs (highest versus lowest quartile: B=−16.2 [95% CI −31.5 to −0.9], P=0.038). CONCLUSIONS: Preceding 60 months of CRI is associated with increased risk of coronary calcification and altered OCN expression in circulating EPCs. John Wiley and Sons Inc. 2019-05-25 /pmc/articles/PMC6585350/ /pubmed/31130038 http://dx.doi.org/10.1161/JAHA.118.011540 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Chan, Yap‐Hang
Ngai, Michael Cheong
Chen, Yan
Wu, Mei‐Zhen
Yu, Yu‐Juan
Zhen, Zhe
Lai, Kevin
Cheung, Tommy
Ho, Lai‐Ming
Chung, Ho‐Yin
Lau, Chak‐Sing
Tse, Hung‐Fat
Yiu, Kai‐Hang
Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title_full Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title_fullStr Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title_full_unstemmed Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title_short Cumulative Rheumatic Inflammation Modulates the Bone–Vascular Axis and Risk of Coronary Calcification
title_sort cumulative rheumatic inflammation modulates the bone–vascular axis and risk of coronary calcification
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585350/
https://www.ncbi.nlm.nih.gov/pubmed/31130038
http://dx.doi.org/10.1161/JAHA.118.011540
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