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Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort

BACKGROUND: Soluble CD14 (sCD14), a circulating pattern recognition receptor, has been suggested as a cardiovascular disease risk factor. Prospective studies evaluating sCD14 with incident cardiovascular disease events are limited, particularly among racially diverse populations. METHODS AND RESULTS...

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Autores principales: Olson, Nels C., Koh, Insu, Reiner, Alex P., Judd, Suzanne E., Irvin, Marguerite R., Howard, George, Zakai, Neil A., Cushman, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335508/
https://www.ncbi.nlm.nih.gov/pubmed/32157955
http://dx.doi.org/10.1161/JAHA.119.014241
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author Olson, Nels C.
Koh, Insu
Reiner, Alex P.
Judd, Suzanne E.
Irvin, Marguerite R.
Howard, George
Zakai, Neil A.
Cushman, Mary
author_facet Olson, Nels C.
Koh, Insu
Reiner, Alex P.
Judd, Suzanne E.
Irvin, Marguerite R.
Howard, George
Zakai, Neil A.
Cushman, Mary
author_sort Olson, Nels C.
collection PubMed
description BACKGROUND: Soluble CD14 (sCD14), a circulating pattern recognition receptor, has been suggested as a cardiovascular disease risk factor. Prospective studies evaluating sCD14 with incident cardiovascular disease events are limited, particularly among racially diverse populations. METHODS AND RESULTS: Between 2003 and 2007, the REGARDS (Reasons for Geographic and Racial Differences in Stroke) study recruited 30 239 black and white participants across the United States. In a nested case–cohort study, sCD14 was measured in baseline serum from 548 cases of incident ischemic stroke, 612 cases of incident coronary heart disease (CHD), and a cohort random sample (n=1039). Cox models estimated hazards ratios (HR) of incident ischemic stroke or CHD per 1 SD higher sCD14, adjusting for cardiovascular disease risk factors. There was a differential association of sCD14 with ischemic stroke and CHD risk by race. Among blacks, the adjusted HR of stroke per SD increment of sCD14 was 1.42 (95% CI: 1.12, 1.80), with no association among whites (HR 1.02 [95% CI: 0.82, 1.27]). Higher sCD14 was associated with increased CHD risk in blacks but not whites, and relationships between sCD14 and CHD were stronger at younger ages. Adjusted for risk factors, the HR of CHD per SD higher sCD14 among blacks at age 45 years was 2.30 (95% CI: 1.45, 3.65) compared with 1.56 (95% CI: 0.94, 2.57) among whites. At age 65 years, the CHD HR was 1.51 (95% CI: 1.20, 1.91) among blacks and 1.02 (95% CI: 0.80, 1.31) among whites. CONCLUSIONS: sCD14 may be a race‐specific stroke and CHD risk marker.
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spelling pubmed-73355082020-07-08 Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort Olson, Nels C. Koh, Insu Reiner, Alex P. Judd, Suzanne E. Irvin, Marguerite R. Howard, George Zakai, Neil A. Cushman, Mary J Am Heart Assoc Original Research BACKGROUND: Soluble CD14 (sCD14), a circulating pattern recognition receptor, has been suggested as a cardiovascular disease risk factor. Prospective studies evaluating sCD14 with incident cardiovascular disease events are limited, particularly among racially diverse populations. METHODS AND RESULTS: Between 2003 and 2007, the REGARDS (Reasons for Geographic and Racial Differences in Stroke) study recruited 30 239 black and white participants across the United States. In a nested case–cohort study, sCD14 was measured in baseline serum from 548 cases of incident ischemic stroke, 612 cases of incident coronary heart disease (CHD), and a cohort random sample (n=1039). Cox models estimated hazards ratios (HR) of incident ischemic stroke or CHD per 1 SD higher sCD14, adjusting for cardiovascular disease risk factors. There was a differential association of sCD14 with ischemic stroke and CHD risk by race. Among blacks, the adjusted HR of stroke per SD increment of sCD14 was 1.42 (95% CI: 1.12, 1.80), with no association among whites (HR 1.02 [95% CI: 0.82, 1.27]). Higher sCD14 was associated with increased CHD risk in blacks but not whites, and relationships between sCD14 and CHD were stronger at younger ages. Adjusted for risk factors, the HR of CHD per SD higher sCD14 among blacks at age 45 years was 2.30 (95% CI: 1.45, 3.65) compared with 1.56 (95% CI: 0.94, 2.57) among whites. At age 65 years, the CHD HR was 1.51 (95% CI: 1.20, 1.91) among blacks and 1.02 (95% CI: 0.80, 1.31) among whites. CONCLUSIONS: sCD14 may be a race‐specific stroke and CHD risk marker. John Wiley and Sons Inc. 2020-03-11 /pmc/articles/PMC7335508/ /pubmed/32157955 http://dx.doi.org/10.1161/JAHA.119.014241 Text en © 2020 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Olson, Nels C.
Koh, Insu
Reiner, Alex P.
Judd, Suzanne E.
Irvin, Marguerite R.
Howard, George
Zakai, Neil A.
Cushman, Mary
Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title_full Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title_fullStr Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title_full_unstemmed Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title_short Soluble CD14, Ischemic Stroke, and Coronary Heart Disease Risk in a Prospective Study: The REGARDS Cohort
title_sort soluble cd14, ischemic stroke, and coronary heart disease risk in a prospective study: the regards cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7335508/
https://www.ncbi.nlm.nih.gov/pubmed/32157955
http://dx.doi.org/10.1161/JAHA.119.014241
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