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Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study

BACKGROUND: Associations between subtle changes in cardiac and cerebral structure and function are not well understood, with some studies suggesting that subclinical cardiac changes may be associated with markers of vascular brain insult. METHODS AND RESULTS: Data from the ARIC (Atherosclerosis Risk...

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Autores principales: Johansen, Michelle C., Shah, Amil M., Lirette, Seth T., Griswold, Michael, Mosley, Thomas H., Solomon, Scott D., Gottesman, Rebecca F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405621/
https://www.ncbi.nlm.nih.gov/pubmed/30526268
http://dx.doi.org/10.1161/JAHA.118.008992
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author Johansen, Michelle C.
Shah, Amil M.
Lirette, Seth T.
Griswold, Michael
Mosley, Thomas H.
Solomon, Scott D.
Gottesman, Rebecca F.
author_facet Johansen, Michelle C.
Shah, Amil M.
Lirette, Seth T.
Griswold, Michael
Mosley, Thomas H.
Solomon, Scott D.
Gottesman, Rebecca F.
author_sort Johansen, Michelle C.
collection PubMed
description BACKGROUND: Associations between subtle changes in cardiac and cerebral structure and function are not well understood, with some studies suggesting that subclinical cardiac changes may be associated with markers of vascular brain insult. METHODS AND RESULTS: Data from the ARIC (Atherosclerosis Risk in Communities) Study (5th ARIC visit; 2011‐2013; N=1974) were used to explore relationships between abnormalities of cardiac structure/function and subclinical brain disease and to test specific associations between those cardiac and vascular brain changes that share a common mechanism. In adjusted models white matter hyperintensities were 0.66 cm(3) greater (95% confidence interval [CI] 0.08‐1.25) for every 1‐mm increase in left ventricular LV wall thickness and 0.64 cm(3) greater (95% CI 0.19‐1.08) for every 10 g/m(2) increase in LV mass index, both markers of LV structure. Odds of brain infarction also increased with greater LV wall thickness (odds ratio 1.11, 95% CI 1.01‐1.23 per 1 mm) and larger LV mass (odds ratio 1.08, 95% CI 1.00‐1.17 per 10 g/m(2)). Higher ejection fraction (per 5%), a marker of systolic function, was significantly associated with decreased odds of overall infarct (odds ratio 0.85, 95% CI0.77‐0.95), but not with cortical infarction (odds ratio 0.92, 95% CI0.78‐1.08). CONCLUSIONS: Among elderly participants in a large cohort study, subclinical markers of LV structure and LV systolic dysfunction were associated with increased odds of brain infarction and more white matter hyperintensities, independent of other vascular risk factors. This suggests end‐organ dysfunction occurs in the heart and brain in parallel, with further studies needed to determine causality.
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spelling pubmed-64056212019-03-19 Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study Johansen, Michelle C. Shah, Amil M. Lirette, Seth T. Griswold, Michael Mosley, Thomas H. Solomon, Scott D. Gottesman, Rebecca F. J Am Heart Assoc Original Research BACKGROUND: Associations between subtle changes in cardiac and cerebral structure and function are not well understood, with some studies suggesting that subclinical cardiac changes may be associated with markers of vascular brain insult. METHODS AND RESULTS: Data from the ARIC (Atherosclerosis Risk in Communities) Study (5th ARIC visit; 2011‐2013; N=1974) were used to explore relationships between abnormalities of cardiac structure/function and subclinical brain disease and to test specific associations between those cardiac and vascular brain changes that share a common mechanism. In adjusted models white matter hyperintensities were 0.66 cm(3) greater (95% confidence interval [CI] 0.08‐1.25) for every 1‐mm increase in left ventricular LV wall thickness and 0.64 cm(3) greater (95% CI 0.19‐1.08) for every 10 g/m(2) increase in LV mass index, both markers of LV structure. Odds of brain infarction also increased with greater LV wall thickness (odds ratio 1.11, 95% CI 1.01‐1.23 per 1 mm) and larger LV mass (odds ratio 1.08, 95% CI 1.00‐1.17 per 10 g/m(2)). Higher ejection fraction (per 5%), a marker of systolic function, was significantly associated with decreased odds of overall infarct (odds ratio 0.85, 95% CI0.77‐0.95), but not with cortical infarction (odds ratio 0.92, 95% CI0.78‐1.08). CONCLUSIONS: Among elderly participants in a large cohort study, subclinical markers of LV structure and LV systolic dysfunction were associated with increased odds of brain infarction and more white matter hyperintensities, independent of other vascular risk factors. This suggests end‐organ dysfunction occurs in the heart and brain in parallel, with further studies needed to determine causality. John Wiley and Sons Inc. 2018-12-10 /pmc/articles/PMC6405621/ /pubmed/30526268 http://dx.doi.org/10.1161/JAHA.118.008992 Text en © 2018 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
Johansen, Michelle C.
Shah, Amil M.
Lirette, Seth T.
Griswold, Michael
Mosley, Thomas H.
Solomon, Scott D.
Gottesman, Rebecca F.
Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title_full Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title_fullStr Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title_full_unstemmed Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title_short Associations of Echocardiography Markers and Vascular Brain Lesions: The ARIC Study
title_sort associations of echocardiography markers and vascular brain lesions: the aric study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405621/
https://www.ncbi.nlm.nih.gov/pubmed/30526268
http://dx.doi.org/10.1161/JAHA.118.008992
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