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WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT

Cardiovascular disease (CVD) and frailty have been linked at the mechanistic and epidemiological levels. Our goal is to identify if subclinical markers such as atherosclerosis, body composition, and fibrofatty infiltration measured from non-contrast whole-body magnetic resonance imaging (MRI) are ma...

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Autores principales: Ambale-Venkatesh, Bharath, Sesso, Jaclyn, Walston, Jeremy, Bandeen-Roche, Karen, Lima, Joao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845055/
http://dx.doi.org/10.1093/geroni/igz038.336
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author Ambale-Venkatesh, Bharath
Sesso, Jaclyn
Walston, Jeremy
Bandeen-Roche, Karen
Lima, Joao
author_facet Ambale-Venkatesh, Bharath
Sesso, Jaclyn
Walston, Jeremy
Bandeen-Roche, Karen
Lima, Joao
author_sort Ambale-Venkatesh, Bharath
collection PubMed
description Cardiovascular disease (CVD) and frailty have been linked at the mechanistic and epidemiological levels. Our goal is to identify if subclinical markers such as atherosclerosis, body composition, and fibrofatty infiltration measured from non-contrast whole-body magnetic resonance imaging (MRI) are markers of physical frailty. Community dwelling older adults with frailty status ascertained by Fried measurement are being recruited from an aging studies registry. MRI is performed using a Canon Galan3T with dedicated coils. Preliminary analysis from 4 frail individuals (86±15 years, 3 female, BMI=22±3kg/m2) and 2 age-matched robust controls (86±1 years, 1 female, BMI=28±0.2kg/m2) is presented. Of 4 frail one had a prior heart attack; one was previously diagnosed with heart failure. Mean atheroma score from 28 vessel segments (0.42±0.26 vs 0.18±0.10) and aortic tortuosity (2.3±0.4 vs 2.1±0.1) were higher in frail compared to robust indicative of higher atherosclerotic burden and vascular stiffness. Mean subcutaneous and visceral adipose tissue volumes were lower in frail compared to robust. However, mean myocardial (1113±27 vs 1089±2), liver (729±92 vs 683±104) and skeletal muscle (1106±25 vs 1072±64) T1 times (milliseconds) were each higher indicative of greater diffuse interstitial fibrosis. Averaged intramuscular fat percent measured across the pelvis, forearm, pectus, thigh, and calf was higher in frail compared to robust (14.8±4.1% vs 8.5±2.3%) indicative of higher fatty infiltration. Although these early results do not reach statistical significance, they support further study to determine cardiovascular and tissue related differences between physically frail and robust older adults, which in turn may inform intervention developments for frailty and CVD.
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spelling pubmed-68450552019-11-18 WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT Ambale-Venkatesh, Bharath Sesso, Jaclyn Walston, Jeremy Bandeen-Roche, Karen Lima, Joao Innov Aging Session 820 (Poster) Cardiovascular disease (CVD) and frailty have been linked at the mechanistic and epidemiological levels. Our goal is to identify if subclinical markers such as atherosclerosis, body composition, and fibrofatty infiltration measured from non-contrast whole-body magnetic resonance imaging (MRI) are markers of physical frailty. Community dwelling older adults with frailty status ascertained by Fried measurement are being recruited from an aging studies registry. MRI is performed using a Canon Galan3T with dedicated coils. Preliminary analysis from 4 frail individuals (86±15 years, 3 female, BMI=22±3kg/m2) and 2 age-matched robust controls (86±1 years, 1 female, BMI=28±0.2kg/m2) is presented. Of 4 frail one had a prior heart attack; one was previously diagnosed with heart failure. Mean atheroma score from 28 vessel segments (0.42±0.26 vs 0.18±0.10) and aortic tortuosity (2.3±0.4 vs 2.1±0.1) were higher in frail compared to robust indicative of higher atherosclerotic burden and vascular stiffness. Mean subcutaneous and visceral adipose tissue volumes were lower in frail compared to robust. However, mean myocardial (1113±27 vs 1089±2), liver (729±92 vs 683±104) and skeletal muscle (1106±25 vs 1072±64) T1 times (milliseconds) were each higher indicative of greater diffuse interstitial fibrosis. Averaged intramuscular fat percent measured across the pelvis, forearm, pectus, thigh, and calf was higher in frail compared to robust (14.8±4.1% vs 8.5±2.3%) indicative of higher fatty infiltration. Although these early results do not reach statistical significance, they support further study to determine cardiovascular and tissue related differences between physically frail and robust older adults, which in turn may inform intervention developments for frailty and CVD. Oxford University Press 2019-11-08 /pmc/articles/PMC6845055/ http://dx.doi.org/10.1093/geroni/igz038.336 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Session 820 (Poster)
Ambale-Venkatesh, Bharath
Sesso, Jaclyn
Walston, Jeremy
Bandeen-Roche, Karen
Lima, Joao
WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title_full WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title_fullStr WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title_full_unstemmed WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title_short WHOLE-BODY MRI TO ASSESS SUBCLINICAL CARDIOVASCULAR DISEASE AND FRAILTY DEVELOPMENT
title_sort whole-body mri to assess subclinical cardiovascular disease and frailty development
topic Session 820 (Poster)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845055/
http://dx.doi.org/10.1093/geroni/igz038.336
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