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Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?

Aging has important deleterious effects on the cardiovascular system. We sought to compare intraventricular kinetic energy (KE) in healthy subjects of varying ages with subjects with ventricular dysfunction to understand if changes in energetic momentum may predispose individuals to heart failure. F...

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Autores principales: Wong, James, Chabiniok, Radomir, deVecchi, Adelaide, Dedieu, Nathalie, Sammut, Eva, Schaeffter, Tobias, Razavi, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867343/
https://www.ncbi.nlm.nih.gov/pubmed/26747496
http://dx.doi.org/10.1152/ajpheart.00075.2015
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author Wong, James
Chabiniok, Radomir
deVecchi, Adelaide
Dedieu, Nathalie
Sammut, Eva
Schaeffter, Tobias
Razavi, Reza
author_facet Wong, James
Chabiniok, Radomir
deVecchi, Adelaide
Dedieu, Nathalie
Sammut, Eva
Schaeffter, Tobias
Razavi, Reza
author_sort Wong, James
collection PubMed
description Aging has important deleterious effects on the cardiovascular system. We sought to compare intraventricular kinetic energy (KE) in healthy subjects of varying ages with subjects with ventricular dysfunction to understand if changes in energetic momentum may predispose individuals to heart failure. Four-dimensional flow MRI was acquired in 35 healthy subjects (age: 1–67 yr) and 10 patients with left ventricular (LV) dysfunction (age: 28–79 yr). Healthy subjects were divided into age quartiles (1st quartile: <16 yr, 2nd quartile: 17–32 yr, 3rd quartile: 33–48 yr, and 4th quartile: 49–64 yr). KE was measured in the LV throughout the cardiac cycle and indexed to ventricular volume. In healthy subjects, two large peaks corresponding to systole and early diastole occurred during the cardiac cycle. A third smaller peak was seen during late diastole in eight adults. Systolic KE (P = 0.182) and ejection fraction (P = 0.921) were preserved through all age groups. Older adults showed a lower early peak diastolic KE compared with children (P < 0.0001) and young adults (P = 0.025). Subjects with LV dysfunction had reduced ejection fraction (P < 0.001) and compared with older healthy adults exhibited a similar early peak diastolic KE (P = 0.142) but with the addition of an elevated KE in diastasis (P = 0.029). In healthy individuals, peak diastolic KE progressively decreases with age, whereas systolic peaks remain constant. Peak diastolic KE in the oldest subjects is comparable to those with LV dysfunction. Unique age-related changes in ventricular diastolic energetics might be physiological or herald subclinical pathology.
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spelling pubmed-48673432016-05-24 Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation? Wong, James Chabiniok, Radomir deVecchi, Adelaide Dedieu, Nathalie Sammut, Eva Schaeffter, Tobias Razavi, Reza Am J Physiol Heart Circ Physiol Integrative Cardiovascular Physiology and Pathophysiology Aging has important deleterious effects on the cardiovascular system. We sought to compare intraventricular kinetic energy (KE) in healthy subjects of varying ages with subjects with ventricular dysfunction to understand if changes in energetic momentum may predispose individuals to heart failure. Four-dimensional flow MRI was acquired in 35 healthy subjects (age: 1–67 yr) and 10 patients with left ventricular (LV) dysfunction (age: 28–79 yr). Healthy subjects were divided into age quartiles (1st quartile: <16 yr, 2nd quartile: 17–32 yr, 3rd quartile: 33–48 yr, and 4th quartile: 49–64 yr). KE was measured in the LV throughout the cardiac cycle and indexed to ventricular volume. In healthy subjects, two large peaks corresponding to systole and early diastole occurred during the cardiac cycle. A third smaller peak was seen during late diastole in eight adults. Systolic KE (P = 0.182) and ejection fraction (P = 0.921) were preserved through all age groups. Older adults showed a lower early peak diastolic KE compared with children (P < 0.0001) and young adults (P = 0.025). Subjects with LV dysfunction had reduced ejection fraction (P < 0.001) and compared with older healthy adults exhibited a similar early peak diastolic KE (P = 0.142) but with the addition of an elevated KE in diastasis (P = 0.029). In healthy individuals, peak diastolic KE progressively decreases with age, whereas systolic peaks remain constant. Peak diastolic KE in the oldest subjects is comparable to those with LV dysfunction. Unique age-related changes in ventricular diastolic energetics might be physiological or herald subclinical pathology. American Physiological Society 2016-01-08 2016-03-15 /pmc/articles/PMC4867343/ /pubmed/26747496 http://dx.doi.org/10.1152/ajpheart.00075.2015 Text en Copyright © 2016 the American Physiological Society http://creativecommons.org/licenses/by/3.0/deed.en_US Licensed under Creative Commons Attribution CC-BY 3.0 (http://creativecommons.org/licenses/by/3.0/deed.en_US) : © the American Physiological Society.
spellingShingle Integrative Cardiovascular Physiology and Pathophysiology
Wong, James
Chabiniok, Radomir
deVecchi, Adelaide
Dedieu, Nathalie
Sammut, Eva
Schaeffter, Tobias
Razavi, Reza
Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title_full Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title_fullStr Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title_full_unstemmed Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title_short Age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
title_sort age-related changes in intraventricular kinetic energy: a physiological or pathological adaptation?
topic Integrative Cardiovascular Physiology and Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867343/
https://www.ncbi.nlm.nih.gov/pubmed/26747496
http://dx.doi.org/10.1152/ajpheart.00075.2015
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