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Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women

Hypertension is associated with development of white matter hyperintensities (WMH) in the brain, which are risk factors for mild cognitive impairment. Hormonal shifts at menopause alter vascular function putting women at risk for both hypertension and WMH. Elevations in aortic hemodynamics precede t...

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Autores principales: Barnes, Jill N., Harvey, Ronée E., Zuk, Samantha M., Lundt, Emily S., Lesnick, Timothy G., Gunter, Jeffrey L., Senjem, Matthew L., Shuster, Lynne T., Miller, Virginia M., Jack, Clifford R., Joyner, Michael J., Kantarci, Kejal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413519/
https://www.ncbi.nlm.nih.gov/pubmed/28389742
http://dx.doi.org/10.1007/s00415-017-8476-1
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author Barnes, Jill N.
Harvey, Ronée E.
Zuk, Samantha M.
Lundt, Emily S.
Lesnick, Timothy G.
Gunter, Jeffrey L.
Senjem, Matthew L.
Shuster, Lynne T.
Miller, Virginia M.
Jack, Clifford R.
Joyner, Michael J.
Kantarci, Kejal
author_facet Barnes, Jill N.
Harvey, Ronée E.
Zuk, Samantha M.
Lundt, Emily S.
Lesnick, Timothy G.
Gunter, Jeffrey L.
Senjem, Matthew L.
Shuster, Lynne T.
Miller, Virginia M.
Jack, Clifford R.
Joyner, Michael J.
Kantarci, Kejal
author_sort Barnes, Jill N.
collection PubMed
description Hypertension is associated with development of white matter hyperintensities (WMH) in the brain, which are risk factors for mild cognitive impairment. Hormonal shifts at menopause alter vascular function putting women at risk for both hypertension and WMH. Elevations in aortic hemodynamics precede the appearance of clinically defined hypertension but the relationship of aortic hemodynamics to development of WMH in women is not known. Therefore, this study aimed to characterize aortic hemodynamics in relationship to WMH in postmenopausal women. Aortic systolic and diastolic blood pressure (BP), aortic augmentation index (Alx) and aortic round trip travel time (Aortic T (R)) by tonometry were examined in 53 postmenopausal women (age 60 ± 2 years). WMH was calculated from fluid-attenuated inversion recovery MRI using a semi-automated segmentation algorithm. WMH as a fraction of total white matter volume positively associated with aortic systolic BP (regression coefficient = 0.018; p = 0.04) after adjusting for age. In addition, WMH fraction was positively associated with AIx (0.025; p = 0.04), and inversely associated with Aortic T (R) (−0.015; p = 0.04) after adjusting for age. Our results suggest that assessing aortic hemodynamics may identify individuals at risk for accelerated development of WMH and guide early treatment to reduce WMH burden and cognitive impairment in the future.
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spelling pubmed-54135192017-05-19 Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women Barnes, Jill N. Harvey, Ronée E. Zuk, Samantha M. Lundt, Emily S. Lesnick, Timothy G. Gunter, Jeffrey L. Senjem, Matthew L. Shuster, Lynne T. Miller, Virginia M. Jack, Clifford R. Joyner, Michael J. Kantarci, Kejal J Neurol Original Communication Hypertension is associated with development of white matter hyperintensities (WMH) in the brain, which are risk factors for mild cognitive impairment. Hormonal shifts at menopause alter vascular function putting women at risk for both hypertension and WMH. Elevations in aortic hemodynamics precede the appearance of clinically defined hypertension but the relationship of aortic hemodynamics to development of WMH in women is not known. Therefore, this study aimed to characterize aortic hemodynamics in relationship to WMH in postmenopausal women. Aortic systolic and diastolic blood pressure (BP), aortic augmentation index (Alx) and aortic round trip travel time (Aortic T (R)) by tonometry were examined in 53 postmenopausal women (age 60 ± 2 years). WMH was calculated from fluid-attenuated inversion recovery MRI using a semi-automated segmentation algorithm. WMH as a fraction of total white matter volume positively associated with aortic systolic BP (regression coefficient = 0.018; p = 0.04) after adjusting for age. In addition, WMH fraction was positively associated with AIx (0.025; p = 0.04), and inversely associated with Aortic T (R) (−0.015; p = 0.04) after adjusting for age. Our results suggest that assessing aortic hemodynamics may identify individuals at risk for accelerated development of WMH and guide early treatment to reduce WMH burden and cognitive impairment in the future. Springer Berlin Heidelberg 2017-04-07 2017 /pmc/articles/PMC5413519/ /pubmed/28389742 http://dx.doi.org/10.1007/s00415-017-8476-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Communication
Barnes, Jill N.
Harvey, Ronée E.
Zuk, Samantha M.
Lundt, Emily S.
Lesnick, Timothy G.
Gunter, Jeffrey L.
Senjem, Matthew L.
Shuster, Lynne T.
Miller, Virginia M.
Jack, Clifford R.
Joyner, Michael J.
Kantarci, Kejal
Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title_full Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title_fullStr Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title_full_unstemmed Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title_short Aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
title_sort aortic hemodynamics and white matter hyperintensities in normotensive postmenopausal women
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413519/
https://www.ncbi.nlm.nih.gov/pubmed/28389742
http://dx.doi.org/10.1007/s00415-017-8476-1
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