Cargando…
Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions
Cerebral small-vessel damage manifests as white matter hyperintensities and cerebral atrophy on brain MRI and is associated with aging, cognitive decline and dementia. We sought to examine the interrelationship of these imaging biomarkers and the influence of hypertension in older individuals. We us...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430031/ https://www.ncbi.nlm.nih.gov/pubmed/28555103 http://dx.doi.org/10.3389/fnagi.2017.00132 |
_version_ | 1783236146749243392 |
---|---|
author | Kern, Kyle C. Wright, Clinton B. Bergfield, Kaitlin L. Fitzhugh, Megan C. Chen, Kewei Moeller, James R. Nabizadeh, Nooshin Elkind, Mitchell S. V. Sacco, Ralph L. Stern, Yaakov DeCarli, Charles S. Alexander, Gene E. |
author_facet | Kern, Kyle C. Wright, Clinton B. Bergfield, Kaitlin L. Fitzhugh, Megan C. Chen, Kewei Moeller, James R. Nabizadeh, Nooshin Elkind, Mitchell S. V. Sacco, Ralph L. Stern, Yaakov DeCarli, Charles S. Alexander, Gene E. |
author_sort | Kern, Kyle C. |
collection | PubMed |
description | Cerebral small-vessel damage manifests as white matter hyperintensities and cerebral atrophy on brain MRI and is associated with aging, cognitive decline and dementia. We sought to examine the interrelationship of these imaging biomarkers and the influence of hypertension in older individuals. We used a multivariate spatial covariance neuroimaging technique to localize the effects of white matter lesion load on regional gray matter volume and assessed the role of blood pressure control, age and education on this relationship. Using a case-control design matching for age, gender, and educational attainment we selected 64 participants with normal blood pressure, controlled hypertension or uncontrolled hypertension from the Northern Manhattan Study cohort. We applied gray matter voxel-based morphometry with the scaled subprofile model to (1) identify regional covariance patterns of gray matter volume differences associated with white matter lesion load, (2) compare this relationship across blood pressure groups, and (3) relate it to cognitive performance. In this group of participants aged 60–86 years, we identified a pattern of reduced gray matter volume associated with white matter lesion load in bilateral temporal-parietal regions with relative preservation of volume in the basal forebrain, thalami and cingulate cortex. This pattern was expressed most in the uncontrolled hypertension group and least in the normotensives, but was also more evident in older and more educated individuals. Expression of this pattern was associated with worse performance in executive function and memory. In summary, white matter lesions from small-vessel disease are associated with a regional pattern of gray matter atrophy that is mitigated by blood pressure control, exacerbated by aging, and associated with cognitive performance. |
format | Online Article Text |
id | pubmed-5430031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54300312017-05-29 Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions Kern, Kyle C. Wright, Clinton B. Bergfield, Kaitlin L. Fitzhugh, Megan C. Chen, Kewei Moeller, James R. Nabizadeh, Nooshin Elkind, Mitchell S. V. Sacco, Ralph L. Stern, Yaakov DeCarli, Charles S. Alexander, Gene E. Front Aging Neurosci Neuroscience Cerebral small-vessel damage manifests as white matter hyperintensities and cerebral atrophy on brain MRI and is associated with aging, cognitive decline and dementia. We sought to examine the interrelationship of these imaging biomarkers and the influence of hypertension in older individuals. We used a multivariate spatial covariance neuroimaging technique to localize the effects of white matter lesion load on regional gray matter volume and assessed the role of blood pressure control, age and education on this relationship. Using a case-control design matching for age, gender, and educational attainment we selected 64 participants with normal blood pressure, controlled hypertension or uncontrolled hypertension from the Northern Manhattan Study cohort. We applied gray matter voxel-based morphometry with the scaled subprofile model to (1) identify regional covariance patterns of gray matter volume differences associated with white matter lesion load, (2) compare this relationship across blood pressure groups, and (3) relate it to cognitive performance. In this group of participants aged 60–86 years, we identified a pattern of reduced gray matter volume associated with white matter lesion load in bilateral temporal-parietal regions with relative preservation of volume in the basal forebrain, thalami and cingulate cortex. This pattern was expressed most in the uncontrolled hypertension group and least in the normotensives, but was also more evident in older and more educated individuals. Expression of this pattern was associated with worse performance in executive function and memory. In summary, white matter lesions from small-vessel disease are associated with a regional pattern of gray matter atrophy that is mitigated by blood pressure control, exacerbated by aging, and associated with cognitive performance. Frontiers Media S.A. 2017-05-15 /pmc/articles/PMC5430031/ /pubmed/28555103 http://dx.doi.org/10.3389/fnagi.2017.00132 Text en Copyright © 2017 Kern, Wright, Bergfield, Fitzhugh, Chen, Moeller, Nabizadeh, Elkind, Sacco, Stern, DeCarli and Alexander. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kern, Kyle C. Wright, Clinton B. Bergfield, Kaitlin L. Fitzhugh, Megan C. Chen, Kewei Moeller, James R. Nabizadeh, Nooshin Elkind, Mitchell S. V. Sacco, Ralph L. Stern, Yaakov DeCarli, Charles S. Alexander, Gene E. Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title | Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title_full | Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title_fullStr | Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title_full_unstemmed | Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title_short | Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions |
title_sort | blood pressure control in aging predicts cerebral atrophy related to small-vessel white matter lesions |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430031/ https://www.ncbi.nlm.nih.gov/pubmed/28555103 http://dx.doi.org/10.3389/fnagi.2017.00132 |
work_keys_str_mv | AT kernkylec bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT wrightclintonb bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT bergfieldkaitlinl bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT fitzhughmeganc bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT chenkewei bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT moellerjamesr bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT nabizadehnooshin bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT elkindmitchellsv bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT saccoralphl bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT sternyaakov bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT decarlicharless bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions AT alexandergenee bloodpressurecontrolinagingpredictscerebralatrophyrelatedtosmallvesselwhitematterlesions |