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Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study
BACKGROUND: Central arterial stiffening and increased pulsatility, with consequent cerebral hypoperfusion, may result in structural brain damage and cognitive impairment. METHODS AND RESULTS: We analyzed a cross‐sectional sample of ARIC‐NCS (Atherosclerosis Risk in Communities–Neurocognitive Study)...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497348/ https://www.ncbi.nlm.nih.gov/pubmed/30646799 http://dx.doi.org/10.1161/JAHA.118.011045 |
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author | Palta, Priya Sharrett, A. Richey Wei, Jingkai Meyer, Michelle L. Kucharska‐Newton, Anna Power, Melinda C. Deal, Jennifer A. Jack, Clifford R. Knopman, David Wright, Jacqueline Griswold, Michael Tanaka, Hirofumi Mosley, Thomas H. Heiss, Gerardo |
author_facet | Palta, Priya Sharrett, A. Richey Wei, Jingkai Meyer, Michelle L. Kucharska‐Newton, Anna Power, Melinda C. Deal, Jennifer A. Jack, Clifford R. Knopman, David Wright, Jacqueline Griswold, Michael Tanaka, Hirofumi Mosley, Thomas H. Heiss, Gerardo |
author_sort | Palta, Priya |
collection | PubMed |
description | BACKGROUND: Central arterial stiffening and increased pulsatility, with consequent cerebral hypoperfusion, may result in structural brain damage and cognitive impairment. METHODS AND RESULTS: We analyzed a cross‐sectional sample of ARIC‐NCS (Atherosclerosis Risk in Communities–Neurocognitive Study) participants (aged 67–90 years, 60% women) with measures of cognition (n=3703) and brain magnetic resonance imaging (n=1255). Central arterial hemodynamics were assessed as carotid‐femoral pulse wave velocity and pressure pulsatility (central pulse pressure). We derived factor scores for cognitive domains. Brain magnetic resonance imaging using 3‐Tesla scanners quantified lacunar infarcts; cerebral microbleeds; and volumes of white matter hyperintensities, total brain, and the Alzheimer disease signature region. We used logistic regression, adjusted for demographics, apolipoprotein E ɛ4, heart rate, mean arterial pressure, and select cardiovascular risk factors, to estimate the odds of lacunar infarcts or cerebral microbleeds. Linear regression, additionally adjusted for intracranial volume, estimated the difference in log‐transformed volumes of white matter hyperintensities, total brain, and the Alzheimer disease signature region. We estimated the mean difference in cognitive factor scores across quartiles of carotid‐femoral pulse wave velocity or central pulse pressure using linear regression. Compared with participants in the lowest carotid‐femoral pulse wave velocity quartile, participants in the highest quartile of carotid‐femoral pulse wave velocity had a greater burden of white matter hyperintensities (P=0.007 for trend), smaller total brain volumes (−18.30 cm(3); 95% CI, −27.54 to −9.07 cm(3)), and smaller Alzheimer disease signature region volumes (−1.48 cm(3); 95% CI, −2.27 to −0.68 cm(3)). These participants also had lower scores in executive function/processing speed (β=−0.04 z score; 95% CI, −0.07 to −0.01 z score) and general cognition (β=−0.09 z score; 95% CI, −0.15 to −0.03 z score). Similar results were observed for central pulse pressure. CONCLUSIONS: Central arterial hemodynamics were associated with structural brain damage and poorer cognitive performance among older adults. |
format | Online Article Text |
id | pubmed-6497348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64973482019-05-07 Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study Palta, Priya Sharrett, A. Richey Wei, Jingkai Meyer, Michelle L. Kucharska‐Newton, Anna Power, Melinda C. Deal, Jennifer A. Jack, Clifford R. Knopman, David Wright, Jacqueline Griswold, Michael Tanaka, Hirofumi Mosley, Thomas H. Heiss, Gerardo J Am Heart Assoc Original Research BACKGROUND: Central arterial stiffening and increased pulsatility, with consequent cerebral hypoperfusion, may result in structural brain damage and cognitive impairment. METHODS AND RESULTS: We analyzed a cross‐sectional sample of ARIC‐NCS (Atherosclerosis Risk in Communities–Neurocognitive Study) participants (aged 67–90 years, 60% women) with measures of cognition (n=3703) and brain magnetic resonance imaging (n=1255). Central arterial hemodynamics were assessed as carotid‐femoral pulse wave velocity and pressure pulsatility (central pulse pressure). We derived factor scores for cognitive domains. Brain magnetic resonance imaging using 3‐Tesla scanners quantified lacunar infarcts; cerebral microbleeds; and volumes of white matter hyperintensities, total brain, and the Alzheimer disease signature region. We used logistic regression, adjusted for demographics, apolipoprotein E ɛ4, heart rate, mean arterial pressure, and select cardiovascular risk factors, to estimate the odds of lacunar infarcts or cerebral microbleeds. Linear regression, additionally adjusted for intracranial volume, estimated the difference in log‐transformed volumes of white matter hyperintensities, total brain, and the Alzheimer disease signature region. We estimated the mean difference in cognitive factor scores across quartiles of carotid‐femoral pulse wave velocity or central pulse pressure using linear regression. Compared with participants in the lowest carotid‐femoral pulse wave velocity quartile, participants in the highest quartile of carotid‐femoral pulse wave velocity had a greater burden of white matter hyperintensities (P=0.007 for trend), smaller total brain volumes (−18.30 cm(3); 95% CI, −27.54 to −9.07 cm(3)), and smaller Alzheimer disease signature region volumes (−1.48 cm(3); 95% CI, −2.27 to −0.68 cm(3)). These participants also had lower scores in executive function/processing speed (β=−0.04 z score; 95% CI, −0.07 to −0.01 z score) and general cognition (β=−0.09 z score; 95% CI, −0.15 to −0.03 z score). Similar results were observed for central pulse pressure. CONCLUSIONS: Central arterial hemodynamics were associated with structural brain damage and poorer cognitive performance among older adults. John Wiley and Sons Inc. 2019-01-16 /pmc/articles/PMC6497348/ /pubmed/30646799 http://dx.doi.org/10.1161/JAHA.118.011045 Text en © 2019 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-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Palta, Priya Sharrett, A. Richey Wei, Jingkai Meyer, Michelle L. Kucharska‐Newton, Anna Power, Melinda C. Deal, Jennifer A. Jack, Clifford R. Knopman, David Wright, Jacqueline Griswold, Michael Tanaka, Hirofumi Mosley, Thomas H. Heiss, Gerardo Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title | Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title_full | Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title_fullStr | Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title_full_unstemmed | Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title_short | Central Arterial Stiffness Is Associated With Structural Brain Damage and Poorer Cognitive Performance: The ARIC Study |
title_sort | central arterial stiffness is associated with structural brain damage and poorer cognitive performance: the aric study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497348/ https://www.ncbi.nlm.nih.gov/pubmed/30646799 http://dx.doi.org/10.1161/JAHA.118.011045 |
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