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High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis

BACKGROUND: Research of hypertension‐related risk factors for Alzheimer's disease has typically focused on blood pressure (BP) levels, despite evidence that high blood pressure variability (BPV) over time may predict poorer cardiovascular, neuropathological, and neurocognitive outcomes. We eval...

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Autores principales: Daniel, George D., Chen, Haiying, Bertoni, Alain G., Hughes, Timothy M., Hayden, Kathleen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310191/
https://www.ncbi.nlm.nih.gov/pubmed/35898668
http://dx.doi.org/10.1002/trc2.12342
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author Daniel, George D.
Chen, Haiying
Bertoni, Alain G.
Hughes, Timothy M.
Hayden, Kathleen M.
author_facet Daniel, George D.
Chen, Haiying
Bertoni, Alain G.
Hughes, Timothy M.
Hayden, Kathleen M.
author_sort Daniel, George D.
collection PubMed
description BACKGROUND: Research of hypertension‐related risk factors for Alzheimer's disease has typically focused on blood pressure (BP) levels, despite evidence that high blood pressure variability (BPV) over time may predict poorer cardiovascular, neuropathological, and neurocognitive outcomes. We evaluated associations between BPV and cognitive function in the Multi‐Ethnic Study of Atherosclerosis (MESA). METHODS: Multivariable linear and logistic regression analyses of BP data across six examinations were used to determine associations that BPV (average real variability [ARV], variability independent of the mean [VIM]) and group‐based latent BP trajectories have with cognitive function, decline, and impairment, measured by the Cognitive Abilities Screening Instrument (CASI), Digit Symbol Coding (DSC), and Digit Span tests. RESULTS: Participants (N = 1314; mean baseline age = 57) were 50% female, and 48% White. Higher systolic (β = −0.06, 95% confidence interval [CI]: −0.12, −0.0001) and diastolic (β = −0.08, 95% CI: −0.14, −0.02) ARV predicted increased global cognitive decline after covariate adjustment. Stronger relationships between BPV and global cognition were in older, White and Black participants, apolipoprotein E (APOE) ε4 non‐carriers, male participants, and non‐antihypertensive medication users. CONCLUSION: Results suggest that higher systolic and diastolic BPV is an independent risk factor for cognitive dysfunction and decline in this multi‐ethnic cohort. This relationship differs across demographic and clinical characteristics.
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spelling pubmed-93101912022-07-26 High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis Daniel, George D. Chen, Haiying Bertoni, Alain G. Hughes, Timothy M. Hayden, Kathleen M. Alzheimers Dement (N Y) Research Articles BACKGROUND: Research of hypertension‐related risk factors for Alzheimer's disease has typically focused on blood pressure (BP) levels, despite evidence that high blood pressure variability (BPV) over time may predict poorer cardiovascular, neuropathological, and neurocognitive outcomes. We evaluated associations between BPV and cognitive function in the Multi‐Ethnic Study of Atherosclerosis (MESA). METHODS: Multivariable linear and logistic regression analyses of BP data across six examinations were used to determine associations that BPV (average real variability [ARV], variability independent of the mean [VIM]) and group‐based latent BP trajectories have with cognitive function, decline, and impairment, measured by the Cognitive Abilities Screening Instrument (CASI), Digit Symbol Coding (DSC), and Digit Span tests. RESULTS: Participants (N = 1314; mean baseline age = 57) were 50% female, and 48% White. Higher systolic (β = −0.06, 95% confidence interval [CI]: −0.12, −0.0001) and diastolic (β = −0.08, 95% CI: −0.14, −0.02) ARV predicted increased global cognitive decline after covariate adjustment. Stronger relationships between BPV and global cognition were in older, White and Black participants, apolipoprotein E (APOE) ε4 non‐carriers, male participants, and non‐antihypertensive medication users. CONCLUSION: Results suggest that higher systolic and diastolic BPV is an independent risk factor for cognitive dysfunction and decline in this multi‐ethnic cohort. This relationship differs across demographic and clinical characteristics. John Wiley and Sons Inc. 2022-07-25 /pmc/articles/PMC9310191/ /pubmed/35898668 http://dx.doi.org/10.1002/trc2.12342 Text en © 2022 The Authors. Alzheimer's & Dementia: Translational Research & Clinical Interventions published by Wiley Periodicals LLC on behalf of Alzheimer's Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Daniel, George D.
Chen, Haiying
Bertoni, Alain G.
Hughes, Timothy M.
Hayden, Kathleen M.
High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title_full High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title_fullStr High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title_full_unstemmed High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title_short High visit‐to‐visit blood pressure variability predicts global cognitive decline: The Multi‐Ethnic Study of Atherosclerosis
title_sort high visit‐to‐visit blood pressure variability predicts global cognitive decline: the multi‐ethnic study of atherosclerosis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310191/
https://www.ncbi.nlm.nih.gov/pubmed/35898668
http://dx.doi.org/10.1002/trc2.12342
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