Evidence mapPaperPMID 39910813Full record

ArticleNeuropathology : official journal of the Japanese Society of Neuropathology2025

Associations of late-life blood pressure with CERAD, Braak, and Thal: Findings from the National Alzheimer's coordinating center neuropathology dataset.

Mo-Kyung Sin, N Maritza Dowling, Jeffrey M Roseman, Ali Ahmed, Edward Zamrini

Abstract read
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Article in Neuropathology : official journal of the Japanese Society of Neuropathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mo-Kyung SinCollege of Nursing, Seattle University, Seattle, Washington, USA.ORCID https://orcid.org/0000-0001-7482-1782
N Maritza DowlingSchool of Nursing, Milken School of Public Health, George Washington University, Washington, DC, USA.
Jeffrey M RosemanSchool of Public Health, University of Alabama, Birmingham, Alabama, USA.
Ali AhmedVeterans Affairs Medical Center, George Washington University and Georgetown University, Washington, DC, USA.
Edward ZamriniIrvine Clinical Research, Irvine, California, USA.ORCID https://orcid.org/0000-0002-3685-4580

Funding

National Alzheimer's Coordinating CenterU24AG072122 · UNIVERSITY OF WASHINGTON · 2025 to 2025
$9.3M
NIA NIH HHS R03 AG070579NIA NIH HHS R03 AG072110NIA NIH HHS U24 AG072122NIH HHS R03AG070579NIH HHS R03AG072110NIH HHS U24 AG072122
6 · The paper itself

Abstract

Mid-life high blood pressure (BP) is a risk factor for Alzheimer's disease (AD). CERAD amyloid β (Aβ) plaques, Braak tau neurofibrillary tangles, and Thal Aβ plaque location are major scoring systems for quantifying neuropathological features of AD. We examined the association of late-life systolic BP (SBP) with CERAD, Braak, and Thal in the National Alzheimer's Coordinating Center (NACC) Neuropathology Dataset. Of 1978 participants with data on CERAD, 762 had scores 0-1 (none to sparse) and 1216 had 2-3 (moderate to frequent). Of 1947 with data on Braak, 411 had stages 0-II (normal to mild) and 1536 had III-VI (moderately to very severe). Of 2132 with data on Thal, 438 had phases 0-I, 428 II-III, and 1266 IV-V. Using the mean of the last four SBP before death, SBP was categorized into <120 (references), 120-139, and ≥140 mmHg. Age-sex-adjusted ORs (95% CIs) associated with SBP ≥140 mmHg for CERAD 2-3 and Braak III-VI were 1.37 (1.03, 1.83, P = 0.03) and 1.26 (0.89, 1.78, P = 0.20), respectively. Similar association was observed for Thal II-III and IV-V. These associations essentially remained unchanged after additional adjustment for APOE and Lewy Body pathology. These findings suggest that higher late-life SBP is associated with markers of presence and severity of neuropathological features of AD. Further studies with larger sample sizes are necessary to confirm the findings.

Indexed as

Alzheimer DiseaseBlood PressureBrainHypertensionNeurofibrillary TanglesPlaque, AmyloidAgedAged, 80 and overFemaleHumansMaleMiddle AgedAlzheimer's diseaseBraakCERADlate‐life blood pressureThal

Identifiers

PMID39910813
PMCPMC12279460

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.