Evidence map›Paper›PMID 41942821›Full record

ArticleActa neuropathologica2026

Contribution of health history and neuropathologic changes to the likelihood of dementia in those with intermediate/high Alzheimer's pathology: findings from The 90 + Study.

Zarui A Melikyan, Zeinah Al-Darsani, Luohua Jiang, Katherine A Colcord, Annlia Paganini-Hill, Syed A Bukhari, Thomas J Montine, Claudia H Kawas, María M Corrada

Abstract read
In one paragraph

Article in Acta neuropathologica, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zarui A Melikyan *Department of Neurobiology and Behavior, University of California, 1400 Bio Sci III, Irvine, CA, 92697, USA. zmelikya@uci.edu.
Zeinah Al-Darsani *Department of Epidemiology and Biostatistics, Temple University College of Public Health, 1210 W. Berks Street, 3Rd Floor Paley Hall, Philadelphia, PA, 19122, USA.
Luohua JiangDepartment of Epidemiology and Biostatistics, University of California, 856 Health Sciences Road, Suite 3400, Irvine, CA, 92617, USA.
Katherine A ColcordDepartment of Epidemiology and Biostatistics, University of California, 856 Health Sciences Road, Suite 3400, Irvine, CA, 92617, USA.
Annlia Paganini-HillBeckman Laser Institute & Medical Clinic, University of California, 1002 Health Sciences Rd, Irvine, CA, 92612, USA.
Syed A BukhariDepartment of Pathology, Stanford University School of Medicine, Lane Building300 Pasteur Drive, Stanford, CA, L23594305, USA.
Thomas J MontineDepartment of Pathology, Stanford University School of Medicine, Lane Building300 Pasteur Drive, Stanford, CA, L23594305, USA.
Claudia H KawasDepartment of Neurobiology and Behavior, University of California, 1400 Bio Sci III, Irvine, CA, 92697, USA.
María M CorradaDepartment of Epidemiology and Biostatistics, University of California, 856 Health Sciences Road, Suite 3400, Irvine, CA, 92617, USA.

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
Diversity Supplement to R01AG021055; Clinical, Imaging, and Pathological Studies in the Oldest Old: The 90+ StudyR01AG021055 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI CORRADA, MARIA, KAWAS, CLAUDIA H. · 2002 to 2024
$36.9M
The Alzheimer's Disease Research Center at the University of California, IrvineP30AG066519 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Elizabeth Head · 2020 to 2026
$27.9M
Neuropathologic substrates for motor and cognitive impairment in three existing cohort studies of Alzheimer's disease and related dementiasUF1AG057707 · NIA · STANFORD UNIVERSITY · PI MONTINE, THOMAS J, WHITE, LON RAY · 2017 to 2017
$3.9M
NIA NIH HHS P30 AG066519NIA NIH HHS R01 AG021055NIA NIH HHS U24 AG021886NIA NIH HHS UF1 AG057707
6 · The paper itself

Abstract

Although intermediate/high Alzheimer's Disease Neuropathologic Change (ADNC) is associated with dementia in many older adults, some remain cognitively normal and are often referred to as resilient to ADNC. We aim to examine health, lifestyle, and neuropathologic factors that distinguish older adults with dementia vs. normal cognition in the presence of intermediate/high ADNC. Participants were from The 90 + Study, a longitudinal study of aging in southern California. This cross-sectional analysis included participants with an intermediate/high ADNC on neuropathologic exam and normal cognition or dementia diagnosis on case conference. We analyzed 11 neuropathologic changes, both vascular and neurodegenerative, dichotomized as present/absent, and the total number of neuropathologies. To examine the association of health and lifestyle factors and neuropathologic changes (predictors) with cognitive diagnosis at consensus case conference, dementia vs. normal cognition, (outcome), we used logistic regression adjusted for demographics. Among 235 participants (mean age at death = 98 years, 70% women), 33% maintained normal cognition. Participants with heart disease (OR = 0.45; 95% CI = 0.25, 0.81) and hypertension (OR = 0.53; 95% CI = 0.29, 0.95) had lower likelihood of dementia. In contrast, participants with a history of transient ischemic attacks (OR = 3.00; 95% CI = 1.46, 6.18), Lewy Body Disease (OR = 2.73; 95% CI = 1.14, 6.58), hippocampal sclerosis (OR = 2.70; 95% CI = 1.06, 6.86), Limbic-predominant Age-related TDP-43 Encephalopathy neuropathologic change (OR = 2.80; 95% CI = 1.53, 5.12), and a high number of non-ADNCs (OR = 4.46; 95% CI = 2.01, 9.92) had higher likelihood of dementia. Arteriolosclerosis, atherosclerosis, cerebral amyloid angiopathy, and microvascular lesions were not associated with dementia. In this study, the presence of neurodegenerative neuropathologic changes other than ADNC and the absence of hypertension distinguish oldest old individuals with dementia from those with normal cognition. Understanding mechanisms underlying normal cognition in those with ADNC may provide important clues to prevention and resilience to the effects of AD neuropathology.

Indexed as

Alzheimer DiseaseBrainDementiaAged, 80 and overAgingCross-Sectional StudiesFemaleHumansLife StyleLongitudinal StudiesMaleDementia vs. normal cognition in the presence of intermediate/high ADNCNeuropathologic changeNon-ADNCOldest old

Identifiers

PMID41942821
PMCPMC13053464

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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 OpenQuestion graph.