Evidence map›Paper›PMID 40613686›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2025

Identifying motor resilience proteins associated with motor decline in older adults.

Aron S Buchman, Tianhao Wang, Katia de Paiva Lopes, Andrea R Zammit, Shahram Oveisgharan, Nicholas Seyfried, Yanling Wang, Phil DeJager, Sukriti Nag, Shinya Tasaki and 2 more

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

12 authors.

Aron S BuchmanRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.ORCID 0000-0002-6426-2742
Tianhao WangRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
Katia de Paiva LopesRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
Andrea R ZammitRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.ORCID 0000-0002-2749-1239
Shahram OveisgharanRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.ORCID 0000-0001-6841-4830
Nicholas SeyfriedDepartment of Neurology, Emory University School of Medicine, Atlanta, Georgia, United States.
Yanling WangRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
Phil DeJagerDepartment of Neurology, Center for Translational and Computational Neuroimmunology, Columbia University Medical Center, New York, New York, United States.
Sukriti NagRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
Shinya TasakiRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
Lei YuRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.
David A BennettRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, Illinois, United States.ORCID 0000-0003-3689-554X

Funding

EPIDEMIOLOGY OF NEURAL RESERVE AND NEUROBIOLOGY IN AGINGR01AG017917 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI BENNETT, DAVID ALAN · 2001 to 2023
$43.3M
Rush Alzheimer's Disease Research CenterP30AG072975 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI Lisa L Barnes, Julie A. Schneider · 2021 to 2026
$24.7M
RISK FACTORS, PATHOLOGY, AND CLINICAL EXPRESSIONS OF ADR01AG015819 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI BENNETT, DAVID ALAN · 1998 to 2024
$21.4M
Multi-omic network-directed proteoform discovery, dissection and functional validation to prioritize novel AD therapeutic targetsU01AG061356 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BENNETT, DAVID ALAN, DE JAGER, PHILIP L · 2018 to 2022
$13.7M
Identifying resilience proteins in key motor tissues that drive motor and cognitive decline and offset the negative effects of ADRD pathologies within and outside the brainR01AG075728 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI ARON S BUCHMAN · 2022 to 2026
$6.9M
Elucidating the molecular drivers of impaired mobility within and outside the CNS in Alzheimer’s disease and related disordersR01AG059732 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI BUCHMAN, ARON S · 2019 to 2023
$2.8M
NIA NIH HHS P30 AG072975NIA NIH HHS P30AG10161NIA NIH HHS R01 AG015819NIA NIH HHS R01 AG017917NIA NIH HHS R01 AG059732NIA NIH HHS R01 AG075728NIA NIH HHS R01AG15819NIA NIH HHS R01AG17917NIA NIH HHS R01AG56352, A.S.BNIA NIH HHS R01AG59732NIA NIH HHS R01AG75728NIA NIH HHS R01AG79133NIA NIH HHS U01 AG061356
6 · The paper itself

Abstract

backgroundThis study will identify cortical proteins that may provide motor resilience, the capacity to maintain motor function despite underlying Alzheimer's disease and related dementias (ADRD) pathologies.

methodsWe studied 850 decedents with postmortem indices of 10 ADRD pathologies and proteome from dorsal lateral prefrontal cortex. Annual parkinsonian signs were assessed using a modified Unified Parkinson Disease Rating Scale. First, we adjusted linear models for ADRD pathologies to isolate resilience proteins, unrelated to ADRD pathologies, but that were related to linear motor decline. Next, functional mixed effects (FMEs) models were used to determine if resilience proteins were related to non-linear motor decline. Exploratory functional enrichment was then used to assess pathways underlying motor resilience proteins.

resultsMean age at death was 90 years (SD = 6.4), 69% female and 7 years follow-up. Adjusting linear models for age, sex, and ADRD pathologies, we isolated thirteen proteins that may provide motor resilience (Bonferroni correction p < 5 × 10-6). FME models showed, that on average, progression of parkinsonian signs was non-linear from 25 to 12 years before death, followed by accelerated linear decline until death. Five of thirteen resilience proteins were also related to non-linear decline. Motor resilience may be supported by a coordinated network of proteins that help to preserve neuronal structure, cellular transport, and synaptic integrity, functions critical for diverse aging phenotypes.

conclusionsCortical proteins may provide motor resilience for both linear and non-linear motor decline. Further drug discovery targeting resilience proteins may yield therapies that can reduce motor impairment even in the absence of treatments for ADRD pathologies.

Indexed as

DementiaDorsolateral Prefrontal CortexProteomePsychomotor PerformanceAged, 80 and overAlzheimer DiseaseAutopsyDisease ProgressionFemaleHumansLinear ModelsMaleParkinson DiseaseResilience, PsychologicalProteomeADRD pathologiesmotor declineparkinsonismresilience proteinstime course

Identifiers

PMID40613686
PMCPMC12569409

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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.