Evidence map›Paper›PMID 41201009›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Neurometabolic and vascular dysfunction as an early diagnostic for Alzheimer's disease and related dementias.

Juan Antonio K Chong Chie, Scott A Persohn, Ravi S Pandey, Greg W Carter, Olivia R Simcox, Paul Salama, Paul R Territo, Alzheimer's Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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  10. Review
  11. Neurometabolic and vascular dysfunction as an early diagnostic for Alzheimer's disease and related dementias.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Juan Antonio K Chong ChieStark Neuroscience Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID 0000-0003-3111-2294
Scott A PersohnStark Neuroscience Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Ravi S PandeyThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Greg W CarterThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Olivia R SimcoxWood College of Osteopathic Medicine, Marian University, Indianapolis, Indiana, USA.
Paul SalamaSchool of Electrical and Computer Engineering, Purdue University, Indianapolis, Indiana, USA.
Paul R TerritoStark Neuroscience Research Institute, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Alzheimer's Disease Neuroimaging Initiative

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Training Grant on Alzheimer's Disease and ADRD at Indiana UniversityT32AG071444 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI GARY E. LANDRETH, Bruce T Lamb · 2021 to 2026
$2.8M
Initiative ADNINIA NIH HHS T32 AG071444NIA NIH HHS T32AG071444NIA NIH HHS U01 AG024904NIH HHS U01 AG024904NIH HHS W81XWH-12-2-0012
6 · The paper itself

Abstract

introductionRecent studies suggest that the brain undergoes anatomical and functional restructuring, resulting in neurometabolic and vascular dysregulation (MVD) prior to amyloid beta accumulation, which begins at an early age and leads to the onset of Alzheimer's disease (AD).

methodsUsing a retrospective clinical population (n = 403) from the Alzheimer's Disease Neuroimaging Initiative, cerebral perfusion and metabolism changes across 59 brain regions were evaluated from clinical studies. Results were verified by transcriptomic signatures and clinical cognitive assessments.

resultsOur findings suggest that disease progression follows a stage-dependent MVD pattern that can identify at-risk regions. Although each region progresses at a different pace, regions related to memory, cognition, and motor function showed significant early dysregulation. Importantly, these changes aligned with transcriptomic and cognitive signatures. DISCUSSION: This study underscores that MVD in brain regions varies by sex and disease stage, making it a sensitive tool for early AD diagnosis. This approach could improve patient monitoring, stratification, and therapeutic testing. HIGHLIGHTS: The potential of metabolic and vascular dysfunction as an early biomarker was assessed. An analytical method to assess dysregulation via imaging was developed. An analytical and graphical method to visualize the changes across disease spectrum was developed. Brain regions progress at different rates across Alzheimer's disease progression. Results were aligned with transcriptomics and cognitive signatures.

Indexed as

Alzheimer DiseaseBrainAgedAged, 80 and overBiomarkersDisease ProgressionEarly DiagnosisFemaleHumansMaleNeuroimagingRetrospective StudiesBiomarkersAlzheimer's diseasebiomarkersdysregulationearly detectionmetabolismperfusionuncoupling

Identifiers

PMID41201009
PMCPMC12593541

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Registered trials

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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.