Evidence map›Paper›PMID 40507850›Full record

ArticleInternational journal of molecular sciences2025

Dementia from Small Vessel Disease Versus Alzheimer's Disease: Separate Diseases or Distinct Manifestations of Cerebral Capillopathy Due to Blood-Brain Barrier Dysfunction? A Pilot Study.

Charles R Joseph, Davis A Melin, Lindsay K Wanner, Bryant Hartman, Jason Badelita, Lucy C Conser, Harrison D Kline, Pranav M Pradhan, Kim Love

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Charles R JosephDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.ORCID 0000-0002-8057-8704
Davis A MelinDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.ORCID 0009-0001-8322-2287
Lindsay K WannerDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.ORCID 0009-0001-5995-6467
Bryant HartmanDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.ORCID 0009-0000-8865-9093
Jason BadelitaDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.
Lucy C ConserDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.ORCID 0009-0007-7475-842X
Harrison D KlineDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.
Pranav M PradhanDepartment of Internal Medicine and Neurology, Liberty University College of Osteopathic Medicine, Lynchburg, VA 24502, USA.
Kim LoveK. R. Love Quantitative Consulting and Collaboration, Athens, GA 30605, USA.ORCID 0000-0002-5912-9525

Funding

Liberty University College of Osteopathic Medicine MR2402- MR2402-B3C98-711099-20
6 · The paper itself

Abstract

Pathophysiological differences separating small vessel disease (SVD) from Alzheimer's disease (AD) may alter treatment approach. Investigating peak-arterial and late-capillary perfusion may differentiate SVD from AD. 14 Subjects with MoCA scores of 11-24 were divided into 2 groups. Group one: 6 AD likely subjects positive for 1 or 2 copies of APOE 4+. Group two: 8 SVD likely subjects APOE-. Group three: 7 age-matched controls (MoCA 26-30). All underwent 3D PASL MRI, FLAIR, and SWI axial MRI. Arterial phase peak amplitude and latency, late capillary inflow/clearance rates, and anatomic abnormalities quantitated using microhemorrhage count, Fazekas, Koedam, and Schelton scales were compared. Arterial perfusion demonstrated no statistical differences among SVD, AD, and controls, suggesting normal arterial flow. Late phase perfusion showed significant localized reduction in capillary flow/clearance rates in SVD and AD compared to controls. Absent arterial phase but significant capillary inflow/clearance differences from controls suggest SVD and AD share common impaired blood-brain barrier origins.

Indexed as

Alzheimer DiseaseBlood-Brain BarrierCerebral Small Vessel DiseasesAgedAged, 80 and overCapillariesCase-Control StudiesCerebrovascular CirculationFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPilot Projects3D PASL MRIAlzheimer diseasearterial perfusion phasecapillary perfusion phaseFazekas scaleKoedam scaleMontreal Cognitive AssessmentScheltens scalesmall vessel disease dementia

Identifiers

PMID40507850
PMCPMC12154280

What OpenQuestion holds

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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.