Evidence mapPaperPMID 41724678Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2026

Spatially resolved transcriptomic profiling identifies distinct signatures in parenchymal and vascular microenvironments in Alzheimer's Disease with Cerebral Amyloid Angiopathy.

Enrique Chimal-Juárez, Nur Jury-Garfe, Laura Gomez-Isaza, Juan C Troncoso, Cristian A Lasagna-Reeves

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2026. 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

5 authors.

Enrique Chimal-JuárezDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA.
Nur Jury-GarfeDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA.
Laura Gomez-IsazaDivision of Neuropathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Juan C TroncosoDivision of Neuropathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Cristian A Lasagna-ReevesDepartment of Neurology, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-5499-3082

Funding

Alzheimer's Association ALZDISCOVERY-1049108Cure Alzheimer's FundFulbright U.S. Scholar ProgramNIA NIH HHS 1RF1AG059639NIA NIH HHS RF1 AG059639NINDS NIH HHS 1R01NS119280NINDS NIH HHS R01 NS119280Rainwater Charitable Foundation
6 · The paper itself

Abstract

introductionAlzheimer's disease (AD) pathology frequently coexists with cerebral amyloid angiopathy (CAA), in which amyloid beta (Aβ) deposits in cerebral blood vessels. Although anti-Aβ immunotherapies can reduce parenchymal plaques, they often exacerbate vascular pathology. This study investigates compartment-specific microenvironmental responses to parenchymal versus vascular amyloid deposition.

methodsWe performed spatial whole-transcriptomic profiling on postmortem brain tissue from individuals with mixed AD/CAA pathology. Gene expression signatures were compared between parenchymal and vascular compartments to identify microenvironment-specific responses to amyloid deposition.

resultsAnalysis revealed that the vascular amyloid microenvironment is distinct from that of parenchymal amyloid, particularly in how shared pathways are differentially upregulated. Notably, although elements of the matrisome were activated in both contexts, they exhibited distinct expression patterns depending on the microenvironment. DISCUSSION: These findings highlight the dynamic and context-dependent nature of the microenvironment in AD/CAA. Our results emphasize the need for compartment-specific therapeutic strategies to mitigate amyloid pathology and reduce treatment-related complications.

Indexed as

Alzheimer DiseaseBrainCerebral Amyloid AngiopathyParenchymal TissueAgedAged, 80 and overAmyloid beta-PeptidesFemaleGene Expression ProfilingHumansMaleSpatial TranscriptomicsTranscriptomeAmyloid beta-PeptidesAlzheimer's diseasecerebral amyloid angiopathymatrisomemicroenvironmentspatial transcriptomicsvascular amyloid

Identifiers

PMID41724678
PMCPMC12928031

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.