Evidence map›Paper›PMID 42659615›Full record

Observational studyNeurology2026

Lesion-Level Subtypes of White Matter Hyperintensity Evolution Beyond Spatial Location.

Raul Gonzalez-Gomez, Enzo Tagliazuchi, Cecilia Gonzalez Campo, Vicente Medel, David A Bennett, Yasser Iturria-Medina

Abstract readObservational Study
In one paragraph

Observational study in Neurology, 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

6 authors.

Raul Gonzalez-GomezNeuroinformatics for Personalized Medicine Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute-Hospital, McGill University, Quebec, Canada.ORCID 0000-0003-2341-011X
Enzo TagliazuchiDepartamento de Física, Universidad de Buenos Aires, Argentina.
Cecilia Gonzalez CampoCognitive Neuroscience Center, Universidad de San Andrés, Victoria, Buenos Aires, Argentina.ORCID 0000-0003-2639-3570
Vicente MedelPontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0003-2443-8683
David A BennettRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL.ORCID 0000-0003-3689-554X
Yasser Iturria-MedinaNeuroinformatics for Personalized Medicine Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute-Hospital, McGill University, Quebec, Canada.ORCID 0000-0002-9345-0347

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesWhite matter hyperintensities (WMHs) are common neuroimaging markers of cerebrovascular pathology in aging and neurodegeneration. Despite their clinical relevance, WMH are typically quantified using global burden measures that assume a relatively homogeneous pathologic process. However, growing evidence suggests substantial biological heterogeneity across lesions. We aimed to identify lesion-level WMH subtypes beyond anatomic location and evaluate their associations with neurodegeneration and vascular risk.

methodsWe conducted a longitudinal observational study analyzing 3224 MRI scans from 403 participants spanning cognitively normal aging, mild cognitive impairment, Alzheimer, and Parkinson disease. Imaging at baseline and 2-year follow-up included structural, diffusion, and resting-state MRI. A total of 2107 WMH lesions were identified, and lesion-wise longitudinal changes were used to derive subtypes using unsupervised clustering. Associations with neurodegeneration and vascular risk factors were assessed using multivariable models with false discovery rate correction.

resultsThree lesion subtypes (L DISCUSSION: WMH are not a homogeneous entity but comprise biologically distinct lesion subtypes with differential neurobiological and clinical significance. Lesion composition may therefore offer a more informative framework than global WMH burden for understanding cerebrovascular contributions to aging and neurodegeneration, with potential implications for risk stratification, clinical interpretation, and targeted interventions.

Indexed as

AgingAlzheimer DiseaseBrainCognitive DysfunctionParkinson DiseaseWhite MatterAgedAged, 80 and overFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMale

Identifiers

PMID42659615
PMCPMC13528905

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.