Evidence map›Paper›PMID 41117445›Full record

ArticleAnnals of neurology2026

Disruption of the Blood-Brain Barrier Predicts Progression of Cerebral Small Vessel Disease White Matter Hyperintensities.

Richard Leigh, Kyle C Kern, Nae-Yuh Wang, Rebecca F Gottesman, Clinton B Wright

Abstract read
In one paragraph

Article in Annals of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

5 authors.

Richard LeighDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0002-8285-1815
Kyle C KernDepartment of Neurology, University of California Los Angeles David Geffen School of Medicine, West Los Angeles VA Medical Center, Los Angeles, CA.ORCID 0000-0002-2703-7669
Nae-Yuh WangDepartments of Medicine, Biostatistics, and Epidemiology, The Johns Hopkins University, Baltimore, MD.
Rebecca F GottesmanNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-9504-1256
Clinton B WrightNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD.

Funding

Global Blood-Brain Barrier Disruption and Post-Stroke Cognitive DeclineR01NS123386 · NINDS · JOHNS HOPKINS UNIVERSITY · PI RICHARD LEIGH · 2022 to 2026
$3.1M
NINDS NIH HHS R01 NS123386NINDS NIH HHS R01NS123386
6 · The paper itself

Abstract

objectiveThe objective of this study was to test if blood-brain barrier (BBB) disruption, detected using dynamic susceptibility contrast (DSC) imaging, would predict progression of white matter hyperintensities (WMHs) over the subsequent year in patients with chronic cerebrovascular disease.

methodsThe study included patients with a history of stroke and at least early confluence of WMH. Magnetic resonance imaging (MRI) scans performed at baseline (> 3 months from stroke) and again 1 year later were segmented to calculate the WMH volume expressed as a fraction of the total brain volume. Change in WMH volume between the 2 timepoints and progression of WMH were the outcome measures. BBB disruption was measured using DSC imaging on the baseline MRI. WMH masks were dilated by 3 mm to create a mask of the adjacent normal appearing white matter (penumbra). BBB disruption was averaged within the WMH and the penumbra.

resultsFifty patients were included; median age was 69 years, and 46% were women. The mean WMH fraction was 1.25% at baseline and 1.36% at 1 year. The mean baseline BBB disruption was 0.20% in the WMH and 0.22% in the penumbra. More severe BBB disruption was associated with greater WMH progression when measured in the WMH (ß = 0.95, confidence interval [CI] = 0.39-1.51, r

interpretationMore severe BBB disruption was predictive of greater WMH progression in patients with chronic cerebrovascular disease. ANN NEUROL 2026;99:437-448.

Indexed as

Blood-Brain BarrierCerebral Small Vessel DiseasesWhite MatterAgedAged, 80 and overDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle Aged

Identifiers

PMID41117445
PMCPMC12894497

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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.