Evidence map›Paper›PMID 41160787›Full record

ArticleNeurology2025

DWI-Positive Lesions in Acute Intracerebral Hemorrhage and Their Correlation With Small Vessel Disease: A Cohort Study.

Satoshi Hosoki, Tomotaka Tanaka, Yuki Kawamura, Sonu M M Bhaskar, Soshiro Ogata, Takehito Kuroda, Satoshi Saito, Kanta Tanaka, Kunihiro Nishimura, Kazunori Toyoda and 3 more

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

13 authors.

Satoshi HosokiDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-4241-3677
Tomotaka TanakaDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-6023-236X
Yuki KawamuraSchool of Clinical Medicine, University of Cambridge, United Kingdom.ORCID 0000-0003-2137-6464
Sonu M M BhaskarDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-9783-3628
Soshiro OgataDepartment of Preventive Medicine and Epidemiology, National Cerebral and Cardiovascular Center, Osaka, Japan; and.
Takehito KurodaDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-3711-9983
Satoshi SaitoDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0001-8608-058X
Kanta TanakaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-3291-5083
Kunihiro NishimuraDepartment of Preventive Medicine and Epidemiology, National Cerebral and Cardiovascular Center, Osaka, Japan; and.
Kazunori ToyodaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-8346-9845
Masatoshi KogaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-6758-4026
Perminder S SachdevCentre for Healthy Brain Ageing, Discipline of Psychiatry and Mental Health, School of Clinical Medicine, Faculty of Medicine and Health, University of New South Wales, Sydney, Australia.ORCID 0000-0002-9595-3220
Masafumi IharaDepartment of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-7102-4048

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesDiffusion-weighted imaging (DWI)-positive lesions are identified in 11%-45% of patients with acute intracerebral hemorrhage (ICH); however, their underlying mechanisms and clinical implications remain unclear. Moreover, the prevalence of these lesions before blood pressure lowering remains elusive. The aim of this study was to evaluate the prevalence, time-dependent changes, and associations of DWI-positive lesions with small vessel disease (SVD) markers and clinical outcomes in patients with acute ICH.

methodsThis retrospective cohort study analyzed data from the National Cerebral and Cardiovascular Center stroke registry. Overall, 872 patients with acute ICH who underwent MRI between January 2015 and January 2021 were evaluated. The patients were characterized based on whether MRI was performed before or after acute-phase blood pressure lowering. Multivariable logistic regression was used to assess the correlation between DWI-positive lesions and factors related to blood pressure reduction and time from ICH onset to imaging, as well as correlation with SVD markers. Furthermore, the relationship between DWI-positive lesions and unfavorable clinical outcomes (modified Rankin Scale scores 3-6 at 90 days) was examined.

resultsAmong 872 patients, 114 patients (13.1%) exhibited DWI-positive lesions (mean age: 71.5 ± 12.9 years; female, 36.0%). The number of patients with DWI-positive lesions was lower among those who underwent MRI before acute-phase blood pressure lowering (45/444 patients [10.1%]) than among those who underwent MRI after blood pressure lowering (69/428 patients [16.1%]). Multivariable analysis revealed that DWI-positive lesions were significantly associated with time from ICH onset to imaging (adjusted odds ratio [aOR], 1.41; 95% CI 1.08-1.84), but not with blood pressure lowering (aOR, 0.92; 95% CI 0.51-1.65). DWI-positive lesions were also strongly associated with SVD markers and higher SVD severity scores. Furthermore, DWI-positive lesions were linked to unfavorable outcomes at 90 days (aOR, 1.70; 95% CI 1.04-2.80). DISCUSSION: DWI-positive lesions are observed before blood pressure lowering, and their frequency increases over time. Their association with SVD markers highlights the role of advanced SVD in lesion formation. These lesions may worsen clinical outcomes, can potentially be helpful as prognostic imaging biomarkers, and may help guide optimal acute ICH management.

Indexed as

Antihypertensive AgentsCerebral HemorrhageCerebral Small Vessel DiseasesDiffusion Magnetic Resonance ImagingHypertensionAcute DiseaseAgedAged, 80 and overBiomarkersBlood PressureFemaleHumansLogistic ModelsMaleMiddle AgedOutcome Assessment, Health CareAntihypertensive AgentsBiomarkers

Identifiers

PMID41160787
PMCPMC12576840

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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.