Evidence map›Paper›PMID 42220244›Full record

Observational studyStroke2026

Impact of Cerebral Small Vessel Disease on Functional Decline: Bleeding With Antithrombotic Therapy 2 Study.

Yoshito Arakaki, Kaori Miwa, Masatoshi Koga, Sohei Yoshimura, Kanta Tanaka, Jin Nakahara, Yusuke Yakushiji, Makoto Sasaki, Shigeru Fujimoto, Masayuki Shiozawa and 7 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Stroke, 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

17 authors.

Yoshito ArakakiDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0003-0097-6049
Kaori MiwaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-7948-3636
Masatoshi KogaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-6758-4026
Sohei YoshimuraDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-4751-3538
Kanta TanakaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-3291-5083
Jin NakaharaDepartment of Neurology, Keio University, School of Medicine, Tokyo, Japan (Y.A., J.N., K. Toyoda).ORCID 0000-0002-5858-0998
Yusuke YakushijiDivision of Neurology, Department of Internal Medicine, Saga University Faculty of Medicine, Japan (Y.Y.).
Makoto SasakiInstitute for Biomedical Sciences, Iwate Medical University, Yahaba, Japan (M. Sasaki).ORCID 0000-0002-3108-4361
Shigeru FujimotoDivision of Neurology, Department of Medicine, Jichi Medical University, Tochigi, Japan (S.F.).ORCID 0000-0002-6295-4737
Masayuki ShiozawaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-8071-7284
Satoshi OkudaDepartment of Neurology, National Hospital Organization Higashi Nagoya Hospital, Japan (S.O.).
Toru IwamaDepartment of Neurosurgery, Gifu Municipal Hospital, Japan (T.I.).ORCID 0000-0002-9426-284X
Masafumi IharaDepartment of Neurology, National Cerebral and Cardiovascular Center, Suita, Japan (M.I.).ORCID 0000-0002-7102-4048
Kazutoshi NishiyamaDepartment of Neurology, Kitasato University School of Medicine, Kanagawa, Japan (K.N.).
Teruyuki HiranoDepartment of Stroke and Cerebrovascular Medicine, Kyorin University, Mitaka, Japan (T.H.).ORCID 0000-0003-2094-2428
Kazunori ToyodaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan (Y.A., K.M., M.K., S.Y., K. Tanaka, M. Shiozawa, K. Toyoda).ORCID 0000-0002-8346-9845
for BAT2 Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo what extent cerebral small vessel disease (SVD) contributes to functional disability remains unclear. We investigated the longitudinal effect of SVD burden on functional decline.

methodsIn this investigator-initiated, prospective, multicenter, and observational study, patients receiving oral antithrombotic therapy for cerebrovascular or cardiovascular diseases were enrolled from 52 hospitals across Japan (2016-2019) and followed for 24 months. SVD score (range, 0-4) was calculated on baseline magnetic resonance imaging obtained under prespecified conditions. The outcomes were an increase in modified Rankin Scale (mRS) score from baseline to end of follow-up (ΔmRS score ≥1). Logistic regression evaluated the association between ΔmRS score ≥1 and SVD score, adjusting for age, sex, premorbid mRS, vascular risk factors, antithrombotic therapy, magnetic resonance imaging field strength, and bleeding or ischemic events during follow-up. Bleeding and ischemic events were treated as time-dependent covariates. Causal mediation analyses using a 4-way decomposition separated the effects of SVD score ≥3 on ΔmRS score ≥1 into direct and indirect effects (mediated by major bleeding or ischemic events).

resultsOf 5378 patients enrolled, 613 were excluded mainly due to the lack of clinical or imaging data. Finally, 4765 patients were analyzed (1573 women; median age, 73 years); ΔmRS score ≥1 was observed in 13.2% of patients with SVD score 0, 16.1% with 1, 20.7% with 2, 28.1% with 3, and 28.2% with 4. SVD score of 3 (adjusted odds ratio, 1.65 [95% CI, 1.27-2.15]) and SVD score of 4 (1.62 [95% CI, 1.19-2.19]) were associated with ΔmRS score ≥1 compared with SVD score of 0. Causal mediation analysis indicated that 73.05% of the total effect of SVD score ≥3 on ΔmRS score ≥1 was attributed to the controlled direct effect (coefficient, 0.497 [95% CI, 0.26-0.73]).

conclusionsSVD burden was associated with functional decline beyond significant bleeding or ischemic events.

Indexed as

Cerebral Small Vessel DiseasesFibrinolytic AgentsHemorrhageAgedAged, 80 and overFemaleHumansJapanMagnetic Resonance ImagingMaleMiddle AgedProspective StudiesRisk FactorsFibrinolytic Agentscardiovascular diseaseslife expectancymagnetic resonance imagingodds ratiorisk factors

Identifiers

PMID42220244
PMCPMC13281974

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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.