Evidence map›Paper›PMID 42227730›Full record

Observational studyEuropean journal of neurology2026

Impact of Intracranial Atherosclerosis and Cerebral Small Vessel Disease on Overt Vascular Events During Antithrombotic Therapy.

Kaori Miwa, Masatoshi Koga, Kanta Tanaka, Yusuke Yakushiji, Makoto Sasaki, Kohsuke Kudo, Sohei Yoshimura, Masafumi Ihara, Shigeru Fujimoto, Tadashi Terasaki and 9 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in European journal of 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

19 authors.

Kaori MiwaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.ORCID https://orcid.org/0000-0002-7948-3636
Masatoshi KogaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
Kanta TanakaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.ORCID https://orcid.org/0000-0002-3291-5083
Yusuke YakushijiDivision of Neurology, Department of Internal Medicine, Saga University Faculty of Medicine, Saga, Japan.
Makoto SasakiInstitute for Biomedical Sciences, Iwate Medical University, Yahaba, Japan.
Kohsuke KudoDepartment of Diagnostic Imaging, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Sohei YoshimuraDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
Masafumi IharaDepartment of Neurology, National Cerebral and Cardiovascular Center, Suita, Japan.
Shigeru FujimotoDivision of Neurology, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Tadashi TerasakiDivision of Neurology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
Yukako YazawaDepartment of Stroke Neurology, Kohnan Hospital, Sendai, Japan.
Yoshinari NagakaneDepartment of Neurology, Kyoto Second Red Cross Hospital, Kyoto, Japan.ORCID https://orcid.org/0000-0003-2203-7077
Hiroshi YamagamiDivision of Stroke Prevention and Treatment, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.
Kazutoshi NishiyamaDepartment of Neurology, Kitasato University School of Medicine, Sagamihara, Japan.
Yoshiki YagitaDepartment of Stroke Medicine, Kawasaki Medical School, Kurashiki, Japan.
Shinichi YoshimuraDepartment of Neurosurgery, Hyogo Medical University, Nishinomiya, Japan.
Teruyuki HiranoDepartment of Stroke and Cerebrovascular Medicine, Kyorin University, Mitaka, Japan.
Kazunori ToyodaDepartment of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
BAT2 Investigators

Funding

Japan Agency for Medical Research and Development JP18ek0210055Japan Agency for Medical Research and Development JP24lk0221171Japan Agency for Medical Research and Development JP24lk0221186Japan Society for the Promotion of Science 19 K17023Japan Society for the Promotion of Science JP23K27522
6 · The paper itself

Abstract

introductionTo investigate the association of intracranial atherosclerotic disease (ICAD), alone and comorbid with cerebral small vessel disease (SVD), with ischemic or hemorrhagic events in patients receiving antithrombotic therapy. PATIENTS AND

methodsIn this prospective, multicenter, observational study, baseline brain MRI was performed to assess SVD (white matter hyperintensities, cerebral microbleeds, lacunes, enlarged perivascular spaces [PVS]), nonlacunar infarcts, and ICAD. SVD burden was defined as SVD score > 2. ICAD was classified as normal-to-mild, moderate, and severe stenosis-to-occlusion. The outcomes were any ischemic event, ischemic stroke, major bleeding, intracranial hemorrhage, and all-cause mortality. We assessed associations of ICAD with outcomes via Cox regression and mediation analyses, adjusting for SVD burden.

resultsAmong 5250 patients (mean age: 71 ± 11 years, 33% women), 3947 (75%) received antiplatelets and 1304 (25%) anticoagulants at baseline. ICAD was normal-to-mild in 3781 (72%), moderate in 571 (11%), and severe-to-occluded in 894 (17%). SVD burden was observed in 1400 (27%). ICAD was associated with a higher frequency of non-lacunar infarcts and a lower frequency of PVS. There was no graded association between ICAD severity and SVD burden. During a median follow-up of 2 years, 278 ischemic events, 197 ischemic strokes, 97 major bleedings, 55 intracranial hemorrhages, and 217 deaths occurred. Severe-to-occluded ICAD independently increased the risk of any ischemic event (adjusted hazard ratio: 1.39 [1.03-1.86]) and mortality (2.01 [1.48-2.74]); coexisting SVD burden further increased the risk of all outcomes. ICAD directly affected ischemic events, while mortality was mainly driven by its additive interaction with SVD.

conclusionsICAD increases the risk of any ischemic events and, with comorbid SVD, contributes to hemorrhagic events and excess mortality.

Indexed as

Cerebral Small Vessel DiseasesFibrinolytic AgentsIntracranial ArteriosclerosisIntracranial HemorrhagesIschemic StrokeAgedAged, 80 and overFemaleHumansMaleMiddle AgedProspective StudiesFibrinolytic Agentsantithrombotic therapycerebral‐small vessel diseaseintracranial atherosclerotic diseaseischemic strokemajor bleeding

Identifiers

PMID42227730
PMCPMC13239194

What OpenQuestion holds

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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.