Evidence map›Paper›PMID 40957669›Full record

ArticleStroke and vascular neurology2026

Characteristics of brain structural damage related to cerebral small vessel disease in general population with intracranial artery stenosis.

Zi-Ang Pan, Zi-Yue Liu, Xing-Qi Pan, Fei-Fei Zhai, Ding-Ding Zhang, Ming Yao, Li-Xin Zhou, Jun Ni, Zheng-Yu Jin, Shu-Yang Zhang and 3 more

Abstract read
In one paragraph

Article in Stroke and vascular neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Zi-Ang PanDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-0204-8150
Zi-Yue LiuDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Xing-Qi PanDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Fei-Fei ZhaiDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Ding-Ding ZhangChinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Ming YaoDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Li-Xin ZhouDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Jun NiDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Zheng-Yu JinChinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shu-Yang ZhangChinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Li-Ying CuiDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China.
Fei HanDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China zhuych910@163.com lourahan@163.com.
Yi-Cheng ZhuDepartment of Neurology, Peking Union Medical College Hospital, Beijing, China zhuych910@163.com lourahan@163.com.ORCID http://orcid.org/0000-0002-8966-1379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsCovert MRI markers of cerebral small vessel disease (CSVD) can coexist with large artery atherosclerosis. We aimed to explore whether the spatial distributions of these markers were diverse in people with or without intracranial artery stenosis (ICAS).

methodsThis cross-sectional analysis included 1206 stroke-free participants (aged 55.69±9.27, 62.94% female) with brain MRI and MR angiography from community-based Shunyi cohort. We analysed the relationships between ICAS and CSVD markers. We also compared the probability maps of lacunes, cerebral microbleeds (CMB), white matter hyperintensities (WMH) and cortex morphology at a voxel/vertex-wise level in groups with and without ICAS.

resultsICAS increased the risk of lacunes by 2.99-fold (95% CI 1.99 to 4.50, p<0.001), lacunes ≥3 by 5.32 times (95% CI 2.76 to 10.28, p<0.001), correlated with WMH volume (β=0.332, SE=0.059, p<0.001), WMH Fazekas scores ≥5 (OR 4.50, 95% CI 2.44 to 8.29, p<0.001) and brain parenchymal fraction (β=-0.012, SE=0.002, p<0.001), but not with CMB. ICAS is associated with lacunes in the corresponding blood supply area. Lacunes that coexist with ICAS were prone in basal ganglia, while the lacunes without ICAS appeared in centrum semiovale more often. WMH with ICAS was prone to present in deep white matter involving the bilateral pyramidal tracts and superior thalamic radiation. People with ICAS were susceptible to worse cortical atrophy of right superior frontal and left rostral anterior cingulate. No obvious distributional differences were found for CMB between the two groups.

conclusionsSince ICAS may be involved in the upstream pathogenesis of lacunes, white matter lesions and cortical atrophy, the impact of ICAS should not be ignored when evaluating MRI markers of CSVD.

Indexed as

BrainCerebral HemorrhageCerebral Small Vessel DiseasesLeukoencephalopathiesMagnetic Resonance AngiographyMagnetic Resonance ImagingStroke, LacunarAdultAgedAtrophyCerebral AngiographyChinaConstriction, PathologicCross-Sectional StudiesFemaleHumansArteriesAtherosclerosisMagnetic Resonance AngiographyMagnetic Resonance ImagingStroke

Identifiers

PMID40957669
PMCPMC13347908

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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.