Evidence map›Paper›PMID 41638756›Full record

ArticleStroke and vascular neurology2026

Multimodal MRI habitat atlas for personalised re-haemorrhage risk prediction in brainstem cavernous malformations.

Haohuai Gui, Xuchen Dong, Zongze Li, Zun Liu, Ying Xiao, Jiaxi Zhou, Yuchuan Zhao, Hongfei Zhang, Ganglei Li, Kai Quan and 2 more

Abstract readValidation Study
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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Haohuai Gui *College of Biomedical Engineering, Fudan University, Shanghai, China.
Xuchen Dong *Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Zongze Li *Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Zun Liu *Department of Radiology, Huashan Hospital, Fudan University, Shanghai, China.
Ying XiaoCollege of Biomedical Engineering, Fudan University, Shanghai, China.
Jiaxi ZhouCollege of Biomedical Engineering, Fudan University, Shanghai, China.
Yuchuan ZhaoCollege of Biomedical Engineering, Fudan University, Shanghai, China.
Hongfei ZhangDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.ORCID http://orcid.org/0009-0008-0500-0989
Ganglei LiDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Kai QuanDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China neurosurgeryzhuw@163.com mayu@fudan.edu.cn quankai@fudan.edu.cn.ORCID http://orcid.org/0000-0002-6483-2434
Yu MaCollege of Biomedical Engineering, Fudan University, Shanghai, China neurosurgeryzhuw@163.com mayu@fudan.edu.cn quankai@fudan.edu.cn.
Wei ZhuDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China neurosurgeryzhuw@163.com mayu@fudan.edu.cn quankai@fudan.edu.cn.ORCID http://orcid.org/0000-0001-7190-7476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop an MRI habitat atlas that is robust across different haemorrhage stages for haemorrhagic brainstem cavernous malformations (BSCMs) and to integrate habitat-derived imaging biomarkers with clinical variables for precise prediction of symptomatic re-haemorrhage.

methodsA retrospective cohort of 205 eligible patients from Huashan Main Campus (2015-2020) was randomly divided into a discovery set (n=147) for model development and an internal validation set (n=58). External validation was performed using a prospective temporal cohort from Huashan West Campus (2021-2023, n=94). Each lesion was segmented into six biologically distinct habitats via unsupervised clustering of multiparametric MRI. Habitat-derived radiomic features were combined with clinical variables into a multimodal logistic regression model, which was rigorously validated both internally and temporally.

resultsThe 2-year cumulative re-haemorrhage rate was 81% in high-risk lesions versus 26% in low-risk lesions. The combined habitat-clinical model achieved an area under the curve (AUC) of 0.833 (95% CI 0.777 to 0.889) in the training set and 0.851 in the external validation set, significantly outperforming both imaging-only (∆AUC+0.07, p=0.008) and clinical-only models (∆AUC+0.17, p<0.001). The model demonstrated excellent calibration and provided net clinical benefit across decision thresholds of 5%-75%.

conclusionThe multimodal MRI habitat atlas provides a robust and reproducible tool for individualised re-haemorrhage risk stratification in BSCMs, facilitating clinical decision-making for surveillance or intervention while reducing the likelihood of overtreatment.

Indexed as

Brain StemHemangioma, Cavernous, Central Nervous SystemIntracranial HemorrhagesMagnetic Resonance ImagingAdultFemaleHumansMaleMiddle AgedPredictive Value of TestsRadiomicsRecurrenceReproducibility of ResultsRetrospective StudiesRisk AssessmentRisk FactorsCerebrovascular DisordersMagnetic Resonance ImagingMalformationStrokeVascular Malformations

Identifiers

PMID41638756
PMCPMC13540293

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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.