Evidence map›Paper›PMID 41449311›Full record

ArticleTranslational stroke research2025

Development and Validation of an Interpretable Hemodynamics-Based Machine Learning Model for Predicting Cerebral Arteriovenous Malformation Rupture.

Chengzhuo Wang, Tzak Sing Lau, Heze Han, Ruinan Li, Zhipeng Li, Qinghui Zhu, Yu Chen, Xiaolin Chen, Registry of Multimodality Treatment for Brain Arteriovenous Malformation in Mainland China (MATCH)

Abstract readValidation StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in Translational stroke research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

9 authors.

Chengzhuo WangDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Tzak Sing LauDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Heze HanDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Ruinan LiDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Zhipeng LiDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Qinghui ZhuDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China.
Yu ChenDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China. chenyu_tiantan@126.com.
Xiaolin ChenDepartment of Neurosurgery, Beijing Tiantan Hospital and Beijing Neurosurgical Institute, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing, 100070, China. cxl_bjtth@163.com.
Registry of Multimodality Treatment for Brain Arteriovenous Malformation in Mainland China (MATCH)

Funding

CFH-brain 2024-3-2051National Key Research and Development Program of China 2021YFC2501101Natural Science Foundation of China 82202244
6 · The paper itself

Abstract

Cerebral arteriovenous malformation (AVM) is a cerebrovascular disease associated with a risk of intracranial hemorrhage. Currently, most risk prediction models for AVM rupture are based on demographic characteristics and lesion morphology, while quantitative hemodynamics-based models remain scarce. This study aims to identify potential biomarkers associated with hemorrhagic risk through quantitative analysis of hemodynamic parameters within AVM lesions, and to develop a predictive model for AVM rupture risk. This study was based on a nationwide, multicenter registry (the MATCH study), enrolling untreated patients who underwent digital subtraction angiography (DSA) between January 2018 and December 2021. The model was trained using an internally derived cohort and validated with both internal and external center cohorts, as well as with follow-up data from patients who received conservative management. Quantitative hemodynamic parameters were extracted using quantitative angiography. Model performance was evaluated using confusion matrix-related metrics. A total of 857 patients with AVM were included in this study and were allocated into an internal cohort (n = 523; 418 for training and 105 for internal validation), an external validation cohort (n = 140), and a longitudinal validation cohort (n = 194). For each patient, 63 quantitative hemodynamic features were extracted. Based on variable importance ranking, the 10 most significant hemodynamic features were selected for model development. Thirteen individual machine learning models were constructed and evaluated. The best models achieved an area under the curve (AUC) of 0.754 in the training set (out-of-fold cross-validation), 0.750 in the internal validation cohort, 0.748 in the external validation cohort, demonstrating robust predictive performance. Furthermore, the SHapley Additive exPlanations (SHAP) framework was employed to interpret the contribution of individual variables within the model, providing insights into the underlying decision-making process. In the conservative treatment cohort, the prediction model results were used to divide patients into high-risk and low-risk groups for rupture, and there was a significant difference in actual risk between the two groups (P = 0.028). This comprehensive approach highlights the potential of quantitative hemodynamic analysis combined with advanced machine learning techniques for individualized risk prediction in AVM patients. This study demonstrates that quantitative hemodynamic features, when integrated with advanced machine learning algorithms, can effectively predict the risk of AVM rupture. The developed model exhibited robust performance across internal, external, and longitudinal validation cohorts. These findings suggest that quantitative hemodynamic analysis holds significant promise for improving individualized risk stratification and clinical decision-making in patients with cerebral arteriovenous malformations.

Indexed as

HemodynamicsIntracranial Arteriovenous MalformationsIntracranial HemorrhagesMachine LearningAdultAgedAngiography, Digital SubtractionCohort StudiesFemaleHumansMaleMiddle AgedRegistriesArteriovenous malformationsHemodynamicsMachine learningPredict modelRupture

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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.