Evidence map›Paper›PMID 41645049›Full record

ArticleInternational journal for numerical methods in biomedical engineering2026

A Statistical Shape Modeling Approach for the Derivation of a Data-Driven Geometry-Aware Lumped Arterial Stenosis Model.

P L J Hilhorst, S C F P M Verstraeten, K Zając, R Ganesan, M van 't Veer, F N van de Vosse, W Huberts

Abstract read
In one paragraph

Article in International journal for numerical methods in biomedical engineering, 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

7 authors.

P L J HilhorstDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0003-1764-1536
S C F P M VerstraetenDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-1011-6627
K ZającSano Centre for Computational Medicine, Kraków, Poland.ORCID https://orcid.org/0000-0003-1393-8236
R GanesanDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-9666-5925
M van 't VeerDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-5006-0111
F N van de VosseDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-4084-2064
W HubertsDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-0779-4785

Funding

European Union's Horizon 2020 Research and Innovation Programme 101016503European Union's Horizon 2020 Research and Innovation Programme 101017578Polish High-Performance Computing Infrastructure PLGrid (HPC Center: ACK Cyfronet AGH) PLG/2024/017022Polish High-Performance Computing Infrastructure PLGrid (HPC Center: ACK Cyfronet AGH) PLG/2024/01710
6 · The paper itself

Abstract

Existing lumped arterial stenosis models struggle to accurately capture the pressure and flow relationship of complex lesion morphologies, thereby limiting their ability to accurately evaluate lesions. To overcome these limitations, we introduce a geometry-informed, data-driven lumped stenosis model that incorporates realistic lesion shapes using statistical shape modeling (SSM). By generating a large dataset of synthetic coronary stenoses, hence focusing on epicardial lesions, and evaluating them through high-fidelity 3D computational fluid dynamics (CFD), we derived reference pressure drops across a diverse range of lesion geometries and flow regimes. These CFD-derived pressures and flows, along with their corresponding shape coefficients, were used to train a lumped parameter model capable of rapidly estimating trans-lesional pressure drops. Remarkably, only five shape modes were necessary to effectively describe the geometric variability, underscoring the efficiency of the approach. Compared to a conventional lumped model, our approach significantly improved pressure drop prediction accuracy, especially in the case of irregular stenosis morphologies. Integration of the new data-driven lumped stenosis model within a 1D pulse wave propagation framework was also successful, aligning simulated pressure and flow waveforms much closer with high-fidelity CFD-coupled results. In turn, the estimation of the fractional flow reserve, a clinically validated index of lesion-specific ischemia, also improved by 18% compared to a conventional lumped model. Although only validated using synthetic lesion data, the model's architecture allows easy integration of additional shape features and lesion-specific parameters, paving the way for future validation on patient-derived geometries.

Indexed as

Coronary StenosisModels, CardiovascularModels, StatisticalComputer SimulationConstriction, PathologicHemodynamicsHumansHydrodynamicscomputational fluid dynamicscoronary hemodynamicspressure drop predictionreduced‐order modelingstatistical shape modeling

Identifiers

PMID41645049
PMCPMC12876559

What Socratic 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 Socratic graph.