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CellViT++: Energy-efficient and adaptive cell segmentation and classification using foundation models CellViT++:基于基础模型的节能和自适应细胞分割和分类
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-09 DOI: 10.1016/j.cmpb.2025.109206
Fabian Hörst , Moritz Rempe , Helmut Becker , Lukas Heine , Julius Keyl , Jens Kleesiek
<div><h3>Background and Objective:</h3><div>Deep learning-based cell segmentation and classification methods in digital pathology are critical for diagnostics but are hampered by models that require extensive annotated datasets, are computationally expensive, and lack adaptability to new cell types. This creates a significant bottleneck in research and clinical workflows. This study introduces <span><math><msup><mrow><mtext>CellViT</mtext></mrow><mrow><mo>+</mo><mo>+</mo></mrow></msup></math></span>, a data-efficient and lightweight framework for generalized cell segmentation that allows for rapid adaptation to novel cell taxonomies with minimal data.</div></div><div><h3>Methods:</h3><div><span><math><msup><mrow><mtext>CellViT</mtext></mrow><mrow><mo>+</mo><mo>+</mo></mrow></msup></math></span> leverages a Vision Transformer with a frozen pretrained foundation model for segmentation. It simultaneously extracts deep cell embeddings from the transformer tokens during the forward pass at no extra computational cost. To adapt to new cell types, only a lightweight classifier is trained on these embeddings, bypassing the need to retrain the segmentation model. We also demonstrate an automated workflow to generate training data from registered H&E and immunofluorescence (IF) slides. The framework was validated on seven public datasets.</div></div><div><h3>Results:</h3><div>The framework achieves remarkable zero-shot segmentation results and data efficiency. On the CoNSeP dataset for colon cancer, we achieved superior results with only 10% of the training data. On all other datasets, we outperformed competing methods or at least approached their performance, all in one model. The classifier approach, based on zero-shot segmentation models, drastically reduces computational costs, with training times of minutes versus hours for baseline models, decreasing CO<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> emission by 96.93%. Models trained on automatically generated labels from IF-staining achieved performance comparable to (lymphocytes, <span><math><mrow><mi>Δ</mi><msub><mrow><mtext>F</mtext></mrow><mrow><mn>1</mn></mrow></msub><mo>:</mo><mspace></mspace><mo>−</mo><mn>0</mn><mo>.</mo><mn>042</mn></mrow></math></span>) or even exceeding (plasma cells, <span><math><mrow><mi>Δ</mi><msub><mrow><mtext>F</mtext></mrow><mrow><mn>1</mn></mrow></msub><mo>:</mo><mspace></mspace><mo>+</mo><mn>0</mn><mo>.</mo><mn>108</mn></mrow></math></span>) those trained on expert-annotated datasets.</div></div><div><h3>Conclusions:</h3><div><span><math><msup><mrow><mtext>CellViT</mtext></mrow><mrow><mo>+</mo><mo>+</mo></mrow></msup></math></span> provides a robust and efficient open-source framework that addresses key limitations in computational pathology by decoupling segmentation from classification. Its ability to adapt to new cell types with minimal data and its support for automated dataset generation from IF slides significantly reduce the r
背景和目的:数字病理学中基于深度学习的细胞分割和分类方法对诊断至关重要,但由于模型需要大量注释数据集,计算成本高,对新细胞类型缺乏适应性,因此受到阻碍。这在研究和临床工作流程中造成了重大瓶颈。本研究介绍了CellViT++,这是一种数据高效且轻量级的通用细胞分割框架,可以用最少的数据快速适应新的细胞分类。方法:CellViT++利用Vision Transformer和冻结的预训练基础模型进行分割。它在向前传递期间同时从变压器令牌中提取深度单元嵌入,而不需要额外的计算成本。为了适应新的细胞类型,只在这些嵌入上训练轻量级分类器,而不需要重新训练分割模型。我们还演示了从注册的H&;E和免疫荧光(IF)幻灯片生成训练数据的自动化工作流程。该框架在七个公共数据集上进行了验证。结果:该框架取得了显著的零镜头分割效果和数据效率。在结肠癌的CoNSeP数据集上,我们仅使用10%的训练数据就取得了优异的结果。在所有其他数据集上,我们的表现都优于竞争对手的方法,或者至少接近他们的表现,所有这些都是在一个模型中实现的。基于零采样分割模型的分类器方法大大降低了计算成本,基线模型的训练时间为几分钟,而基线模型的训练时间为几小时,二氧化碳排放量减少了96.93%。在if染色自动生成的标签上训练的模型的性能与(淋巴细胞,ΔF1:−0.042)相当,甚至超过(浆细胞,ΔF1:+0.108)在专家注释数据集上训练的模型。结论:CellViT++提供了一个强大而高效的开源框架,通过将分割与分类分离,解决了计算病理学的关键限制。它能够以最少的数据适应新的单元类型,并支持从IF幻灯片自动生成数据集,大大减少了对耗时的专家注释的依赖。这项工作为加速研究、加强诊断工作流程和实现更深入的队列分析提供了基础工具。该代码可从https://github.com/TIO-IKIM/CellViT-plus-plus和PyPI包中获得。
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引用次数: 0
In silico modelling of aortic annuloplasty: hemodynamic assessment through in vitro experiments and in vivo MRI 主动脉环成形术的计算机模拟:通过体外实验和体内MRI进行血流动力学评估
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-09 DOI: 10.1016/j.cmpb.2026.109246
Marta Zattoni , Luca Bontempi , Steffen Ringgaard , Giulia Luraghi , Leila Louise Benhassen , Peter Johansen , Monika Colombo
Aortic annuloplasty (AA) is an innovative surgical technique for aortic root (AR) enlargement. It is performed by implanting sutures, bands, or rings, either externally or internally the AR, hereby reducing its diameter. This study evaluates the impact of AA approaches on AR hemodynamic by employing a porcine-specific workflow combining in vivo magnetic resonance imaging (MRI), in vitro experiments and in silico fluid-structure interaction (FSI) simulations investigating external single ring AA. CAD models of native and post-annuloplasty ARs were segmented from in vivo porcine MRI data and served as the basis for fabricating 3D-printed resin phantoms and implementing computational digital twins. The former were tested on a pulsatile flow-loop, whereas the latter were integrated in FSI simulations, with time-dependent boundary conditions based on the resultant experimental pressure waveforms. Additionally, a proof-of-concept validation of the in silico model against in vivo data is proposed. Computational results of the two cases were compared in terms of fluid velocity, vorticity, helicity, and wall shear stresses, providing a step towards understanding the complex interactions between the AR and blood flow dynamics. Results suggested that the presence of the ring increased the systolic jet flow and post-valve velocities (three-fold increase), reduced the backward, vortical flow during diastole (∼ 9% decrease), and induced modifications in bulk flow and wall shear stresses distribution. Furthermore, the development of an animal-specific digital twin of a post-AA AR represents a significant advancement in the field, providing a valuable tool for future research and for clinical applications to aid AA decision-making process.
主动脉环成形术(AA)是主动脉根部(AR)扩大的一种创新手术技术。它是通过在AR外部或内部植入缝合线、带或环来实现的,从而减小其直径。本研究采用猪特异性工作流程,结合体内磁共振成像(MRI)、体外实验和硅流固耦合(FSI)模拟研究外部单环AA,评估AA方法对AR血流动力学的影响。从猪体内MRI数据中分割出原生和环成形术后ar的CAD模型,并作为制造3d打印树脂模型和实现计算数字双胞胎的基础。前者在脉动流环上进行了测试,而后者则集成在FSI模拟中,并根据所得的实验压力波形设置了随时间变化的边界条件。此外,提出了针对体内数据的硅模型的概念验证。两种情况下的计算结果在流体速度、涡度、螺旋度和壁面剪切应力方面进行了比较,为理解AR和血流动力学之间复杂的相互作用提供了一步。结果表明,环的存在增加了收缩射流和阀后速度(增加了3倍),减少了舒张期的反向和垂直流动(减少了9%),并引起了体积流动和壁面剪切应力分布的改变。此外,动物特异性后AA AR数字孪生体的开发代表了该领域的重大进步,为未来的研究和临床应用提供了有价值的工具,以帮助AA决策过程。
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引用次数: 0
A novel multi-field interaction cutting model for ultrasonically activated surgical devices 一种新型超声激活手术器械多场相互作用切割模型
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-12 DOI: 10.1016/j.cmpb.2026.109241
Shilun Du, Yingda Hu, Fan Wei, Yong Lei

Background and Objectives:

Ultrasonically activated surgical devices (UASDs) are widely used in surgery due to their cutting, hemostatic, and thermal control capabilities. Modeling the UASD cutting process enhances understanding of these surgical procedures, aiding in surgery planning and design optimization. However, existing models lack consideration for the high-frequency cutting interactions, limiting their predictive accuracy. This study aims to develop a UASD-tissue interaction cutting model that considers high-frequency interactions and enhances prediction accuracy for multi-physical fields during cutting.

Methods:

This paper models the multi-field interaction process during the soft tissue cutting in UASD. First, a novel multi-field interaction cutting model is proposed, designed to predict cutting force, deformation, temperature, and tissue damage. Second, a LuGre-based interactive force module considering cellular rupture lubrication effects is developed for characterizing high-frequency UASD-tissue interactions. Third, a localized contact algorithm utilizing position-based dynamics and an adaptive time solver are proposed to achieve stable contact and solve the multi-time scale mechanism equations. Numerical experiments and physical experiments on phantoms and porcine livers are conducted.

Results:

The simulated force, temperature, damage, and deformation are consistent with the physical experimental results. The model captures the negative correlation between cutting speed and lubrication with temperature and friction, and shows increased vibration amplitude can lead to higher friction and heat generation, while maintaining stability across different cutting scenarios.

Conclusions:

The proposed model can robustly and accurately predict the multi-physical interactions during cutting, providing insights into the UASDs cutting process, thereby facilitating surgical planning and instrument design.
背景与目的:超声激活手术装置(uasd)因其切割、止血和热控制等功能在外科手术中得到广泛应用。对UASD切割过程进行建模可以增强对这些手术过程的理解,有助于手术计划和设计优化。然而,现有模型缺乏对高频切削相互作用的考虑,限制了其预测精度。本研究旨在建立一种考虑高频相互作用的uasd -组织相互作用切割模型,提高切割过程中多物理场的预测精度。方法:模拟UASD软组织切割过程中的多场相互作用过程。首先,提出了一种新的多场相互作用切削模型,用于预测切削力、变形、温度和组织损伤。其次,考虑细胞破裂润滑效应,开发了基于lugre的交互力模块,用于表征高频uasd -组织相互作用。第三,提出了一种基于位置动力学和自适应时间求解器的局部接触算法,以实现稳定接触和求解多时间尺度机构方程。对模型和猪肝进行了数值实验和物理实验。结果:模拟的受力、温度、损伤、变形与物理实验结果一致。该模型捕获了切削速度和润滑与温度和摩擦之间的负相关关系,并表明增加的振动幅值可以导致更高的摩擦和热量产生,同时在不同的切削情景下保持稳定性。结论:所建立的模型可以稳健、准确地预测切割过程中的多物理相互作用,为了解uasd切割过程提供依据,从而为手术计划和器械设计提供依据。
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引用次数: 0
Multi-scale heart simulation augments the explainability of artificial intelligence-enabled electrocardiogram through provision of an electrocardiogram database labelled with cellular pathologies 通过提供标记有细胞病理的心电图数据库,多尺度心脏模拟增强了人工智能心电图的可解释性
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-10 DOI: 10.1016/j.cmpb.2026.109247
Jun-ichi Okada , Katsuhito Fujiu , Eriko Hasumi , Ying Chen , Takumi Washio , Toshiaki Hisada , Seiryo Sugiura

Background and Objectives

Although artificial-intelligence-enhanced electrocardiograms (AI-ECGs) offer prediction and diagnosis capabilities superior to those of humans, they exhibit poor explainability and interpretability because of their complex-neural-network-derived black-box characteristics. To augment the explainability of artificial intelligence-enhanced electrocardiogram (AI-ECG) analysis, we proposed a method combining AI-ECG and synthetic ECG database created by a multi-scale heart simulator.

Methods

Using the “UT-Heart” multi-scale heart simulator running on the supercomputer Fugaku, we simulated 30,720 12-lead ECG recordings. This dataset comprises an exhaustive combination of 12 cellular and subcellular pathologies reportedly associated with heart failure and was analysed using a previously developed AI-ECG system that accurately classifies ECGs into New York Heart Association (NYHA) functional classes. By analysing the relationship between HF severity and labelled pathology in each simulated ECG recording, we elucidated the origin of abnormalities detected using AI-ECG.

Results

AI-ECG classified 30,618 ECGs (excluding 102 arrhythmia cases) into 2234 control and 28,384 HF cases. A separate three-group classification identified 2234 control, 18,444 NYHA I/II, and 9940 NYHA III/IV cases. In the two-group classification, significant differences (p < 0.01) were observed in sodium (Na) and Na–calcium exchanger currents and the transmural distribution of distinct cell types. Although the three-group classification revealed a severity-dependent progression of the Na current abnormality, the cell distribution in NYHA III/IV was closer to that of normal cases than to that of NYHA I/II. These findings did not explain the changes in the ECG waveform that the AI-ECG identified as notable features of heart failure in the heatmap analysis.

Conclusions

The ECG dataset generated using the multi-scale heart simulator can enhance the explainability of AI-ECGs by elucidating the mechanisms underlying HF-severity-specific changes in ECGs of heart failure.
背景和目的虽然人工智能增强心电图(AI-ECGs)提供了优于人类的预测和诊断能力,但由于其复杂的神经网络衍生的黑箱特征,它们表现出较差的可解释性和可解释性。为了提高人工智能增强心电图(AI-ECG)分析的可解释性,我们提出了一种将AI-ECG与由多尺度心脏模拟器创建的合成心电数据库相结合的方法。方法采用在Fugaku超级计算机上运行的“UT-Heart”多尺度心脏模拟器,对30720例12导联心电图进行模拟。该数据集包括与心力衰竭相关的12种细胞和亚细胞病理的详尽组合,并使用先前开发的AI-ECG系统进行分析,该系统将心电图准确地分类为纽约心脏协会(NYHA)的功能类别。通过分析每个模拟心电图记录中HF严重程度与标记病理之间的关系,我们阐明了AI-ECG检测到的异常的来源。结果ai - ecg将30618例心电图(不包括102例心律失常)分为对照组2234例和心衰28384例。一个单独的三组分类确定了2234例对照,18444例NYHA I/II和9940例NYHA III/IV。在两组分类中,钠(Na)和钠钙交换电流以及不同类型细胞的跨壁分布存在显著差异(p < 0.01)。虽然三组分类显示Na电流异常的进展是严重依赖的,但NYHA III/IV组的细胞分布比NYHA I/II组更接近正常病例。这些发现并不能解释AI-ECG在热图分析中识别为心力衰竭显著特征的ECG波形变化。结论使用多尺度心脏模拟器生成的ECG数据集可以通过阐明心力衰竭心电图中hf严重程度特异性变化的机制来增强ai -ECG的可解释性。
{"title":"Multi-scale heart simulation augments the explainability of artificial intelligence-enabled electrocardiogram through provision of an electrocardiogram database labelled with cellular pathologies","authors":"Jun-ichi Okada ,&nbsp;Katsuhito Fujiu ,&nbsp;Eriko Hasumi ,&nbsp;Ying Chen ,&nbsp;Takumi Washio ,&nbsp;Toshiaki Hisada ,&nbsp;Seiryo Sugiura","doi":"10.1016/j.cmpb.2026.109247","DOIUrl":"10.1016/j.cmpb.2026.109247","url":null,"abstract":"<div><h3>Background and Objectives</h3><div>Although artificial-intelligence-enhanced electrocardiograms (AI-ECGs) offer prediction and diagnosis capabilities superior to those of humans, they exhibit poor explainability and interpretability because of their complex-neural-network-derived black-box characteristics. To augment the explainability of artificial intelligence-enhanced electrocardiogram (AI-ECG) analysis, we proposed a method combining AI-ECG and synthetic ECG database created by a multi-scale heart simulator.</div></div><div><h3>Methods</h3><div>Using the “UT-Heart” multi-scale heart simulator running on the supercomputer Fugaku, we simulated 30,720 12-lead ECG recordings. This dataset comprises an exhaustive combination of 12 cellular and subcellular pathologies reportedly associated with heart failure and was analysed using a previously developed AI-ECG system that accurately classifies ECGs into New York Heart Association (NYHA) functional classes. By analysing the relationship between HF severity and labelled pathology in each simulated ECG recording, we elucidated the origin of abnormalities detected using AI-ECG.</div></div><div><h3>Results</h3><div>AI-ECG classified 30,618 ECGs (excluding 102 arrhythmia cases) into 2234 control and 28,384 HF cases. A separate three-group classification identified 2234 control, 18,444 NYHA I/II, and 9940 NYHA III/IV cases. In the two-group classification, significant differences (<em>p</em> &lt; 0.01) were observed in sodium (Na) and Na–calcium exchanger currents and the transmural distribution of distinct cell types. Although the three-group classification revealed a severity-dependent progression of the Na current abnormality, the cell distribution in NYHA III/IV was closer to that of normal cases than to that of NYHA I/II. These findings did not explain the changes in the ECG waveform that the AI-ECG identified as notable features of heart failure in the heatmap analysis.</div></div><div><h3>Conclusions</h3><div>The ECG dataset generated using the multi-scale heart simulator can enhance the explainability of AI-ECGs by elucidating the mechanisms underlying HF-severity-specific changes in ECGs of heart failure.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"277 ","pages":"Article 109247"},"PeriodicalIF":4.8,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145975339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
HeartUnloadNet: A cycle-consistent graph network with reduced supervision for predicting unloaded cardiac geometry from diastolic states HeartUnloadNet:一个周期一致的图网络,具有较少的监督,用于预测舒张状态下的无负荷心脏几何形状。
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-08 DOI: 10.1016/j.cmpb.2026.109243
Siyu Mu, Wei Xuan Chan, Choon Hwai Yap

Background and Objective:

The unloaded cardiac geometry, representing the zero-stress and zero-strain reference state of the heart, is fundamental for personalized biomechanical modeling of cardiac function. However, this state cannot be directly observed in vivo, as clinical imaging only captures pressure-loaded geometries such as those at end-diastole. Traditional inverse finite element solvers are commonly used to reconstruct the unloaded geometry, but they require iterative optimization, are computationally expensive, and may suffer from convergence issues. The objective of this study was to develop an efficient and accurate deep learning framework to predict the unloaded left ventricular geometry directly from clinical end-diastolic states.

Methods:

We propose HeartUnloadNet, a graph attention-based neural network that incorporates both mesh topology and physiological parameters, including pressure, myocardial stiffness, and fiber orientation. The framework employs a cycle-consistent bidirectional training strategy, allowing reduced supervision by enforcing that the predicted unloaded state can reconstruct the original end-diastolic geometry. The model was trained and validated on 10,350 finite element simulations generated across diverse anatomical shapes and physiological conditions. Performance was evaluated using geometric metrics such as Dice similarity coefficient, Hausdorff distance, mean distance, and standard deviation of nodal errors.

Results:

HeartUnloadNet achieved sub-millimeter accuracy, with a Dice similarity coefficient of 0.986 ± 0.023 and a Hausdorff distance of 0.083 ± 0.028 cm. Compared to conventional inverse finite element solvers, the framework was over 100,000 times faster, with an average inference time of 0.02 seconds per case. Ablation studies demonstrated that cycle consistency enabled the model to maintain high accuracy even when only 3% of the training data were labeled. The method consistently outperformed baseline architectures across all evaluation metrics.

Conclusions:

HeartUnloadNet provides a scalable and accurate alternative to traditional inverse finite element approaches for estimating the unloaded cardiac geometry. By combining mesh-aware learning with physiological conditioning and reduced supervision, the framework achieves real-time performance while maintaining biomechanical fidelity. This work establishes a foundation for future integration of learning-based surrogates into clinical workflows, supporting patient-specific cardiac modeling and real-time functional assessment.
背景与目的:无负荷心脏几何图形代表心脏的零应力和零应变参考状态,是心功能个性化生物力学建模的基础。然而,这种状态不能在体内直接观察到,因为临床成像只能捕获压力加载的几何形状,例如舒张末期的几何形状。传统的逆有限元求解器通常用于重建未加载的几何结构,但它们需要迭代优化,计算成本高,并且可能存在收敛问题。本研究的目的是开发一个有效和准确的深度学习框架,以直接从临床舒张末期状态预测无负荷左心室几何形状。方法:我们提出了HeartUnloadNet,这是一个基于图形注意力的神经网络,结合了网格拓扑和生理参数,包括压力、心肌刚度和纤维方向。该框架采用循环一致的双向训练策略,通过强制预测的卸载状态可以重建原始的舒张末期几何形状,从而减少了监督。该模型在10,350个不同解剖形状和生理条件下的有限元模拟中进行了训练和验证。使用几何指标如Dice相似系数、Hausdorff距离、平均距离和节点误差的标准偏差来评估性能。结果:HeartUnloadNet达到亚毫米精度,Dice相似系数为0.986±0.023,Hausdorff距离为0.083±0.028 cm。与传统的逆有限元求解器相比,该框架的速度要快10万倍以上,平均推理时间为0.02秒。消融研究表明,周期一致性使模型即使只有3%的训练数据被标记也能保持高精度。该方法始终优于所有评估度量的基线体系结构。结论:HeartUnloadNet提供了一种可扩展的、准确的替代传统的逆向有限元方法来估计无负荷心脏几何形状。通过将网格感知学习与生理条件调节和减少监督相结合,该框架在保持生物力学保真度的同时实现了实时性能。这项工作为未来将基于学习的替代品整合到临床工作流程中奠定了基础,支持针对患者的心脏建模和实时功能评估。
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引用次数: 0
Beyond a single mode: GAN ensembles for diverse medical data generation 超越单一模式:GAN集成多种医疗数据生成
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-02 DOI: 10.1016/j.cmpb.2026.109234
Lorenzo Tronchin , Tommy Löfstedt , Paolo Soda , Valerio Guarrasi

Background and Objective:

The advancement of generative AI in medical imaging faces the trilemma of simultaneously achieving high fidelity and diversity in synthetic data generation. Although Generative Adversarial Networks (GANs) have demonstrated significant potential, they are often hindered by limitations such as mode collapse and poor coverage of real data distributions. This study investigates the use of GAN ensembles as a solution to these challenges, with the goal of enhancing the quality and utility of synthetic medical images.

Methods:

We formulate a multi-objective optimisation problem to select an optimal ensemble of GANs that balances fidelity and diversity. The ensemble comprises models that contribute uniquely to the synthetic data space, ensuring minimal redundancy. A comprehensive evaluation was conducted using three distinct medical imaging datasets. We tested 22 GAN architectures, incorporating various loss functions and regularisation techniques. By sampling models at different training epochs, we crafted 110 unique configurations for ensemble selection.

Results:

The selected GAN ensembles demonstrated improved performance in generating synthetic medical images that closely resemble real data distributions. These ensembles preserved image fidelity while increasing diversity. In some settings, downstream models trained on synthetic data achieved slightly higher accuracy than those trained on real data alone. This effect arises because the synthetic images act as a targeted data augmentation mechanism that enhances class balance and diversity rather than replacing real data.

Conclusions:

GAN ensembles offer a robust solution to the fidelity–diversity–efficiency trade-off in medical image synthesis. By integrating multiple complementary models, the proposed approach improves the representativeness and utility of synthetic medical data, potentially advancing a wide range of clinical and research applications in diagnostic AI.
背景与目的:生成式人工智能在医学成像领域的发展面临着在合成数据生成中同时实现高保真度和多样性的三难选择。尽管生成对抗网络(GANs)已经显示出巨大的潜力,但它们经常受到模式崩溃和真实数据分布覆盖不足等限制的阻碍。本研究探讨了使用GAN集成作为解决这些挑战的方法,目的是提高合成医学图像的质量和实用性。方法:我们制定了一个多目标优化问题,以选择一个最优的gan集合,平衡保真度和多样性。集成包括对合成数据空间做出独特贡献的模型,确保了最小的冗余。使用三种不同的医学成像数据集进行综合评估。我们测试了22种GAN架构,结合了各种损失函数和正则化技术。通过对不同训练时期的模型进行采样,我们为集成选择制作了110种独特的配置。结果:所选择的GAN集成在生成与真实数据分布非常相似的合成医学图像方面表现出改进的性能。这些组合保留了图像的保真度,同时增加了多样性。在某些情况下,使用合成数据训练的下游模型的准确性略高于仅使用真实数据训练的模型。产生这种效果是因为合成图像充当了一种有针对性的数据增强机制,增强了类的平衡和多样性,而不是取代了真实数据。结论:GAN集成为医学图像合成中的保真度-多样性-效率权衡提供了一个强大的解决方案。通过整合多个互补模型,该方法提高了合成医疗数据的代表性和实用性,有望推动诊断人工智能的广泛临床和研究应用。
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引用次数: 0
Towards open-set myoelectric gesture recognition via dual-perspective inconsistency learning 基于双视角不一致学习的开放式肌电手势识别
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-16 DOI: 10.1016/j.cmpb.2026.109258
Chen Liu , Can Han , Chengfeng Zhou , Yaqi Wang , Crystal Cai , Dahong Qian

Background and Objective:

Gesture recognition based on surface electromyography (sEMG) has achieved significant progress in human-machine interaction (HMI), especially in prosthetic control and movement rehabilitation. However, accurately recognizing predefined gestures within a closed set is still inadequate in practice; a robust open-set system needs to effectively reject unknown gestures while correctly classifying known ones, which is rarely explored in the field of myoelectric gesture recognition.

Methods:

To handle this challenge, we first report a significant distinction in prediction inconsistency discovered for unknown classes, which arises from perspective differences and can substantially enhance open-set recognition performance. Based on this insight, we propose a novel dual-perspective inconsistency learning approach, PredIN, to explicitly magnify the prediction inconsistency by enhancing the inconsistency of class feature distribution within different perspectives. Specifically, PredIN maximizes the class feature distribution inconsistency among the dual perspectives to enhance their differences. Meanwhile, it optimizes inter-class separability within an individual perspective to maintain individual performance.

Results:

We evaluate our method on four public benchmark sEMG datasets. Comprehensive experiments demonstrate that the PredIN outperforms state-of-the-art methods by a clear margin.

Conclusion:

Our proposed method simultaneously achieves accurate closed-set classification for predefined gestures and effective rejection for unknown gestures, exhibiting its efficacy and superiority in open-set gesture recognition based on sEMG.
背景与目的:基于表面肌电图(sEMG)的手势识别在人机交互(HMI)方面取得了重大进展,特别是在假肢控制和运动康复方面。然而,在实践中,准确识别封闭集合中的预定义手势仍然是不够的;鲁棒的开集系统需要在对已知手势进行正确分类的同时,对未知手势进行有效的拒绝,这在肌电手势识别领域研究较少。方法:为了应对这一挑战,我们首先报告了未知类的预测不一致性的显著区别,这是由视角差异引起的,可以大大提高开集识别的性能。基于这一认识,我们提出了一种新的双视角不一致学习方法PredIN,通过增强不同视角内类特征分布的不一致性来显式放大预测不一致。具体而言,PredIN最大化了双视角之间的类特征分布不一致性,从而增强了它们之间的差异性。同时,它在单个透视图中优化类间可分离性,以保持单个性能。结果:我们在四个公共基准表面肌电信号数据集上评估了我们的方法。综合实验表明,PredIN的性能明显优于最先进的方法。结论:该方法在对预定义手势进行准确的闭集分类的同时,对未知手势进行有效的拒绝,在基于表面肌电信号的开放集手势识别中显示出其有效性和优越性。
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引用次数: 0
Prey capture enhanced Harris hawks optimizer for wrapper-based feature selection in high-dimensional medical data 猎物捕获增强哈里斯鹰优化器包装为基础的特征选择在高维医疗数据
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-04 DOI: 10.1016/j.cmpb.2026.109237
Mohammed Batis , Yi Chen , Lei Liu , Ali Asghar Heidari , Huiling Chen

Background and Objective

While the Harris Hawks Optimizer (HHO) is widely utilized for wrapper-based Feature Selection (FS) due to its efficiency and ease of implementation, existing HHO-based FS approaches encounter challenges when handling high-dimensional datasets, such as falling into local optima and high computational costs. In the HHO algorithm, the Harris hawks engage in surprise attacks on the identified prey according to the prey's escape energy. However, there may be scenarios where the prey could escape due to the algorithm's limitations. To enhance the algorithm's prey-capture ability, this article introduces an enhanced HHO algorithm termed Prey Capture Harris Hawks Optimizer (PCHHO).

Methods

The prey capture strategy incorporates crossover and mutation operators to enhance the algorithm's exploratory-exploitative capabilities. The performance of PCHHO is evaluated on the CEC2017 benchmark suite, where it is compared to HHO, with three enhanced HHO algorithms, nine classical metaheuristic algorithms, and nine improved metaheuristic algorithms. The experimental comparison results are synthesized using the Wilcoxon signed-rank and Friedman tests. Ultimately, a binary form of PCHHO (bPCHHO) is designed for wrapper-based FS and compared with six excellent binary metaheuristics using 15 high-dimensional medical datasets.

Results

The results demonstrate the excellent performance of the proposed algorithm on the CEC2017 benchmark suite compared to other algorithms, as well as the effectiveness of bPCHHO in evolving a subset of features with 77% reduction in classification error, 8% reduction in computational time, and 73% fewer features selected compared to bHHO.

Conclusions

The proposed PCHHO and its binary variant bPCHHO exhibit superior performance in both benchmark optimization and wrapper-based FS for high-dimensional medical data, highlighting their potential for practical applications.
背景与目的Harris Hawks Optimizer (HHO)因其高效和易于实现而被广泛应用于基于包装器的特征选择(FS)中,但现有的基于HHO的特征选择方法在处理高维数据集时面临陷入局部最优和计算成本高的挑战。在HHO算法中,哈里斯鹰根据猎物的逃跑能量对已识别的猎物进行突然袭击。然而,由于算法的局限性,可能会出现猎物逃跑的情况。为了提高算法的猎物捕获能力,本文介绍了一种增强型的HHO算法,称为猎物捕获哈里斯鹰优化器(PCHHO)。方法在捕获策略中引入交叉算子和变异算子,增强算法的探索利用能力。在CEC2017基准测试套件上评估了PCHHO的性能,并将其与HHO进行了比较,其中包括三种增强的HHO算法,九种经典的元启发式算法和九种改进的元启发式算法。采用Wilcoxon符号秩检验和Friedman检验对实验结果进行了综合。最后,针对基于包装器的FS设计了一种二进制形式的PCHHO (bPCHHO),并使用15个高维医疗数据集与6种优秀的二进制元启发式方法进行了比较。结果表明,与其他算法相比,该算法在CEC2017基准测试集上表现优异,并且bPCHHO在进化特征子集方面的有效性,与bHHO相比,分类误差减少77%,计算时间减少8%,选择的特征减少73%。结论所提出的PCHHO及其二进制变体bPCHHO在高维医疗数据的基准优化和基于包装器的FS方面均表现出优异的性能,具有实际应用潜力。
{"title":"Prey capture enhanced Harris hawks optimizer for wrapper-based feature selection in high-dimensional medical data","authors":"Mohammed Batis ,&nbsp;Yi Chen ,&nbsp;Lei Liu ,&nbsp;Ali Asghar Heidari ,&nbsp;Huiling Chen","doi":"10.1016/j.cmpb.2026.109237","DOIUrl":"10.1016/j.cmpb.2026.109237","url":null,"abstract":"<div><h3>Background and Objective</h3><div>While the Harris Hawks Optimizer (HHO) is widely utilized for wrapper-based Feature Selection (FS) due to its efficiency and ease of implementation, existing HHO-based FS approaches encounter challenges when handling high-dimensional datasets, such as falling into local optima and high computational costs. In the HHO algorithm, the Harris hawks engage in surprise attacks on the identified prey according to the prey's escape energy. However, there may be scenarios where the prey could escape due to the algorithm's limitations. To enhance the algorithm's prey-capture ability, this article introduces an enhanced HHO algorithm termed Prey Capture Harris Hawks Optimizer (PCHHO).</div></div><div><h3>Methods</h3><div>The prey capture strategy incorporates crossover and mutation operators to enhance the algorithm's exploratory-exploitative capabilities. The performance of PCHHO is evaluated on the CEC2017 benchmark suite, where it is compared to HHO, with three enhanced HHO algorithms, nine classical metaheuristic algorithms, and nine improved metaheuristic algorithms. The experimental comparison results are synthesized using the Wilcoxon signed-rank and Friedman tests. Ultimately, a binary form of PCHHO (bPCHHO) is designed for wrapper-based FS and compared with six excellent binary metaheuristics using 15 high-dimensional medical datasets.</div></div><div><h3>Results</h3><div>The results demonstrate the excellent performance of the proposed algorithm on the CEC2017 benchmark suite compared to other algorithms, as well as the effectiveness of bPCHHO in evolving a subset of features with 77% reduction in classification error, 8% reduction in computational time, and 73% fewer features selected compared to bHHO.</div></div><div><h3>Conclusions</h3><div>The proposed PCHHO and its binary variant bPCHHO exhibit superior performance in both benchmark optimization and wrapper-based FS for high-dimensional medical data, highlighting their potential for practical applications.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"277 ","pages":"Article 109237"},"PeriodicalIF":4.8,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145975338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Decoding metabolic reprogramming heterogeneity across bladder cancer stages using single-cell and spatial multi-omics approaches 利用单细胞和空间多组学方法解码膀胱癌分期的代谢重编程异质性
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-21 DOI: 10.1016/j.cmpb.2026.109261
Jiang Zhao , Jingwei Zhao , Wei Huang , Weijie Lin , Kuangzheng Jie , Zihang Wu , Benyi Li , Lixin Fan , Xiangwei Wang

Background

Reprogramming of metabolic pathways represents a central indicator in cancer pathogenesis, but the metabolic heterogeneity of bladder cancer (BLCA) at different stages is not well understood. This study aims to analyze metabolic reprogramming in BLCA across stages and its impact on patient survival.

Methods

Single-cell sequencing data were used to examine metabolic heterogeneity of epithelial cells and cell subpopulation differentiation in BLCA at various clinical stages. Spatial transcriptome data were analyzed for copy number variability and riboflavin metabolism in BLCA epithelial cells. Bulk RNA sequencing data from BLCA patients were used for riboflavin pathway expression analysis and prognostic biomarker identification. The effects of three biomarkers (ENPP1, ACP1, and RFK) on BLCA risk were validated using RT-qPCR, Mendelian randomization and co-localization analysis.

Results

Epithelial cells exhibited significant metabolic heterogeneity during bladder cancer progression. Compared to normal control stage, riboflavin metabolic activity progressively increased with disease stage, as validated by spatial transcriptomics and bulk RNA-seq. High expression of ENPP1, ACP1, and RFK (riboflavin pathway) strongly correlated with poor overall survival. RT-qPCR confirmed their high expression in tumours, increasing with stage. Mendelian randomisation/co-localisation indicated these genes localise to bladder epithelium, and their genetic variation associates negatively with BLCA risk.

Conclusion

Increased riboflavin metabolism is likely to be an important marker of malignant progression in BLCA. The ENPP1, ACP1 and RFK genes in this pathway may serve as valuable prognostic biomarkers for BLCA, with potential implications for early diagnosis, monitoring disease progression, and guiding personalized treatment strategies.
代谢途径的编程是癌症发病机制的中心指标,但膀胱癌(BLCA)在不同阶段的代谢异质性尚不清楚。本研究旨在分析不同阶段BLCA的代谢重编程及其对患者生存的影响。方法利用单细胞测序数据检测BLCA不同临床阶段上皮细胞的代谢异质性和细胞亚群分化。分析了BLCA上皮细胞的拷贝数变异性和核黄素代谢的空间转录组数据。来自BLCA患者的大量RNA测序数据用于核黄素途径表达分析和预后生物标志物鉴定。采用RT-qPCR、孟德尔随机化和共定位分析验证三种生物标志物(ENPP1、ACP1和RFK)对BLCA风险的影响。结果上皮细胞在膀胱癌进展过程中表现出明显的代谢异质性。空间转录组学和大量RNA-seq证实,与正常对照期相比,核黄素代谢活性随着疾病分期逐渐增加。ENPP1、ACP1和RFK(核黄素途径)的高表达与较差的总生存率密切相关。RT-qPCR证实了它们在肿瘤中的高表达,随分期增加而增加。孟德尔随机化/共定位表明,这些基因定位于膀胱上皮,其遗传变异与BLCA风险呈负相关。结论核黄素代谢增高可能是BLCA恶性进展的重要标志。该通路中的ENPP1、ACP1和RFK基因可能作为BLCA的有价值的预后生物标志物,具有早期诊断、监测疾病进展和指导个性化治疗策略的潜在意义。
{"title":"Decoding metabolic reprogramming heterogeneity across bladder cancer stages using single-cell and spatial multi-omics approaches","authors":"Jiang Zhao ,&nbsp;Jingwei Zhao ,&nbsp;Wei Huang ,&nbsp;Weijie Lin ,&nbsp;Kuangzheng Jie ,&nbsp;Zihang Wu ,&nbsp;Benyi Li ,&nbsp;Lixin Fan ,&nbsp;Xiangwei Wang","doi":"10.1016/j.cmpb.2026.109261","DOIUrl":"10.1016/j.cmpb.2026.109261","url":null,"abstract":"<div><h3>Background</h3><div>Reprogramming of metabolic pathways represents a central indicator in cancer pathogenesis, but the metabolic heterogeneity of bladder cancer (BLCA) at different stages is not well understood. This study aims to analyze metabolic reprogramming in BLCA across stages and its impact on patient survival.</div></div><div><h3>Methods</h3><div>Single-cell sequencing data were used to examine metabolic heterogeneity of epithelial cells and cell subpopulation differentiation in BLCA at various clinical stages. Spatial transcriptome data were analyzed for copy number variability and riboflavin metabolism in BLCA epithelial cells. Bulk RNA sequencing data from BLCA patients were used for riboflavin pathway expression analysis and prognostic biomarker identification. The effects of three biomarkers (ENPP1, ACP1, and RFK) on BLCA risk were validated using RT-qPCR, Mendelian randomization and co-localization analysis.</div></div><div><h3>Results</h3><div>Epithelial cells exhibited significant metabolic heterogeneity during bladder cancer progression. Compared to normal control stage, riboflavin metabolic activity progressively increased with disease stage, as validated by spatial transcriptomics and bulk RNA-seq. High expression of ENPP1, ACP1, and RFK (riboflavin pathway) strongly correlated with poor overall survival. RT-qPCR confirmed their high expression in tumours, increasing with stage. Mendelian randomisation/co-localisation indicated these genes localise to bladder epithelium, and their genetic variation associates negatively with BLCA risk.</div></div><div><h3>Conclusion</h3><div>Increased riboflavin metabolism is likely to be an important marker of malignant progression in BLCA. The ENPP1, ACP1 and RFK genes in this pathway may serve as valuable prognostic biomarkers for BLCA, with potential implications for early diagnosis, monitoring disease progression, and guiding personalized treatment strategies.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"277 ","pages":"Article 109261"},"PeriodicalIF":4.8,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146074614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Doppler ultrasound and high-frame-rate ultrasound particle image velocimetry derived inlet boundary conditions on wall shear stress parameters in the stented superficial femoral artery 多普勒超声和高帧率超声粒子图像测速导出的入口边界条件对支架内股浅动脉壁剪应力参数的影响
IF 4.8 2区 医学 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS Pub Date : 2026-04-01 Epub Date: 2026-01-17 DOI: 10.1016/j.cmpb.2026.109259
Lisa Rutten , Lennart van de Velde , Lente Pol , Kartik Jain , Michel M.P.J. Reijnen , Michel Versluis

Background and Objectives

Hemodynamic predictions by computational fluid dynamics (CFD) strongly depend on inlet boundary conditions (IBC). One-dimensional Doppler ultrasound (DUS) is typically used for estimating flow IBCs, despite its sensitivity to the operator, ultrasound hardware and assumptions in flow rate computation. An alternative is two-dimensional high-frame-rate ultrasound particle image velocimetry (echoPIV). This study investigated the differences between DUS and echoPIV-derived IBCs and their effect on wall shear stress parameters in the stented superficial femoral artery.

Methods

CFD simulations using DUS and echoPIV-derived IBCs were performed for three patients with a superficial femoral artery stenosis that were treated with a stent. Spatiotemporal velocity profiles were compared at 0 – 50 mm from the inlet. Differences were quantified with the root-mean-square error (RMSE). Regions of low time-averaged wall shear stress (TAWSS) and high oscillatory shear index (OSI) using a literature-based threshold of 0.4 Pa and 0.2, respectively, and an IBC-specific threshold (lower third and upper third, respectively) were determined. Co-localization was quantified using the Jaccard similarity index.

Results

The DUS and echoPIV-derived IBCs differed in flow rate and velocity profile, with the largest difference found at peak systole (RMSE: > 50 cm/s). Using the literature-based threshold, similarity in low TAWSS was high for two patients (0.85 – 0.88) and low for one (0.57). Agreement in high OSI was low in two patients (0.45 – 0.48) and high in one patient (0.83). The IBC-specific threshold increased the agreement for both low TAWSS and high OSI (≥0.75).

Conclusions

Differences in DUS and echoPIV-derived IBCs affected the TAWSS and OSI magnitudes. Regions of low TAWSS and high OSI corresponded well using an IBC-specific threshold. The literature-based threshold resulted in lower similarity values and different interpretations of restenosis risk that may cause differences in follow-up intensity or medical management.
背景与目的计算流体力学(CFD)的血流动力学预测在很大程度上依赖于入口边界条件(IBC)。一维多普勒超声(DUS)通常用于估计流量ibc,尽管它对操作员、超声硬件和流量计算中的假设很敏感。另一种选择是二维高帧率超声粒子图像测速(echoPIV)。本研究探讨了DUS和echopiv衍生的IBCs的差异及其对支架股浅动脉壁剪切应力参数的影响。方法采用DUS和echopiv衍生IBCs对3例经支架治疗的股浅动脉狭窄患者进行scfd模拟。在距离进气道0 ~ 50mm处比较了时空速度分布。差异用均方根误差(RMSE)量化。采用基于文献的阈值分别为0.4 Pa和0.2,以及ibc特定阈值(分别为下三分之一和上三分之一)确定了低时间平均壁剪应力(TAWSS)和高振荡剪切指数(OSI)区域。采用Jaccard相似性指数对共定位进行量化。结果DUS和echopiv衍生的IBCs在流速和速度分布上存在差异,在收缩期峰值差异最大(RMSE: 50 cm/s)。使用基于文献的阈值,低TAWSS的相似性在2例患者中较高(0.85 - 0.88),在1例患者中较低(0.57)。高OSI的一致性在2例患者中较低(0.45 - 0.48),在1例患者中较高(0.83)。ibc特异性阈值增加了低TAWSS和高OSI(≥0.75)的一致性。结论DUS和echopiv源性IBCs的差异影响TAWSS和OSI的大小。使用ibc特定阈值,低TAWSS和高OSI区域对应良好。基于文献的阈值导致较低的相似值和对再狭窄风险的不同解释,这可能导致随访强度或医疗管理的差异。
{"title":"Effect of Doppler ultrasound and high-frame-rate ultrasound particle image velocimetry derived inlet boundary conditions on wall shear stress parameters in the stented superficial femoral artery","authors":"Lisa Rutten ,&nbsp;Lennart van de Velde ,&nbsp;Lente Pol ,&nbsp;Kartik Jain ,&nbsp;Michel M.P.J. Reijnen ,&nbsp;Michel Versluis","doi":"10.1016/j.cmpb.2026.109259","DOIUrl":"10.1016/j.cmpb.2026.109259","url":null,"abstract":"<div><h3>Background and Objectives</h3><div>Hemodynamic predictions by computational fluid dynamics (CFD) strongly depend on inlet boundary conditions (IBC). One-dimensional Doppler ultrasound (DUS) is typically used for estimating flow IBCs, despite its sensitivity to the operator, ultrasound hardware and assumptions in flow rate computation. An alternative is two-dimensional high-frame-rate ultrasound particle image velocimetry (echoPIV). This study investigated the differences between DUS and echoPIV-derived IBCs and their effect on wall shear stress parameters in the stented superficial femoral artery.</div></div><div><h3>Methods</h3><div>CFD simulations using DUS and echoPIV-derived IBCs were performed for three patients with a superficial femoral artery stenosis that were treated with a stent. Spatiotemporal velocity profiles were compared at 0 – 50 mm from the inlet. Differences were quantified with the root-mean-square error (RMSE). Regions of low time-averaged wall shear stress (TAWSS) and high oscillatory shear index (OSI) using a literature-based threshold of 0.4 Pa and 0.2, respectively, and an IBC-specific threshold (lower third and upper third, respectively) were determined. Co-localization was quantified using the Jaccard similarity index.</div></div><div><h3>Results</h3><div>The DUS and echoPIV-derived IBCs differed in flow rate and velocity profile, with the largest difference found at peak systole (RMSE: &gt; 50 cm/s). Using the literature-based threshold, similarity in low TAWSS was high for two patients (0.85 – 0.88) and low for one (0.57). Agreement in high OSI was low in two patients (0.45 – 0.48) and high in one patient (0.83). The IBC-specific threshold increased the agreement for both low TAWSS and high OSI (≥0.75).</div></div><div><h3>Conclusions</h3><div>Differences in DUS and echoPIV-derived IBCs affected the TAWSS and OSI magnitudes. Regions of low TAWSS and high OSI corresponded well using an IBC-specific threshold. The literature-based threshold resulted in lower similarity values and different interpretations of restenosis risk that may cause differences in follow-up intensity or medical management.</div></div>","PeriodicalId":10624,"journal":{"name":"Computer methods and programs in biomedicine","volume":"277 ","pages":"Article 109259"},"PeriodicalIF":4.8,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146024464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Computer methods and programs in biomedicine
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