无监督学习自动分析心脏多模态影像,识别心肌病变区域。
A novel unsupervised machine learning strategy to handle multimodal cardiac PET/MRI data

- 通过两步聚类整合多种影像数据生成超体素,实现患者间图像关联。
- 在99名患者中达到0.76±0.04的平衡准确率,167个模拟数据验证效果更优。
- 自动生成图文报告,辅助医生发现纤维化或炎症等异常区域。
心律失常性左心室心肌病是一种难以诊断的遗传性心肌病,缺乏金标准诊断依据。同步PET/MR成像结合多参数定量分析,有助于揭示疾病表型与进展特征。本研究提出一种方法学策略,用于处理PET/MRI数据,包括跨患者数据关联与区域分析。对99例经基因确诊的患者,分别对T1、T2图、LGE和18F-FDG-PET图像进行独立z-score标准化后合并为单一体积,并通过超体素聚类生成32组跨患者簇。每簇与各模态赋予“异常”评分,可视化可能与疾病相关的异常区域。该方法生成每位患者的自动化文本及弹道图健康报告,经重复嵌套交叉验证与心内科医生评估对比,平衡准确率达0.76±0.04;在167个数值幻影数据集上进一步验证,准确率≥0.8。聚类结果与医生视觉观察高度一致,可有效识别不同程度的纤维化或炎症。该方法实现了对多模态PET/MRI数据的系统化处理,助力刻画心肌异质性。
原文摘要 · Abstract (English)
Arrhythmogenic left ventricular cardiomyopathy is a genetic myocardial disease difficult to diagnose due to the lack of gold standard criteria. Simultaneous PET/MR imaging, combined with multiparametric quantitative analysis, could facilitate the identification of different profiles related to the phenotype and progression of cardiomyopathy. This preliminary study focuses on a methodological strategy for dealing with PET/MRI data, including inter-patient data linkage and regional analysis. Two-step clustering was applied to T1 and T2 maps, LGE, and 18F-FDG-PET images of 99 patients genetically diagnosed with arrhythmogenic left ventricular cardiomyopathy. Each patient's images were independently z-scored and summed into a single volume, which was clustered into supervoxels. Thirty-two inter-patient groups of supervoxels were obtained by spectral clustering. An "abnormality" score was assigned to each cluster and modality, and used to visualise abnormal regions likely associated with disease. They enabled the generation of automated textual and bullseye health reports for each patient, which were compared with cardiac imager assessments using balanced accuracy in repeated nested cross-validation. This approach was further validated on a larger cohort of 167 numerical phantoms. The reports generated by clustering accurately identified most of the cardiac physicians' observations (BA = 0.76 $\pm$ 0.04 in repeated nested cross-validation on patients, and BA $\ge$ 0.8 on phantoms). Furthermore, the identified abnormal clusters closely matched their visual observations, facilitating the identification of varying degrees of fibrosis or inflammation on the images. This approach enables a more systematic handling of multimodal PET/MRI data to characterise myocardial heterogeneity in arrhythmogenic left ventricular cardiomyopathy patients.
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