Mathieu Bottier, Andreia Lucia Do Nascimento Pinto, Britt J Van Akker, Oliver Hamilton, Ioannis Katramados, Amelia Shoemark, Claire Hogg, Thomas Burgoyne
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In collaboration with Intel®, we have used an Artificial Intelligence platform (Intel® Geti™), to develop a workflow called PCD-AID (PCD- Artificial Intelligence Diagnosis) that uses computer vision to aid in the diagnosis of PCD. This work is part of an organised ERS Clinical Research Collaboration with BEAT-PCD. The system was tested alongside the PCD diagnostic pathway (n=158) to determine diagnostic accuracy. The model has been trained with TEM images from over 21,000 cilia cross-sections to detect cilia and then classify them based on normal or abnormal ultrastructure or ‘unusable’ for diagnostic purposes (tilted or distorted images). Using retrospective and prospective patient samples, we have found PCD-AID can reliably identify ciliary ultrastructural defects (sensitivity of 0.87 and specificity of 0.88) and assess TEM images in under 1 minute per patient. It has good agreement with diagnostic specialists (> 75%) at identifying a range of ultrastructural defects and strikingly outperforms specialists at identifying subtle central pair defects associated with pathogenic mutations in <i>HYDIN</i>. 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引用次数: 0
摘要
早期和准确的诊断原发性纤毛运动障碍(PCD)允许适当的多学科管理和减少肺功能下降。在诊断PCD时,透射电子显微镜(TEM)在确定纤毛超微结构缺陷方面是必不可少的。这需要具有丰富经验的高技能专家。机器学习提供了一个很好的机会,可以减少专家评估纤毛的时间(1-2小时),提高诊断的准确性。与英特尔®合作,我们使用人工智能平台(英特尔®Geti™)开发了一个名为PCD- aid (PCD-人工智能诊断)的工作流程,该流程使用计算机视觉来帮助诊断PCD。这项工作是与BEAT-PCD组织的ERS临床研究合作的一部分。该系统与PCD诊断途径(n=158)一起进行测试,以确定诊断准确性。该模型使用来自21,000多个纤毛横截面的TEM图像进行训练,以检测纤毛,然后根据正常或异常的超微结构或“不可用”的诊断目的(倾斜或扭曲的图像)对它们进行分类。通过回顾性和前瞻性患者样本,我们发现PCD-AID可以可靠地识别纤毛超微结构缺陷(灵敏度为0.87,特异性为0.88),并在每位患者不到1分钟的时间内评估TEM图像。它与诊断专家(>75%)在识别一系列超微结构缺陷方面,在识别与HYDIN致病性突变相关的细微中心对缺陷方面,他们的表现明显优于专家。在诊断路径中实现计算机视觉人工智能,提高了PCD的诊断效果。
PCD-AID: artificial intelligence diagnosis of primary ciliary dyskinesia
Early and accurate diagnosis of Primary Ciliary Dyskinesia (PCD) allows appropriate multidisciplinary management and a reduction in lung function decline. Transmission Electron Microscopy (TEM) is essential in determining ciliary ultrastructural defects, when diagnosing PCD. This requires highly skilled specialists with considerable experience. Machine learning provides an excellent opportunity to reduce the time experts spend assessing cilia (1–2 hours) and improve accuracy of diagnosis. In collaboration with Intel®, we have used an Artificial Intelligence platform (Intel® Geti™), to develop a workflow called PCD-AID (PCD- Artificial Intelligence Diagnosis) that uses computer vision to aid in the diagnosis of PCD. This work is part of an organised ERS Clinical Research Collaboration with BEAT-PCD. The system was tested alongside the PCD diagnostic pathway (n=158) to determine diagnostic accuracy. The model has been trained with TEM images from over 21,000 cilia cross-sections to detect cilia and then classify them based on normal or abnormal ultrastructure or ‘unusable’ for diagnostic purposes (tilted or distorted images). Using retrospective and prospective patient samples, we have found PCD-AID can reliably identify ciliary ultrastructural defects (sensitivity of 0.87 and specificity of 0.88) and assess TEM images in under 1 minute per patient. It has good agreement with diagnostic specialists (> 75%) at identifying a range of ultrastructural defects and strikingly outperforms specialists at identifying subtle central pair defects associated with pathogenic mutations in HYDIN. Implementing computer vision artificial intelligence in the diagnostic pathway improved diagnosis of PCD.