Deep learning segmentation model for quantification of infarct size in pigs with myocardial ischemia/reperfusion

IF 8 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Basic Research in Cardiology Pub Date : 2024-09-30 DOI:10.1007/s00395-024-01081-x
Felix Braczko, Andreas Skyschally, Helmut Lieder, Jakob Nikolas Kather, Petra Kleinbongard, Gerd Heusch
{"title":"Deep learning segmentation model for quantification of infarct size in pigs with myocardial ischemia/reperfusion","authors":"Felix Braczko, Andreas Skyschally, Helmut Lieder, Jakob Nikolas Kather, Petra Kleinbongard, Gerd Heusch","doi":"10.1007/s00395-024-01081-x","DOIUrl":null,"url":null,"abstract":"<p>Infarct size (IS) is the most robust end point for evaluating the success of preclinical studies on cardioprotection. The gold standard for IS quantification in ischemia/reperfusion (I/R) experiments is triphenyl tetrazolium chloride (TTC) staining, typically done manually. This study aimed to determine if automation through deep learning segmentation is a time-saving and valid alternative to standard IS quantification. High-resolution images from TTC-stained, macroscopic heart slices were retrospectively collected from pig experiments (<i>n</i> = 390) with I/R without/with cardioprotection to cover a wide IS range. Existing IS data from pig experiments, quantified using a standard method of manual and subsequent digital labeling of film-scan annotations, were used as reference. To automate the evaluation process with the aim to be more objective and save time, a deep learning pipeline was implemented; the collected images (<i>n</i> = 3869) were pre-processed by cropping and labeled (image annotations). To ensure their usability as training data for a deep learning segmentation model, IS was quantified from image annotations and compared to IS quantified using the existing film-scan annotations. A supervised deep learning segmentation model based on dynamic U-Net architecture was developed and trained. The evaluation of the trained model was performed by fivefold cross-validation (<i>n</i> = 220 experiments) and testing on an independent test set (<i>n</i> = 170 experiments). Performance metrics (Dice similarity coefficient [DSC], pixel accuracy [ACC], average precision [mAP]) were calculated. IS was then quantified from predictions and compared to IS quantified from image annotations (linear regression, Pearson’s <i>r</i>; analysis of covariance; Bland–Altman plots). Performance metrics near 1 indicated a strong model performance on cross-validated data (DSC: 0.90, ACC: 0.98, mAP: 0.90) and on the test set data (DSC: 0.89, ACC: 0.98, mAP: 0.93). IS quantified from predictions correlated well with IS quantified from image annotations in all data sets (cross-validation: <i>r</i> = 0.98; test data set: <i>r</i> = 0.95) and analysis of covariance identified no significant differences. The model reduced the IS quantification time per experiment from approximately 90 min to 20 s. The model was further tested on a preliminary test set from experiments in isolated, saline-perfused rat hearts with regional I/R without/with cardioprotection (<i>n</i> = 27). There was also no significant difference in IS between image annotations and predictions, but the performance on the test set data from rat hearts was lower (DSC: 0.66, ACC: 0.91, mAP: 0.65). IS quantification using a deep learning segmentation model is a valid and time-efficient alternative to manual and subsequent digital labeling.</p>","PeriodicalId":8723,"journal":{"name":"Basic Research in Cardiology","volume":"45 1","pages":""},"PeriodicalIF":8.0000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Basic Research in Cardiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00395-024-01081-x","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Infarct size (IS) is the most robust end point for evaluating the success of preclinical studies on cardioprotection. The gold standard for IS quantification in ischemia/reperfusion (I/R) experiments is triphenyl tetrazolium chloride (TTC) staining, typically done manually. This study aimed to determine if automation through deep learning segmentation is a time-saving and valid alternative to standard IS quantification. High-resolution images from TTC-stained, macroscopic heart slices were retrospectively collected from pig experiments (n = 390) with I/R without/with cardioprotection to cover a wide IS range. Existing IS data from pig experiments, quantified using a standard method of manual and subsequent digital labeling of film-scan annotations, were used as reference. To automate the evaluation process with the aim to be more objective and save time, a deep learning pipeline was implemented; the collected images (n = 3869) were pre-processed by cropping and labeled (image annotations). To ensure their usability as training data for a deep learning segmentation model, IS was quantified from image annotations and compared to IS quantified using the existing film-scan annotations. A supervised deep learning segmentation model based on dynamic U-Net architecture was developed and trained. The evaluation of the trained model was performed by fivefold cross-validation (n = 220 experiments) and testing on an independent test set (n = 170 experiments). Performance metrics (Dice similarity coefficient [DSC], pixel accuracy [ACC], average precision [mAP]) were calculated. IS was then quantified from predictions and compared to IS quantified from image annotations (linear regression, Pearson’s r; analysis of covariance; Bland–Altman plots). Performance metrics near 1 indicated a strong model performance on cross-validated data (DSC: 0.90, ACC: 0.98, mAP: 0.90) and on the test set data (DSC: 0.89, ACC: 0.98, mAP: 0.93). IS quantified from predictions correlated well with IS quantified from image annotations in all data sets (cross-validation: r = 0.98; test data set: r = 0.95) and analysis of covariance identified no significant differences. The model reduced the IS quantification time per experiment from approximately 90 min to 20 s. The model was further tested on a preliminary test set from experiments in isolated, saline-perfused rat hearts with regional I/R without/with cardioprotection (n = 27). There was also no significant difference in IS between image annotations and predictions, but the performance on the test set data from rat hearts was lower (DSC: 0.66, ACC: 0.91, mAP: 0.65). IS quantification using a deep learning segmentation model is a valid and time-efficient alternative to manual and subsequent digital labeling.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
用于量化猪心肌缺血/再灌注梗死面积的深度学习分割模型
梗死面积(IS)是评估心脏保护临床前研究成功与否的最可靠终点。在缺血/再灌注(I/R)实验中,IS量化的黄金标准是三苯基氯化四氮唑(TTC)染色,通常由人工完成。本研究旨在确定通过深度学习分割实现自动化是否是一种省时且有效的标准 IS 定量替代方法。从猪实验(n = 390)中回顾性地收集了TTC染色的高分辨率宏观心脏切片图像,这些实验包括无/有心脏保护的I/R实验,以覆盖广泛的IS范围。猪实验中的现有 IS 数据采用手动量化的标准方法,随后对胶片扫描注释进行数字标注,作为参考。为了使评估过程自动化,从而更加客观并节省时间,我们实施了一个深度学习管道;通过裁剪和标注(图像注释)对收集到的图像(n = 3869)进行了预处理。为确保其作为深度学习分割模型训练数据的可用性,根据图像注释对 IS 进行了量化,并与使用现有胶片扫描注释量化的 IS 进行了比较。开发并训练了一个基于动态 U-Net 架构的有监督深度学习分割模型。通过五重交叉验证(n = 220 次实验)和在独立测试集(n = 170 次实验)上测试,对训练好的模型进行了评估。计算了性能指标(骰子相似系数 [DSC]、像素精度 [ACC]、平均精度 [mAP])。然后根据预测结果量化 IS,并与根据图像注释量化的 IS 进行比较(线性回归、Pearson's r;协方差分析;Bland-Altman 图)。性能指标接近 1 表明模型在交叉验证数据(DSC:0.90,ACC:0.98,mAP:0.90)和测试集数据(DSC:0.89,ACC:0.98,mAP:0.93)上表现优异。在所有数据集中,通过预测量化的 IS 与通过图像注释量化的 IS 相关性良好(交叉验证:r = 0.98;测试数据集:r = 0.95),协方差分析没有发现显著差异。该模型将每次实验的 IS 定量时间从大约 90 分钟减少到 20 秒。该模型在离体、生理盐水灌注的大鼠心脏实验的初步测试集上进行了进一步测试,实验中大鼠心脏区域 I/R(无/有心脏保护)(n = 27)。图像注释和预测之间在 IS 方面也没有明显差异,但在大鼠心脏测试集数据上的性能较低(DSC:0.66;ACC:0.91;mAP:0.65)。使用深度学习分割模型进行IS量化是替代人工和后续数字标注的有效、省时的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Basic Research in Cardiology
Basic Research in Cardiology 医学-心血管系统
CiteScore
16.30
自引率
5.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Basic Research in Cardiology is an international journal for cardiovascular research. It provides a forum for original and review articles related to experimental cardiology that meet its stringent scientific standards. Basic Research in Cardiology regularly receives articles from the fields of - Molecular and Cellular Biology - Biochemistry - Biophysics - Pharmacology - Physiology and Pathology - Clinical Cardiology
期刊最新文献
Peripheral chemoreceptors sustain central chemoreflex potentiation and cardiorespiratory abnormalities in high-output heart failure. From kidney injury to cardiac dysfunction: the central role of oxidative stress in diabetes and CKD. Treadmill exercise activates mechanosensitive Piezo1 to inhibit cardiomyocyte apoptosis and improve cardiac function after myocardial infarction in mice. NLGN3 contributes to angiogenesis in myocardial infarction via activation of the Gαi1/3-Akt pathway. Coronary microvascular dysfunction is a determinant of perfusion-contraction matching during ischemia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1