启动时间:基于ct的儿童肺部疾病放射组学

Y. Zhang, X. Ma, C. Zhao
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Accurate diagnosis is a difficult problem in pediatric imaging. In the era of precision medicine, the development of CT-basted radiomics brings challenges and opportunities for the accurate diagnosis and treatment of children’s lung diseases. At present, the application of radiomics to the thorax is almost exclusively focused on lung cancer, specifically, the detection of lung cancer, prediction of histology and subtype, prediction of prognosis, and assessment of treatment effect [5], which has shown independent prognosis and prediction capacity in many tumors and played a very important role in increasing the accuracy of diagnosis, reducing the application rate of invasive examination, and assessing the risk of lung cancer progression [6,7]. In addition, imageology has also been used to predict lung cancer gene phenotype and mutation [8]. Some studies have been carried out in pulmonary inflammation disease including infectious pneumonia, interstitial pneumonie, chronic lung injury and chronic pulmonary diseases. By extracting characteristics of image area of lesion and using computer-assisted texture-based image analysis, quantitative assessment of highresolution computed tomography and disease assessment can be realized adequately in general interstitial pneumonie [9]. the accuracy rate of classification for the image area of ground-glass opacity lesion was 70.7%.In addition, different image group labels can extract different image group characteristics, which can be used to identify chronic lung injury and pneumonia [10]. Chronic Obstructive Pulmonary Disease (COPD), as a common disease in respiratory department, is caused by small airway disease (obstructive bronchitis) and lung parenchymal destruction (emphysema). However, the proportions of lesion in COPD patients were different [11]. As the development of CT-basted radiomics, the mathematical model of airway function based on standard vital capacity can be used to analyze the existence and severity of emphysema in patients with COPD [12]. The volume of pulmonary emphysema and air-trapping retention in patients with COPD can also be quantified and positioned relatively by using the parameters of the low attenuation area in CT scans [13]. The visual manifestations and severity of emphysema, which may reflect the severity of small airway disease, are significantly correlated with the risk of death [14,15]. The study of Charbonnier JP et al. also has been proved that the parametric spectrum of lung (PRM) is a tool for the classification of quantitative density of COPD [16]. Cho MH et al. showed the relationship between gene and image subtypes in 12031 patients with COPD, which opened a new field for the differential genetics of COPD phenotype [17]. Asthma, as a heterogeneous disease, is easily confused with COPD and can benefit from the classification of subtypes. Improving the prognosis of asthmatic patients by using personalized clinical and imaging biomarkers has been one of the primary goals of the Severe Asthma Research Program (SARP) Project [18]. Quantitative study of CT providing structural and functional information of lung has been a useful tool for the study of asthma [19,20], This technique can identify the unique structure and functional phenotype of asthma and COPD successfully [21]. Research findings airway remodeling and air retention in Quantitative study of CT were associated with lung function, severity of asthma and histology, which can be used to distinguish asthma subgroups and served as the basis for the development of new therapies [22,23]. Quantitative analysis of chest CT images can identify and quantify Interstitial Lung Disease (ILD) [24]. The main imaging features of ILD on CT images are ground glass shadow, honeycomb shadow, reticular shadow, and consolidation shadow etc. Pulmonary Quantitative Analysis (QA) of CT images can objectively quantify specific patterns of ILD changes during treatment in patients with SSc-ILD [25]. With the understanding of different modes of IFP, which can find subtle changes, it may be helpful not only to reduce the invasive operation, but also to precisely treat patients and evaluate the therapeutic effects [26]. Therefore, based on the theory and clinical applications of radiomics, CT-basted radiomics will serve as a new radiological analysis tool for treatment prediction in lung diseases of children [27]. However, the application of accurate radiomic in children’s lung diseases is rare. Only a few studies have focus on the semiquantitative CT measurements to quantitatively assess the extent of air trapping [28,29]. The characteristic CT findings in BO included mosaic air retention, bronchiectasis and atelectasis, which were not evenly distributed throughout the lung [30]. Quantitative detection of CT in post-transplant BO patients with air retention is associated with airway obstruction in PFT [28]. A previous study showed the value of the quantitative CT analysis in predicting severity and longitudinal changes of inhalation lung injury. The quantitative CT analysis could also help to assess pulmonary function by some CT indicators, including Normally Aerated Volume Ratio (NAVR) and Reductively Aerated Volume Ratio (RAVR) [31]. Some studies also focused on unique structural abnormalities in chest CT scans of Bronchopulmonary Dysplasia (BPD) patients, and found that the scope of lesions in image correlates with the clinical manifestations and lung function in children with BPD. Currently, radiomics has become a challenge in pediatrics and also proposes some problems need to be further solved. 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At present, the application of radiomics to the thorax is almost exclusively focused on lung cancer, specifically, the detection of lung cancer, prediction of histology and subtype, prediction of prognosis, and assessment of treatment effect [5], which has shown independent prognosis and prediction capacity in many tumors and played a very important role in increasing the accuracy of diagnosis, reducing the application rate of invasive examination, and assessing the risk of lung cancer progression [6,7]. In addition, imageology has also been used to predict lung cancer gene phenotype and mutation [8]. Some studies have been carried out in pulmonary inflammation disease including infectious pneumonia, interstitial pneumonie, chronic lung injury and chronic pulmonary diseases. By extracting characteristics of image area of lesion and using computer-assisted texture-based image analysis, quantitative assessment of highresolution computed tomography and disease assessment can be realized adequately in general interstitial pneumonie [9]. the accuracy rate of classification for the image area of ground-glass opacity lesion was 70.7%.In addition, different image group labels can extract different image group characteristics, which can be used to identify chronic lung injury and pneumonia [10]. Chronic Obstructive Pulmonary Disease (COPD), as a common disease in respiratory department, is caused by small airway disease (obstructive bronchitis) and lung parenchymal destruction (emphysema). However, the proportions of lesion in COPD patients were different [11]. As the development of CT-basted radiomics, the mathematical model of airway function based on standard vital capacity can be used to analyze the existence and severity of emphysema in patients with COPD [12]. The volume of pulmonary emphysema and air-trapping retention in patients with COPD can also be quantified and positioned relatively by using the parameters of the low attenuation area in CT scans [13]. The visual manifestations and severity of emphysema, which may reflect the severity of small airway disease, are significantly correlated with the risk of death [14,15]. The study of Charbonnier JP et al. also has been proved that the parametric spectrum of lung (PRM) is a tool for the classification of quantitative density of COPD [16]. Cho MH et al. showed the relationship between gene and image subtypes in 12031 patients with COPD, which opened a new field for the differential genetics of COPD phenotype [17]. Asthma, as a heterogeneous disease, is easily confused with COPD and can benefit from the classification of subtypes. Improving the prognosis of asthmatic patients by using personalized clinical and imaging biomarkers has been one of the primary goals of the Severe Asthma Research Program (SARP) Project [18]. Quantitative study of CT providing structural and functional information of lung has been a useful tool for the study of asthma [19,20], This technique can identify the unique structure and functional phenotype of asthma and COPD successfully [21]. Research findings airway remodeling and air retention in Quantitative study of CT were associated with lung function, severity of asthma and histology, which can be used to distinguish asthma subgroups and served as the basis for the development of new therapies [22,23]. Quantitative analysis of chest CT images can identify and quantify Interstitial Lung Disease (ILD) [24]. The main imaging features of ILD on CT images are ground glass shadow, honeycomb shadow, reticular shadow, and consolidation shadow etc. Pulmonary Quantitative Analysis (QA) of CT images can objectively quantify specific patterns of ILD changes during treatment in patients with SSc-ILD [25]. With the understanding of different modes of IFP, which can find subtle changes, it may be helpful not only to reduce the invasive operation, but also to precisely treat patients and evaluate the therapeutic effects [26]. Therefore, based on the theory and clinical applications of radiomics, CT-basted radiomics will serve as a new radiological analysis tool for treatment prediction in lung diseases of children [27]. However, the application of accurate radiomic in children’s lung diseases is rare. Only a few studies have focus on the semiquantitative CT measurements to quantitatively assess the extent of air trapping [28,29]. The characteristic CT findings in BO included mosaic air retention, bronchiectasis and atelectasis, which were not evenly distributed throughout the lung [30]. Quantitative detection of CT in post-transplant BO patients with air retention is associated with airway obstruction in PFT [28]. A previous study showed the value of the quantitative CT analysis in predicting severity and longitudinal changes of inhalation lung injury. The quantitative CT analysis could also help to assess pulmonary function by some CT indicators, including Normally Aerated Volume Ratio (NAVR) and Reductively Aerated Volume Ratio (RAVR) [31]. Some studies also focused on unique structural abnormalities in chest CT scans of Bronchopulmonary Dysplasia (BPD) patients, and found that the scope of lesions in image correlates with the clinical manifestations and lung function in children with BPD. Currently, radiomics has become a challenge in pediatrics and also proposes some problems need to be further solved. 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引用次数: 0

摘要

放射组学是一门新兴的交叉学科,是大数据技术和医学影像辅助诊断的融合产物。放射组学可以从不同的医学影像(如CT、PET、MRI、超声)中收集信息,进行更深入的挖掘,预测分析,量化疾病特征,建立疾病模型,识别新的诊断和预后生物标志物,协助医生做出最准确的诊断[1,2]。近年来,它已发展成为一种由影像、基因和临床信息组成的辅助诊断、分析和预测的方法。基于ct的放射组学对肺组织的分辨率高,在肺部疾病的研究中具有显著优势,为肺部疾病的准确诊断和治疗提供了巨大的潜力[3,4]。准确诊断是儿科影像学的一个难题。在精准医疗时代,基于ct的放射组学的发展为儿童肺部疾病的准确诊断和治疗带来了挑战和机遇。目前,放射组学在胸腔的应用几乎全部集中在肺癌上,具体来说,在肺癌的检测、组织学及亚型的预测、预后的预测、治疗效果的评估[5]等方面,已经在许多肿瘤中显示出独立的预后和预测能力,在提高诊断准确率、降低有创检查的应用率方面发挥了非常重要的作用。以及评估肺癌进展的风险[6,7]。此外,影像学也被用于预测肺癌基因表型和突变[8]。对感染性肺炎、间质性肺炎、慢性肺损伤和慢性肺部疾病等肺部炎症疾病进行了一些研究。通过提取病变图像区域特征,利用计算机辅助的基于纹理的图像分析,可以充分实现对一般间质性肺炎bb0的高分辨率计算机断层成像定量评估和疾病评估。对毛玻璃混浊病变图像区域的分类准确率为70.7%。此外,不同的图像组标签可以提取不同的图像组特征,可用于识别慢性肺损伤和肺炎[10]。慢性阻塞性肺疾病(Chronic Obstructive Pulmonary Disease, COPD)是由小气道疾病(阻塞性支气管炎)和肺实质破坏(肺气肿)引起的呼吸内科常见病。然而,慢性阻塞性肺病患者的病变比例不同。随着ct放射组学的发展,基于标准肺活量的气道功能数学模型可用于分析COPD患者肺气肿的存在及严重程度。利用CT扫描低衰减区参数[13],也可以量化COPD患者肺气肿的体积和空气潴留量,并进行相对定位。肺气肿的视觉表现和严重程度与死亡风险显著相关,可反映小气道疾病的严重程度[14,15]。Charbonnier JP等人的研究也证明了肺参数谱(parameter spectrum of lung, PRM)是COPD bbb定量密度分类的工具0。Cho MH等在12031例COPD患者中显示了基因与图像亚型之间的关系,为COPD表型[17]的差异遗传学开辟了新的领域。哮喘作为一种异质性疾病,很容易与COPD混淆,并且可以从亚型分类中获益。通过使用个性化的临床和成像生物标志物来改善哮喘患者的预后是严重哮喘研究计划(SARP)[18]项目的主要目标之一。提供肺结构和功能信息的CT定量研究已成为哮喘研究的有用工具[19,20],该技术可以成功识别哮喘和COPD独特的结构和功能表型[21]。研究发现CT定量研究中气道重塑和空气潴留与肺功能、哮喘严重程度和组织学相关,可用于区分哮喘亚群,是开发新疗法的基础[22,23]。定量分析胸部CT图像可以识别和量化间质性肺疾病(ILD)[24]。CT图像上ILD的主要成像特征有磨玻璃影、蜂窝影、网状影、实变影等。CT图像的肺部定量分析(QA)可以客观地量化SSc-ILD患者治疗期间ILD变化的特定模式。 了解不同的IFP模式,发现细微的变化,不仅有助于减少手术的侵入性,而且有助于对患者进行精准治疗,评估治疗效果[26]。因此,基于放射组学的理论和临床应用,基于ct的放射组学将成为一种新的放射学分析工具,用于儿童肺部疾病的治疗预测。然而,精确放射组学在儿童肺部疾病中的应用很少。只有少数研究关注于半定量CT测量来定量评估空气捕获的程度[28,29]。BO的特征性CT表现为弥散性空气潴留、支气管扩张和肺不张,且在肺内分布不均匀。移植后BO患者伴空气潴留的CT定量检测与PFT[28]气道阻塞相关。先前的研究显示定量CT分析在预测吸入性肺损伤的严重程度和纵向变化方面的价值。定量CT分析还可以通过正常充气容积比(NAVR)和还原性充气容积比(RAVR)[31]等CT指标评估肺功能。一些研究还关注了支气管肺发育不良(BPD)患者胸部CT扫描中独特的结构异常,发现图像上病变的范围与BPD患儿的临床表现和肺功能相关。目前,放射组学已经成为儿科学的一个挑战,也提出了一些需要进一步解决的问题。首先,需要对扫描方案、研究方法、参数等多因素制定标准化方案,建立多病、大样本数据。其次,图像的稳定性和放射组学模型建立的准确性也有待进一步研究。最后,放射组学、组织病理学和基因之间的关系需要在儿科学中进一步探讨。综上所述,放射组学可以帮助识别新的生物标志物,为了解未知疾病的表型提供新的见解,减少或避免创伤性手术,为准确诊断和个性化治疗提供广阔的前景。基于CT在肺部疾病中的优势,我们的目标是关注基于CT的儿童肺部疾病放射组学,为儿童肺部疾病的精准医疗提供准确的信息支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time to Start Up: CT-Basted Radiomics in Children’s Lung Diseases
Radiomics is a new interdisciplinary field and a fusion product consisting by large data technology and medical image to aid diagnosis. Radiomics can gather information from different medical imaging (i.e. CT, PET, MRI, ultrasound) for deeper excavation, predict and analyse to quantify disease characteristics, establish disease models, and identify new diagnostic and prognostic biomarkers to assist physicians in making the most accurate diagnosis [1,2]. Recently, it has evolved into a method which consisted of imaging, gene, and clinical information for auxiliary diagnosis, analysis and prediction. CT-basted radiomics has significant advantages in the study of lung diseases due to its high resolution for lung tissue, which represents a great potential for accurate diagnosis and treatment of lung diseases [3,4]. Accurate diagnosis is a difficult problem in pediatric imaging. In the era of precision medicine, the development of CT-basted radiomics brings challenges and opportunities for the accurate diagnosis and treatment of children’s lung diseases. At present, the application of radiomics to the thorax is almost exclusively focused on lung cancer, specifically, the detection of lung cancer, prediction of histology and subtype, prediction of prognosis, and assessment of treatment effect [5], which has shown independent prognosis and prediction capacity in many tumors and played a very important role in increasing the accuracy of diagnosis, reducing the application rate of invasive examination, and assessing the risk of lung cancer progression [6,7]. In addition, imageology has also been used to predict lung cancer gene phenotype and mutation [8]. Some studies have been carried out in pulmonary inflammation disease including infectious pneumonia, interstitial pneumonie, chronic lung injury and chronic pulmonary diseases. By extracting characteristics of image area of lesion and using computer-assisted texture-based image analysis, quantitative assessment of highresolution computed tomography and disease assessment can be realized adequately in general interstitial pneumonie [9]. the accuracy rate of classification for the image area of ground-glass opacity lesion was 70.7%.In addition, different image group labels can extract different image group characteristics, which can be used to identify chronic lung injury and pneumonia [10]. Chronic Obstructive Pulmonary Disease (COPD), as a common disease in respiratory department, is caused by small airway disease (obstructive bronchitis) and lung parenchymal destruction (emphysema). However, the proportions of lesion in COPD patients were different [11]. As the development of CT-basted radiomics, the mathematical model of airway function based on standard vital capacity can be used to analyze the existence and severity of emphysema in patients with COPD [12]. The volume of pulmonary emphysema and air-trapping retention in patients with COPD can also be quantified and positioned relatively by using the parameters of the low attenuation area in CT scans [13]. The visual manifestations and severity of emphysema, which may reflect the severity of small airway disease, are significantly correlated with the risk of death [14,15]. The study of Charbonnier JP et al. also has been proved that the parametric spectrum of lung (PRM) is a tool for the classification of quantitative density of COPD [16]. Cho MH et al. showed the relationship between gene and image subtypes in 12031 patients with COPD, which opened a new field for the differential genetics of COPD phenotype [17]. Asthma, as a heterogeneous disease, is easily confused with COPD and can benefit from the classification of subtypes. Improving the prognosis of asthmatic patients by using personalized clinical and imaging biomarkers has been one of the primary goals of the Severe Asthma Research Program (SARP) Project [18]. Quantitative study of CT providing structural and functional information of lung has been a useful tool for the study of asthma [19,20], This technique can identify the unique structure and functional phenotype of asthma and COPD successfully [21]. Research findings airway remodeling and air retention in Quantitative study of CT were associated with lung function, severity of asthma and histology, which can be used to distinguish asthma subgroups and served as the basis for the development of new therapies [22,23]. Quantitative analysis of chest CT images can identify and quantify Interstitial Lung Disease (ILD) [24]. The main imaging features of ILD on CT images are ground glass shadow, honeycomb shadow, reticular shadow, and consolidation shadow etc. Pulmonary Quantitative Analysis (QA) of CT images can objectively quantify specific patterns of ILD changes during treatment in patients with SSc-ILD [25]. With the understanding of different modes of IFP, which can find subtle changes, it may be helpful not only to reduce the invasive operation, but also to precisely treat patients and evaluate the therapeutic effects [26]. Therefore, based on the theory and clinical applications of radiomics, CT-basted radiomics will serve as a new radiological analysis tool for treatment prediction in lung diseases of children [27]. However, the application of accurate radiomic in children’s lung diseases is rare. Only a few studies have focus on the semiquantitative CT measurements to quantitatively assess the extent of air trapping [28,29]. The characteristic CT findings in BO included mosaic air retention, bronchiectasis and atelectasis, which were not evenly distributed throughout the lung [30]. Quantitative detection of CT in post-transplant BO patients with air retention is associated with airway obstruction in PFT [28]. A previous study showed the value of the quantitative CT analysis in predicting severity and longitudinal changes of inhalation lung injury. The quantitative CT analysis could also help to assess pulmonary function by some CT indicators, including Normally Aerated Volume Ratio (NAVR) and Reductively Aerated Volume Ratio (RAVR) [31]. Some studies also focused on unique structural abnormalities in chest CT scans of Bronchopulmonary Dysplasia (BPD) patients, and found that the scope of lesions in image correlates with the clinical manifestations and lung function in children with BPD. Currently, radiomics has become a challenge in pediatrics and also proposes some problems need to be further solved. Firstly, It is necessary to establish standardization programme for many factors, such as scanning scheme, research method, parameters, and establish multiple diseases and large sample data. Secondly, the stability of image and the accuracy of radiomics model building also needs further study. Lastly, the relationship between radiomics, histopathology, and gene, needs to be further explored in pediatrics. In summary, radiomics can help to identify new biomarkers, provide new insights for understanding the phenotypic of unknown diseases, reduce or avoid traumatic operations, and provide broad prospects for accurate diagnosis and personalized treatment. Based on the advantages of CT in lung diseases, we aim to focuse attention on the CT-basted radiomics in lung diseases of children to provide accurate information support for accurate medical of children’s lung diseases.
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