基于双能谱CT材料分解图像的放射组学增强机会性骨状态评估。

IF 3.8 3区 医学 Q2 ENGINEERING, BIOMEDICAL Bioengineering Pub Date : 2024-12-12 DOI:10.3390/bioengineering11121257
Qiye Cheng, Jingyi Zhang, Mengting Hu, Shigeng Wang, Yijun Liu, Jianying Li, Wei Wei
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引用次数: 0

摘要

双能谱CT (DEsCT)采用材料分解(MD)技术,为骨状态的机会性评估开辟了新的途径。放射组学是一种阐明骨骼结构和质地特征的强大工具,有助于检测矿物质损失。因此,本研究旨在比较骨密度测量和基于MD图像的放射组学模型对骨状态评估的效果,并进一步探讨放射组学模型的临床价值。方法:回顾性收集了307例在我院接受定量计算机断层扫描(QCT)和全腹部DEsCT扫描的患者的资料。根据QCT测量结果,将患者分为三类:正常骨密度(BMD)、骨质减少和骨质疏松症。利用腹部DEsCT数据重建6种MD图像,包括HAP (Water)、HAP (Fat)、Ca (Water)、Ca (Fat)、Fat (Ca)和Fat (HAP)。将患者随机分为训练组(n = 214)和验证组(n = 93),比例为7:3。聚焦于L1至L3椎体,测量6张MD图像的密度值。利用随机森林分类器构建了6个密度值模型和6个放射组学模型。采用受试者工作特征(ROC)曲线评估这些模型在评估骨状态方面的性能,并采用DeLong检验比较模型之间的性能差异。结果:基于HAP (Water)、HAP (Fat)、Ca (Water)和Ca (Fat) MD图像的密度值模型的宏观曲线下面积(AUC)分别为0.870、0.870、0.847和0.765,优于Fat (Ca) (AUC = 0.623)和Fat (HAP) (AUC = 0.618)密度值模型。在放射组学模型的比较中,模型性能的趋势与6张MD图像的密度值模型一致。然而,基于HAP (Water)、Ca (Water)、HAP (Fat)、Ca (Fat)、Fat (Ca)和Fat (HAP)图像的密度值模型的性能优于基于MD图像的密度值模型,其值分别为0.946、0.941、0.934、0.926、0.831和0.824。结论:利用HAP (Water)、HAP (Fat)、Ca (Water)和Ca (Fat) MD图像的密度值可以准确地评估骨状态。然而,来自MD图像的放射组学模型在评估骨骼状态方面优于传统的密度测量方法,突出了其优越的诊断潜力。
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Enhancing the Opportunistic Bone Status Assessment Using Radiomics Based on Dual-Energy Spectral CT Material Decomposition Images.

The dual-energy spectral CT (DEsCT) employs material decomposition (MD) technology, opening up novel avenues for the opportunistic assessment of bone status. Radiomics, a powerful tool for elucidating the structural and textural characteristics of bone, aids in the detection of mineral loss. Therefore, this study aims to compare the efficacy of bone status assessment using both bone density measurements and radiomics models derived from MD images and to further explore the clinical value of radiomics models.

Methods: Retrospective data were collected from 307 patients who underwent both quantitative computed tomography (QCT) and full-abdomen DEsCT scans at our institution. Based on QCT measurements, patients were divided into three categories: normal bone mineral density (BMD), osteopenia, and osteoporosis. Using the abdominal DEsCT data, six types of MD images were reconstructed, including HAP (Water), HAP (Fat), Ca (Water), Ca (Fat), Fat (Ca), and Fat (HAP). Patients were randomly divided into a training cohort (n = 214) and a validation cohort (n = 93) at a ratio of 7:3. Focusing on the L1 to L3 vertebrae, density values from the six MD images were measured. Six density value models and six radiomics models were constructed using a random forest (RF) classifier. The performance of these models in assessing bone status was evaluated using the receiver operating characteristic (ROC) curves, and the DeLong test was employed to compare performance differences between the models.

Results: The macro-area under the curve (AUC) values for the density value models based on HAP (Water), HAP (Fat), Ca (Water), and Ca (Fat) MD images were 0.870, 0.870, 0.847, and 0.765, respectively, which outperformed those of Fat (Ca) (AUC = 0.623) and Fat (HAP) (AUC = 0.618) density value models. In the comparison of radiomics models, the trends of model performance were consistent with the density value models across the six MD images. However, the models based on HAP (Water), Ca (Water), HAP (Fat), Ca (Fat), Fat (Ca), and Fat (HAP) images exhibited superior performance than those of the density value models with the corresponding MD images, with values of 0.946, 0.941, 0.934, 0.926, 0.831, and 0.824, respectively.

Conclusions: Bone status assessment can be accurately conducted using density values from HAP (Water), HAP (Fat), Ca (Water), and Ca (Fat) MD images. However, radiomics models derived from MD images surpass traditional density measurement methods in evaluating bone status, highlighting their superior diagnostic potential.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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