The diagnostic value of a nomogram based on enhanced CT radiomics for differentiating between intrahepatic cholangiocarcinoma and early hepatic abscess.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2024-08-23 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1409060
Meng-Chen Yang, Hai-Yang Liu, Yan-Ming Zhang, Yi Guo, Shang-Yu Yang, Hua-Wei Zhang, Bao Cui, Tian-Min Zhou, Hao-Xiang Guo, Dan-Wei Hou
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Abstract

Objective: This study aimed to investigate the value of a CT-enhanced scanning radiomics nomogram in distinguishing between early hepatic abscess (EHA) and intrahepatic cholangiocarcinoma (ICC) and to validate its diagnostic efficacy.

Materials and methods: Clinical and imaging data on 112 patients diagnosed with EHA and ICC who underwent double-phase CT-enhanced scanning at our hospital were collected. The contours of the lesions were delineated layer by layer across the three phases of CT scanning and enhancement using 3D Slicer software to define the region of interest (ROI). Subsequently, the contours were merged into 3D models, and radiomics features were extracted using the Radiomics plug-in. The data were randomly divided into training (n = 78) and validation (n = 34) cohorts at a 7:3 ratio, using the R programming language. Standardization was performed using the Z-score method, and LASSO regression was used to select the best λ-value for screening variables, which were then used to establish prediction models. The rad-score was calculated using the best radiomics model, and a joint model was constructed based on the rad-score and clinical scores. A nomogram was developed based on the joint model. The diagnostic efficacy of the models for distinguishing ICC and EHA was assessed using receiver operating characteristic (ROC) curve and area under the curve (AUC) analyses. Calibration curves were used to evaluate the reliability and accuracy of the nomograms, while decision curves and clinical impact curves were utilized to assess their clinical value.

Results: Compared with the ICC group, significant differences were observed in clinical data and imaging characteristics in the EHA group, including age, centripetal enhancement, hepatic pericardial depression sign, arterial perfusion abnormality, arterial CT value, and arteriovenous enhancement (p < 0.05). Logistic regression analysis identified centripetal enhancement, hepatic pericardial depression sign, arterial perfusion abnormality, arterial CT value, and arteriovenous enhancement as independent influencing factors. Three, five, and four radiomics features were retained in the scanning, arterial, and venous phases, respectively. Single-phase models were constructed, with the radiomics model from the arterial phase demonstrating the best diagnostic efficacy. The rad-score was calculated using the arterial-phase radiomics model, and nomograms were drawn in conjunction with the clinical model. The nomogram based on the combined model exhibited the highest differential diagnostic efficacy between EHA and ICC (training cohort: AUC of 0.972; validation cohort: AUC of 0.868). The calibration curves indicated good agreement between the predicted and pathological results, while decision curves and clinical impact curves demonstrated higher clinical utility of the nomograms.

Conclusion: The CT-enhanced scanning radiomics nomogram demonstrates high clinical value in distinguishing between EHA and ICC, thereby enhancing the accuracy of preoperative diagnosis.

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基于增强 CT 放射成像的提名图在区分肝内胆管癌和早期肝脓肿方面的诊断价值。
研究目的本研究旨在探讨 CT 增强扫描放射组学提名图在区分早期肝脓肿(EHA)和肝内胆管癌(ICC)方面的价值,并验证其诊断效果:收集了在我院接受双相 CT 增强扫描的 112 例 EHA 和 ICC 患者的临床和影像学资料。使用 3D Slicer 软件在 CT 扫描和增强的三个阶段逐层描绘病变轮廓,以确定感兴趣区(ROI)。随后,将轮廓合并为三维模型,并使用 Radiomics 插件提取放射组学特征。使用 R 编程语言将数据按 7:3 的比例随机分为训练组(n = 78)和验证组(n = 34)。使用 Z 分数法进行标准化,并使用 LASSO 回归法为筛选变量选择最佳 λ 值,然后用于建立预测模型。使用最佳放射组学模型计算辐射评分,并根据辐射评分和临床评分构建联合模型。根据联合模型制定了一个提名图。利用接收者操作特征曲线(ROC)和曲线下面积(AUC)分析评估了这些模型在区分 ICC 和 EHA 方面的诊断效果。校准曲线用于评估提名图的可靠性和准确性,而决策曲线和临床影响曲线则用于评估其临床价值:与 ICC 组相比,EHA 组的临床数据和影像学特征存在显著差异,包括年龄、向心性增强、肝包膜凹陷征、动脉灌注异常、动脉 CT 值和动静脉增强(P < 0.05)。逻辑回归分析确定向心性增强、肝包膜凹陷征、动脉灌注异常、动脉 CT 值和动静脉增强为独立影响因素。扫描、动脉和静脉阶段分别保留了三个、五个和四个放射组学特征。构建了单阶段模型,其中动脉阶段的放射组学模型显示出最佳诊断效果。使用动脉期放射组学模型计算放射评分,并结合临床模型绘制提名图。基于组合模型的提名图在 EHA 和 ICC 之间显示出最高的鉴别诊断效果(训练队列:AUC 为 0.972;验证队列:AUC 为 0.868)。校准曲线表明预测结果与病理结果之间具有良好的一致性,而决策曲线和临床影响曲线则表明提名图具有更高的临床实用性:结论:CT 增强扫描放射组学提名图在区分 EHA 和 ICC 方面具有很高的临床价值,从而提高了术前诊断的准确性。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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