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Machine Learning-Based CT Radiomics Model to Predict the Risk of Hip Fragility Fracture.
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-03 DOI: 10.1016/j.acra.2025.01.023
Jinglei Yuan, Bing Li, Chu Zhang, Jing Wang, Bingsheng Huang, Liheng Ma

Rationale and objectives: This research aimed to develop a combined model based on proximal femur attenuation values and radiomics features at routine CT to predict hip fragility fracture using machine learning methods.

Method: A total of 254 patients (training cohort, n=132; test cohort 1, n=56;test cohort 2, n=66) who underwent hip or pelvic CT scans were included. Three different machine learning methods were used to build the Support Vector Machine (SVM) model, Logistic Regression (LR) model and Random Forest (RF) model respectively. The method that exhibited the best performance in the training cohort and test cohort 1 was selected to represent the radiomics model for subsequent studies. The mean CT Hounsfield unit of three-dimensional CT images at the proximal femur was extracted to construct the mean CTHU model. Multivariate logistic regression was performed using mean CT Hounsfield unit together with radiomics features, and the combined model was subsequently developed with a visualized nomogram.

Results: Among the radiomics models based on three machine learning methods, the LR model showed the best performance in the training cohort (AUC=0.875, 95% CI=0.806-0.926) and in the test cohort 1 (AUC=0.851, 95% CI=0.730-0.932). Compared to the mean CT model and the LR model, the combined model showed superior discriminatory power in the training cohort (AUC=0.934, 95% CI=0.895-0.972), the test cohort 1 (AUC=0.893, 95% CI=0.812-0.974) and the test cohort 2 (AUC=0.851, 95% CI=0.742-0.927).

Conclusion: The combined model, based on the mean CT Hounsfield unit of the proximal femur and radiomics features, can provide an accurate quantitative imaging basis for individualized risk prediction of hip fragility fracture.

{"title":"Machine Learning-Based CT Radiomics Model to Predict the Risk of Hip Fragility Fracture.","authors":"Jinglei Yuan, Bing Li, Chu Zhang, Jing Wang, Bingsheng Huang, Liheng Ma","doi":"10.1016/j.acra.2025.01.023","DOIUrl":"https://doi.org/10.1016/j.acra.2025.01.023","url":null,"abstract":"<p><strong>Rationale and objectives: </strong>This research aimed to develop a combined model based on proximal femur attenuation values and radiomics features at routine CT to predict hip fragility fracture using machine learning methods.</p><p><strong>Method: </strong>A total of 254 patients (training cohort, n=132; test cohort 1, n=56;test cohort 2, n=66) who underwent hip or pelvic CT scans were included. Three different machine learning methods were used to build the Support Vector Machine (SVM) model, Logistic Regression (LR) model and Random Forest (RF) model respectively. The method that exhibited the best performance in the training cohort and test cohort 1 was selected to represent the radiomics model for subsequent studies. The mean CT Hounsfield unit of three-dimensional CT images at the proximal femur was extracted to construct the mean CTHU model. Multivariate logistic regression was performed using mean CT Hounsfield unit together with radiomics features, and the combined model was subsequently developed with a visualized nomogram.</p><p><strong>Results: </strong>Among the radiomics models based on three machine learning methods, the LR model showed the best performance in the training cohort (AUC=0.875, 95% CI=0.806-0.926) and in the test cohort 1 (AUC=0.851, 95% CI=0.730-0.932). Compared to the mean CT model and the LR model, the combined model showed superior discriminatory power in the training cohort (AUC=0.934, 95% CI=0.895-0.972), the test cohort 1 (AUC=0.893, 95% CI=0.812-0.974) and the test cohort 2 (AUC=0.851, 95% CI=0.742-0.927).</p><p><strong>Conclusion: </strong>The combined model, based on the mean CT Hounsfield unit of the proximal femur and radiomics features, can provide an accurate quantitative imaging basis for individualized risk prediction of hip fragility fracture.</p>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":" ","pages":""},"PeriodicalIF":3.8,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143191351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Radiomics Analysis of Different Machine Learning Models based on Multiparametric MRI to Identify Benign and Malignant Testicular Lesions.
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-03 DOI: 10.1016/j.acra.2025.01.026
Yuanxi Jian, Suping Yang, Rui Liu, Xin Tan, Qian Zhao, Junlin Wu, Yuan Chen

Rationale and objectives: To develop and validate a machine learning-based prediction model for the use of multiparametric magnetic resonance imaging(MRI) to predict benign and malignant lesions in the testis.

Materials and methods: The study retrospectively enrolled 148 patients with pathologically confirmed benign and malignant testicular lesions, dividing them into: training set (n=103) and validation set (n=45). Radiomics characteristics were derived from T2-weighted(T2WI)、contrast-enhanced T1-weighted(CE-T1WI)、diffusion-weighted imaging(DWI) and Apparent diffusion coefficient(ADC) MRI images, followed by feature selection. A machine learning-based combined model was developed by incorporating radiomics scores (rad scores) from the optimal radiomics model along with clinical predictors. Draw the receiver operating characteristic (ROC) curve and use the area under the curve (AUC) to evaluate and compare the predictive performance of each model. The diagnostic efficacy of the various machine learning models was evaluated using the Delong test.

Results: Radiomics features were extracted from four sequence-based groups(CE-T1WI+DWI+ADC+T2WI), and the model that combined Logistic Regression(LR) machine learning showed the best performance in the radiomics model. The clinical model identified one independent predictors. The combined clinical-radiomics model showed the best performance, whose AUC value was 0.932(95% confidence intervals(CI)0.868-0.978), sensitivity was 0.875, specificity was 0.871 and accuracy was 0.884 in validation set.

Conclusion: The combined clinical-radiomics model can be used as a reliable tool to predict benign and malignant testicular lesions and provide a reference for clinical treatment method decisions.

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引用次数: 0
A Deep Radiomics Model for Lymph Node Metastasis Prediction of Early-Stage Gastric Cancer Based on CT Images.
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-03 DOI: 10.1016/j.acra.2024.12.036
Xiaoping Cen, Jingyang He, Yahan Tong, Huanming Yang, Youyong Lu, Yixue Li, Wei Dong, Can Hu
{"title":"A Deep Radiomics Model for Lymph Node Metastasis Prediction of Early-Stage Gastric Cancer Based on CT Images.","authors":"Xiaoping Cen, Jingyang He, Yahan Tong, Huanming Yang, Youyong Lu, Yixue Li, Wei Dong, Can Hu","doi":"10.1016/j.acra.2024.12.036","DOIUrl":"https://doi.org/10.1016/j.acra.2024.12.036","url":null,"abstract":"","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":" ","pages":""},"PeriodicalIF":3.8,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143191348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
MR Imaging Techniques for Microenvironment Mapping of the Glioma Tumors: A Systematic Review.
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2025.01.024
Fateme Shahedi, Shahrokh Naseri, Mahdi Momennezhad, Hoda Zare

Rationale and objectives: The tumor microenvironment (TME) is a critical regulator of cancer progression, metastasis, and treatment response. Currently, various imaging approaches exist to assess the pathophysiological features of the TME. This systematic review provides an overview of magnetic resonance imaging (MRI) methods used in clinical practice to characterize the pathophysiological features of the gliomas TME.

Methods: This review involved a systematic comprehensive search of original open-access articles reporting the clinical use of MR imaging in glioma patients of all ages in the PubMed, Scopus, and Web of Science databases between January 2010 and December 2023. We restricted our research to papers published in the English language.

Results: A total of 1137 studies were preliminarily identified through electronic database searches. After duplicate studies were removed, 44 studies met the eligibility criteria. The glioma TME was accompanied by alterations in metabolism, pH, vascularity, oxygenation, and extracellular matrix components, including tumor-associated macrophages, and sodium concentration.

Conclusion: Multiparametric MRI is capable of noninvasively assessing the pathophysiological features and tumor-supportive niches of the TME, which is in line with its application in personalized medicine.

{"title":"MR Imaging Techniques for Microenvironment Mapping of the Glioma Tumors: A Systematic Review.","authors":"Fateme Shahedi, Shahrokh Naseri, Mahdi Momennezhad, Hoda Zare","doi":"10.1016/j.acra.2025.01.024","DOIUrl":"https://doi.org/10.1016/j.acra.2025.01.024","url":null,"abstract":"<p><strong>Rationale and objectives: </strong>The tumor microenvironment (TME) is a critical regulator of cancer progression, metastasis, and treatment response. Currently, various imaging approaches exist to assess the pathophysiological features of the TME. This systematic review provides an overview of magnetic resonance imaging (MRI) methods used in clinical practice to characterize the pathophysiological features of the gliomas TME.</p><p><strong>Methods: </strong>This review involved a systematic comprehensive search of original open-access articles reporting the clinical use of MR imaging in glioma patients of all ages in the PubMed, Scopus, and Web of Science databases between January 2010 and December 2023. We restricted our research to papers published in the English language.</p><p><strong>Results: </strong>A total of 1137 studies were preliminarily identified through electronic database searches. After duplicate studies were removed, 44 studies met the eligibility criteria. The glioma TME was accompanied by alterations in metabolism, pH, vascularity, oxygenation, and extracellular matrix components, including tumor-associated macrophages, and sodium concentration.</p><p><strong>Conclusion: </strong>Multiparametric MRI is capable of noninvasively assessing the pathophysiological features and tumor-supportive niches of the TME, which is in line with its application in personalized medicine.</p>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":" ","pages":""},"PeriodicalIF":3.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143080828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrigendum to: “Developing a Nomogram to Stratify Intracranial Solitary Fibrous Tumor Recurrence” Academic Radiology Volume 31, Issue 3, March 2024, Pages 1044–1054 更正:"颅内单发纤维性肿瘤复发分层提名图的开发》,《放射学术》第 31 卷第 3 期,2024 年 3 月,第 1044-1054 页。
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.06.019
Xiaohong Liang , Xiaoai Ke , Jian Jiang , Shenglin Li , Caiqiang Xue , Cheng Yan , Mingzi Gao , Junlin Zhou , Liqin Zhao
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引用次数: 0
Evaluating Artificial Intelligence Competency in Education: Performance of ChatGPT-4 in the American Registry of Radiologic Technologists (ARRT) Radiography Certification Exam 评估人工智能在教育方面的能力:ChatGPT-4 在美国放射技师注册机构 (ARRT) 放射学认证考试中的表现。
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.08.009
Yousif Al-Naser MRT(R) , Felobater Halka , Boris Ng BEng , Dwight Mountford MRT(R) MSc , Sonali Sharma , Ken Niure MRT(R) , Charlotte Yong-Hing MD , Faisal Khosa MD , Christian Van der Pol MD

Rationale and Objectives

The American Registry of Radiologic Technologists (ARRT) leads the certification process with an exam comprising 200 multiple-choice questions. This study aims to evaluate ChatGPT-4's performance in responding to practice questions similar to those found in the ARRT board examination.

Materials and Methods

We used a dataset of 200 practice multiple-choice questions for the ARRT certification exam from BoardVitals. Each question was fed to ChatGPT-4 fifteen times, resulting in 3000 observations to account for response variability.

Results

ChatGPT's overall performance was 80.56%, with higher accuracy on text-based questions (86.3%) compared to image-based questions (45.6%). Response times were longer for image-based questions (18.01 s) than for text-based questions (13.27 s). Performance varied by domain: 72.6% for Safety, 70.6% for Image Production, 67.3% for Patient Care, and 53.4% for Procedures. As anticipated, performance was best on on easy questions (78.5%).

Conclusion

ChatGPT demonstrated effective performance on the BoardVitals question bank for ARRT certification. Future studies could benefit from analyzing the correlation between BoardVitals scores and actual exam outcomes. Further development in AI, particularly in image processing and interpretation, is necessary to enhance its utility in educational settings.
理由和目标:美国放射技师注册委员会 (ARRT) 主导认证程序,考试包括 200 道选择题。本研究旨在评估 ChatGPT-4 在回答与 ARRT 委员会考试类似的练习题时的表现:我们使用了 BoardVitals 提供的 200 道 ARRT 认证考试练习选择题数据集。每道题都向 ChatGPT-4 发送了 15 次,共观察了 3000 次,以考虑反应的可变性:ChatGPT 的总体性能为 80.56%,其中文本问题(86.3%)的准确率高于图像问题(45.6%)。图像问题的回复时间(18.01 秒)比文本问题的回复时间(13.27 秒)长。不同领域的成绩各不相同:安全 72.6%,图像制作 70.6%,病人护理 67.3%,程序 53.4%。正如预期的那样,简单问题的成绩最好(78.5%):ChatGPT 在 ARRT 认证的 BoardVitals 题库中表现出色。分析 BoardVitals 分数与实际考试结果之间的相关性将有助于今后的研究。有必要进一步发展人工智能,尤其是在图像处理和解读方面,以提高其在教育环境中的实用性。
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引用次数: 0
18F-FDG-PET/CT Uptake by Noncancerous Lung as a Predictor of Interstitial Lung Disease Induced by Immune Checkpoint Inhibitors 非癌肺的 18F-FDG-PET/CT 摄取可预测免疫检查点抑制剂诱发的间质性肺病
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.08.043
Motohiko Yamazaki , Satoshi Watanabe MD, PhD , Masaki Tominaga , Takuya Yagi , Yukari Goto , Naohiro Yanagimura , Masashi Arita , Aya Ohtsubo , Tomohiro Tanaka , Koichiro Nozaki , Yu Saida , Rie Kondo , Toshiaki Kikuchi , Hiroyuki Ishikawa

Rationale and Objectives

Immune checkpoint inhibitors (ICIs) have improved lung cancer prognosis; however, ICI-related interstitial lung disease (ILD) is fatal and difficult to predict. Herein, we hypothesized that pre-existing lung inflammation on radiological imaging can be a potential risk factor for ILD onset. Therefore, we investigated the association between high uptake in noncancerous lung (NCL) on 18F- FDG-PET/CT and ICI-ILD in lung cancer.

Methods

Patients with primary lung cancer who underwent FDG-PET/CT within three months prior to ICI therapy were retrospectively included. Artificial intelligence was utilized for extracting the NCL regions (background lung) from the lung contralateral to the primary tumor. FDG uptake by the NCL was assessed via the SUVmax (NCL-SUVmax), SUVmean (NCL-SUVmean), and total glycolytic activity (NCL-TGA) defined as NCL-SUVmean × NCL volume [mL]. NCL-SUVmean and NCL-TGA were calculated using the following four SUV thresholds: 0.5, 1.0, 1.5, and 2.0.

Results

Of the 165 patients, 28 (17.0%) developed ILD. Univariate analysis showed that high values of NCL-SUVmax, NCL-SUVmean2.0 (SUV threshold = 2.0), and NCL-TGA1.0 (SUV threshold = 1.0) were significantly associated with ILD onset (all p = 0.003). Multivariate analysis adjusted for age, tumor FDG uptake, and pre-existing interstitial lung abnormalities revealed that a high NCL-TGA1.0 (≥ 149.45) was independently associated with ILD onset (odds ratio, 6.588; p = 0.002). Two-year cumulative incidence of ILD was significantly higher in the high NCL-TGA1.0 group than in the low group (58.4% vs. 14.4%; p < 0.001).

Conclusion

High uptake of NCL on FDG-PET/CT is correlated with ICI-ILD development, which could serve as a risk stratification tool before ICI therapy in primary lung cancer.
理由和目标:免疫检查点抑制剂(ICIs)改善了肺癌的预后;然而,与 ICI 相关的间质性肺病(ILD)是致命的,而且难以预测。在此,我们假设放射影像学上已有的肺部炎症可能是 ILD 发病的潜在风险因素。因此,我们研究了18F- FDG-PET/CT在非癌肺(NCL)中的高摄取与肺癌ICI-ILD之间的关联:方法:回顾性纳入在接受 ICI 治疗前三个月内接受 FDG-PET/CT 的原发性肺癌患者。利用人工智能从原发肿瘤对侧肺中提取 NCL 区域(背景肺)。NCL 的 FDG 摄取通过 SUVmax(NCL-SUVmax)、SUVmean(NCL-SUVmean)和总糖酵解活性(NCL-TGA)进行评估,总糖酵解活性定义为 NCL-SUVmean×NCL 体积[mL]。NCL-SUVmean和NCL-TGA使用以下四个SUV阈值计算:结果:在 165 名患者中,28 人(17.0%)出现了 ILD。单变量分析显示,NCL-SUVmax、NCL-SUVmean2.0(SUV阈值=2.0)和NCL-TGA1.0(SUV阈值=1.0)的高值与ILD发病显著相关(均为P = 0.003)。调整了年龄、肿瘤 FDG 摄取和原有肺间质异常的多变量分析显示,NCL-TGA1.0 高(≥149.45)与 ILD 发病独立相关(几率比为 6.588;P = 0.002)。NCL-TGA1.0高分组的两年累积ILD发病率明显高于低分组(58.4% vs. 14.4%;P 结论:NCL-TGA1.0高分组的两年累积ILD发病率明显高于低分组(58.4% vs. 14.4%):FDG-PET/CT上NCL的高摄取与ICI-ILD的发展相关,可作为原发性肺癌ICI治疗前的风险分层工具。
{"title":"18F-FDG-PET/CT Uptake by Noncancerous Lung as a Predictor of Interstitial Lung Disease Induced by Immune Checkpoint Inhibitors","authors":"Motohiko Yamazaki ,&nbsp;Satoshi Watanabe MD, PhD ,&nbsp;Masaki Tominaga ,&nbsp;Takuya Yagi ,&nbsp;Yukari Goto ,&nbsp;Naohiro Yanagimura ,&nbsp;Masashi Arita ,&nbsp;Aya Ohtsubo ,&nbsp;Tomohiro Tanaka ,&nbsp;Koichiro Nozaki ,&nbsp;Yu Saida ,&nbsp;Rie Kondo ,&nbsp;Toshiaki Kikuchi ,&nbsp;Hiroyuki Ishikawa","doi":"10.1016/j.acra.2024.08.043","DOIUrl":"10.1016/j.acra.2024.08.043","url":null,"abstract":"<div><h3>Rationale and Objectives</h3><div>Immune checkpoint inhibitors (ICIs) have improved lung cancer prognosis; however, ICI-related interstitial lung disease (ILD) is fatal and difficult to predict. Herein, we hypothesized that pre-existing lung inflammation on radiological imaging can be a potential risk factor for ILD onset. Therefore, we investigated the association between high uptake in noncancerous lung (NCL) on <sup>18</sup>F- FDG-PET/CT and ICI-ILD in lung cancer.</div></div><div><h3>Methods</h3><div>Patients with primary lung cancer who underwent FDG-PET/CT within three months prior to ICI therapy were retrospectively included. Artificial intelligence was utilized for extracting the NCL regions (background lung) from the lung contralateral to the primary tumor. FDG uptake by the NCL was assessed via the SUVmax (NCL-SUVmax), SUVmean (NCL-SUVmean), and total glycolytic activity (NCL-TGA)<!--> <!-->defined as NCL-SUVmean<!--> <!-->×<!--> <!-->NCL volume [mL]. NCL-SUVmean and NCL-TGA were calculated using the following four SUV thresholds: 0.5, 1.0, 1.5, and 2.0.</div></div><div><h3>Results</h3><div>Of the 165 patients, 28 (17.0%) developed ILD. Univariate analysis showed that high values of NCL-SUVmax, NCL-SUVmean<sub>2.0</sub> (SUV threshold<!--> <!-->=<!--> <!-->2.0), and NCL-TGA<sub>1.0</sub> (SUV threshold<!--> <!-->=<!--> <!-->1.0) were significantly associated with ILD onset (all <em>p</em> = 0.003). Multivariate analysis adjusted for age, tumor FDG uptake, and pre-existing interstitial lung abnormalities revealed that a high NCL-TGA<sub>1.0</sub> (≥<!--> <!-->149.45) was independently associated with ILD onset (odds ratio, 6.588; <em>p</em> = 0.002). Two-year cumulative incidence of ILD was significantly higher in the high NCL-TGA<sub>1.0</sub> group than in the low group (58.4% vs. 14.4%; <em>p</em> &lt; 0.001).</div></div><div><h3>Conclusion</h3><div>High uptake of NCL on FDG-PET/CT is correlated with ICI-ILD development, which could serve as a risk stratification tool before ICI therapy in primary lung cancer.</div></div>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":"32 2","pages":"Pages 1026-1035"},"PeriodicalIF":3.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142127245","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preoperative CT and Radiomics Nomograms for Distinguishing Bronchiolar Adenoma and Early-Stage Lung Adenocarcinoma 用于区分支气管腺瘤和早期肺腺癌的术前 CT 和放射omics Nomogram。
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.08.047
Xiulan Liu , Yanqiong Xu , Jiajia Shu , Yan Zuo , Zhi Li , Meng Lin , Chenrong Li , Yuqi Liu , Xianhong Wang , Ying Zhao , Zihong Du , Gang Wang , Wenjia Li

Rationale and Objectives

Evaluating the capability of CT nomograms and CT-based radiomics nomograms to differentiate between Bronchiolar Adenoma (BA) and Early-stage Lung Adenocarcinoma (LUAD).

Materials and Methods

In this retrospective study; we analyzed data from 226 patients who were treated at our institution and pathologically confirmed to have either BA or Early-stage LUAD. Patients were randomly divided into a training cohort (n = 158) and a testing cohort (n = 68). All CT images were independently analyzed and measured by two radiologists using conventional computed tomography. Clinical predictive factors were identified using logistic regression. Multivariable logistic regression analysis was used to construct differential diagnostic models for BA and early-stage LUAD, including traditional CT and radiomics models. The performance of the models was determined based on the area under the receiver operating characteristic curve, discrimination ability, and decision curve analysis (DCA).

Results

Lesion shape, tumor-lung interface, and pleural retraction signs were identified as independent clinical predictors. The areas under the curve for the CT nomogram, radiomic features, and radiomics nomogram were 0.854, 0.769, and 0.901, respectively. Both the CT nomogram and the radiomics nomogram demonstrated good generalizability in distinguishing between the two entities. DCA indicated that the nomograms achieved a higher net benefit compared to the use of radiomic features alone.

Conclusion

The two preoperative nomograms hold significant value in differentiating between patients with BA and those with Early-stage LUAD, and they contribute to informed clinical treatment decision-making.
材料与方法在这项回顾性研究中,我们分析了在本院接受治疗并经病理证实患有支气管腺瘤(BA)或早期肺腺癌(LUAD)的 226 名患者的数据。患者被随机分为训练组(158 人)和测试组(68 人)。所有 CT 图像均由两名放射科医生使用传统计算机断层扫描进行独立分析和测量。采用逻辑回归法确定临床预测因素。多变量逻辑回归分析用于构建 BA 和早期 LUAD 的差异诊断模型,包括传统 CT 模型和放射组学模型。结果肿块形状、肿瘤-肺界面和胸膜回缩征被确定为独立的临床预测因素。CT提名图、放射学特征和放射学提名图的曲线下面积分别为0.854、0.769和0.901。CT 提名图和放射组学提名图在区分两种实体方面都表现出良好的普适性。结论 这两个术前提名图在区分 BA 患者和早期 LUAD 患者方面具有重要价值,有助于做出明智的临床治疗决策。
{"title":"Preoperative CT and Radiomics Nomograms for Distinguishing Bronchiolar Adenoma and Early-Stage Lung Adenocarcinoma","authors":"Xiulan Liu ,&nbsp;Yanqiong Xu ,&nbsp;Jiajia Shu ,&nbsp;Yan Zuo ,&nbsp;Zhi Li ,&nbsp;Meng Lin ,&nbsp;Chenrong Li ,&nbsp;Yuqi Liu ,&nbsp;Xianhong Wang ,&nbsp;Ying Zhao ,&nbsp;Zihong Du ,&nbsp;Gang Wang ,&nbsp;Wenjia Li","doi":"10.1016/j.acra.2024.08.047","DOIUrl":"10.1016/j.acra.2024.08.047","url":null,"abstract":"<div><h3>Rationale and Objectives</h3><div>Evaluating the capability of CT nomograms and CT-based radiomics nomograms to differentiate between Bronchiolar Adenoma (BA) and Early-stage Lung Adenocarcinoma (LUAD).</div></div><div><h3>Materials and Methods</h3><div>In this retrospective study; we analyzed data from 226 patients who were treated at our institution and pathologically confirmed to have either BA or Early-stage LUAD. Patients were randomly divided into a training cohort (<em>n<!--> </em>=<!--> <!-->158) and a testing cohort (<em>n<!--> </em>=<!--> <!-->68). All CT images were independently analyzed and measured by two radiologists using conventional computed tomography. Clinical predictive factors were identified using logistic regression. Multivariable logistic regression analysis was used to construct differential diagnostic models for BA and early-stage LUAD, including traditional CT and radiomics models. The performance of the models was determined based on the area under the receiver operating characteristic curve, discrimination ability, and decision curve analysis (DCA).</div></div><div><h3>Results</h3><div>Lesion shape, tumor-lung interface, and pleural retraction signs were identified as independent clinical predictors. The areas under the curve for the CT nomogram, radiomic features, and radiomics nomogram were 0.854, 0.769, and 0.901, respectively. Both the CT nomogram and the radiomics nomogram demonstrated good generalizability in distinguishing between the two entities. DCA indicated that the nomograms achieved a higher net benefit compared to the use of radiomic features alone.</div></div><div><h3>Conclusion</h3><div>The two preoperative nomograms hold significant value in differentiating between patients with BA and those with Early-stage LUAD, and they contribute to informed clinical treatment decision-making.</div></div>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":"32 2","pages":"Pages 1054-1066"},"PeriodicalIF":3.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142261934","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improving the Assessment of Axonal Injury in Early Multiple Sclerosis 改进对早期多发性硬化症轴突损伤的评估。
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.08.048
Ahmad A. Toubasi M.D. , Gary Cutter Ph.D. , Caroline Gheen B.S. , Taegan Vinarsky B.S. , Keejin Yoon B.S. , Salma AshShareef M.S. , Pragnya Adapa , Olivia Gruder M.D. , Stephanie Taylor M.D. , James E. Eaton M.D. , Junzhong Xu Ph.D. , Francesca Bagnato M.D., Ph.D.

Rationale and Objectives

Several quantitative magnetic resonance imaging (MRI) methods are available to measure tissue injury in multiple sclerosis (MS), but their pathological specificity remains limited. The multi-compartment diffusion imaging using the spherical mean technique (SMT) overcomes several technical limitations of the diffusion-weighted image signal, thus delivering metrics with increased pathological specificity. Given these premises, here we assess whether the SMT-derived apparent axonal volume (Vax) provides a better tissue classifier than the diffusion tensor imaging (DTI)-derived axial diffusivity (AD) in the white matter (WM) of MS brains.

Methods

Forty-three treatment-naïve people with newly diagnosed MS, clinically isolated syndrome, or radiologically isolated syndrome and 18 healthy controls (HCs) underwent a 3.0 Tesla MRI inclusive of T1-weighted (T1-w) and T2-w fluid-attenuated inversion recovery (FLAIR) sequences, and multi-b shell diffusion-weighted imaging. In patients only, pre- and post-gadolinium diethylenetriamine penta-acetic acid T1-w sequences were obtained for the evaluation of contrast-active lesions (CELs). Vax and AD were calculated in T2-lesions, chronic black holes (cBHs), and normal appearing (NAWM) in patients and normal WM (NWM) in HCs. Vax and AD values were compared across all the possible combinations of these regions. CELs were excluded from the analyses.

Results

Vax differed in all comparisons (p ≤ 0.047 by paired t-test); AD differed in most comparisons (p < 0.001) except between NAWM and NWM, and between cBHs and T2-lesions. Vax had higher accuracy (p ≤ 0.029 by DeLong test) and larger effect size (p ≤ 0.038 by paired t-test) than AD in differentiating areas with even minimal tissue injury.

Conclusions

Vax provides a better radiological quantitative discriminator of different degrees of axonal-mediated tissue injury even between areas with expected minimal pathology. Our data support further studies to assess the readiness of Vax as a measure of outcome for clinical trials on neuroprotection in MS.
理由和目标:目前有几种定量磁共振成像(MRI)方法可用于测量多发性硬化症(MS)的组织损伤,但其病理特异性仍然有限。使用球面均值技术(SMT)进行的多室弥散成像克服了弥散加权图像信号的一些技术局限性,从而提供了病理特异性更强的指标。鉴于这些前提,我们在此评估在多发性硬化症大脑白质(WM)中,SMT得出的表观轴突体积(Vax)是否比扩散张量成像(DTI)得出的轴向扩散率(AD)提供了更好的组织分类器:43名未经治疗的新诊断多发性硬化症、临床孤立综合征或放射学孤立综合征患者和18名健康对照组(HCs)接受了3.0特斯拉核磁共振成像(MRI)检查,包括T1加权(T1-w)和T2-w流体衰减反转恢复(FLAIR)序列以及多B壳扩散加权成像。仅对患者进行了二乙烯三胺五乙酸钆前和后 T1-w 序列检查,以评估造影剂活性病变(CEL)。计算了患者 T2- 病变、慢性黑洞(cBHs)和正常显示(NAWM)以及 HCs 正常 WM(NWM)的 Vax 和 AD。在这些区域的所有可能组合中比较了 Vax 和 AD 值。分析中不包括CEL:在所有比较中,Vax 均有差异(通过配对 t 检验,p ≤ 0.047);在大多数比较中,AD 均有差异(p 2-裂隙)。在区分组织损伤最小的区域方面,Vax 比 AD 具有更高的准确性(通过 DeLong 检验,p ≤ 0.029)和更大的效应大小(通过配对 t 检验,p ≤ 0.038):结论:Vax 是轴突介导的不同组织损伤程度的更好的放射学定量判别指标,即使在预期病理程度极轻的区域之间也是如此。我们的数据支持进一步的研究,以评估 Vax 是否可作为多发性硬化症神经保护临床试验的结果测量指标。
{"title":"Improving the Assessment of Axonal Injury in Early Multiple Sclerosis","authors":"Ahmad A. Toubasi M.D. ,&nbsp;Gary Cutter Ph.D. ,&nbsp;Caroline Gheen B.S. ,&nbsp;Taegan Vinarsky B.S. ,&nbsp;Keejin Yoon B.S. ,&nbsp;Salma AshShareef M.S. ,&nbsp;Pragnya Adapa ,&nbsp;Olivia Gruder M.D. ,&nbsp;Stephanie Taylor M.D. ,&nbsp;James E. Eaton M.D. ,&nbsp;Junzhong Xu Ph.D. ,&nbsp;Francesca Bagnato M.D., Ph.D.","doi":"10.1016/j.acra.2024.08.048","DOIUrl":"10.1016/j.acra.2024.08.048","url":null,"abstract":"<div><h3>Rationale and Objectives</h3><div>Several quantitative magnetic resonance imaging (MRI) methods are available to measure tissue injury in multiple sclerosis (MS), but their pathological specificity remains limited. The multi-compartment diffusion imaging using the spherical mean technique (SMT) overcomes several technical limitations of the diffusion-weighted image signal, thus delivering metrics with increased pathological specificity. Given these premises, here we assess whether the SMT-derived apparent axonal volume (V<sub>ax</sub>) provides a better tissue classifier than the diffusion tensor imaging (DTI)-derived axial diffusivity (AD) in the white matter (WM) of MS brains.</div></div><div><h3>Methods</h3><div>Forty-three treatment-naïve people with newly diagnosed MS, clinically isolated syndrome, or radiologically isolated syndrome and 18 healthy controls (HCs) underwent a 3.0 Tesla MRI inclusive of T<sub>1</sub>-weighted (T<sub>1</sub>-w) and T<sub>2</sub>-w fluid-attenuated inversion recovery (FLAIR) sequences, and multi-b shell diffusion-weighted imaging. In patients only, pre- and post-gadolinium diethylenetriamine penta-acetic acid T<sub>1</sub>-w sequences were obtained for the evaluation of contrast-active lesions (CELs). V<sub>ax</sub> and AD were calculated in T<sub>2</sub>-lesions, chronic black holes (cBHs), and normal appearing (NAWM) in patients and normal WM (NWM) in HCs. V<sub>ax</sub> and AD values were compared across all the possible combinations of these regions. CELs were excluded from the analyses.</div></div><div><h3>Results</h3><div>V<sub>ax</sub> differed in all comparisons (p ≤ 0.047 by paired t-test); AD differed in most comparisons (p &lt; 0.001) except between NAWM and NWM, and between cBHs and T<sub>2</sub>-lesions. V<sub>ax</sub> had higher accuracy (p ≤ 0.029 by DeLong test) and larger effect size (p ≤ 0.038 by paired t-test) than AD in differentiating areas with even minimal tissue injury.</div></div><div><h3>Conclusions</h3><div>V<sub>ax</sub> provides a better radiological quantitative discriminator of different degrees of axonal-mediated tissue injury even between areas with expected minimal pathology. Our data support further studies to assess the readiness of V<sub>ax</sub> as a measure of outcome for clinical trials on neuroprotection in MS.</div></div>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":"32 2","pages":"Pages 1002-1014"},"PeriodicalIF":3.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142300173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
MRI Radiomics Nomogram for Predicting Disease Transition Time and Risk Stratification in Preclinical Alzheimer's Disease 用于预测临床前阿尔茨海默病的疾病转变时间和风险分层的核磁共振成像放射组学提名图。
IF 3.8 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-02-01 DOI: 10.1016/j.acra.2024.08.059
Shuai Lin , Ming Xue , Jiali Sun , Chang Xu , Tianqi Wang , Jianxiu Lian , Min Lv , Ping Yang , Chenjun Sheng , Zijian Cheng , Wei Wang

Rationale and Objectives

Accurate prediction of the progression of preclinical Alzheimer's disease (AD) is crucial for improving clinical management and disease prognosis. The objective of this study was to develop and validate clinical-radimoics integrated model to predict the time to progression (TTP) and disease risk stratification of preclinical AD.

Materials and Methods

A total of 244 cases (mean age: 73.8 ± 5.5 years, 120 women) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database were randomly divided into the training cohort (n = 172) and validation cohort (n = 72) using a 7:3 ratio. Clinical factors were identified by univariate and multivariate COX regression. Radiomics features were extracted from GM, WM and CSF of T1WI images and selected by Spearman correlation analysis and least absolute shrinkage and selection operator (LASSO). Using selected clinical factors and radiomics features, the clinical, radimocis and clinical-radiomics nomogram models were developed for predicting the TTP. The performance of each model was assessed by C-index. The risk stratification ability and predicting efficacy of the clinical-radiomics model were utilizing the Kaplan-Meier curve and receiver operator characteristic (ROC) curve.

Results

The C-index of clinical, radimocis and clinical-radiomics models were 0.852 (95% confidence interval[CI]:0.810–0.893), 0.863 (95%CI:0.816–0.910) and 0.903 (95%:0.870–0.936) in the training cohort and 0.725 (95%CI:0.630–0.820), 0.788 (95%CI:0.678–0.898), 0.813(95%CI:0.734–0.892) in the validation cohort. The AUCs of the multi-predictor nomogram at 1-, 3-, 5- and 7-year were 0.894, 0.908, 0.930, 0.979 in the training cohort and 0.671, 0.726, 0.839, 0.931 in the validation cohort.

Conclusion

In this study, we constructed a clinical-radimoics integrated model to predict the progression of preclinical AD and stratified the risk of disease progression in preclinical AD.
理由和目标:准确预测临床前阿尔茨海默病(AD)的进展对于改善临床管理和疾病预后至关重要。本研究旨在开发和验证临床-放射学综合模型,以预测临床前阿尔茨海默病的进展时间(TTP)和疾病风险分层:将阿尔茨海默病神经影像学倡议(ADNI)数据库中的244例病例(平均年龄:73.8 ± 5.5岁,女性120例)按7:3的比例随机分为训练队列(n = 172)和验证队列(n = 72)。通过单变量和多变量 COX 回归确定临床因素。从 T1WI 图像的 GM、WM 和 CSF 中提取放射组学特征,并通过斯皮尔曼相关性分析和最小绝对收缩和选择算子(LASSO)进行筛选。利用选定的临床因素和放射组学特征,建立了用于预测 TTP 的临床、放射组学和临床-放射组学提名图模型。每个模型的性能由 C-index 评估。临床-放射组学模型的风险分层能力和预测效果采用卡普兰-梅耶曲线和接收者操作特征曲线(ROC)进行评估:临床模型、放射肿瘤学模型和临床-放射肿瘤学模型的C指数分别为0.852(95%置信区间[CI]:0.810-0.893)、0.863(95%CI:0.816-0.910)和0.在训练队列中为 903(95%:0.870-0.936),在验证队列中为 0.725(95%CI:0.630-0.820)、0.788(95%CI:0.678-0.898)、0.813(95%CI:0.734-0.892)。多预测因子提名图在1年、3年、5年和7年的AUC值在训练队列中分别为0.894、0.908、0.930和0.979,在验证队列中分别为0.671、0.726、0.839和0.931:本研究构建了一个临床-放射学综合模型来预测临床前AD的进展,并对临床前AD的疾病进展风险进行了分层。
{"title":"MRI Radiomics Nomogram for Predicting Disease Transition Time and Risk Stratification in Preclinical Alzheimer's Disease","authors":"Shuai Lin ,&nbsp;Ming Xue ,&nbsp;Jiali Sun ,&nbsp;Chang Xu ,&nbsp;Tianqi Wang ,&nbsp;Jianxiu Lian ,&nbsp;Min Lv ,&nbsp;Ping Yang ,&nbsp;Chenjun Sheng ,&nbsp;Zijian Cheng ,&nbsp;Wei Wang","doi":"10.1016/j.acra.2024.08.059","DOIUrl":"10.1016/j.acra.2024.08.059","url":null,"abstract":"<div><h3>Rationale and Objectives</h3><div>Accurate prediction of the progression of preclinical Alzheimer's disease (AD) is crucial for improving clinical management and disease prognosis. The objective of this study was to develop and validate clinical-radimoics integrated model to predict the time to progression (TTP) and disease risk stratification of preclinical AD.</div></div><div><h3>Materials and Methods</h3><div>A total of 244 cases (mean age: 73.8 ± 5.5 years, 120 women) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database were randomly divided into the training cohort (n = 172) and validation cohort (n = 72) using a 7:3 ratio. Clinical factors were identified by univariate and multivariate COX regression. Radiomics features were extracted from GM, WM and CSF of T<sub>1</sub>WI images and selected by Spearman correlation analysis and least absolute shrinkage and selection operator (LASSO). Using selected clinical factors and radiomics features, the clinical, radimocis and clinical-radiomics nomogram models were developed for predicting the TTP. The performance of each model was assessed by C-index. The risk stratification ability and predicting efficacy of the clinical-radiomics model were utilizing the Kaplan-Meier curve and receiver operator characteristic (ROC) curve.</div></div><div><h3>Results</h3><div>The C-index of clinical, radimocis and clinical-radiomics models were 0.852 (95% confidence interval[CI]:0.810–0.893), 0.863 (95%CI:0.816–0.910) and 0.903 (95%:0.870–0.936) in the training cohort and 0.725 (95%CI:0.630–0.820), 0.788 (95%CI:0.678–0.898), 0.813(95%CI:0.734–0.892) in the validation cohort. The AUCs of the multi-predictor nomogram at 1-, 3-, 5- and 7-year were 0.894, 0.908, 0.930, 0.979 in the training cohort and 0.671, 0.726, 0.839, 0.931 in the validation cohort.</div></div><div><h3>Conclusion</h3><div>In this study, we constructed a clinical-radimoics integrated model to predict the progression of preclinical AD and stratified the risk of disease progression in preclinical AD.</div></div>","PeriodicalId":50928,"journal":{"name":"Academic Radiology","volume":"32 2","pages":"Pages 951-962"},"PeriodicalIF":3.8,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142331771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Academic Radiology
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