Texture analysis of cardiovascular MRI native T1 mapping in patients with Duchenne muscular dystrophy.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Mary Luz Mojica-Pisciotti, Tomáš Holeček, Věra Feitová, Lukáš Opatřil, Roman Panovský
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引用次数: 0

Abstract

Background: Duchenne muscular dystrophy (DMD) patients are monitored periodically for cardiac involvement, including cardiac MRI with gadolinium-based contrast agents (GBCA). Texture analysis (TA) offers an alternative approach to assess late gadolinium enhancement (LGE) without relying on GBCA administration, impacting DMD patients' care. The study aimed to evaluate the prognostic value of selected TA features in the LGE assessment of DMD patients.

Results: We developed a pipeline to extract TA features of native T1 parametric mapping and evaluated their prognostic value in assessing LGE in DMD patients. For this evaluation, five independent TA features were selected using Boruta to identify relevant features based on their importance, least absolute shrinkage and selection operator (LASSO) to reduce the number of features, and hierarchical clustering to target multicollinearity and identify independent features. Afterward, logistic regression was used to determine the features with better discrimination ability. The independent feature inverse difference moment normalized (IDMN), which measures the pixel values homogeneity in the myocardium, achieved the highest accuracy in classifying LGE (0.857 (0.572-0.982)) and also was significantly associated with changes in the likelihood of LGE in a subgroup of patients with three yearly examinations (estimate: 23.35 (8.7), p-value = 0.008). Data are presented as mean (SD) or median (IQR) for normally and non-normally distributed continuous variables and numbers (percentages) for categorical ones. Variables were compared with the Welch t-test, Wilcoxon rank-sum, and Chi-square tests. A P-value < 0.05 was considered statistically significant.

Conclusion: IDMN leverages the information native T1 parametric mapping provides, as it can detect changes in the pixel values of LGE images of DMD patients that may reflect myocardial alterations, serving as a supporting tool to reduce GBCA use in their cardiac MRI examinations.

杜氏肌营养不良患者心血管MRI原生T1定位的纹理分析。
背景:杜氏肌营养不良(DMD)患者定期监测心脏受损伤,包括使用钆基对比剂(GBCA)进行心脏MRI检查。质地分析(TA)提供了一种替代方法来评估晚期钆增强(LGE),而不依赖GBCA给药,影响DMD患者的护理。本研究旨在评价选定TA特征在DMD患者LGE评估中的预后价值。结果:我们开发了一个管道来提取原生T1参数映射的TA特征,并评估其在评估DMD患者LGE中的预后价值。为了进行评估,采用Boruta方法根据TA的重要性选择5个独立TA特征,采用最小绝对收缩和选择算子(LASSO)方法减少特征数量,采用分层聚类方法针对多重共线性并识别独立特征。然后,使用逻辑回归来确定识别能力较好的特征。测量心肌像素值均匀性的独立特征逆差矩归一化(IDMN)对LGE的分类准确率最高(0.857(0.572-0.982)),并且与每年检查3次的亚组患者LGE发生可能性的变化显著相关(估计:23.35 (8.7),p值= 0.008)。对于正态分布和非正态分布的连续变量,数据以平均值(SD)或中位数(IQR)表示,对于分类变量,数据以数字(百分比)表示。变量比较采用Welch t检验、Wilcoxon秩和和卡方检验。结论:IDMN利用原生T1参数映射提供的信息,可以检测DMD患者LGE图像中可能反映心肌改变的像素值变化,作为辅助工具减少GBCA在心脏MRI检查中的使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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