按 D50 进展模型分层的肌萎缩侧索硬化症患者的 T1 加权磁共振成像纹理分析。

IF 4.1 Q1 CLINICAL NEUROLOGY Brain communications Pub Date : 2024-11-05 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae389
Pedram Parnianpour, Robert Steinbach, Isabelle Jana Buchholz, Julian Grosskreutz, Sanjay Kalra
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引用次数: 0

摘要

肌萎缩侧索硬化症是一种进行性神经退行性疾病,由于其异质性,在预测个体疾病轨迹方面存在挑战。本研究探讨了纹理分析在肌萎缩侧索硬化症患者 T1 加权 MRI 上的应用,并根据 D50 疾病进展模型进行了分层。与传统的线性指标相比,D50 模型能更细致地反映疾病的进展情况,它计算功能衰退的西格玛曲线,并对疾病的侵袭性和累积性进行独立量化。在这项研究中,我们使用 D50 模型和核磁共振成像的纹理分析对一组具有代表性的 116 名肌萎缩侧索硬化症患者进行了研究。纹理分析是一种用于量化核磁共振成像中体素强度模式的技术,它被用来辨别与肌萎缩侧索硬化症相关的脑组织变化。这项研究根据疾病的积累、侵袭性和首次发病部位,以及与积累/侵袭性的直接回归,检查了不同亚组患者纹理特征自相关性的改变。研究结果表明,根据疾病累积程度分层的患者,其灰质和白质的纹理自相关性模式各不相同,双侧皮质脊髓束、右侧海马和左侧颞极的纹理自相关性增加,而运动和运动外脑区的纹理自相关性则普遍降低。在回归分析中,左侧扣带回白质、脑干、左侧小脑扁桃体灰质和右侧前枕下束内的灰质和白质群的自相关性改变也与疾病积累呈负相关。此外,疾病的侵袭性仅与右颞上回和扣带回白质右后部的两个小群相关。研究结果表明,纹理分析可作为肌萎缩侧索硬化症疾病分期的潜在生物标志物,并有可能在使用T1加权图像的基础上进行快速评估。
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T1-weighted MRI texture analysis in amyotrophic lateral sclerosis patients stratified by the D50 progression model.

Amyotrophic lateral sclerosis, a progressive neurodegenerative disease, presents challenges in predicting individual disease trajectories due to its heterogeneous nature. This study explores the application of texture analysis on T1-weighted MRI in patients with amyotrophic lateral sclerosis, stratified by the D50 disease progression model. The D50 model, which offers a more nuanced representation of disease progression than traditional linear metrics, calculates the sigmoidal curve of functional decline and provides independent quantifications of disease aggressiveness and accumulation. In this research, a representative cohort of 116 patients with amyotrophic lateral sclerosis was studied using the D50 model and texture analysis on MRI images. Texture analysis, a technique used for quantifying voxel intensity patterns in MRI images, was employed to discern alterations in brain tissue associated with amyotrophic lateral sclerosis. This study examined alterations of the texture feature autocorrelation across sub-groups of patients based on disease accumulation, aggressiveness and the first site of onset, as well as in direct regressions with accumulation/aggressiveness. The findings revealed distinct patterns of the texture-derived autocorrelation in grey and white matter, increase in bilateral corticospinal tract, right hippocampus and left temporal pole as well as widespread decrease within motor and extra-motor brain regions, of patients stratified based on their disease accumulation. Autocorrelation alterations in grey and white matter, in clusters within the left cingulate gyrus white matter, brainstem, left cerebellar tonsil grey matter and right inferior fronto-occipital fasciculus, were also negatively associated with disease accumulation in regression analysis. Otherwise, disease aggressiveness correlated with only two small clusters, within the right superior temporal gyrus and right posterior division of the cingulate gyrus white matter. The findings suggest that texture analysis could serve as a potential biomarker for disease stage in amyotrophic lateral sclerosis, with potential for quick assessment based on using T1-weighted images.

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