Age-appropriate or delayed myelination? Scoring myelination in routine clinical MRI

IF 2.3 3区 医学 Q3 CLINICAL NEUROLOGY
Inga Harting , Sven F. Garbade , Stefan D. Roosendaal , Hannah Fels-Palesandro , Clara Raudonat , Alexander Mohr , Nicole I. Wolf
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引用次数: 0

Abstract

Background

Assessment of myelination is a core issue in paediatric neuroimaging and can be challenging, particularly in settings without dedicated paediatric neuroradiologists. Deep learning models have recently been shown to be able to estimate myelination age in children with normal MRI, but currently lack validation for patients with myelination delay and implementation including pre-processing suitable for local imaging is not trivial. Standardized myelination scores, which have been successfully used as biomarkers for myelination in hypomyelinating diseases, rely on visual, semiquantitative scoring of myelination on routine clinical MRI and may offer an easy-to-use alternative for assessment of myelination.

Methods

Myelination was scored in 13 anatomic sites (items) on conventional T2w and T1w images in controls (n = 253, 0–2 years). Items for the score were selected based on inter-rater variability, practicability of scoring, and importance for correctly identifying validation scans.

Results

The resulting myelination score consisting of 7 T2- and 5 T1-items delineated myelination from term-equivalent to advanced, incomplete myelination which 50 % and 99 % of controls had reached by 19.1 and 32.7 months, respectively. It correctly identified 20/20 new control MRIs and 40/43 with myelination delay, missing one patient with borderline myelination delay at 8.6 months and 2 patients with incomplete T2-myelination of subcortical temporopolar white matter at 28 and 34 months.

Conclusions

The proposed myelination score provides an easy to use, standardized, and versatile tool to delineate myelination normally occurring during the first 1.5 years of life.

适龄髓鞘化还是延迟髓鞘化?常规临床磁共振成像中的髓鞘化评分。
背景髓鞘化评估是儿科神经影像学的一个核心问题,具有一定的挑战性,尤其是在没有专门儿科神经放射科医生的情况下。最近的研究表明,深度学习模型能够估算出核磁共振成像正常儿童的髓鞘化年龄,但目前还缺乏对髓鞘化延迟患者的验证,而且包括适合局部成像的预处理在内的实施也并非易事。标准化的髓鞘化评分已成功用作髓鞘功能减退疾病的髓鞘化生物标志物,它依靠常规临床磁共振成像对髓鞘化进行可视化、半定量评分,可为髓鞘化评估提供一种易于使用的替代方法。方法在对照组(n = 253,0-2 岁)的常规 T2w 和 T1w 图像上对 13 个解剖部位(项目)的髓鞘化进行评分。结果由7个T2-和5个T1-项目组成的髓鞘化评分将髓鞘化划分为等效期髓鞘化和晚期不完全髓鞘化,分别有50%和99%的对照组患者在19.1个月和32.7个月时达到了等效期髓鞘化和晚期不完全髓鞘化。它能正确识别 20/20 例新的对照组 MRI 和 40/43 例髓鞘化延迟患者,但漏诊了一名 8.6 个月时有边缘髓鞘化延迟的患者和两名 28 个月和 34 个月时皮层下颞极白质 T2 髓鞘化不完全的患者。
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来源期刊
CiteScore
6.30
自引率
3.20%
发文量
115
审稿时长
81 days
期刊介绍: The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies. Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability. Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.
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