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通过定性纵向成像技术追踪面肩肱型肌营养不良症的肌肉萎缩和疾病活动。

Tracking muscle wasting and disease activity in facioscapulohumeral muscular dystrophy by qualitative longitudinal imaging.

机构信息

Unità Operativa Complessa di Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Istituto di Neurologia, Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

J Cachexia Sarcopenia Muscle. 2019 Dec;10(6):1258-1265. doi: 10.1002/jcsm.12473. Epub 2019 Oct 30.

Abstract

BACKGROUND

Facioscapulohumeral muscular dystrophy (FSHD) is one of the most frequent late-onset muscular dystrophies, characterized by progressive fatty replacement and degeneration involving single muscles in an asynchronous manner. With clinical trials at the horizon in this disease, the knowledge of its natural history is of paramount importance to understand the impact of new therapies. The aim of this study was to assess disease progression in FSHD using qualitative muscle magnetic resonance imaging, with a focus on the evolution of hyperintense lesions identified on short-tau inversion recovery (STIR+) sequences, hypothesized to be markers of active muscle injury.

METHODS

One hundred genetically confirmed consecutive FSHD patients underwent lower limb muscle magnetic resonance imaging at baseline and after 365 ± 60 days in this prospective longitudinal study. T1 weighted (T1w) and STIR sequences were used to assess fatty replacement using a semiquantitative visual score and muscle oedema. The baseline and follow-up scans of each patient were also evaluated by unblinded direct comparison to detect the changes not captured by the scoring system.

RESULTS

Forty-nine patients showed progression on T1w sequences after 1 year, and 30 patients showed at least one new STIR+ lesion. Increased fat deposition at follow-up was observed in 13.9% STIR+ and in only 0.21% STIR- muscles at baseline (P < 0.001). Overall, 89.9% of the muscles that showed increased fatty replacement were STIR+ at baseline and 7.8% were STIR+ at 12 months. A higher number of STIR+ muscles at baseline was associated with radiological worsening (odds ratio 1.17, 95% confidence interval 1.06-1.30, P = 0.003).

CONCLUSIONS

Our study confirms that STIR+ lesions represent prognostic biomarkers in FSHD and contributes to delineate its radiological natural history, providing useful information for clinical trial design. Given the peculiar muscle-by-muscle involvement in FSHD, MRI represents an invaluable tool to explore the modalities and rate of disease progression.

摘要

背景

面肩肱型肌营养不良症(FSHD)是最常见的迟发性肌营养不良症之一,其特征为单块肌肉进行性脂肪替代和退化,且方式不同步。随着该病临床试验的出现,了解其自然病史对于理解新疗法的影响至关重要。本研究旨在使用定性肌肉磁共振成像评估 FSHD 的疾病进展,重点关注在短反转时间(STIR+)序列上识别出的高信号病变的演变,这些病变被假设为活跃性肌肉损伤的标志物。

方法

在这项前瞻性纵向研究中,100 名经基因确诊的连续 FSHD 患者在基线时和 365 ± 60 天后接受了下肢肌肉磁共振成像检查。使用半定量视觉评分和肌肉水肿评估 T1 加权(T1w)和 STIR 序列评估脂肪替代。每位患者的基线和随访扫描也通过盲法直接比较进行评估,以发现评分系统无法捕捉到的变化。

结果

1 年后,49 名患者在 T1w 序列上显示出进展,30 名患者显示出至少一个新的 STIR+病变。在随访中,13.9%的 STIR+肌肉和仅 0.21%的 STIR-肌肉观察到脂肪沉积增加(P < 0.001)。总体而言,89.9%在基线时显示脂肪替代增加的肌肉在 STIR+,7.8%在 12 个月时显示 STIR+。基线时 STIR+肌肉数量较多与影像学恶化相关(优势比 1.17,95%置信区间 1.06-1.30,P = 0.003)。

结论

我们的研究证实,STIR+病变是 FSHD 的预后生物标志物,并有助于描绘其影像学自然病史,为临床试验设计提供有用信息。鉴于 FSHD 肌肉呈独特的肌肉受累方式,MRI 是探索疾病进展方式和速度的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9c/6903444/cfce460b26a7/JCSM-10-1258-g001.jpg

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