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直面肌病:包涵体肌炎的面肌受累解读

Face to Face: deciphering facial involvement in inclusion body myositis.

机构信息

Referral Centre for Neuromuscular Diseases and ALS (Amyotrophic Lateral Sclerosis), Timone University Hospital, Marseille, France.

Aix-Marseille University, Inserm, GMGF, Marseille, France.

出版信息

J Neurol. 2024 Jan;271(1):410-418. doi: 10.1007/s00415-023-11986-7. Epub 2023 Sep 23.

DOI:10.1007/s00415-023-11986-7
PMID:37740740
Abstract

OBJECTIVE

The objective of this study is to evaluate the frequency and characteristics of facial involvement in inclusion body myositis (IBM) patients and to compare it to the one previously described in facioscapulohumeral dystrophy (FSHD) patients.

METHODS

Thirty-two IBM patients were included and compared to 29 controls and 39 FSHD patients. All participants were recorded in a video as they performed a series of seven facial tasks. Five raters independently assessed facial weakness using both a qualitative evaluation and a semi-quantitative facial weakness score (FWS).

RESULTS

IBM patients had higher FWS than controls (7.89 ± 7.56 vs 1.06 ± 0.88, p < 0.001). Twenty IBM patients (63%) had a facial weakness with a FWS above the maximum value for controls. All facial tasks were significantly more impaired in IBM patients compared to controls (p < 0.001), task 2 evaluating orbiculari oculi muscle weakness being the most affected. IBM patients with facial weakness reported more swallowing troubles than IBM patients without facial weakness (p = 0.03). FSHD patients displayed higher FWS than IBM patients (12.16 ± 8.37 vs 7.89 ± 7.56, p = 0.01) with more pronounced facial asymmetry (p = 0.01). FWS inter-rater ICC was 0.775.

CONCLUSION

This study enabled us to estimate the frequency of facial impairment in IBM in more than half of patients, to detail its characteristics and to compare them with those of FSHD patients. The standardized, semi-quantitative FWS is an interesting diagnostic help in IBM as it appeared more sensitive than qualitative evaluation to detect mild facial weakness.

摘要

目的

本研究旨在评估包涵体肌炎(IBM)患者面部受累的频率和特征,并将其与先前描述的面肩肱型肌营养不良症(FSHD)患者进行比较。

方法

纳入 32 名 IBM 患者,并与 29 名对照组和 39 名 FSHD 患者进行比较。所有参与者均在视频中记录,以完成一系列 7 项面部任务。5 名评分者分别使用定性评估和半定量面部无力评分(FWS)对面部无力进行独立评估。

结果

IBM 患者的 FWS 高于对照组(7.89±7.56 对 1.06±0.88,p<0.001)。20 名 IBM 患者(63%)的面部无力 FWS 高于对照组的最大值。与对照组相比,IBM 患者的所有面部任务均明显受损(p<0.001),评估眼轮匝肌无力的任务 2 受影响最严重。有面部无力的 IBM 患者比无面部无力的 IBM 患者报告更多的吞咽困难(p=0.03)。FSHD 患者的 FWS 高于 IBM 患者(12.16±8.37 对 7.89±7.56,p=0.01),且面部不对称更明显(p=0.01)。FWS 评分者间 ICC 为 0.775。

结论

本研究能够评估超过一半 IBM 患者的面部受损频率,详细描述其特征,并将其与 FSHD 患者进行比较。标准化的半定量 FWS 是 IBM 中的一种有趣的诊断辅助手段,因为它比定性评估更能检测到轻度的面部无力。

相似文献

1
Face to Face: deciphering facial involvement in inclusion body myositis.直面肌病:包涵体肌炎的面肌受累解读
J Neurol. 2024 Jan;271(1):410-418. doi: 10.1007/s00415-023-11986-7. Epub 2023 Sep 23.
2
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J Neurol. 2021 Apr;268(4):1342-1350. doi: 10.1007/s00415-020-10281-z. Epub 2020 Oct 28.
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Disabil Rehabil. 2023 May;45(9):1530-1535. doi: 10.1080/09638288.2022.2066208. Epub 2022 May 16.
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Inclusion-body myositis presenting with facial diplegia.包涵体肌炎致面瘫。
Muscle Nerve. 2014 Feb;49(2):287-9. doi: 10.1002/mus.24060. Epub 2013 Dec 18.
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Atypical progression of motor symptoms in facio-scapulo-humeral dystrophy: clinical worsening or overlap?面肩肱型肌营养不良症运动症状的非典型进展:病情恶化还是重叠?
BMJ Case Rep. 2023 May 29;16(5):e253820. doi: 10.1136/bcr-2022-253820.
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Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD.健康对照者和 IBM、FSHD 和 OPMD 患者肌肉活检的定量 MRI 与肌肉组织病理学的相关性。
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本文引用的文献

1
Diagnosing and managing dysphagia in inclusion body myositis: a systematic review.诊断和管理包涵体肌炎伴发的吞咽困难:系统综述。
Rheumatology (Oxford). 2023 Oct 3;62(10):3227-3244. doi: 10.1093/rheumatology/kead194.
2
Facioscapulohumeral Muscular Dystrophy.面肩肱型肌营养不良症
Continuum (Minneap Minn). 2022 Dec 1;28(6):1735-1751. doi: 10.1212/CON.0000000000001155.
3
Inclusion Body Myositis.包涵体肌炎。
Continuum (Minneap Minn). 2022 Dec 1;28(6):1663-1677. doi: 10.1212/CON.0000000000001204.
4
Development and validation of the patient-reported "Facial Function Scale" for facioscapulohumeral muscular dystrophy.用于面肩肱型肌营养不良症的患者报告的“面部功能量表”的开发与验证
Disabil Rehabil. 2023 May;45(9):1530-1535. doi: 10.1080/09638288.2022.2066208. Epub 2022 May 16.
5
Recent Progress in Oculopharyngeal Muscular Dystrophy.眼咽型肌营养不良症的最新进展
J Clin Med. 2021 Mar 29;10(7):1375. doi: 10.3390/jcm10071375.
6
Characterizing the face in facioscapulohumeral muscular dystrophy.描述面肩肱型肌营养不良症的面容。
J Neurol. 2021 Apr;268(4):1342-1350. doi: 10.1007/s00415-020-10281-z. Epub 2020 Oct 28.
7
Facial diplegia as the presenting symptom of inclusion body myositis.面部双侧瘫作为包涵体肌炎的首发症状
Muscle Nerve. 2019 Aug;60(2):E14-E16. doi: 10.1002/mus.26514. Epub 2019 May 23.
8
Inclusion body myositis: clinical features and pathogenesis.包涵体肌炎:临床特征和发病机制。
Nat Rev Rheumatol. 2019 May;15(5):257-272. doi: 10.1038/s41584-019-0186-x.
9
Inclusion Body Myositis: Update on Pathogenesis and Treatment.包涵体肌炎:发病机制和治疗的最新进展。
Neurotherapeutics. 2018 Oct;15(4):995-1005. doi: 10.1007/s13311-018-0658-8.
10
Clinical and genetic features of patients with facial-sparing facioscapulohumeral muscular dystrophy.面肩肱型肌营养不良症患者的临床和遗传学特征。
Eur J Neurol. 2018 Feb;25(2):356-364. doi: 10.1111/ene.13509. Epub 2017 Dec 21.