Pattern of pareses in 5q-spinal muscular atrophy.

IF 4.7 2区 医学 Q1 CLINICAL NEUROLOGY Therapeutic Advances in Neurological Disorders Pub Date : 2024-08-27 eCollection Date: 2024-01-01 DOI:10.1177/17562864241263420
Zeljko Uzelac, Beate Schwäble, Johannes Dorst, Angela Rosenbohm, Kurt Wollinsky, Claudia D Wurster, Janna S Steinbreier, Albert C Ludolph
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Abstract

Background: This prospective study investigates the pattern of pareses in 5q-associated spinal muscular atrophy (SMA) to identify disease-specific characteristics and potential differences from amyotrophic lateral sclerosis (ALS) and spinobulbar muscular atrophy (SBMA). Detailed knowledge about pareses patterns in SMA facilitates differential diagnosis and supports therapeutic monitoring.

Methods: Between January 2021, and June 2021, 66 SMA patients (59.1% male, aged 33.6 ± 15.2 years) were included in the study. Most patients had SMA type II (n = 28) or SMA type III (n = 28), seven patients had SMA type I, and three patients had SMA type IV. We analyzed the pattern of pareses using the UK Medical Research Council (MRC) scoring system.

Results: In both, upper and lower limbs muscle weakness was less pronounced in distal (upper limbs: MRC median 3.0 (interquartile range 1.5-3.5); lower limbs: 1.5 (0.5-3.0)) compared to proximal muscle groups (upper limbs: 2.0 (1.5-2.6); p < 0.001; lower limbs: 0.5 (0.5-1.5); p < 0.001). Thenar muscles were stronger than other small hand muscles (3.0 (2.0-3.5) vs 3.0 (1.5-3.5); p = 0.004). Muscles had more strength in upper (2.3 (1.5-3.1)) compared to lower limbs (1.1 (0.5-2.3); p < 0.001) and in flexors compared to extensors.

Conclusion: We identified a specific pattern of muscle paresis in SMA which is different from the pattern of paresis in ALS and SBMA. As a rule of thumb, the pattern of pareses is similar, but not identical to ALS in distal, but different in proximal muscle groups.

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5q脊髓性肌萎缩症的瘫痪模式。
研究背景这项前瞻性研究调查了5q相关性脊髓性肌萎缩症(SMA)的瘫痪模式,以确定疾病的特异性特征以及与肌萎缩性脊髓侧索硬化症(ALS)和脊髓小脑性肌萎缩症(SBMA)的潜在差异。详细了解 SMA 的瘫痪模式有助于鉴别诊断和支持治疗监测:方法:2021 年 1 月至 2021 年 6 月期间,66 名 SMA 患者(59.1% 为男性,年龄为 33.6 ± 15.2 岁)被纳入研究。大多数患者为 SMA II 型(28 人)或 SMA III 型(28 人),7 名患者为 SMA I 型,3 名患者为 SMA IV 型。我们使用英国医学研究委员会(MRC)的评分系统分析了患者的瘫痪模式:结果:在这两种患者中,上肢和下肢的肌无力在远端(上肢、下肢)都不太明显:MRC 中位数为 3.0(四分位间范围为 1.5-3.5);下肢为 1.5(0.5-3.5):上肢:2.0 (1.5-2.6); p p = 0.004)。与下肢(1.1(0.5-2.3);p)相比,上肢(2.3(1.5-3.1))肌肉的力量更强:我们发现了 SMA 肌肉瘫痪的特殊模式,它不同于 ALS 和 SBMA 的瘫痪模式。根据经验,远端肌肉群的瘫痪模式与 ALS 相似,但不完全相同,而近端肌肉群的瘫痪模式则不同。
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来源期刊
CiteScore
8.30
自引率
1.70%
发文量
62
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Neurological Disorders is a peer-reviewed, open access journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of neurology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in neurology, providing a forum in print and online for publishing the highest quality articles in this area.
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