Enhancing the effects of nusinersen with cybernic treatment using Hybrid Assistive Limb (HAL) in spinal muscular atrophy: a real-world case series and exploratory cohort analysis.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Takashi Nakajima, Toshio Saito, Akihiro Hashiguchi, Taiki Nakabayashi, Kazuki Kodera, Kota Utsumi, Takeshi Kanayama, Haruka Urabe, Satoru Kinoshita
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引用次数: 0

Abstract

Background: Nusinersen therapy for spinal muscular atrophy (SMA) provides significant functional improvement when initiated pre-symptomatically or early in life. However, challenges remain in diverse populations with longer disease duration. In Japan, innovative cybernic therapy with the Hybrid Assistive Limb (HAL) is gaining traction in treating neuromuscular diseases. This observational study investigated whether combining HAL therapy with nusinersen and conventional physiotherapy yields functional improvements in SMA, irrespective of disease duration or age. Functional improvement indicators included the Hammersmith Functional Motor Scale-Expanded (HFMSE) and Revised Upper Limb Module (RULM) scores, and the 2-minute walk test (2MWT), measured 15 months post-nusinersen initiation. A cohort analysis of a selected case series was conducted.

Results: Twelve patients with SMA type 2 or 3 who met the criteria of being able to walk with a hoist and began nusinersen treatment > 40 months post-disease onset were selected for longitudinal clinical assessment. Cohort 1 (n = 5, mean age 36.0 years) underwent HAL therapy, while Cohort 2 (n = 7, 24.6 years) did not. Baseline characteristics, except mean age, were similar across cohorts. In Cohort 1, the period from baseline (nusinersen initiation) to HAL therapy ranged from 0 to 8.8 months. HFMSE scores improved in both cohorts at 15 months; the least squares mean (LSM) change from baseline (95% confidence interval [CI]) was 4.7 points (2.2, 7.3) in Cohort 1 and 2.9 points (0.7, 5.1) in Cohort 2. Clinically meaningful improvement of 3.0 points in HFSME was exceeded by four of five patients in Cohort 1 and three of seven in Cohort 2. The LSM change from baseline in RULM was 2.2 points (95% CI 1.0, 3.3) in Cohort 1, exceeding the minimal clinically important difference of 0.5-1.0 points, but remained unchanged in Cohort 2 due to ceiling effects (- 0.2; -1.5, 1.2; p = 0.016). The LSM change from baseline in the 2MWT had improved in Cohort 1 (34.57 m; 95% CI 4.57, 64.57), but not in Cohort 2 (- 3.86; -37.75, 30.03).

Conclusions: In patients with SMA type 2 and 3, clinically meaningful improvements in multiple indicators were observed when HAL was combined with nusinersen, even when treatment commenced many years after disease onset.

Registration: jRCT1090220400 ( https://jrct.niph.go.jp/en-latest-detail/jRCT1090220400 ).

混合辅助肢(HAL)控制性治疗脊髓性肌萎缩的效果:真实世界的病例系列和探索性队列分析。
背景:Nusinersen治疗脊髓性肌萎缩症(SMA)在症状前或生命早期开始时可提供显着的功能改善。然而,在疾病持续时间较长的不同人群中,挑战仍然存在。在日本,使用混合辅助肢体(HAL)的创新控制论疗法在治疗神经肌肉疾病方面越来越受欢迎。这项观察性研究调查了HAL治疗联合nusinersen和常规物理治疗是否能改善SMA的功能,与疾病持续时间或年龄无关。功能改善指标包括Hammersmith功能运动量表扩展(HFMSE)和修订上肢模块(RULM)评分,以及2分钟步行测试(2MWT),在nusinersen开始后15个月测量。对选定的病例系列进行了队列分析。结果:选择12例2型或3型SMA患者进行纵向临床评估,这些患者在发病后40个月左右开始接受nusinersen治疗,符合能够用起重机行走的标准。队列1 (n = 5,平均年龄36.0岁)接受了HAL治疗,而队列2 (n = 7, 24.6岁)没有接受HAL治疗。除平均年龄外,各队列的基线特征相似。在队列1中,从基线(nusinersen起始)到HAL治疗的时间为0至8.8个月。15个月时,两组患者的HFMSE评分均有所改善;队列1与基线的最小二乘平均(LSM)变化(95%置信区间[CI])为4.7点(2.2,7.3),队列2为2.9点(0.7,5.1)。在队列1的5名患者中有4名和队列2的7名患者中有3名患者的HFSME临床意义改善超过了3.0分。在队列1中,RULM的LSM较基线变化为2.2点(95% CI 1.0, 3.3),超过了0.5-1.0点的最小临床重要差异,但在队列2中由于天花板效应(- 0.2;-1.5、1.2;p = 0.016)。在队列1中,2MWT的LSM较基线变化有所改善(34.57 m;95% CI 4.57, 64.57),但在队列2中没有(- 3.86;-37.75, 30.03)。结论:在2型和3型SMA患者中,即使在发病多年后开始治疗,HAL联合nusinersen也能观察到多项临床有意义的改善。报名:jRCT1090220400 (https://jrct.niph.go.jp/en-latest-detail/jRCT1090220400)。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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