Long-Term Effects of Annual Intensive Rehabilitation in Patients with Hereditary Pure Cerebellar Ataxia: A 7-year Follow-up Study.

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Kyota Bando, Yuki Kondo, Yosuke Ariake, Taro Kato, Mari S Oba, Takatoshi Hara, Yuji Takahashi
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Abstract

Although intensive rehabilitation has achieved short-term benefits in patients with spinocerebellar degeneration, long-term outcomes of periodic intervention remain unclear, particularly in patients with pure spinocerebellar ataxia types 6 (SCA6) and 31 (SCA31). To investigate the longitudinal effects of annual intensive rehabilitation on ataxic symptoms and balance function in patients with pure cerebellar type SCA6 and SCA31. Seven patients with genetically confirmed SCA6 or SCA31 participated in annual 4-week intensive rehabilitation programmes. Each programme consisted of daily physical therapy, occupational/speech therapy, and self-directed balance training. The participants were assessed annually at pre-intervention, post-intervention, and the 6-month follow-up using the Scale for the Assessment and Rating of Ataxia (SARA) and Balance Evaluation Systems Test (BESTest). Changes were analysed using linear mixed-effect models. SARA scores were stable, indicating slower progression than the expected natural history, through year 6, with significant improvement observed post-intervention in year 2 (p = 0.04). Significant deterioration occurred at year 7 based on pre-intervention scores (p = 0.01), suggesting prolonged sustained benefits for coordination. The BESTest scores revealed an earlier decline, with significant deterioration from year 3 (p = 0.04), which progressed until year 7 (p < 0.01). Annual intensive rehabilitation effectively slowed the progression of ataxic symptoms (SARA) for up to six years, while balance function (BESTest) showed a significant decline from the third year. These findings indicate that an annual rehabilitation schedule is valuable for maintaining coordination but may be insufficient to prevent the progressive decline of balance function in patients with pure cerebellar ataxia.

Abstract Image

遗传性单纯小脑共济失调患者每年强化康复的长期效果:一项7年随访研究。
尽管强化康复在脊髓小脑变性患者中获得了短期益处,但定期干预的长期结果尚不清楚,特别是单纯的脊髓小脑性共济失调6型(SCA6)和31型(SCA31)患者。探讨年度强化康复对单纯小脑型SCA6和SCA31患者共济失调症状和平衡功能的纵向影响。7例基因确诊的SCA6或SCA31患者参加了每年4周的强化康复计划。每个项目包括日常物理治疗、职业/语言治疗和自我平衡训练。参与者每年在干预前、干预后和6个月的随访中使用共济失调评估和评级量表(SARA)和平衡评估系统测试(BESTest)进行评估。使用线性混合效应模型分析变化。SARA评分稳定,表明第6年的进展比预期的自然病史慢,干预后第2年观察到显著改善(p = 0.04)。根据干预前评分,在第7年出现了显著的恶化(p = 0.01),表明协调性的持续获益延长了。最佳分数显示较早的下降,从第3年开始显著恶化(p = 0.04),一直持续到第7年(p = 0.04)
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来源期刊
Cerebellum
Cerebellum 医学-神经科学
CiteScore
6.40
自引率
14.30%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Official publication of the Society for Research on the Cerebellum devoted to genetics of cerebellar ataxias, role of cerebellum in motor control and cognitive function, and amid an ageing population, diseases associated with cerebellar dysfunction. The Cerebellum is a central source for the latest developments in fundamental neurosciences including molecular and cellular biology; behavioural neurosciences and neurochemistry; genetics; fundamental and clinical neurophysiology; neurology and neuropathology; cognition and neuroimaging. The Cerebellum benefits neuroscientists in molecular and cellular biology; neurophysiologists; researchers in neurotransmission; neurologists; radiologists; paediatricians; neuropsychologists; students of neurology and psychiatry and others.
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