Non-motor symptoms in patients with isolated dystonia: comparison between the age of onset

Dystonia Pub Date : 2024-02-09 DOI:10.3389/dyst.2024.11468
Yifan Zhou, Lingbing Wang, Hongxia Li, Yiwen Wu
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Abstract

Background: The etiology and motor presentation differs between pediatric- and adult-onset dystonia. Emerging evidence has demonstrated that non-motor symptoms are frequent in adult dystonia, which affect the quality of life. By contrast, little is known about the frequency and severity of such presentations in pediatric-onset individuals. Here, we investigated the motor and non-motor symptoms in a large cohort of Chinese patients with isolated dystonia and compared between pediatric-onset and adult-onset groups.Methods: In this retrospective study, 34 pediatric-onset patients and 197 adult-onset patients with isolated dystonia were recruited. Motor impairment was assessed by the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS). Non-motor symptoms were evaluated through several validated scales, including fatigue (by Fatigue Severity Scale, FSS), excessive daytime sleepiness (by Epworth Sleepiness Scale, ESS), sleep disturbance (by Pittsburgh Sleep Quality Index, PSQI), anxiety (by Beck Anxiety Inventory, BAI) and depression (by Beck Depression Inventory 21, BDI-21).Results: Generalized dystonia was more common in pediatric-onset patients and focal dystonia was more common in adult-onset patients (p < 0.001). Generally, the BFMDRS score in total pediatric-onset group was higher than adult-onset group (p = 0.002). No differences was found in BFMDRS score between pediatric-onset and adult-onset patients with cervical and multifocal subtype dystonia. Compared with adult-onset group, pediatric-onset group had a lower rate of sleep disturbance (p < 0.0001) and similar rates of fatigue, excessive daytime sleepiness, depression and anxiety. Logistic regression analysis on patients with cervical dystonia indicated that the adult-onset and motor severity were independently associated with increased odds of sleep disturbance (p = 0.03) and depression (p = 0.01), respectively.Conclusion: Pediatric-onset dystonia patients were less likely to display focal dystonia. Most non-motor symptoms in pediatric-onset patients were comparable to their adult-onset counterparts. Non-motor presentations may to some extent correlate with motor symptoms, but their underlying pathophysiology need to be investigated further.
孤立性肌张力障碍患者的非运动症状:发病年龄的比较
背景:儿童和成人肌张力障碍的病因和运动表现各不相同。新的证据表明,成人肌张力障碍患者经常出现非运动症状,这些症状会影响患者的生活质量。相比之下,人们对儿童发病者出现非运动症状的频率和严重程度知之甚少。在此,我们调查了一大批中国孤立性肌张力障碍患者的运动和非运动症状,并对儿童发病组和成人发病组进行了比较:在这项回顾性研究中,共招募了 34 名儿童发病型孤立性肌张力障碍患者和 197 名成人发病型孤立性肌张力障碍患者。运动障碍通过伯克-法恩-马斯登肌张力障碍评定量表(Burke-Fahn-Marsden Dystonia Rating Scale,BFMDRS)进行评估。非运动症状通过几种有效量表进行评估,包括疲劳(疲劳严重程度量表,FSS)、白天过度嗜睡(埃普沃斯嗜睡量表,ESS)、睡眠障碍(匹兹堡睡眠质量指数,PSQI)、焦虑(贝克焦虑量表,BAI)和抑郁(贝克抑郁量表21,BDI-21):结果:全身性肌张力障碍在儿童患者中更为常见,而局灶性肌张力障碍在成人患者中更为常见(P < 0.001)。总体而言,儿童发病组的 BFMDRS 总分高于成人发病组(P = 0.002)。颈性肌张力障碍和多灶性肌张力障碍儿童发病组和成人发病组的 BFMDRS 评分没有差异。与成人发病组相比,儿童发病组的睡眠障碍发生率较低(P < 0.0001),疲劳、白天过度嗜睡、抑郁和焦虑的发生率相似。对颈性肌张力障碍患者进行的逻辑回归分析表明,成人发病率和运动严重程度分别与睡眠障碍(p = 0.03)和抑郁(p = 0.01)几率增加独立相关:结论:小儿肌张力障碍患者较少表现出局灶性肌张力障碍。结论:小儿肌张力障碍患者较少表现出局灶性肌张力障碍,大多数小儿患者的非运动症状与成人患者相当。非运动症状可能在一定程度上与运动症状相关,但其潜在的病理生理学还需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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