Neurology Unit, Movement Disorders Division, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, P.le Scuro 10, 37134, Verona, Italy.
Center for Neurodegenerative Diseases (CEMAND), Department of Medicine, Surgery and Dentistry-Scuola Medica Salernitana, University of Salerno, Baronissi, SA, Italy.
J Neurol. 2021 Dec;268(12):4737-4743. doi: 10.1007/s00415-021-10583-w. Epub 2021 May 7.
Functional motor disorders (FMDs) are usually categorized according to the predominant phenomenology; however, it is unclear whether this phenotypic classification mirrors the underlying pathophysiologic mechanisms.
To compare the characteristics of patients with different FMDs phenotypes and without co-morbid neurological disorders, aiming to answer the question of whether they represent different expressions of the same disorder or reflect distinct entities.
Consecutive outpatients with a clinically definite diagnosis of FMDs were included in the Italian registry of functional motor disorders (IRFMD), a multicenter data collection platform gathering several clinical and demographic variables. To the aim of the current work, data of patients with isolated FMDs were extracted.
A total of 176 patients were included: 58 with weakness, 40 with tremor, 38 with dystonia, 23 with jerks/facial FMDs, and 17 with gait disorders. Patients with tremor and gait disorders were older than the others. Patients with functional weakness had more commonly an acute onset (87.9%) than patients with tremor and gait disorders, a shorter time lag from symptoms onset and FMDs diagnosis (2.9 ± 3.5 years) than patients with dystonia, and had more frequently associated functional sensory symptoms (51.7%) than patients with tremor, dystonia and gait disorders. Patients with dystonia complained more often of associated pain (47.4%) than patients with tremor. No other differences were noted between groups in terms of other variables including associated functional neurological symptoms, psychiatric comorbidities, and predisposing or precipitating factors.
Our data support the evidence of a large overlap between FMD phenotypes.
功能性运动障碍(FMD)通常根据主要表现进行分类;然而,尚不清楚这种表型分类是否反映了潜在的病理生理机制。
比较不同 FMD 表型且无共患神经障碍患者的特征,旨在回答它们是否代表同一疾病的不同表现,还是反映不同实体。
连续纳入意大利功能性运动障碍登记处(IRFMD)的临床明确诊断为 FMD 的门诊患者,该登记处是一个收集多种临床和人口统计学变量的多中心数据收集平台。为了当前工作的目的,提取了患有孤立性 FMD 的患者的数据。
共纳入 176 例患者:58 例为无力,40 例为震颤,38 例为肌张力障碍,23 例为抽搐/面肌 FMD,17 例为步态障碍。震颤和步态障碍患者年龄较大。与震颤和步态障碍患者相比,功能性无力患者更常见急性起病(87.9%),从症状发作到 FMD 诊断的时间间隔更短(2.9±3.5 年),且更常伴有功能性感觉症状(51.7%),与震颤、肌张力障碍和步态障碍患者相比。震颤患者中,伴有相关功能性感觉症状的比例更高(51.7%)。在其他变量方面,如相关功能性神经症状、精神共病和诱发或促发因素,各组之间无其他差异。
我们的数据支持 FMD 表型之间存在广泛重叠的证据。