Hannah Kelly , Rongyi Sun , Mohamed Elkasaby , Alexander Wang , Hesham Abboud
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引用次数: 0
Abstract
Background
Recent studies suggest that movement disorders are common in early MS. However, the frequency and clinical characteristics of movement disorders at all stages of MS remain unknown.
Objectives
To evaluate the frequency, clinical characteristics, and anatomical generators of movement disorders in relapsing and progressive MS.
Methods
We conducted a prospective study of adult MS patients from 2016 to 2022 at a neuroimmunology clinic. Patients were evaluated for demyelination-related movement disorders via a survey and focused examination. We classified movement disorders based on phenomenology and identified anatomic correlates according to lesion locations and relation to relapses. Findings were compared between relapsing and progressive MS.
Results
Of 327 patients, 211 (64.5 %) had demyelination-related movement disorders (median age 35.3, Q1 28.5, Q3 44.8; 72.5 % female). Spinal movement disorders were the most common and occurred in 177 patients (54.1 %). Brainstem/cerebellar movement disorders occurred in 59 (18 %), and striatal/thalamic movement disorders occurred in 8 (2.4 %). The most common movement subtypes were tonic spasms (39.4 %) and tremor (24.5 %). We observed 21 cases (6.4 %) in which movement disorders represented a new relapse including the first attack of the disease. Patients with progressive MS were more likely to have demyelination-related movement disorders (chi square, p < 0.001), including spinal (chi square, p = 0.0003), brainstem/cerebellar (chi square, p = 0.009), and striatal/thalamic movement disorders (fisher exact, p = 0.03).
Discussion
Demyelination-related movement disorders are very common in all stages of MS, especially in patients with progressive disease and those with spinal lesions. In some, movement disorders may be the presenting symptom of the disease.
期刊介绍:
The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials).
JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.