Corticobasal Syndrome: Are There Central or Peripheral Triggers?

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200365
Abhishek Lenka, Joseph Jankovic
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引用次数: 0

Abstract

Background and objectives: Corticobasal syndrome (CBS) is a complex of symptoms and signs comprising limb rigidity, bradykinesia, dystonia, myoclonus, apraxia, cortical sensory loss, and a variety of cognitive and language impairments. CBS is commonly seen in tauopathies. Striking asymmetry in clinical and imaging findings in CBS raises questions about potential triggers initiating neurodegeneration. The objective of this study was to investigate potential central or peripheral triggers preceding CBS symptoms.

Methods: In this retrospective observational study, we reviewed medical records of patients with CBS at our Parkinson's Disease Center and Movement Disorders Clinic, focusing on evidence of possible central or peripheral "trigger" occurring within a year before the onset of CBS. We also reviewed records of patients with Parkinson disease (PD) for comparison.

Results: Of the 72 patients with CBS, 15 (20.8%) reported potential focal triggers before the onset of CBS-related neurologic symptoms. By contrast, only 1 of 72 patients with PD (1.4%) had a documented trigger before the onset of PD-related symptoms (p < 0.001). Of potential triggers, 13 were peripheral (related to hand or shoulder surgeries or trauma) and 2 were central (stroke and head trauma). Patients with CBS with triggers were younger, had earlier symptom onset, comprised a higher proportion of men, and had a higher likelihood of limb onset of symptoms than those without.

Discussion: Our finding of relatively high frequency of focal triggers in CBS compared with PD suggests potential central or peripheral triggers initiating neurodegeneration, possibly explaining asymmetric clinical and imaging features in CBS. Further research is necessary to validate and explore this observation's implications for CBS pathogenesis.

皮质基底综合征:是中枢诱因还是外周诱因?
背景和目的:皮质基底综合征(CBS)是由肢体僵硬、运动迟缓、肌张力障碍、肌阵挛、失能、皮质感觉缺失以及各种认知和语言障碍组成的症状和体征综合征。CBS 常见于陶陶病。CBS 的临床和影像学发现具有显著的不对称性,这引发了人们对引发神经变性的潜在诱因的疑问。本研究的目的是调查 CBS 症状出现前的潜在中枢或外周诱因:在这项回顾性观察研究中,我们查阅了帕金森病中心和运动障碍门诊的 CBS 患者的医疗记录,重点关注 CBS 发病前一年内可能发生的中枢或外周 "诱发因素 "的证据。我们还查阅了帕金森病(PD)患者的病历,以进行对比:在 72 名 CBS 患者中,有 15 人(20.8%)在出现 CBS 相关神经症状之前报告了潜在的病灶触发因素。相比之下,72 名帕金森病患者中只有 1 人(1.4%)在出现帕金森病相关症状之前有记录的诱发因素(P < 0.001)。在潜在的触发因素中,13 个是外周触发因素(与手部或肩部手术或外伤有关),2 个是中枢触发因素(中风和头部外伤)。与无诱发因素的患者相比,有诱发因素的CBS患者更年轻、症状出现更早、男性比例更高、肢端发病的可能性更大:讨论:我们发现,与帕金森病相比,CBS中局灶性诱发因素的频率相对较高,这表明潜在的中枢或外周诱发因素可能会引发神经变性,从而解释了CBS不对称的临床和影像学特征。有必要开展进一步研究,以验证和探讨这一观察结果对 CBS 发病机制的影响。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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