Multiple Sclerosis Patients with Markedly Low Intrathecal Antibody Response in Sri Lanka.

IF 2.2 Q3 CLINICAL NEUROLOGY
Multiple Sclerosis International Pub Date : 2018-02-28 eCollection Date: 2018-01-01 DOI:10.1155/2018/5342936
S M K Gamage, I Wijeweera, S B Adikari, Katharina Fink, Jan Hillert, Anna Fogdell-Hahn, H M A Sominanda
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引用次数: 6

Abstract

Multiple sclerosis (MS) is a heterogeneous disease which is poorly studied in Asia, where the disease is known to be rare with significant differences in clinical and radiological presentations and intrathecal antibody response. Therefore the objective of this study was to determine clinical presentation, radiological and neurophysiological characteristics, and oligoclonal band status in Sri Lankan MS patients, following careful exclusion of patients with neuromyelitis optica spectrum disorders and other conditions mimicking multiple sclerosis. Sixty-nine MS patients were recruited to the study adhering to McDonald 2010 criteria. Their clinical presentation, characteristics of central nervous system lesions in magnetic resonance imaging, visual evoked potential (VEP) results, oligoclonal bands (OCB), and AQP4 antibody status were studied. Of 69 MS patients, 54%, 6%, and 1% were relapsing remitting, secondary progressive, and primary progressive, respectively, and 39% were patients with clinically isolated syndrome. The commonest clinical presentations were cerebral motor followed by cerebral sensory and optic neuritis. Majority had typical periventricular and infratentorial lesions in MRI. Though not clinically apparent, bilateral delay of P100 wave latency was present in 52%. OCB positivity was 42% and AQP4 antibody was positive in only one patient. In conclusion, this group of Sri Lankan MS patients shares most of the clinical and radiological features of Caucasian MS patients. However, the OCB positivity is lower in this group, when compared to the Caucasian MS populations.

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斯里兰卡多发性硬化症患者鞘内抗体反应明显低。
多发性硬化症(MS)是一种异质性疾病,在亚洲研究甚少,该疾病在临床和放射学表现以及鞘内抗体反应方面存在显着差异。因此,本研究的目的是确定斯里兰卡MS患者的临床表现、放射学和神经生理学特征以及寡克隆带状态,仔细排除患有视神经脊髓炎谱系障碍和其他类似多发性硬化症的患者。69名MS患者被纳入遵循McDonald 2010标准的研究。研究了他们的临床表现、中枢神经系统病变的磁共振特征、视觉诱发电位(VEP)结果、寡克隆带(OCB)和AQP4抗体状态。在69例MS患者中,分别有54%、6%和1%为复发缓解型、继发性进展型和原发性进展型,39%为临床孤立综合征患者。最常见的临床表现是大脑运动,其次是大脑感觉和视神经炎。多数MRI表现为典型的脑室周围和幕下病变。虽然临床不明显,但52%的患者存在双侧P100波延迟。OCB阳性42%,AQP4抗体阳性1例。总之,这组斯里兰卡MS患者具有高加索MS患者的大部分临床和影像学特征。然而,与高加索MS人群相比,该组的OCB阳性较低。
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来源期刊
Multiple Sclerosis International
Multiple Sclerosis International CLINICAL NEUROLOGY-
自引率
0.00%
发文量
6
审稿时长
15 weeks
期刊介绍: Multiple Sclerosis International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to all aspects of multiple sclerosis, including clinical neurology, neuroimaging, neuropathology, therapeutics, genetics, neuroimmunology, biomarkers, psychology and neurorehabilitation.
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