Joseph F G, Hirst C L, Pickersgill T P, Ben-Shlomo Y, Robertson N P, Scolding N J
University of Bristol Institute of Clinical Neurosciences, Frenchay Hospital, Bristol BS16 1LE, UK.
J Neurol Neurosurg Psychiatry. 2009 Mar;80(3):292-6. doi: 10.1136/jnnp.2008.150896. Epub 2008 Oct 1.
Oligoclonal band (OCB) negative multiple sclerosis (MS) is well recognised but uncommon, studied in only a few usually small case series. These reached differing conclusions on whether its clinical features or course differ from OCB positive disease. The study hypothesis was that a definitive study would not only be of clinical and prognostic value but also potentially offer information about the possible role of CSF oligoclonal immunoglobulins in MS disease processes.
A collaborative cohort of well documented patients in southwest England and south Wales was used to identify and analyse a large group of patients with OCB negative MS and make comparisons with age and sex matched OCB positive controls.
An approximate minimum 3% of patients with MS were OCB negative. They were significantly more likely to exhibit neurological or systemic clinical features atypical of MS (headaches, neuropsychiatric features and skin changes). Non-specific MRI, blood and (other) CSF abnormalities were also more common, emphasising the need for continued diagnostic vigilance, although the incautious application of McDonald diagnostic criteria in OCB negative cases renders categorisation as "definite" MS more likely. Studying the uniformly assessed Cardiff group (69 patients), we found the prognosis for neurological disability was significantly better for OCB negative cases. The age adjusted hazard ratio for OCB negative and OCB positive subjects to reach Disability Scale Status (DSS) 4 and DSS 6 was, respectively, 0.60 (95% CI 0.39 to 0.93; p = 0.02) and 0.51 (95% CI 0.27 to 0.94; p = 0.03).
There are clear clinical differences between OCB negative and OCB positive MS, in particular a better prognosis for disability. This is consistent with a secondary but nonetheless contributory role in disease process for intrathecally synthesised immunoglobulins.
寡克隆带(OCB)阴性的多发性硬化症(MS)已得到充分认识,但并不常见,仅在少数通常规模较小的病例系列中进行过研究。这些研究对于其临床特征或病程是否与OCB阳性疾病不同得出了不同结论。该研究的假设是,一项确定性研究不仅具有临床和预后价值,还可能提供有关脑脊液寡克隆免疫球蛋白在MS疾病过程中可能作用的信息。
利用英格兰西南部和南威尔士记录完善的患者协作队列,识别并分析一大组OCB阴性MS患者,并与年龄和性别匹配的OCB阳性对照进行比较。
约3%的MS患者为OCB阴性。他们更有可能表现出MS非典型的神经或全身临床特征(头痛、神经精神特征和皮肤变化)。非特异性MRI、血液和(其他)脑脊液异常也更常见,这强调了持续进行诊断警惕的必要性,尽管在OCB阴性病例中不谨慎地应用麦克唐纳诊断标准更有可能将其归类为“明确的”MS。研究统一评估的加的夫组(69例患者)时,我们发现OCB阴性病例的神经功能障碍预后明显更好。OCB阴性和OCB阳性受试者达到残疾量表状态(DSS)4和DSS 6的年龄调整风险比分别为0.60(95%CI 0.39至0.93;p = 0.02)和0.51(95%CI 0.27至0.94;p = 0.03)。
OCB阴性和OCB阳性MS之间存在明显的临床差异,尤其是残疾预后更好。这与鞘内合成免疫球蛋白在疾病过程中的次要但仍有贡献的作用一致。