Kamińska Joanna, Koper Olga M, Piechal Kinga, Kemona Halina
Zakład Laboratoryjnej Diagnostyki Klinicznej, Uniwersytet Medyczny w Białymstoku.
Laboratorium RH+, Piaseczno.
Postepy Hig Med Dosw (Online). 2017 Jun 30;71(0):551-563. doi: 10.5604/01.3001.0010.3836.
Multiple sclerosis (MS) is a chronic inflammatory and demyelinating disease of autoimmune originate. The main agents responsible for the MS development include exogenous, environmental, and genetic factors. MS is characterized by multifocal and temporally scattered central nervous system (CNS) damage which lead to the axonal damage. Among clinical courses of MS it can be distinguish relapsing-remitting multiple sclerosis (RRMS), secondary progressive multiple sclerosis (SPSM), primary progressive multiple sclerosis (PPMS), and progressive-relapsing multiple sclerosis (RPMS). Depending on the severity of signs and symptoms MS can be described as benign MS or malignant MS. MS diagnosis is based on McDonald's diagnostic criteria, which link clinical manifestation with characteristic lesions demonstrated by magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, and visual evoked potentials. Among CSF laboratory tests used to the MS diagnosis are applied: Tibbling & Link IgG index, reinbegrams, and CSF isoelectrofocusing for oligoclonal bands detection. It should be emphasized, that despite huge progress regarding MS as well as the availability of different diagnostics methods this disease is still a diagnostic challenge. It may result from fact that MS has diverse clinical course and there is a lack of single test, which would be of appropriate diagnostic sensitivity and specificity for quick and accurate diagnosis.
多发性硬化症(MS)是一种起源于自身免疫的慢性炎症性脱髓鞘疾病。导致MS发生的主要因素包括外源性、环境和遗传因素。MS的特征是多灶性且在时间上分散的中枢神经系统(CNS)损伤,进而导致轴突损伤。在MS的临床病程中,可以区分复发缓解型多发性硬化症(RRMS)、继发进展型多发性硬化症(SPMS)、原发进展型多发性硬化症(PPMS)和进展复发型多发性硬化症(PRMS)。根据体征和症状的严重程度,MS可被描述为良性MS或恶性MS。MS的诊断基于麦克唐纳诊断标准,该标准将临床表现与磁共振成像(MRI)、脑脊液(CSF)分析和视觉诱发电位所显示的特征性病变联系起来。用于MS诊断的CSF实验室检测方法包括:蒂布林和林克IgG指数、重复检测以及用于检测寡克隆带的CSF等电聚焦。应该强调的是,尽管在MS方面取得了巨大进展以及有多种诊断方法可用,但这种疾病仍然是一个诊断挑战。这可能是因为MS有多种临床病程,并且缺乏一种对快速准确诊断具有适当诊断敏感性和特异性的单一检测方法。