Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Mult Scler. 2013 Sep;19(10):1249-54. doi: 10.1177/1352458513500554.
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system with an unknown etiology. The clinical disease course is variable, with the majority of patients experiencing reversible episodes of neurological disability in the third or fourth decade of life, eventually followed by a state of irreversible progression. Continuous axonal and neuronal loss is thought to be the major cause of this progression. Over the last decade, extensive research has targeted the gray matter and its role in MS pathogenesis. While pathological and imaging studies have begun to reveal important clues about the role of cortical pathology, gene expression studies in MS cortex are still emerging. Microarray-based comparative gene expression profiling provides a snapshot of genes underlying a particular condition and has been performed using brain tissues from patients with progressive MS. In this review, we summarize existing data from gene expression changes in cortical tissues from MS brains and how they may provide clues to the pathogenesis.
多发性硬化症(MS)是一种中枢神经系统的慢性炎症性脱髓鞘疾病,病因不明。临床疾病过程是多变的,大多数患者在生命的第三或第四个十年经历可逆性神经功能障碍发作,最终进入不可逆进展状态。持续的轴突和神经元丢失被认为是这种进展的主要原因。在过去的十年中,大量研究针对灰质及其在 MS 发病机制中的作用。虽然病理和影像学研究已经开始揭示皮质病变作用的重要线索,但 MS 皮质的基因表达研究仍在出现。基于微阵列的比较基因表达谱提供了特定条件下潜在基因的快照,并已使用进行性 MS 患者的脑组织进行了研究。在这篇综述中,我们总结了来自 MS 大脑皮质组织中基因表达变化的现有数据,以及它们如何为发病机制提供线索。