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多发性硬化症中的皮质脱髓鞘和弥漫性白质损伤。

Cortical demyelination and diffuse white matter injury in multiple sclerosis.

作者信息

Kutzelnigg Alexandra, Lucchinetti Claudia F, Stadelmann Christine, Brück Wolfgang, Rauschka Helmut, Bergmann Markus, Schmidbauer Manfred, Parisi Joseph E, Lassmann Hans

机构信息

Center for Brain Research, Medical University of Vienna, Vienna, Austria.

出版信息

Brain. 2005 Nov;128(Pt 11):2705-12. doi: 10.1093/brain/awh641. Epub 2005 Oct 17.

DOI:10.1093/brain/awh641
PMID:16230320
Abstract

Focal demyelinated plaques in white matter, which are the hallmark of multiple sclerosis pathology, only partially explain the patient's clinical deficits. We thus analysed global brain pathology in multiple sclerosis, focusing on the normal-appearing white matter (NAWM) and the cortex. Autopsy tissue from 52 multiple sclerosis patients (acute, relapsing-remitting, primary and secondary progressive multiple sclerosis) and from 30 controls was analysed using quantitative morphological techniques. New and active focal inflammatory demyelinating lesions in the white matter were mainly present in patients with acute and relapsing multiple sclerosis, while diffuse injury of the NAWM and cortical demyelination were characteristic hallmarks of primary and secondary progressive multiple sclerosis. Cortical demyelination and injury of the NAWM, reflected by diffuse axonal injury with profound microglia activation, occurred on the background of a global inflammatory response in the whole brain and meninges. There was only a marginal correlation between focal lesion load in the white matter and diffuse white matter injury, or cortical pathology, respectively. Our data suggest that multiple sclerosis starts as a focal inflammatory disease of the CNS, which gives rise to circumscribed demyelinated plaques in the white matter. With chronicity, diffuse inflammation accumulates throughout the whole brain, and is associated with slowly progressive axonal injury in the NAWM and cortical demyelination.

摘要

白质中的局灶性脱髓鞘斑块是多发性硬化症病理学的标志,但只能部分解释患者的临床缺陷。因此,我们分析了多发性硬化症的全脑病理学,重点关注外观正常的白质(NAWM)和皮质。使用定量形态学技术分析了52例多发性硬化症患者(急性、复发缓解型、原发进展型和继发进展型多发性硬化症)以及30例对照的尸检组织。白质中新发的活动性局灶性炎性脱髓鞘病变主要见于急性和复发型多发性硬化症患者,而NAWM的弥漫性损伤和皮质脱髓鞘是原发进展型和继发进展型多发性硬化症的特征性标志。皮质脱髓鞘和NAWM损伤表现为弥漫性轴突损伤伴小胶质细胞深度激活,这发生在全脑和脑膜的全身性炎症反应背景下。白质中的局灶性病变负荷与弥漫性白质损伤或皮质病理学之间仅存在微弱的相关性。我们的数据表明,多发性硬化症始于中枢神经系统的局灶性炎症性疾病,导致白质中出现局限性脱髓鞘斑块。随着疾病的慢性化,弥漫性炎症在全脑累积,并与NAWM中缓慢进展的轴突损伤和皮质脱髓鞘相关。

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