Schmahmann Jeremy D, Smith Eric E, Eichler Florian S, Filley Christopher M
Ataxia Unit, Cognitive/Behavioral Neurology Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA.
Ann N Y Acad Sci. 2008 Oct;1142:266-309. doi: 10.1196/annals.1444.017.
Lesions of the cerebral white matter (WM) result in focal neurobehavioral syndromes, neuropsychiatric phenomena, and dementia. The cerebral WM contains fiber pathways that convey axons linking cerebral cortical areas with each other and with subcortical structures, facilitating the distributed neural circuits that subserve sensorimotor function, intellect, and emotion. Recent neuroanatomical investigations reveal that these neural circuits are topographically linked by five groupings of fiber tracts emanating from every neocortical area: (1) cortico-cortical association fibers; (2) corticostriatal fibers; (3) commissural fibers; and cortico-subcortical pathways to (4) thalamus and (5) pontocerebellar system, brain stem, and/or spinal cord. Lesions of association fibers prevent communication between cortical areas engaged in different domains of behavior. Lesions of subcortical structures or projection/striatal fibers disrupt the contribution of subcortical nodes to behavior. Disconnection syndromes thus result from lesions of the cerebral cortex, subcortical structures, and WM tracts that link the nodes that make up the distributed circuits. The nature and the severity of the clinical manifestations of WM lesions are determined, in large part, by the location of the pathology: discrete neurological and neuropsychiatric symptoms result from focal WM lesions, whereas cognitive impairment across multiple domains--WM dementia--occurs in the setting of diffuse WM disease. We present a detailed review of the conditions affecting WM that produce these neurobehavioral syndromes, and consider the pathophysiology, clinical effects, and broad significance of the effects of aging and vascular compromise on cerebral WM, in an attempt to help further the understanding, diagnosis, and treatment of these disorders.
脑白质(WM)病变会导致局灶性神经行为综合征、神经精神现象和痴呆。脑白质包含纤维通路,这些通路传递着连接大脑皮质区域彼此以及与皮质下结构的轴突,促进了有助于感觉运动功能、智力和情感的分布式神经回路。最近的神经解剖学研究表明,这些神经回路通过从每个新皮质区域发出的五组纤维束在地形上相互连接:(1)皮质 - 皮质联合纤维;(2)皮质纹状体纤维;(3)连合纤维;以及通向(4)丘脑和(5)脑桥小脑系统、脑干和/或脊髓的皮质下通路。联合纤维病变会阻止参与不同行为领域的皮质区域之间的交流。皮质下结构或投射/纹状体纤维的病变会破坏皮质下节点对行为的贡献。因此,分离综合征是由大脑皮质、皮质下结构以及连接构成分布式回路的节点的白质束病变引起的。白质病变临床表现的性质和严重程度在很大程度上取决于病变的位置:局灶性白质病变会导致离散的神经和神经精神症状,而在弥漫性白质疾病的情况下会出现跨多个领域的认知障碍——白质痴呆。我们对影响白质并导致这些神经行为综合征的病症进行了详细综述,并考虑了衰老和血管损伤对脑白质影响的病理生理学、临床效应和广泛意义,以期有助于进一步理解、诊断和治疗这些疾病。