Lotspeich L J, Ciaranello R D
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, California 94305.
Int Rev Neurobiol. 1993;35:87-129. doi: 10.1016/s0074-7742(08)60569-3.
Autism is a syndrome with multiple etiologies, as is made clear both by the evidence of neurobiological research and by the catalog of disorders that present with autistic behaviors. What remains unclear are the specific neuropathological mechanisms that produce autistic behaviors; for example, is there a common neuroanatomic pathology for all cases of autism, or can autistic behaviors emerge from different pathological sequences within the brain? Although it is premature to generalize, neuropathological studies appear to have identified common abnormalities in the cerebellum and limbic system of at least five autistic subjects. These subjects, with variable levels of mental retardation, demonstrated marked Purkinje cell loss in the cerebellar hemispheres, together with retained fetal neuronal circuitry in cerebellar nuclei and increased neuronal packing in specific regions of the limbic system, amygdala, and hippocampus. The architecture of the cerebral cortex was not affected. Although our knowledge of brain functioning is incomplete, alterations of the kind noted in the cerebellum and limbic system could reasonably produce autistic behaviors. For more detail, readers are directed to a review of cerebellar contributions to higher functions by Schmahmann (1991). Neuroimaging studies allow less resolution of brain structure than do neuroanatomic studies, and the reported findings from neuroimaging are somewhat contradictory. However, a number of investigators have reported structural abnormalities in ventricle size and cerebral hemispheric asymmetry using CT. MRI, which offers greater resolution, has uncovered some consistent findings, along with a variety of nonspecific abnormalities. Common abnormalities include reduced volume of cerebellar hemispheres and vermal lobules--findings not inconsistent with the above-mentioned neuropathological defects. It is also interesting to note that individuals with fragile X syndrome have similar cerebellar findings. PET and NMR studies of autism are at a preliminary stage, but these methodologies allow insight into the functioning of the brain, rather than simply brain anatomy. Recent PET studies indicating decreased association between paired regions of the brains of autistic subjects are of interest, particularly if they can be confirmed and refined by additional studies. Neurophysiological studies also offer insight into brain function, but are subject to numerous methodological criticisms. Nevertheless, recent reports of diminished P300 waves and absent NC components in autistic subjects seem to indicate fundamental defects in attention and secondary processing, which could help explain the self-stimulatory behaviors often seen in autism. The disturbances in brain development associated with autism can be produced in a number of ways, and at different times during development of the nervous system.(ABSTRACT TRUNCATED AT 400 WORDS)
自闭症是一种具有多种病因的综合征,神经生物学研究的证据以及呈现出自闭症行为的疾病目录都清楚地表明了这一点。尚不清楚的是产生自闭症行为的具体神经病理机制;例如,所有自闭症病例是否存在共同的神经解剖学病理,或者自闭症行为是否可以从大脑内不同的病理序列中出现?尽管现在进行概括还为时过早,但神经病理学研究似乎已经在至少五名自闭症患者的小脑和边缘系统中发现了共同的异常。这些患者智力发育迟缓程度各异,其小脑半球出现明显的浦肯野细胞丢失,同时小脑核中保留了胎儿神经元回路,边缘系统、杏仁核和海马体的特定区域神经元堆积增加。大脑皮层的结构未受影响。尽管我们对大脑功能的了解并不完整,但在小脑和边缘系统中发现的这类改变有可能导致自闭症行为。欲了解更多细节,读者可查阅施马曼(1991年)关于小脑对高级功能贡献的综述。神经影像学研究对大脑结构的分辨率不如神经解剖学研究,而且神经影像学报告的结果也有些相互矛盾。然而,一些研究人员使用CT报告了脑室大小和大脑半球不对称方面的结构异常。分辨率更高的MRI发现了一些一致的结果,以及各种非特异性异常。常见的异常包括小脑半球和蚓部小叶体积减小——这一发现与上述神经病理学缺陷并不矛盾。同样有趣的是,脆性X综合征患者也有类似的小脑表现。对自闭症的PET和NMR研究尚处于初步阶段,但这些方法能够洞察大脑的功能,而不仅仅是大脑解剖结构。最近的PET研究表明自闭症患者大脑配对区域之间的关联减少,这一点很有意思,特别是如果能通过更多研究得到证实和完善的话。神经生理学研究也有助于洞察大脑功能,但受到众多方法学上的批评。尽管如此,最近关于自闭症患者P300波减弱和NC成分缺失的报告似乎表明存在注意力和次级加工方面的根本缺陷,这有助于解释自闭症中常见的自我刺激行为。与自闭症相关的大脑发育障碍可以通过多种方式产生,并且发生在神经系统发育的不同时期。(摘要截选至400字)