Woods B T
Department of Medicine, Texas A&M University School of Medicine and Central Texas Veterans Health Care System, Temple 76502, USA.
Am J Psychiatry. 1998 Dec;155(12):1661-70. doi: 10.1176/ajp.155.12.1661.
The author 1) reassesses the case against a neuronal degeneration hypothesis for schizophrenia; 2) demonstrates that the hypothesis that schizophrenia is a disorder caused by early (i.e., pre- or perinatal) and static (i.e., fixed, nonprogressive) damage to the brain is unsatisfactory because it cannot readily account for brain imaging results from schizophrenic patients and lacks both satisfactory clinical examples and experimental models of early, static developmental disorders resulting in the late spontaneous functional deterioration that characterizes schizophrenia; and 3) offers an alternative pathogenetic hypothesis for schizophrenia that is consistent with the available imaging and neuropathological data.
Published data on schizophrenia and relevant clinical and experimental studies of neurodevelopment and its disorders are reviewed.
The neuropathological studies provide strong evidence against a classic neurodegenerative pathogenesis of schizophrenia and moderate support for prenatal developmental abnormalities. The imaging data provide strong evidence that excessive brain volume loss occurs after maximum brain volume expansion and equivocal evidence that it continues after onset of overt illness. The available clinical and experimental models of late deterioration after static, early brain lesions are unconvincing. A progressive developmental mechanism can reconcile the neuropathological and imaging data, while being compatible with both early onset and late deterioration.
It matters whether the pathogenetic agent in schizophrenia is static or progressive, since if it is the latter it is worthwhile to search not only for means of prevention but also for interventions that will arrest progression as early as possible.
1)重新评估反对精神分裂症神经元退化假说的证据;2)证明精神分裂症是一种由大脑早期(即产前或围产期)和静态(即固定、非进行性)损伤引起的疾病这一假说并不令人满意,因为它无法轻易解释精神分裂症患者的脑成像结果,且缺乏令人满意的临床实例以及早期静态发育障碍导致精神分裂症特征性晚期自发功能衰退的实验模型;3)为精神分裂症提供一种与现有成像和神经病理学数据一致的替代性发病机制假说。
回顾已发表的关于精神分裂症以及神经发育及其障碍的相关临床和实验研究数据。
神经病理学研究提供了有力证据反对精神分裂症经典的神经退行性发病机制,并适度支持产前发育异常。成像数据提供了有力证据表明在脑容量最大扩张后出现了过度的脑容量损失,以及不明确的证据表明在明显疾病发作后仍在继续。现有的早期静态脑损伤后晚期衰退的临床和实验模型并不令人信服。一种渐进性发育机制可以协调神经病理学和成像数据,同时与早期发病和晚期衰退都兼容。
精神分裂症的致病因素是静态的还是进行性的很重要,因为如果是后者,那么不仅值得寻找预防方法,还值得寻找尽早阻止病情进展的干预措施。