Hansson L O, Waters N, Winblad B, Gottfries C G, Carlsson A
Department of Pharmacology, University of Gothenburg, Sweden.
J Neural Transm Gen Sect. 1994;98(3):217-35. doi: 10.1007/BF01276538.
A previously performed post-mortem study comparing monoaminergic indices in the brains of 14 schizophrenic patients and 10 patients with psychosis not diagnosed as schizophrenia, with age-matched control cases without any known neuropsychiatric illness, was re-investigated, using multivariate analysis. The monoaminergic patterns showing up in this analysis suggested the existence of at least two different forms of the disease, both of which could be distinguished from the controls as well as from each other. One of the schizophrenic groups consisted of paranoid cases, and had a relatively mild family history, whereas the other group, mainly consisting of hebephrenic cases, had a severe family history. The former group showed low levels of dopamine and high levels of serotonergic precursor and metabolite, whereas the latter group in some respects tended to show the opposite aberrations. Neuroleptic treatment did not seem to account for the different biochemical profiles, unless one assumes that this treatment can cause completely different monoaminergic aberrations in different individuals. Instead, one could argue that the different biochemical profiles found are characteristic of the disease.
一项先前进行的尸检研究,比较了14名精神分裂症患者、10名未被诊断为精神分裂症的精神病患者以及年龄匹配的无任何已知神经精神疾病的对照病例大脑中的单胺能指标,并采用多变量分析进行了重新研究。该分析中出现的单胺能模式表明存在至少两种不同形式的疾病,这两种形式都可以与对照病例区分开来,且彼此之间也能区分。其中一组精神分裂症患者为偏执型病例,家族病史相对较轻,而另一组主要为青春型病例,家族病史严重。前一组显示多巴胺水平较低,血清素前体和代谢物水平较高,而后一组在某些方面则倾向于表现出相反的异常。抗精神病药物治疗似乎无法解释不同的生化特征,除非假设这种治疗会在不同个体中导致完全不同的单胺能异常。相反,可以认为所发现的不同生化特征是该疾病的特征。