Rafaelsen O J, Gjerris A
Prog Neuropsychopharmacol Biol Psychiatry. 1985;9(5-6):533-8. doi: 10.1016/0278-5846(85)90013-2.
Concentrations of vasoactive intestinal polypeptide (VIP), cholecystokinin (CCK) and gastrin in the cerebrospinal fluid (CSF) was studied in patients with endogenous depression, non-endogenous depression, mania, schizophrenia and a control group. All patients were classified according to various diagnostic systems. In the group of non-endogenously depressed patients CSF-VIP levels (median 16 pmol/l) were found significantly lowered compared to controls (median = 32 pmol/l) and endogenous depression (26 pmol/l). Going through the non-endogenous group it appeared that the low CSF-VIP was due to a group of patients with a former diagnosis of endogenous depression or a present diagnosis of possible endogenous depression. Moreover, this group was clinically characterized by 'dysphoric/hysterical features', 'reversed diurnal variation' (i.e. worst in the evening), and 'lack of clearly circumscribed episode'. In many aspects this group seems similar to the atypical depressions described as monoamineoxidase responders. Concerning CSF-CCK and CSF-gastrin no significant differences between the examined groups were demonstrated.
对患有内源性抑郁症、非内源性抑郁症、躁狂症、精神分裂症的患者以及一个对照组的脑脊液(CSF)中血管活性肠肽(VIP)、胆囊收缩素(CCK)和胃泌素的浓度进行了研究。所有患者均根据各种诊断系统进行分类。在非内源性抑郁症患者组中,发现脑脊液VIP水平(中位数为16 pmol/l)与对照组(中位数 = 32 pmol/l)和内源性抑郁症组(26 pmol/l)相比显著降低。在非内源性抑郁症组中进一步研究发现,脑脊液VIP水平低是由于一组既往诊断为内源性抑郁症或目前诊断为可能的内源性抑郁症的患者所致。此外,该组在临床上具有“烦躁/癔症特征”、“昼夜节律颠倒”(即傍晚时症状最严重)和“缺乏明确界定的发作”等特点。在许多方面,该组似乎与被描述为单胺氧化酶反应者的非典型抑郁症相似。关于脑脊液CCK和脑脊液胃泌素,在所检查的组之间未显示出显著差异。