Mathé A A, Agren H, Lindström L, Theodorsson E
Karolinska Institute, Department of Psychiatry, St. Göran's Hospital, Stockholm, Sweden.
Neurosci Lett. 1994 Dec 5;182(2):138-42. doi: 10.1016/0304-3940(94)90782-x.
Cerebrospinal fluid (CSF) was collected under controlled conditions from subjects suffering from major depression (n = 63) or schizophrenia (n = 28) and from healthy controls (n = 20). Following Sep-pak extraction, calcitonin gene-related peptide immunoreactivity (CGRP-LI) was determined by radioimmunoassay in sample aliquots. CGRP-LI concentrations in CSF were increased in the depressed patients compared to the schizophrenic and control subjects (P < 0.001). No CGRP-LI differences were found between the latter two groups. CGRP-LI did not correlate to any of the technical (e.g. storage conditions) or patient (demographic, biochemical, or clinical) variables investigated. In view of the CGRP's discrete distribution and specific effects in brain and the above results, we hypothesize that increased CSF CGRP-LI might be a trait marker of major depression. Regardless of the mechanisms (altered synthesis/release/metabolism in brain or changed fate in CSF) leading to elevated CSF CGRP-LI, the identification of a possible disease trait marker should contribute to the early diagnosis of major depression and identification of family members at risk and may help in differential diagnosis in other disorders with affective symptomatology.
在可控条件下,从患有重度抑郁症的受试者(n = 63)、精神分裂症的受试者(n = 28)以及健康对照者(n = 20)中采集脑脊液(CSF)。经Sep-pak萃取后,采用放射免疫分析法测定样品等分试样中的降钙素基因相关肽免疫反应性(CGRP-LI)。与精神分裂症患者和对照受试者相比,抑郁症患者脑脊液中的CGRP-LI浓度升高(P < 0.001)。后两组之间未发现CGRP-LI存在差异。CGRP-LI与所研究的任何技术(如储存条件)或患者(人口统计学、生化或临床)变量均无相关性。鉴于CGRP在大脑中的离散分布和特定作用以及上述结果,我们推测脑脊液中CGRP-LI升高可能是重度抑郁症的一种特征性标志物。无论导致脑脊液中CGRP-LI升高的机制(大脑中合成/释放/代谢改变或脑脊液中命运改变)如何,确定一种可能的疾病特征性标志物都应有助于重度抑郁症的早期诊断以及识别有患病风险的家庭成员,并可能有助于对其他伴有情感症状的疾病进行鉴别诊断。