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多种神经胶质细胞衍生神经营养因子(GDNF)对躁狂症和精神分裂症的支持作用:四大精神障碍的比较研究。

Diverse glial cell line-derived neurotrophic factor (GDNF) support between mania and schizophrenia: a comparative study in four major psychiatric disorders.

机构信息

Dokuz Eylul University, Medical School, Izmir, Turkey.

Dokuz Eylul University, Medical School, Izmir, Turkey.

出版信息

Eur Psychiatry. 2015 Feb;30(2):198-204. doi: 10.1016/j.eurpsy.2014.11.003. Epub 2014 Dec 24.

DOI:10.1016/j.eurpsy.2014.11.003
PMID:25543333
Abstract

BACKGROUND

Brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) have essential roles in synaptic plasticity which is involved in pathogenesis and treatment of psychiatric disorders. However, it is not clear whether they act simultaneously during illness states in major psychiatric disorders.

METHODS

BDNF and GDNF serum levels were measured concomitantly by enzyme-linked immunosorbent assay (ELISA) method in 171 patients diagnosed with schizophrenia (n=33), bipolar disorder-manic episode (n=39), bipolar/unipolar depression (n=64, 24/40) and obsessive-compulsive disorder (n=35) according to DSM-IV, and 78 healthy volunteers. SCID-I and SCID non-patient version were used for clinical evaluation of the patients and healthy volunteers, respectively. Correlations between the two trophic factor levels, and illness severity scores, duration of illness and medication dosages were studied across different illnesses.

RESULTS

While patients had equally lower BDNF levels in all diagnoses, GDNF levels were significantly higher in mania and lower in schizophrenia compared to healthy controls. BDNF levels were negatively correlated to illness severity scores in affective episodes (mania and depression). Longer duration of illness (>5 years) had an impact on lower GDNF levels in schizophrenia. BDNF levels and antipsychotic drug dosages in schizophrenia, and GDNF levels and antidepressant drug dosages in obsessive-compulsive disorder were positively correlated.

CONCLUSION

Our data confirmed the evidence of equally deficient neuronal support by BDNF in all major psychiatric illnesses, but suggested a diverse glial functioning between schizophrenia and mania.

摘要

背景

脑源性神经营养因子(BDNF)和胶质细胞源性神经营养因子(GDNF)在突触可塑性中起重要作用,而突触可塑性涉及精神疾病的发病机制和治疗。然而,在主要精神疾病的疾病状态下,它们是否同时起作用尚不清楚。

方法

采用酶联免疫吸附法(ELISA)同时检测 171 例精神分裂症(n=33)、双相障碍躁狂发作(n=39)、双相/单相抑郁(n=64,24/40)和强迫症(n=35)患者及 78 名健康志愿者的血清 BDNF 和 GDNF 水平。采用 SCID-I 和 SCID 非患者版对患者和健康志愿者进行临床评估。研究了两种营养因子水平与不同疾病严重程度评分、病程和药物剂量之间的相关性。

结果

尽管所有诊断患者的 BDNF 水平均相等降低,但躁狂症患者的 GDNF 水平明显升高,而精神分裂症患者的 GDNF 水平明显降低。BDNF 水平与情感发作(躁狂和抑郁)中的疾病严重程度评分呈负相关。病程较长(>5 年)对精神分裂症患者的 GDNF 水平有影响。精神分裂症患者的 BDNF 水平与抗精神病药物剂量、强迫症患者的 GDNF 水平与抗抑郁药物剂量呈正相关。

结论

我们的数据证实了 BDNF 在所有主要精神疾病中均存在神经元支持不足的证据,但提示精神分裂症和躁狂症之间的神经胶质功能存在差异。

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