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血清脑源性神经营养因子在未经药物治疗的首发精神分裂症中的水平降低:与临床表型的关系。

Decreased levels of serum brain-derived neurotrophic factor in drug-naïve first-episode schizophrenia: relationship to clinical phenotypes.

机构信息

Beijing Huilongguan Hospital, Beijing, People's Republic of China.

出版信息

Psychopharmacology (Berl). 2009 Dec;207(3):375-80. doi: 10.1007/s00213-009-1665-6. Epub 2009 Sep 29.

Abstract

OBJECTIVE

There is accumulating evidence that brain-derived neurotrophic factor (BDNF) may be involved in the pathophysiology of patients with schizophrenia. Clinical studies show reductions in BDNF in schizophrenic patients treated with first generation antipsychotics or second generation antipsychotics. However, there have been few systematic studies to examine the relationship between BDNF levels and psychopathology in first-episode and drug-naïve patients with schizophrenia.

MATERIALS AND METHODS

Serum BDNF levels were determined using enzyme-linked-immunosorbent assay (ELISA) in the serum of 88 never-medicated first-episode and 90 healthy controls subjects matched for age and gender. The schizophrenia symptomatology and the depressive symptoms were assessed by the positive and negative syndrome scale (PANSS) and the Hamilton rating (HAMD) scale for depression.

RESULTS

The results showed that BDNF levels were significantly lower in first-episode patients with schizophrenia than in healthy control subjects (9.0 +/- 4.2 ng/ml vs 12.1 +/- 2.2 ng/ml; F = 37.6; df = 1, 176; p < 0.0001). A significant positive correlation between BDNF levels and PANSS positive subscore was observed (r = 0.29; df = 88; p = 0.008). Furthermore, higher BDNF levels were observed in patients with paranoid subtype of schizophrenia. However, no significant correlation between BDNF and HAMD total score was found.

CONCLUSION

Low BDNF levels at the onset of psychosis suggest that it may contribute to the pathogenesis of schizophrenia and perhaps, could be a candidate biological marker for positive symptoms.

摘要

目的

越来越多的证据表明脑源性神经营养因子(BDNF)可能参与精神分裂症患者的病理生理学过程。临床研究表明,接受第一代或第二代抗精神病药物治疗的精神分裂症患者的 BDNF 水平降低。然而,很少有系统的研究来检查首发和未经药物治疗的精神分裂症患者的 BDNF 水平与精神病理学之间的关系。

材料和方法

使用酶联免疫吸附试验(ELISA)测定 88 例未经药物治疗的首发精神分裂症患者和 90 例年龄和性别相匹配的健康对照者血清中的 BDNF 水平。阳性和阴性症状量表(PANSS)和汉密尔顿抑郁量表(HAMD)评估精神分裂症症状和抑郁症状。

结果

结果显示,首发精神分裂症患者的 BDNF 水平明显低于健康对照组(9.0±4.2ng/ml 与 12.1±2.2ng/ml;F=37.6;df=1,176;p<0.0001)。BDNF 水平与 PANSS 阳性评分呈显著正相关(r=0.29;df=88;p=0.008)。此外,偏执型精神分裂症患者的 BDNF 水平较高。然而,BDNF 与 HAMD 总分之间没有显著相关性。

结论

精神病发病时的低 BDNF 水平表明它可能有助于精神分裂症的发病机制,并且可能是阳性症状的候选生物标志物。

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