Department of Neurosciences, Mood and Anxiety Disorders Unit, University of Turin, Turin, 10126 Torino, Italy.
J Affect Disord. 2010 Apr;122(1-2):174-8. doi: 10.1016/j.jad.2009.07.009. Epub 2009 Aug 6.
There is lack of data regarding BDNF serum levels in patients with obsessive-compulsive disorder (OCD). The aims of the present study were: 1) to assess the serum BDNF content in a sample of drug-naïve patients with OCD and 2) to assess whether putative alterations in peripheral BDNF may be associated to OCD severity and clinical characteristics.
Twenty-four drug-naïve patients with a principal diagnosis of OCD were recruited. In parallel, a control group of 24 unrelated volunteers matched for gender and age was enrolled. Serum BDNF levels were measured by ELISA method.
The results showed that BDNF levels were decreased in OCD patients when compared to controls (36.90+/-6.42 ng/ml versus 41.59+/-7.82 ng/ml; p=0.043). No correlations were evidenced between serum BDNF content and the severity of OCD symptoms measured as Y-BOCS scores or other clinical variables.
The choice of drug-naïve patients with obsessive-compulsive disorder had limited the size of the sample and excluded the recruitment of patients with a severe symptomatology.
Our findings reveal for the first time in OCD patients a decrease in serum BDNF levels. These data corroborate the hypothesis of a dysfunction in the neurotrophin expression in the OCD pathogenetic mechanism and provide the rationale for further investigations directed to the identification of novel biomarkers and new therapeutic strategies for antiobsessional treatments.
目前缺乏强迫症(OCD)患者血清脑源性神经营养因子(BDNF)水平的数据。本研究的目的是:1)评估药物初治 OCD 患者的血清 BDNF 含量,2)评估外周血 BDNF 可能发生的变化是否与 OCD 严重程度和临床特征相关。
招募了 24 名药物初治 OCD 患者作为实验组,同时招募了 24 名性别和年龄相匹配的无关志愿者作为对照组。通过 ELISA 法检测血清 BDNF 水平。
结果显示,与对照组相比,OCD 患者的 BDNF 水平降低(36.90+/-6.42ng/ml 与 41.59+/-7.82ng/ml;p=0.043)。血清 BDNF 含量与 Y-BOCS 评分或其他临床变量评估的 OCD 症状严重程度之间无相关性。
选择药物初治 OCD 患者限制了样本量,并排除了招募严重症状的患者。
我们的发现首次在 OCD 患者中揭示了血清 BDNF 水平降低。这些数据支持了神经发生在 OCD 发病机制中表达功能障碍的假说,并为进一步研究提供了依据,旨在确定新的生物标志物和新的抗强迫症治疗策略。