Department of Psychiatry, University of California, San Francisco School of Medicine, San Francisco, CA 94143, United States.
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 15;35(7):1623-30. doi: 10.1016/j.pnpbp.2011.06.013. Epub 2011 Jul 3.
The "neurotrophin hypothesis" of depression posits a role of brain-derived neurotrophic factor (BDNF) in depression, although it is unknown whether BDNF is more involved in the etiology of depression or in the mechanism of action of antidepressants. It is also unknown whether pre-treatment serum BDNF levels predict antidepressant response.
Thirty un-medicated depressed subjects were treated with escitalopram (N=16) or sertraline (N=14) for 8 weeks. Twenty-five of the depressed subjects completed 8 weeks of antidepressant treatment and had analyzable data. Twenty-eight healthy controls were also studied. Serum for BDNF assay was obtained at baseline in all subjects and after 8 weeks of treatment in the depressed subjects. Depression ratings were obtained at baseline and after 8 weeks of treatment in the depressed subjects.
Pre-treatment BDNF levels were lower in the depressed subjects than the controls (p=0.001) but were not significantly correlated with pre-treatment depression severity. Depression ratings improved with SSRI treatment (p<0.001), and BDNF levels increased with treatment (p=0.005). Changes in BDNF levels were not significantly correlated with changes in depression ratings. However, pre-treatment BDNF levels were directly correlated with antidepressant responses (p<0.01), and "Responders" to treatment (≥ 50% improvement in depression ratings) had higher pre-treatment BDNF levels than did "Non-responders" (p<0.05).
These results confirm low serum BDNF levels in un-medicated depressed subjects and confirm antidepressant-induced increases in BDNF levels, but they suggest that antidepressants do not work simply by correcting BDNF insufficiency. Rather, these findings are consistent with a permissive or facilitatory role of BDNF in the mechanism of action of antidepressants.
抑郁症的“神经生长因子假说”认为脑源性神经营养因子(BDNF)在抑郁症中起作用,尽管尚不清楚 BDNF 是否更多地参与抑郁症的病因或抗抑郁药的作用机制。也不知道治疗前血清 BDNF 水平是否可以预测抗抑郁反应。
30 名未经治疗的抑郁症患者分别接受艾司西酞普兰(N=16)或舍曲林(N=14)治疗 8 周。其中 25 名抑郁症患者完成了 8 周的抗抑郁治疗且可分析数据。同时还研究了 28 名健康对照者。所有研究对象均在基线时和抑郁症患者治疗 8 周后获得 BDNF 检测血清,抑郁症患者在基线和治疗 8 周后进行抑郁评分。
治疗前,抑郁症患者的 BDNF 水平低于对照组(p=0.001),但与治疗前的抑郁严重程度无显著相关性。SSRI 治疗可改善抑郁评分(p<0.001),并使 BDNF 水平升高(p=0.005)。BDNF 水平的变化与抑郁评分的变化无显著相关性。然而,治疗前的 BDNF 水平与抗抑郁反应直接相关(p<0.01),且“应答者”(抑郁评分改善≥50%)的治疗前 BDNF 水平高于“非应答者”(p<0.05)。
这些结果证实未经治疗的抑郁症患者血清 BDNF 水平较低,并证实抗抑郁药可增加 BDNF 水平,但这表明抗抑郁药并非仅通过纠正 BDNF 不足而起作用。相反,这些发现与 BDNF 在抗抑郁药作用机制中具有许可或促进作用的假说一致。