Chen Shiou-Lan, Lee Sheng-Yu, Chang Yun-Hsuan, Chen Shih-Heng, Chu Chun-Hsien, Wang Tzu-Yun, Chen Po-See, Lee I-Hui, Yang Yen-Kuang, Hong Jau-Shyong, Lu Ru-Band
Department of Neurology, School of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan; Department of Psychiatry, National Cheng Kung University, Taiwan.
Department of Psychiatry, National Cheng Kung University, Taiwan; National Cheng Kung University Hospital, Taiwan; Addiction Research Center, National Cheng Kung University, Taiwan.
Prog Neuropsychopharmacol Biol Psychiatry. 2014 Jun 3;51:99-104. doi: 10.1016/j.pnpbp.2014.01.012. Epub 2014 Jan 25.
Brain-derived neurotropic factor (BDNF) is widely distributed in the peripheral and central nervous systems. BDNF and its gene polymorphism may be important in synaptic plasticity and neuron survival, and may become a key target in the physiopathology of several mental illnesses. To elucidate the role of BDNF, we compared the plasma BDNF levels and the BDNF Val66Met gene variants effect in several mental disorders.
We enrolled 644 participants: 177 patients with bipolar I disorder (BP-I), 190 with bipolar II disorder (BP-II), 151 with schizophrenia, and 126 healthy controls. Their plasma BDNF levels and BDNF Val66Met single nucleotide polymorphisms (SNP) were checked before pharmacological treatment.
Plasma levels of BDNF were significantly lower in patients with schizophrenia than in healthy controls and patients with bipolar disorder (F = 37.667, p<0.001); the distribution of the BDNF Val66Met SNP was not different between groups (χ(2) = 5.289, p = 0.507). Nor were plasma BDNF levels significantly different between Met/Met, Met/Val, and Val/Val carriers in each group, which indicated that the BDNF Val66Met SNP did not influence plasma BDNF levels in our participants. Plasma BDNF levels were, however, significantly negatively correlated with depression scores in patients with bipolar disorder and with negative symptoms in patients with schizophrenia.
We conclude that plasma BDNF profiles in different mental disorders are not affected by BDNF Val66Met gene variants, but by the process and progression of the illness itself.
脑源性神经营养因子(BDNF)广泛分布于外周和中枢神经系统。BDNF及其基因多态性在突触可塑性和神经元存活中可能起重要作用,并可能成为几种精神疾病病理生理学的关键靶点。为阐明BDNF的作用,我们比较了几种精神障碍患者的血浆BDNF水平及BDNF Val66Met基因变异的影响。
我们招募了644名参与者:177例I型双相情感障碍(BP-I)患者、190例II型双相情感障碍(BP-II)患者、151例精神分裂症患者和126名健康对照者。在药物治疗前检测他们的血浆BDNF水平和BDNF Val66Met单核苷酸多态性(SNP)。
精神分裂症患者的血浆BDNF水平显著低于健康对照者和双相情感障碍患者(F = 37.667,p<0.001);BDNF Val66Met SNP在各组间的分布无差异(χ(2) = 5.289,p = 0.507)。每组中Met/Met、Met/Val和Val/Val携带者的血浆BDNF水平也无显著差异,这表明BDNF Val66Met SNP不影响我们研究参与者的血浆BDNF水平。然而,双相情感障碍患者的血浆BDNF水平与抑郁评分显著负相关,精神分裂症患者的血浆BDNF水平与阴性症状显著负相关。
我们得出结论,不同精神障碍患者的血浆BDNF水平不受BDNF Val66Met基因变异的影响,而是受疾病本身的进程和发展的影响。