TY - JOUR
T1 - The BDNF Val66Met polymorphism and plasma brain-derived neurotrophic factor levels in Han Chinese patients with bipolar disorder and schizophrenia
AU - Chen, Shiou Lan
AU - Lee, Sheng Yu
AU - Chang, Yun Hsuan
AU - Chen, Shih Heng
AU - Chu, Chun Hsien
AU - Wang, Tzu Yun
AU - Chen, Po See
AU - Lee, I. Hui
AU - Yang, Yen Kuang
AU - Hong, Jau Shyong
AU - Lu, Ru Band
N1 - Funding Information:
This study was supported in part by grants DOH95-TD-I-111-004 and DOH98-TD-I-111-DD004 from the Taiwan Department of Health ; grants NSC98-2627-B-006-017 , NSC98-2627-B-006-017 , and NSC101-2314-B-006-063-MY3 from the Taiwan National Science Council (to RBL); and by a grant from the National Cheng Kung University Project to Promote Academic Excellence and Develop a World Class Research Center .
PY - 2014/6/3
Y1 - 2014/6/3
N2 - Objective: 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. Method: 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. Results: 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 (χ2=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. Conclusion: 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.
AB - Objective: 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. Method: 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. Results: 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 (χ2=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. Conclusion: 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.
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U2 - 10.1016/j.pnpbp.2014.01.012
DO - 10.1016/j.pnpbp.2014.01.012
M3 - Article
C2 - 24468644
AN - SCOPUS:84893617517
SN - 0278-5846
VL - 51
SP - 99
EP - 104
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
ER -