Juckel Georg, Schumacher Christiane, Giegling Ina, Assion Hans-Jörg, Mavrogiorgou Paraskevi, Pogarell Oliver, Mulert Christoph, Hegerl Ulrich, Norra Christine, Rujescu Dan
Department of Psychiatry, Ruhr University, 44791 Bochum, Germany.
J Psychiatr Res. 2010 Jun;44(8):541-6. doi: 10.1016/j.jpsychires.2009.11.006. Epub 2009 Dec 9.
The serotonergic system plays an important pathophysiological role in various psychiatric disorders. Brain-derived neurotrophic factor (BDNF) is involved in the differentiation and survival of serotonergic neurons. A previous study showed that low serum BDNF levels were associated with strong loudness dependence of auditory evoked potentials (LDAEP) as a reflection of low central serotonergic activity. To evaluate the genetic basis of this relationship, we studied whether the LDAEP is correlated with genetic variants within the BDNF gene.
Ninety five healthy subjects (41 males, 54 females) received electrophysiological recording of LDAEP and blood drawing for BDNF genotyping. Three BDNF markers (including the single nucleotide polymorphism rs6265(Val66Met)) were analyzed.
Haplotype analysis revealed stronger LDAEP values in carriers of the G(Val)-C-T [rs6265(Val66Met)-rs2030324-rs1491850] haplotype within the BDNF gene in comparison to other haplotype carriers. These findings were demonstrated for the LDAEP of both left and right primary auditory cortices as well as for the vertex electrode (Cz).
Subjects with the BDNF haplotype G(Val)-C-T seem to be characterized by low serotonergic activity as well as possibly by low serum BDNF levels. These findings need replication in independent samples.
血清素能系统在多种精神疾病中发挥着重要的病理生理作用。脑源性神经营养因子(BDNF)参与血清素能神经元的分化和存活。先前的一项研究表明,血清BDNF水平低与听觉诱发电位的强响度依赖性(LDAEP)相关,这反映了中枢血清素能活性低。为了评估这种关系的遗传基础,我们研究了LDAEP是否与BDNF基因内的遗传变异相关。
95名健康受试者(41名男性,54名女性)接受了LDAEP的电生理记录,并抽取血液进行BDNF基因分型。分析了三个BDNF标记(包括单核苷酸多态性rs6265(Val66Met))。
单倍型分析显示,与其他单倍型携带者相比,BDNF基因内G(Val)-C-T [rs6265(Val66Met)-rs2030324-rs1491850]单倍型携带者的LDAEP值更强。左右初级听觉皮层以及头顶电极(Cz)的LDAEP均证实了这些发现。
具有BDNF单倍型G(Val)-C-T的受试者似乎具有血清素能活性低以及可能血清BDNF水平低的特征。这些发现需要在独立样本中进行重复验证。