Park Jeong Wook, Han Si Ryung, Yang Dong Won, Kim Yeong In, Lee Kwang Soo
Department of Neurology, Catholic University of Korea, Seoul, Korea.
Headache. 2006 Jun;46(6):991-6. doi: 10.1111/j.1526-4610.2006.00439.x.
To investigate polymorphisms in the serotonin transporter protein gene and harm avoidance personality dimension in patients with migraine without aura (MWOA).
The serotonin transporter protein is a key modulator of serotonergic synaptic neurotransmission. Two polymorphic regions of the gene for serotonin transporter protein have been found, and are associated with variations in the functional activity of serotonin caused by differing transcriptional efficiency. The harm avoidance (HA) personality trait may also be heritable and associated with altered serotonergic neurotransmitter activity.
We amplified the polymorphism in the promoter of serotonin transporter protein (5-HTTLPR) and the variable number of tandem repeats polymorphism within intron 2 (VNTR) using the polymerase chain reaction and performed genotype polymorphism analyses in 97 patients with MWOA and 100 healthy controls. We investigated serotonin-related personality traits by evaluating the HA personality dimension using a tridimensional questionnaire.
The genotype frequencies and allele distributions of 5-HTTLPR did not differ between patients with MWOA and controls. The VNTR genotype STin2.12/STin2.12 was significantly more common in patients with MWOA (90%) than in controls (77%; P= .017). Patients with MWOA also had HA scores (21.9 +/- 6.4) significantly higher than those of controls (16.3 +/- 6.1; P < .001).
Serotonergic activity might be involved in the development of MWOA and VNTR of serotonin transporter gene might be one of the genetically contributing factors.
研究无先兆偏头痛(MWOA)患者血清素转运蛋白基因多态性与回避伤害人格维度。
血清素转运蛋白是血清素能突触神经传递的关键调节因子。已发现血清素转运蛋白基因的两个多态性区域,它们与转录效率不同导致的血清素功能活性变化有关。回避伤害(HA)人格特质也可能具有遗传性,并与血清素能神经递质活性改变有关。
我们使用聚合酶链反应扩增血清素转运蛋白启动子(5-HTTLPR)的多态性和内含子2内可变串联重复多态性(VNTR),并在97例MWOA患者和100例健康对照中进行基因型多态性分析。我们通过使用三维问卷评估HA人格维度来研究血清素相关的人格特质。
5-HTTLPR的基因型频率和等位基因分布在MWOA患者和对照之间没有差异。VNTR基因型STin2.12/STin2.12在MWOA患者中(90%)比在对照中(77%)明显更常见(P = .017)。MWOA患者的HA评分(21.9 +/- 6.4)也显著高于对照(16.3 +/- 6.1;P < .001)。
血清素能活性可能参与了MWOA的发病机制,血清素转运基因的VNTR可能是遗传因素之一。