Inoue Kazuyuki, Itoh Kunihiko, Yoshida Keizo, Higuchi Hisashi, Kamata Mitsuhiro, Takahashi Hitoshi, Shimizu Tetsuo, Suzuki Toshio
Department of Pharmaceutical Science, Akita University Hospital, Japan.
Biol Pharm Bull. 2007 Oct;30(10):1996-8. doi: 10.1248/bpb.30.1996.
Norepinephrinergic neurotransmission in the central nervous system have a major impact on the symptomatology in major depressive disorder (MDD), and genetic polymorphisms of norepinephrine transporter (NET) have a possibility to be involved in susceptibility to MDD. We investigated the association of the G1287A (rs5569) polymorphism of the NET gene and susceptibility to MDD by comparing 145 major depressive patients with 164 healthy individuals first in a Japanese population. The genotype frequencies in depressed patients and health volunteers of the NET G1287A polymorphism were 52.4% (G/G), 39.3% (G/A) and 8.3% (A/A) in depressed patients, 61.6% (G/G), 29.9% (G/A allele) and 8.5% (A/A) in healthy volunteers, respectively. The allele frequencies in depressed patients and health volunteers of the NET G1287A polymorphism were 72.1% (G allele) and 27.9% (A allele) in depressed patients, 76.5% (G allele) and 23.5% (A allele) in healthy volunteers, respectively. The genotype distribution and allele frequencies were not significantly different between major depressive patients and healthy volunteers. NET G1287A polymorphism appears not to be an important factor in susceptibility to MDD in a Japanese population.
中枢神经系统中的去甲肾上腺素能神经传递对重度抑郁症(MDD)的症状学有重大影响,而去甲肾上腺素转运体(NET)的基因多态性可能与MDD的易感性有关。我们首先在日本人群中,通过比较145名重度抑郁症患者和164名健康个体,研究了NET基因的G1287A(rs5569)多态性与MDD易感性之间的关联。NET G1287A多态性在抑郁症患者和健康志愿者中的基因型频率分别为:抑郁症患者中52.4%(G/G)、39.3%(G/A)和8.3%(A/A),健康志愿者中61.6%(G/G)、29.9%(G/A等位基因)和8.5%(A/A)。NET G1287A多态性在抑郁症患者和健康志愿者中的等位基因频率分别为:抑郁症患者中72.1%(G等位基因)和27.9%(A等位基因),健康志愿者中76.5%(G等位基因)和23.5%(A等位基因)。重度抑郁症患者和健康志愿者之间的基因型分布和等位基因频率没有显著差异。在日本人群中,NET G1287A多态性似乎不是MDD易感性的重要因素。