Association analysis between the C-1291G polymorphism in the promoter region of the adrenergic α2A receptor gene and polydipsia in schizophrenia

被引:4
|
作者
Yamaguchi, Wakana [1 ,2 ]
Shinkai, Takahiro [1 ]
Inoue, Yoshiaki [1 ,3 ]
Utsunomiya, Kensuke [1 ,4 ]
Sakata, Shinichi [1 ]
Fukunaka, Yuko [1 ,5 ]
Yamada, Kenji [1 ,6 ]
Chen, Hsin-I [1 ,7 ]
Hwang, Rudi [8 ]
Ohmori, Osamu [1 ,9 ]
Nakamura, Jun [1 ]
机构
[1] Univ Occupat & Environm Hlth, Dept Psychiat, Sch Med, Yahatanishi Ku, Kitakyushu, Fukuoka 8078555, Japan
[2] Komine Eto Hosp, Yahatanishi Ku, Kitakyushu, Fukuoka 8070081, Japan
[3] Toshiba Human Asset Serv Co, Principal Off, Med Ctr, Tokyo, Japan
[4] Mitsubishi Heavy Ind Co Ltd, Dept Hlth Management, Shimonoseki Shipyard & Machinery Works, Shimonoseki, Yamaguchi 7508505, Japan
[5] Tsutsumi Hosp, Fukuoka 8114224, Japan
[6] Kokura Gamou Hosp, Kokuraminami Ku, Kitakyushu, Fukuoka 8020978, Japan
[7] Kaohsiung Med Univ, Dept Publ Hlth, Kaohsiung 807, Taiwan
[8] Univ Toronto, Neurogenet Sect, Ctr Addict & Mental Hlth, Clarke Div,Dept Psychiat, Toronto, ON M5T 1R8, Canada
[9] Wakato Hosp, Wakamatsu Ku, Kitakyushu, Fukuoka 8080132, Japan
关键词
Adrenergic alpha 2A receptors; Association study; Genetics; Polydipsia; Schizophrenia; WATER-INTOXICATION; HYPONATREMIA;
D O I
10.1016/j.pnpbp.2009.01.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several lines of studies have shown the existence of an important inhibitory mechanism for the control of water intake involving adrenergic alpha 2A receptors (ADRA2A). A human study using patients with schizophrenia demonstrated an exacerbation of polydipsia by the administration of clonidine, an ADRA2A-agonist, and a relief of polydipsia by mianserin, an ADRA2A-antagonist, suggesting the involvement of the central adrenergic system in the drinking behavior of patients with schizophrenia. Based on these findings we examined a possible association between the C-1291G polymorphism in the promoter region of the ADRA2A gene and polydipsia in schizophrenia using a Japanese case-control sample. Our sample includes 348 patients with schizophrenia (DSM-IV) (84 with polydipsia and 264 without polydipsia). No significant association between the ADRA2A C-1291G polymorphism and polydipsia was found. Our result suggests that the ADRA2A C-1291G polymorphism may not confer susceptibility to polydipsia in schizophrenia in our sample. Further studies with larger samples are warranted. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:499 / 502
页数:4
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