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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.
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页码:499 / 502
页数:4
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