Family-based association studies of α-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder

被引:6
作者
Abou Jamra, R
Schumacher, J
Golla, A
Richter, C
Otte, ACJ
Schulze, TG
Ohlraun, S
Maier, W
Rietschel, M
Cichon, S
Propping, P
Nöthen, MM
机构
[1] Univ Bonn, Inst Human Genet, D-53111 Bonn, Germany
[2] Univ Bonn, Inst Med Biometry Informat & Epidemiol, D-5300 Bonn, Germany
[3] Cent Inst Mental Hlth, D-6800 Mannheim, Germany
[4] Univ Bonn, Dept Psychiat, D-5300 Bonn, Germany
[5] Univ Antwerp, Dept Med Genet, B-2020 Antwerp, Belgium
关键词
manic-depression; transmission disequilibrium test; adrenergic receptor genes;
D O I
10.1002/ajmg.b.20145
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several lines of evidence suggest an involvement of the noradrenergic neurotransmitter system in the pathogenesis of bipolar affective disorder (BPAD). Three genes for alpha-adrenergic receptors (ADRA) are located in chromosomal regions that showed evidence for linkage: The alpha(1c)-adrenergic (ADRA-1C) receptor gene on 8p21, the alpha(2a)-adrenergic (ADRA-2A) receptor gene on 10q25, and the alpha(2c)-adrenergic (ADRA-2C) receptor on 4p16. In a BPAD sample of 120 parent-offspring triads, we genotyped a 492 Cys/Arg variant in exon 2 of the ADRA-1C gene, a -1291 G/C variant in the 5' UTR of the ADRA-2A gene, and a STR marker (adra2c1) in the 5' UTR of the ADRA-2C gene. Using the Transmission Disequilibrium Test (TDT), no significant differences in transmissions were observed for any of the three ADRA genes. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:79 / 81
页数:3
相关论文
共 23 条
[11]   Two functionally distinct α2-adrenergic receptors regulate sympathetic neurotransmission [J].
Hein, L ;
Altman, JD ;
Kobilka, BK .
NATURE, 1999, 402 (6758) :181-184
[12]  
HOEHE MR, 1995, J MOL MED-JMM, V73, P299
[13]   A noradrenergic and serotonergic hypothesis of the linkage between epilepsy and affective disorders [J].
Jobe, PC ;
Dailey, JW ;
Wernicke, JF .
CRITICAL REVIEWS IN NEUROBIOLOGY, 1999, 13 (04) :317-356
[14]   A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22 [J].
Kelsoe, JR ;
Spence, MA ;
Loetscher, E ;
Foguet, M ;
Sadovnick, AD ;
Remick, RA ;
Flodman, P ;
Khristich, J ;
Mroczkowski-Parker, Z ;
Brown, JL ;
Masser, D ;
Ungerleider, S ;
Rapaport, MH ;
Wishart, WL ;
Luebbert, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :585-590
[15]  
Kruglyak L, 1996, AM J HUM GENET, V58, P1347
[16]   Power and design considerations for a general class of family-based association tests: Quantitative traits [J].
Lange, C ;
DeMeo, DL ;
Laird, NM .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (06) :1330-1341
[17]  
Lario S, 1997, CLIN GENET, V51, P129
[18]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159
[19]  
Riess Olaf, 1992, Human Molecular Genetics, V1, P452, DOI 10.1093/hmg/1.6.452
[20]   alpha(1a)-adrenoceptor polymorphism: Pharmacological characterization and association with benign prostatic hypertrophy [J].
Shibata, K ;
Hirasawa, A ;
Moriyama, N ;
Kawabe, K ;
Ogawa, S ;
Tsujimoto, G .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 118 (06) :1403-1408