Evidence for linkage by transmission disequilibrium test analysis of a chromosome 22 microsatellite marker D22S278 and bipolar disorder in a Palestinian Arab population

被引:0
|
作者
Mujaheed, M
Corbex, M
Lichtenberg, P
Levinson, DF
Deleuze, JF
Mallet, J
Ebstein, RP [1 ]
机构
[1] S Herzog Mem Hosp, Res Lab, POB 35300, IL-91351 Jerusalem, Israel
[2] Palestinian Res Ctr Genet Mental Disorders, Bethlehem, Palestine
[3] CNRS, Lab Genet Mol Neurotransmiss & Proc Neurodegenera, LGN, Paris, France
[4] Univ Penn, Sch Med, Dept Psychiat, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Med, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
[6] Aventis, Iury, France
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2000年 / 96卷 / 06期
关键词
bipolar disorder; schizophrenia; transmission disequilibrium test; ETDT; chromosome; 22; D22S278; Palestinian Arab;
D O I
10.1002/1096-8628(20001204)96:6<836::AID-AJMG28>3.3.CO;2-U
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of linkage studies suggest a schizophrenia susceptibility locus on chromosome 22, particularly with microsatellite marker D22S278 (22q12). In addition to some evidence for linkage to schizophrenia in this region, linkage to bipolar disorder using this marker has also been reported. We tested a group of 60 Bipolar I triads and an expanded group of 79 Bipolar I and Bipolar II: triads recruited from a Palestinian Arab population for linkage with the D22S278 marker. Significant linkage was observed using the extended transmission disequilibrium test for multiallelic markers (ETDT) for both Bipolar I (P = 0.031) and the expanded group of Bipolar I and Bipolar II (P = 0.041). These weakly positive results are at least consistent with the hypothesis that this region of chromosome 22 might harbor a susceptibility locus for both major psychoses and should be considered for more intensive study. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:836 / 838
页数:3
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