Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32

被引:31
作者
Liu, CY
Badner, JA
Christian, SL
Guroff, JJ
Detera-Wadleigh, SD
Gershon, ES
机构
[1] Univ Chicago, Dept Psychiat, Chicago, IL 60637 USA
[2] Cent S Univ, Natl Lab Med Gene, Changsha, Hunan, Peoples R China
[3] NIMH, NIH, Bethesda, MD 20892 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 105卷 / 04期
关键词
bipolar disorder; linkage; association; 13q; map;
D O I
10.1002/ajmg.1358
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A region between D13S71 and D13S274 on 13q32 showed linkage to bipolar disorder (BP) based on a genome scan using markers with an average spacing of similar to6 cM and an average heterozygosity of similar to 60% [Detera-Wadleigh et al., 1999: Proc Natl Acad Sci USA 96:5604-5609]. In an attempt to confirm this finding and achieve fine mapping of the susceptibility region, nine additional microsatellite markers with average heterozygosity of similar to 86%, located between D13S71 and D13S274, were typed in the same sample. The strongest linkage evidence was detected by multipoint linkage analysis (ASPEX program) around D13S779-D13S225 with maximum LOD score of 3.25 under Affection Status Model II (ASM II; P = 0.0000546). Data from additional nine markers resulted in a decrease of the 95% confidence interval of the Linkage region. Association analyses with GASSOC TDT and ASPEX/sib_tdt detect potential linkage disequilibrium with several markers, including D13S280 (ASPEX TDT P = 0.0033, ASM I). These data generated using a higher marker density within the proposed susceptibility region strengthen the validity of our previous findings and suggest a finer localization of the susceptibility gene(s) on 13q32. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:375 / 380
页数:6
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