New segregation analysis of panic disorder

被引:0
作者
Vieland, VJ
Goodman, DW
Chapman, T
Fyer, AJ
机构
[1] NEW YORK STATE PSYCHIAT INST & HOSP,DEPT THERAPEUT,NEW YORK,NY 10032
[2] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PSYCHIAT,NEW YORK,NY 10027
[3] COLUMBIA UNIV,SCH PUBL HLTH,DIV GENET EPIDEMIOL,NEW YORK,NY 10027
[4] CORNELL UNIV,COLL MED,ITHACA,NY 14853
[5] COLUMBIA UNIV,SCH PUBL HLTH,DIV BIOSTAT,NEW YORK,NY 10032
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 67卷 / 02期
关键词
anxiety disorders; panic disorder; genetics; segregation analysis;
D O I
10.1002/(SICI)1096-8628(19960409)67:2<147::AID-AJMG4>3.0.CO;2-P
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We performed simple segregation analyses of panic disorder using 126 families of probands with DSM-III-R panic disorder who were ascertained for a family study of anxiety disorders at an anxiety disorders research clinic. We present parameter estimates for dominant, recessive, and arbitrary single major locus models without sex effects, as well as for a nongenetic transmission model, and compare these models to each other and to models obtained by other investigators. We rejected the nongenetic transmission model when comparing it to the recessive model. Consistent with some previous reports, we find comparable support for dominant and recessive models, and in both cases estimate nonzero phenocopy rates. The effect of restricting the analysis to families of probands without any lifetime history of comorbid major depression (MDD) was also examined. No notable differences in parameter estimates were found in that subsample, although the power of that analysis was low. Consistency between the findings in our sample and in another independently collected sample suggests the possibility of pooling such samples in the future in order to achieve the necessary power for more complex analyses. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:147 / 153
页数:7
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