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双相情感障碍:一个主要基因座的证据。

Bipolar disorder: evidence for a major locus.

作者信息

Spence M A, Flodman P L, Sadovnick A D, Bailey-Wilson J E, Ameli H, Remick R A

机构信息

Department of Pediatrics, University of California, Irvine.

出版信息

Am J Med Genet. 1995 Oct 9;60(5):370-6. doi: 10.1002/ajmg.1320600505.

DOI:10.1002/ajmg.1320600505
PMID:8546148
Abstract

Complex segregation analyses were conducted on families of bipolar I and bipolar II probands to delineate the mode of inheritance. The probands were ascertained from consecutive referrals to the Mood Disorder Service, University Hospital, University of British Columbia and diagnosed by DSM-III-R and Research Diagnostic Criteria. Data were available on over 1,500 first-degree relatives of the 186 Caucasian probands. The purpose of the analyses was to determine if, after correcting for age and birth cohort, there was evidence for a single major locus. Five models were fit to the data using the statistical package SAGE: i) dominant, ii) recessive, iii) arbitrary mendelian inheritance, iv) environmental, and v) no major effects. A single dominant, mendelian major locus was the best fitting of these models for the sample of bipolar I and II probands when only bipolar relatives were defined as affected (polygenic inheritance could not be tested). Adding recurrent major depression to the diagnosis "affected" for relatives reduced the evidence for a major locus effect. Our findings support the undertaking of linkage studies and are consistent with the analyses of the National Institutes of Mental Health (NIMH) Collaborative Study data by Rice et al. (Arch Gen Psychiatry 44: 441-447, 1987) and Blangero and Elston (Genet Epidemiol 6:221-227, 1989).

摘要

对I型双相情感障碍和II型双相情感障碍先证者的家族进行了复杂分离分析,以确定遗传模式。先证者来自不列颠哥伦比亚大学大学医院情绪障碍服务中心连续转诊的患者,并根据《精神疾病诊断与统计手册》第三版修订本(DSM-III-R)和研究诊断标准进行诊断。有186名白种人先证者的1500多名一级亲属的数据。分析的目的是确定在校正年龄和出生队列后,是否有证据支持单一主要基因座的存在。使用统计软件包SAGE对数据拟合了五个模型:i)显性,ii)隐性,iii)任意孟德尔遗传,iv)环境,v)无主要效应。当仅将双相情感障碍亲属定义为患病时(无法检验多基因遗传),单一显性孟德尔主要基因座是这些模型中对I型和II型双相情感障碍先证者样本拟合最好的模型。将复发性重度抑郁症纳入亲属“患病”诊断中,降低了主要基因座效应的证据。我们的研究结果支持进行连锁研究,并且与赖斯等人(《美国精神病学杂志》44:441 - 447, 1987)以及布兰杰罗和埃尔斯顿(《遗传流行病学》6:221 - 227, 1989)对美国国立精神卫生研究所(NIMH)合作研究数据的分析结果一致。

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