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位于4号染色体q35区域的双相情感障碍易感性基因座。

A susceptibility locus for bipolar affective disorder on chromosome 4q35.

作者信息

Adams L J, Mitchell P B, Fielder S L, Rosso A, Donald J A, Schofield P R

机构信息

School of Psychiatry, University of New South Wales, Australia.

出版信息

Am J Hum Genet. 1998 May;62(5):1084-91. doi: 10.1086/301826.

Abstract

Bipolar affective disorder (BAD) affects approximately 1% of the population and shows strong heritability. To identify potential BAD susceptibility loci, we undertook a 15-cM genome screen, using 214 microsatellite markers on the 35 most informative individuals of a large, statistically powerful pedigree. Data were analyzed by parametric two-point linkage methods under several diagnostic models. LOD scores >1.00 were obtained for 21 markers, with four of these >2.00 for at least one model. The remaining 52 individuals in the family were genotyped with these four markers, and LOD scores remained positive for three markers. A more intensive screen was undertaken in these regions, with the most positive results being obtained for chromosome 4q35. Using a dominant model of inheritance with 90% maximum age-specific penetrance and including bipolar I, II, schizoaffective/mania, and unipolar individuals as affected, we obtained a maximum two-point LOD score of 2.20 (theta = .15) at D4S1652 and a maximum three-point LOD score of 3.19 between D4S408 and D4S2924. Nonparametric analyses further supported the presence of a locus on chromosome 4q35. A maximum score of 2.62 (P=.01) was obtained between D4S1652 and D4S171 by use of the GENEHUNTER program, and a maximum score of 3.57 (P=.0002) was obtained at D4S2924 using the affected pedigree member method. Analysis of a further 10 pedigrees suggests the presence of this locus in at least one additional family, indicating a possible predisposing locus and not a pedigree-specific mutation. Our results suggest the presence of a novel BAD susceptibility locus on chromosome 4q35.

摘要

双相情感障碍(BAD)影响着约1%的人口,且具有很强的遗传性。为了确定潜在的BAD易感基因座,我们使用一个大型、具有统计学效力的家系中35个信息最丰富的个体,采用214个微卫星标记进行了一次15厘摩的基因组筛查。数据通过几种诊断模型下的参数两点连锁法进行分析。21个标记获得了大于1.00的LOD分数,其中4个标记在至少一种模型下大于2.00。对该家系中其余52个个体用这4个标记进行基因分型,3个标记的LOD分数仍为阳性。在这些区域进行了更密集的筛查,4号染色体q35区域得到的阳性结果最为显著。采用显性遗传模型,最大年龄特异性外显率为90%,将双相I型、II型、分裂情感性/躁狂型和单相个体均视为患病个体,我们在D4S1652处获得了最大两点LOD分数2.20(θ = 0.15),在D4S408和D4S2924之间获得了最大三点LOD分数3.19。非参数分析进一步支持了4号染色体q35区域存在一个基因座。使用GENEHUNTER程序在D4S1652和D4S171之间获得了最大分数2.62(P = 0.01),使用患病家系成员法在D4S2924处获得了最大分数3.57(P = 0.0002)。对另外10个家系的分析表明,至少在一个其他家系中存在该基因座,这表明存在一个可能的易感基因座,而非家系特异性突变。我们的结果表明在4号染色体q35区域存在一个新的BAD易感基因座。

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