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惊恐障碍全基因组遗传筛查结果。

Results of a genome-wide genetic screen for panic disorder.

作者信息

Knowles J A, Fyer A J, Vieland V J, Weissman M M, Hodge S E, Heiman G A, Haghighi F, de Jesus G M, Rassnick H, Preud'homme-Rivelli X, Austin T, Cunjak J, Mick S, Fine L D, Woodley K A, Das K, Maier W, Adams P B, Freimer N B, Klein D F, Gilliam T C

机构信息

Department of Psychiatry, College of Physicians and Surgeons at Columbia University and New York State Psychiatric Institute, New York 10032, USA.

出版信息

Am J Med Genet. 1998 Mar 28;81(2):139-47. doi: 10.1002/(sici)1096-8628(19980328)81:2<139::aid-ajmg4>3.0.co;2-r.

Abstract

Panic disorder is characterized by spontaneous and recurrent panic attacks, often accompanied by agoraphobia. The results of family, twin, and segregation studies suggest a genetic role in the etiology of the illness. We have genotyped up to 23 families that have a high density of panic disorder with 540 microsatellite DNA markers in a first-pass genomic screen. The thirteen best families (ELOD > 6.0 under the dominant genetic model) have been genotyped with an ordered set of markers encompassing all the autosomes, at an average marker density of 11 cM. Over 110,000 genotypes have been generated on the whole set of families, and the data have been analyzed under both a dominant and a recessive model, and with the program SIBPAIR. No lod scores exceed 2.0 for either parametric model. Two markers give lod scores over 1.0 under the dominant model (chromosomes 1p and 20p), and four do under the recessive model (7p, 17p, 20q, and X/Y). One of these (20p) may be particularly promising. Analysis with SIBPAIR yielded P values equivalent to a lod score of 1.0 or greater (i.e., P < .016, one-sided, uncorrected for multiple tests) for 11 marker loci (2, 7p, 8p, 8q, 9p, 11q, 12q, 16p, 20p and 20q).

摘要

惊恐障碍的特征是自发且反复发作的惊恐发作,常伴有广场恐惧症。家族、双生子和系谱研究结果表明,遗传因素在该疾病的病因中起作用。在首次全基因组筛查中,我们对多达23个惊恐障碍高密度家族进行了基因分型,使用了540个微卫星DNA标记。13个最佳家族(在显性遗传模型下ELOD>6.0)已使用一组有序的标记进行基因分型,这些标记涵盖所有常染色体,平均标记密度为11厘摩。对整个家族集产生了超过110,000个基因型,并在显性和隐性模型下使用SIBPAIR程序对数据进行了分析。对于任何一个参数模型,对数优势比分均未超过2.0。在显性模型下,两个标记的对数优势比分超过1.0(1号染色体短臂和20号染色体短臂),在隐性模型下有四个标记超过1.0(7号染色体短臂、17号染色体短臂、20号染色体长臂和X/Y染色体)。其中一个(20号染色体短臂)可能特别有前景。使用SIBPAIR进行分析时,11个标记位点(2号染色体、7号染色体短臂、8号染色体短臂、8号染色体长臂、9号染色体短臂、11号染色体长臂、12号染色体长臂、16号染色体短臂、20号染色体短臂和20号染色体长臂)产生的P值相当于对数优势比分1.0或更高(即,P<.016,单侧,未针对多次检验进行校正)。

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