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精神分裂症中的假常染色体区域:通过同胞对和对数计分法对七个基因座进行连锁分析。

Pseudoautosomal region in schizophrenia: linkage analysis of seven loci by sib-pair and lod-score methods.

作者信息

d'Amato T, Waksman G, Martinez M, Laurent C, Gorwood P, Campion D, Jay M, Petit C, Savoye C, Bastard C

机构信息

Clinique Assistant des Hôpitaux, SHU de Psychiatrie d'Adultes (Pr. Daléry), Hôpital du Vinatier, Lyon-Bron, France.

出版信息

Psychiatry Res. 1994 May;52(2):135-47. doi: 10.1016/0165-1781(94)90083-3.

Abstract

In a previous study, we reported a nonrandom segregation between schizophrenia and the pseudoautosomal locus DXYS14 in a sample of 33 sibships. That study has been extended by the addition of 16 new sibships from 16 different families. Data from six other loci of the pseudoautosomal region and of the immediately adjacent part of the X specific region have also been analyzed. Two methods of linkage analysis were used: the affected sibling pair (ASP) method and the lod-score method. Lod-score analyses were performed on the basis of three different models--A, B, and C--all shown to be consistent with the epidemiological data on schizophrenia. No clear evidence for linkage was obtained with any of these models. However, whatever the genetic model and the disease classification, maximum lod scores were positive with most of the markers, with the highest scores generally being obtained for the DXYS14 locus. When the ASP method was used, the earlier finding of nonrandom segregation between schizophrenia and the DXYS14 locus was still supported in this larger data set, at an increased level of statistical significance. Findings of ASP analyses were not significant for the other loci. Thus, findings obtained from analyses using the ASP method, but not the lod-score method, were consistent with the pseudoautosomal hypothesis for schizophrenia.

摘要

在之前的一项研究中,我们报告了在一个包含33个同胞对的样本中,精神分裂症与假常染色体位点DXYS14之间存在非随机分离现象。该研究通过增加来自16个不同家庭的16个新同胞对得以扩展。还分析了假常染色体区域的其他六个位点以及X特异性区域紧邻部分的数据。使用了两种连锁分析方法:患病同胞对(ASP)法和对数优势比分法。对数优势比分分析是基于三种不同模型——A、B和C——进行的,所有这些模型都与精神分裂症的流行病学数据一致。使用这些模型均未获得明确的连锁证据。然而,无论遗传模型和疾病分类如何,大多数标记的最大对数优势比分均为正值,其中DXYS14位点通常获得最高分数。当使用ASP方法时,在这个更大的数据集中,精神分裂症与DXYS14位点之间非随机分离的早期发现仍然得到支持,且统计显著性水平有所提高。ASP分析对其他位点的结果不显著。因此,使用ASP方法而非对数优势比分法进行分析所得到的结果与精神分裂症的假常染色体假说一致。

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