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胰岛素依赖型糖尿病(IDDM)异质性的研究:连锁研究、双基因座模型与遗传异质性

The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.

作者信息

Hodge S E, Anderson C E, Neiswanger K, Sparkes R S, Rimoin D L

出版信息

Am J Hum Genet. 1983 Nov;35(6):1139-55.

Abstract

One hundred families with insulin-dependent diabetes mellitus (IDDM) were analyzed for linkage with 27 genetic markers, including HLA, properdin factor B (BF), and glyoxalase 1(GLO) on chromosome 6, and Kidd blood group (Jk) on chromosome 2. The linkage analyses were performed under several different genetic models. An approximate correction for two-locus linkage analysis was developed and applied to four markers. Two different heterogeneity tests were implemented and applied to all the markers. One, the Predivided-Sample Test, utilizes various criteria thought to be relevant to genetic heterogeneity in IDDM. The other, the Admixture Test, looks for heterogeneity without specifying a prior how the sample should be divided. Results continued to support linkage of IDDM with three chromosome 6 markers: HLA, BF, and GLO. The total lod score for Kidd blood group, under the recessive model with 20% penetrance, is 1.63--down 1.2 from the 2.83 reported by us earlier. The only other marker whose lod score exceeded 1.0 under any model was pancreatic amylase (AMY2). The two-locus correction, which involved lowering the penetrance values used in the analysis, affected estimates of theta (recombination fraction) but did not markedly change the lod scores themselves. There was little evidence for heterogeneity within any of the lod scores, under either the Predivided-Sample Test or the Admixture Test.

摘要

对100个胰岛素依赖型糖尿病(IDDM)家庭进行了分析,以研究其与27个遗传标记的连锁关系,这些标记包括位于6号染色体上的HLA、备解素因子B(BF)和乙二醛酶1(GLO),以及位于2号染色体上的基德血型(Jk)。连锁分析在几种不同的遗传模型下进行。开发了一种用于两位点连锁分析的近似校正方法,并应用于四个标记。实施了两种不同的异质性检验,并应用于所有标记。一种是预划分样本检验,它利用了各种被认为与IDDM遗传异质性相关的标准。另一种是混合检验,它在不预先指定样本应如何划分的情况下寻找异质性。结果继续支持IDDM与6号染色体上的三个标记HLA、BF和GLO的连锁关系。在隐性模型下,基德血型的总对数分数为1.63,外显率为20%,比我们之前报道的2.83下降了1.2。在任何模型下,对数分数超过1.0的唯一其他标记是胰腺淀粉酶(AMY2)。两位点校正涉及降低分析中使用的外显率值,影响了θ(重组分数)的估计,但对数分数本身没有明显变化。在预划分样本检验或混合检验下,几乎没有证据表明任何对数分数内存在异质性。

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