首页> 美国卫生研究院文献>American Journal of Human Genetics >A new Graves disease-susceptibility locus maps to chromosome 20q11.2. International Consortium for the Genetics of Autoimmune Thyroid Disease.
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A new Graves disease-susceptibility locus maps to chromosome 20q11.2. International Consortium for the Genetics of Autoimmune Thyroid Disease.

机译:一个新的Graves疾病易感性基因座点映射到20q11.2号染色体。国际自身免疫甲状腺疾病遗传学国际联盟。

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摘要

The autoimmune thyroid diseases (AITDs) include two related disorders, Graves disease (GD) and Hashimoto thyroiditis, in which perturbations of immune regulation result in an immune attack on the thyroid gland. The AITDs are multifactorial and develop in genetically susceptible individuals. However, the genes responsible for this susceptibility remain unknown. Recently, we initiated a whole-genome linkage study of patients with AITD, in order to identify their susceptibility genes. We studied a data set of 53 multiplex, multigenerational AITD families (323 individuals), using highly polymorphic and densely spaced microsatellite markers (intermarker distance <10 cM). Linkage analysis was performed by use of two-point and multipoint parametric methods (classic LOD-score analysis). While studying chromosome 20, we found a locus on chromosome 20q11.2 that was strongly linked to GD. A maximum two-point LOD score of 3.2 was obtained at marker D20S195, assuming a recessive mode of inheritance and a penetrance of.3. The maximum nonparametric LOD score was 2.4 (P=.00043); this score also was obtained at marker D20S195. Multipoint linkage analysis yielded a maximum LOD score of 3.5 for a 6-cM interval between markers D20S195 and D20S107. There was no evidence for heterogeneity in our sample. In our view, these results indicate strong evidence for linkage and suggest the presence of a major GD-susceptibility gene on chromosome 20q11.2.
机译:自身免疫性甲状腺疾病(AITD)包括两种相关的疾病,格雷夫斯病(GD)和桥本甲状腺炎,其中免疫调节的紊乱导致对甲状腺的免疫攻击。 AITD是多因素的,并且在遗传易感人群中发展。然而,导致这种敏感性的基因仍然未知。最近,我们启动了AITD患者全基因组连锁研究,以鉴定其易感基因。我们使用高度多态且间隔紧密的微卫星标记(标记间距离<10 cM)研究了53个多重,多代AITD家族(323个个体)的数据集。通过使用两点和多点参数方法(经典LOD得分分析)进行链接分析。在研究20号染色体时,我们在20q11.2号染色体上发现了一个与GD密切相关的基因座。假设隐性遗传模式和渗透率3,则在标记D20S195上获得的最高两点LOD得分为3.2。非参数LOD最高评分为2.4(P = .00043);该分数也是在标记D20S195上获得的。在标记D20S195和D20S107之间的6 cM间隔内,多点连锁分析得出的最大LOD得分为3.5。在我们的样本中没有证据表明存在异质性。我们认为,这些结果表明存在强有力的连锁证据,并表明在染色体20q11.2上存在主要的GD敏感性基因。

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