A new Graves disease-susceptibility locus maps to chromosome 20q11.2

被引:83
作者
Tomer, Y
Barbesino, G
Greenberg, DA
Concepcion, E
Davies, TF
机构
[1] Mt Sinai Med Ctr, Div Endocrinol & Metab, New York, NY 10029 USA
[2] Mt Sinai Med Ctr, Dept Med, New York, NY 10029 USA
[3] Mt Sinai Med Ctr, Sch Med, Dept Psychiat, New York, NY 10029 USA
[4] Mt Sinai Med Ctr, Sch Med, Dept Biomath, New York, NY 10029 USA
关键词
D O I
10.1086/302146
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The autoimmune thyroid diseases (AITDs) include two related disorders, Craves disease (CD) 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 CD-susceptibility gene on chromosome 20q11.2.
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页码:1749 / 1756
页数:8
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