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Original Studies |
Division of Endocrinology and Metabolism, Departments of Medicine and Psychiatry (D.A.G.), Mount Sinai School of Medicine, New York, New York 10029
Address all correspondence and requests for reprints to: Yaron Tomer, M.D., Division of Endocrinology and Metabolism, Box 1055, Mount Sinai Medical Center, One Gustave L. Levy Place, New York, New York 10029. E-mail: ytomer{at}smtplink.mssm.edu
The autoimmune thyroid diseases [Graves and Hashimotos
diseases (GD and HT)] develop in genetically susceptible individuals,
but the genes responsible for this susceptibility remain unknown. To
identify such genes, we have been testing candidate genes and
chromosomal regions using highly polymorphic microsatellite markers. We
recently reported evidence for the first locus linked to GD (GD-1) on
chromosome 14q31 in a small group of families. We have now extended
these studies and analyzed 53 multiplex families with GD and/or HT (323
individuals). Chromosome 14 was screened using 16 microsatellite
markers spanning the entire chromosome. Three additional markers
located inside candidate genes on chromosome 14 were also studied.
Microsatellite markers were amplified using fluorescent-labeled primers
and separated on an ABI-310 genetic analyzer. The data were analyzed
using LIPED software for two-point logarithm of odds (LOD) score
analysis and GeneHunter software for multipoint linkage analysis. No
linkage of any marker was found to HT or autoimmune thyroid diseases
(GD+HT). The previously identified GD-1 locus on 14q31 continued to
show evidence of linkage to GD in this much larger set of families. The
maximum LOD score was 2.1 obtained for marker D14S81 (
= 0.01),
assuming a recessive mode of inheritance and a penetrance of 0.3.
Multipoint analysis yielded a maximum LOD score of 2.5 between markers
D14S81 and D14S1054. There was no evidence for heterogeneity in our
sample. These data again suggest the presence of a major Graves
disease susceptibility gene (GD-1) on chromosome 14q31. This locus is
close to the recently identified multinodular goiter-1 locus.
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