Linkage of HLA to myasthenia gravis and genetic heterogeneity depending onanti-titin antibodies

Background: MG is an autoimmune disease of the neuromuscular junction. MG w ith thymus hyperplasia has been associated with, but not genetically linked to, the HLA-DR3 haplotype. Objective: To re-evaluate the association of HL A with MG in 656 patients with generalized disease and to test linkage of H ILA to MG with thymus hyperplasia. Methods: Patients were genotyped for HLA -DRB1. Data analysis included case-control comparisons after subgrouping pa tients by thymus histopathology. The transmission of parental alleles to MG offspring with thymus hyperplasia was studied in simplex families using th e transmission/disequilibrium test (TDT) as a test of linkage. Results: MG with thymus hyperplasia was positively associated with DR3 (OR = 4.5, p = 1 X 10(-6)) and negatively associated with DR7 (OR = 0.28, P = 1 X 10(-6)), based on both case-control comparisons and TDT. No association was detected with thymomas. Conversely, patients who lacked thymus anomalies but expres sed anti-titin antibodies (ATA) had an increase of DR7 (OR = 2.08, P = 4 X 10(-3)) and a decrease of DR3 (OR = 0.33, p = 9 X 10(-3)). Conclusions: The authors established linkage of HLA to MG and thymus hyperplasia, defining the MYAS1 locus. Moreover, DR3 and DR7, or closely linked genes, have oppos ing effects on MG phenotypes. Nonthymomatous patients with ATA may be a pat hogenetically distinct subset of MG patients.