ASSOCIATION OF HLA-DQB1-ASTERISK-0201 WITH STIFF-MAN SYNDROME

被引:55
作者
PUGLIESE, A
SOLIMENA, M
AWDEH, ZL
ALPER, CA
BUGAWAN, T
ERLICH, HA
DECAMILLI, P
EISENBARTH, GS
机构
[1] UNIV COLORADO, HLTH SCI CTR, BARBARA DAVIS CTR CHILDHOOD DIABET, DENVER, CO 80262 USA
[2] YALE UNIV, SCH MED,HOWARD HUGHES MED INST,DEPT CELL BIOL, RES LABS, NEW HAVEN, CT USA
[3] HARVARD UNIV, SCH MED, CTR BLOOD RES, BOSTON, MA USA
[4] ROCHE MOLEC SYST INC, DEPT HUMAN GENET, ALAMEDA, CA USA
关键词
D O I
10.1210/jc.77.6.1550
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Stiff-man syndrome (SMS) is a rare disorder of the central nervous system of probable autoimmune origin. Patients with SMS often have other autoimmune diseases, in particular type I (insulin-dependent) diabetes mellitus (IDDM). Approximately 60% of patients with SMS have high titers of autoantibodies against the enzyme glutamic acid decarboxylase, Similar to SMS, the majority of patients with IDDM have autoantibodies against glutamic acid decarboxylase at or before diabetes onset, although usually at a lower titer and with a different reaction pattern than patients with SMS. To investigate the immunogenetic basis of SMS, we HLA-typed 18 patients with the disease. Seventy-two percent carried the DQB1*0201 allele (13 of 18, P = 0.02 vs. 18 of 48 controls), indicating that SMS is associated with this allele. DQB1*0201 is also a susceptibility allele for IDDM and other autoimmune diseases. Patients with SMS carried the IDDM-protective DQB1*0602 allele and other sequence-related DQB1*06 alleles with the same frequency observed in controls. In contrast, these alleles are rarely found in IDDM. Five of 8 (62.5%) SMS patients lacking a DQB1*06 allele were diabetic in contrast to only 2 of 10 (20%) with a DQB1*06 allele (P = 0.08), suggesting that the presence of DQB1*0602 or other DQB1*06 alleles may be associated with a reduced prevalence of diabetes among patients with SMS.
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页码:1550 / 1553
页数:4
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