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High prevalence of GAD(65) (and IA-2) antibodies in Japanese IDDM patients by a new immunoprecipitation assay based on recombinant human GAD(65)
被引:0
|作者:
Akamine, H
Komiya, I
Shimabukuro, T
Asawa, T
Tanaka, H
Yagi, N
Taira, T
Nagata, K
Arakaki, K
Wakugami, T
Takasu, N
Powell, MJ
Furmaniak, J
Smith, BR
机构:
[1] Second Dept. of Internal Medicine, University of the Ryukyus, School of Medicine, Nishihara
[2] FIRS Laboratories, RSR Ltd., Llanishen, Cardiff CF4 5DU, Parc Ty Glas
[3] Department of Medicine, University of Wales, College of Medicine, Cardiff CF4 4XN, Heath Park
[4] Second Dept. of Internal Medicine, University of the Ryukyus, School of Medicine, Nakagami-gun, Okinawa 903-01, 207 Uehara, Nishihara
关键词:
GAD(65) antibody;
IA-2;
antibody;
Japanese IDDM;
autoimmune thyroid disease;
D O I:
10.1002/(SICI)1096-9136(199709)14:9<778::AID-DIA461>3.0.CO;2-7
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Marked differences have been reported in the prevalence of glutamic acid decarboxylase (GAD) antibodies between Caucasian (63-84 %) and Japanese (30-50 %) or Asian (5-50 %) IDDM patients. Using a new immunoprecipitation assay based on I-125-labelled recombinant human GAD(65), we have reassessed prevalence of GAD(65) antibodies in Japanese patients. We also assessed prevalence of IA-2 antibodies. GAD(65) antibodies were detected in 83.3 % of sera taken within 1 year of onset, comparable to the prevalence reported in Caucasian patients. Positivity decreased to 66.7 % after 2 to 3 years and to 54.3 % after 3 years from onset, still higher than previously reported Asian prevalence. Except in one patient, high antibody levels persisted chronically, up to 12 years. There was no difference in the prevalence of GAD(65) antibodies between Japanese IDDM patients with and without autoimmune thyroid disease (AITD). IA-2 antibodies were detected in 64.7 % of sera taken within 1 year of onset. Prevalence of IA-2 antibodies was lower than that of GAD(65) antibodies. The difference in positivity in Asian IDDM patients between present and previous reports arose from the sensitivity of our assay for GAD(65) antibodies. Additionally, the patients we studied had classic IDDM with a well-defined onset. We conclude that prevalence of GAD(65) antibodies in Japanese IDDM patients is comparable to that in Western studies. There was no relationship of GAD(65) antibody positivity to coexistence of AITD. Our results suggest that autoimmunity is the most significant cause of Japanese IDDM. (C) 1997 by John Wiley & Sons, Ltd.
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页码:778 / 784
页数:7
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