Diverging evolution of anti-GAD and anti-IA-2 antibodies in long-standing diabetes mellitus as a function of age at onset: No association with complications

被引:0
|
作者
Hermitte, L [1 ]
Atlan-Gepner, C [1 ]
Mattei, C [1 ]
Dufayet, D [1 ]
Jannot, MF [1 ]
Christofilis, MA [1 ]
Nervi, S [1 ]
Vialettes, B [1 ]
机构
[1] Univ Aix Marseille 2, UPRES EA 2193, Lab Diabetol, Marseille, France
关键词
diabetes mellitus; glutamic acid decarboxylase (GAD); tyrosine phosphatase (IA-2); diabetes complication;
D O I
10.1002/(SICI)1096-9136(199807)15:7<586::AID-DIA624>3.3.CO;2-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glutamic acid decarboxylase autoantibodies (GAD-A) and tyrosine phosphatase IA-2 autoantibodies (IA2-A) were measured in sera of 50 recently diagnosed (<6 wk, 33 % younger than 15 yr), 19 short-term (1 to 9 yr, 35 % with onset age below 15 yr) and 89 long-standing diabetic patients (>10 yr, 57 % with onset age below 15 yr). Complications were assessed by clinical examination, retinal angiographs and microalbuminuria measurement. Both prevalences and levels of CAD-A and IA2-A decreased with increasing duration of diabetes. However even in those with long duration diabetes, 15 to 63 % of the sera were still positive for one or two antibodies. In the group with onset after the age of 15 yr, significantly higher prevalences and levels of CAD-A (but not IA2-A) was observed in comparison with the group with earlier onset. No association was found with any microvascular complications in any group. We conclude that CAD-A and IA2-A persist in some diabetic patients, despite a long duration. Persistence of CAD-A was greatest in those with postpubertal disease onset. We speculate that persistence of some beta-cells or specific environmental factors can sustain one autoimmune reaction especially in some postpubertal-onset diabetic patients. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:586 / 591
页数:6
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