Progress in the characterization of slowly progressive autoimmune diabetes in adult patients (LADA or type 1,5 diabetes)

被引:25
|
作者
Schernthaner, G
Hink, S
Kopp, HP
Muzyka, B
Streit, G
Kroiss, A
机构
[1] Krankenhaus Rudolfstiftung, Med Klin 1, Dept Med 1, A-1030 Vienna, Austria
[2] Rudolfstiftung Hosp, Dept Nucl Med, Vienna, Austria
关键词
LADA; type; 1.5; diabetes; GAD; IA2; islet autoimmunity; insulin deficiency;
D O I
10.1055/s-2001-18573
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
LADA or type 1.5 diabetes is a slowly progressive form of autoimmune diabetes of adults and represents a considerable proportion (about 5-10%) of all diabetic patients. Associations with high risk HLA genotypes and autoimmune phenomena (GAD, IA2, ICA) show similarities with type 1 diabetes, but phenotypical characteristics of these patients do not allow the correct identification without screening of GAD antibodies. The relatively low antibody titers against islet-cell antigens in LADA patients may be sign of a less aggressive form of autoimmune diabetes and could be responsible for the-long non-insulin requirement phase of this diabetes type. Similar as in prediabetic relatives of type 1 diabetic patients the risk for beta cell failure in adult "type 2 diabetic" patients increases with the number of antibodies positive. Consequently, low titers of GAD - in particular in elderly patients - do not predict a progressive and rapid-loss of beta-cell failure, when associations with highrisk genotypes or other islet-cell antibodies are lacking. Patients with LADA share insulin resistance with type 2 diabetic patients, but display a more severe defect in stimulated beta-cell capacity than patients with classical type 2 diabetes. With respect to features of the metabolic syndrome, patients with LADA have lower BMI blood pressure and triglyceride levels compared with classical type 2 diabetes patients. Early identification of LADA patients will be mandatory, when effective immune interventions are available for prevention of the beta-cell destructive process insulin requirement of these patients.
引用
收藏
页码:S94 / S108
页数:15
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