Adult-onset atypical (type 1) diabetes - Additional insights and differences with type 1A diabetes in a European Mediterranean population

被引:29
作者
Aguilera, E
Casamitjana, R
Ercilla, G
Oriola, J
Gomis, R
Conget, I
机构
[1] Hosp Clin & Univ Barcelona, Endocrinol & Diabet Unit, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
[2] Hosp Clin & Univ Barcelona, Hormonal Unit, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
[3] Hosp Clin & Univ Barcelona, Immunol Unit, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
关键词
D O I
10.2337/diacare.27.5.1108
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - In 1997, the American Diabetes Association proposed two subcategories for type 1 diabetes: type 1A or immunomediated diabetes and type 1B or idiopathic diabetes characterized by negative beta-cell autoimmunity markers, lack of association with HLA, and Fluctuating insulinopenia. The aim of this study was to examine clinical characteristics, beta-cell function, HLA typing, and mutations in maturity-onset diabetes of the young (MODY) genes in patients with atypical type 1 diabetes (type 1 diabetes diagnosed at onset, without pancreatic autoantibodies and fluctuating insulinopenia). RESEARCH DESIGN AND METHODS - Eight patients with atypical type 1 diabetes (all men, 30.7 +/- 7.6 years) and 16 newly diagnosed age- and sex-matched patients with type 1A diabetes were studied retrospectively, Islet cell, GAD, tyrosine phosphatase and insulin antibodies, and basal and stimulated plasma C-peptide were measured at onset and after 1 year. HLA-DRB1-DQA1-DQB1 typing and screening for mutations in the HNF-1alpha and HNF-4alpha genes were performed from genomic DNA. RESULTS - Atypical patients displayed significantly higher BMI and better beta-cell function at onset and after 12 months. Three patients carried protective or neutral type 1 diabetes haplotypes, five patients displayed heterozygosity for susceptible and protective haplotypes and seven patients showed Asp. We found a nondescribed variant Pro436Ser in exon 10 of the HNF-4alpha gene in one atypical patient without susceptible haplotypes. CONCLUSIONS - in our population, there are atypical forms of young adult-onset ketosis-prone diabetes initially diagnosed as type 1 diabetes, differing from type 1 diabetes in the absence of beta-cell autoimmunity, persistent beta-cell Function capacity, fluctuating insulin requirements and ketosis-prone episodes, as well as clinical features of type 2 diabetes. Only one subgroup could be strictly classified as having type 1B diabetes. Additional information is still needed to improve our understanding of the mechanisms that finally lead to the disease.
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收藏
页码:1108 / 1114
页数:7
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