The 6?year incidence of diabetes-associated autoantibodies in genetically at-risk children: the TEDDY study
详细信息    查看全文
  • 作者:Jeffrey P. Krischer ; Kristian F. Lynch ; Desmond A. Schatz ; Jorma Ilonen
  • 关键词:Autoimmunity ; Diabetes in young children ; HLA ; DR ; DQ genotypes ; Incidence ; Islet autoantibodies ; Type 1 diabetes
  • 刊名:Diabetologia
  • 出版年:2015
  • 出版时间:May 2015
  • 年:2015
  • 卷:58
  • 期:5
  • 页码:980-987
  • 全文大小:295 KB
  • 参考文献:1. (1997) Report of the expert committee on the diagnosis and classification of diabetes mellitus. Diabetes Care 20:1183-1197
    2. Orban, T, Sosenko, JM, Cuthbertson, D (2009) Pancreatic islet autoantibodies as predictors of type 1 diabetes in the diabetes prevention trial-type 1. Diabetes Care 32: pp. 2269-2274 CrossRef
    3. Ziegler, AG, Rewers, M, Simell, O (2013) Seroconversion to multiple islet autoantibodies and risk of progression to diabetes in children. JAMA 309: pp. 2473-2479 CrossRef
    4. Ziegler, AG, Bonifacio, E (2012) Age-related islet autoantibody incidence in offspring of patients with type 1 diabetes. Diabetologia 55: pp. 1937-1943 CrossRef
    5. Ilonen, J, Hammais, A, Laine, AP (2013) Patterns of beta-cell autoantibody appearance and genetic associations during the first years of life. Diabetes 62: pp. 3636-3640 CrossRef
    The Environmental Determinants of Diabetes in the Young (TEDDY) study: study design. Pediatr Diabetes 8: pp. 286-298 CrossRef
    6. TEDDY Study Group (2008) The Environmental Determinants of Diabetes in the Young (TEDDY) Study. Ann N Y Acad Sci 1150:1-3
    7. Hagopian, WA, Erlich, H, Lernmark, A (2011) The Environmental Determinants of Diabetes in the Young (TEDDY): genetic criteria and international diabetes risk screening of 421 000 infants. Pediatr Diabetes 12: pp. 733-743 CrossRef
    8. Bonifacio, E, Yu, L, Williams, AK (2010) Harmonization of glutamic acid decarboxylase and islet antigen-2 autoantibody assays for national institute of diabetes and digestive and kidney diseases consortia. J Clin Endocrinol Metab 95: pp. 3360-3367 CrossRef
    9. Koczwara, K, Bonifacio, E, Ziegler, AG (2004) Transmission of maternal islet antibodies and risk of autoimmune diabetes in offspring of mothers with type 1 diabetes. Diabetes 53: pp. 1-4 CrossRef
    10. Lynch, KF, Lernmark, B, Merlo, J, Cilio, CM, Ivarsson, SA, Lernmark, A (2008) Cord blood islet autoantibodies and seasonal association with the type 1 diabetes high-risk genotype. J Perinatol 28: pp. 211-217 CrossRef
    11. Ulm, K (1990) A simple method to calculate the confidence interval of a standardized mortality ratio (SMR). Am J Epidemiol 131: pp. 373-375
    12. O’Leary, LA, Dorman, JS, LaPorte, RE (1991) Familial and sporadic insulin-dependent diabetes: evidence for heterogeneous etiologies?. Diabetes Res Clin Pract 14: pp. 183-190 CrossRef
    13. Dahlquist, G, Blom, L, Holmgren, G (1985) The epidemiology of diabetes in Swedish children 0-4?years—a six-year prospective study. Diabetologia 28: pp. 802-808 CrossRef
    14. Graham, J, Hagopian, WA, Kockum, I (2002) Genetic effects on age-dependent onset and islet cell autoantibody markers in type 1 diabetes. Diabetes 51: pp. 1346-1355 CrossRef
    15. M?kinen, A, H?rk?nen, T, Ilonen, J, Knip, M (2008) Characterization of the humoral immune response to islet antigen 2 in children with newly diagnosed type 1 diabetes. Eur J Endocrinol 159: pp. 19-26 CrossRef
    16. Vermeulen, I, Weets, I, Asanghanwa, M (2011) Contribution of antibodies against IA-2beta and zinc transporter 8 to classification of diabetes diagnosed under 40?years of age. Diabetes Care 34: pp. 1760-1765 CrossRef
    17. Torn, C, Hadley, D, Lee, HS (2014) Role of type 1 diabetes associated SNPs on risk of autoantibody positivity in th
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Internal Medicine
    Metabolic Diseases
    Human Physiology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0428
文摘
Aims/hypothesis Islet autoantibodies, in addition to elevated blood glucose, define type 1 diabetes. These autoantibodies are detectable for a variable period of time before diabetes onset. Thus, the occurrence of islet autoantibodies is associated with the beginning of the disease process. The age at, and order in, which autoantibodies appear may be associated with different genetic backgrounds or environmental exposures, or both. Methods Infants with HLA-DR high-risk genotypes (DR3/4, DR4/4, DR4/8 and DR3/3) were enrolled and prospectively followed with standardised autoantibody assessments quarterly throughout the first 4?years of life and then semi-annually thereafter. Results Autoantibodies appeared in 549/8,503 (6.5%) children during 34,091 person-years of follow-up. Autoantibodies at 3 (0.1%) and 6 (0.2%) months of age were rare. Of the 549, 43.7% had islet autoantibodies to insulin (IAA) only, 37.7% had glutamic acid decarboxylase autoantibodies (GADA) only, 13.8% had both GADA and IAA only, 1.6% had insulinoma antigen-2 only and 3.1% had other combinations. The incidence of IAA only peaked within the first year of life and declined over the following 5?years, but GADA only increased until the second year and remained relatively constant. GADA only were more common than IAA only in HLA-DR3/3 children but less common in HLA-DR4/8 children. Conclusions/interpretation Islet autoantibodies can occur very early in life and the order of appearance was related to HLA-DR-DQ genotype.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700