Predicting Type 1 Diabetes Using Biomarkers

被引:124
作者
Bonifacio, Ezio [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Tech Univ Dresden, DFG Ctr Regenerat Therapies Dresden, D-01062 Dresden, Germany
[2] Tech Univ Dresden, Fac Med, D-01062 Dresden, Germany
[3] Tech Univ Dresden, Paul Langerhans Inst Dresden, Helmholtz Ctr Munich, Univ Clin Carl Gustav Carus, D-01062 Dresden, Germany
[4] German Ctr Diabet Res DZD eV, Neuherberg, Germany
[5] Forschergrp Diabet eV, Neuherberg, Germany
[6] Helmholtz Zentrum Munchen, Inst Diabet & Obes, Neuherberg, Germany
关键词
GLUTAMIC-ACID DECARBOXYLASE; TRIAL-TYPE; T-CELLS; ISLET AUTOIMMUNITY; CESAREAN-SECTION; INCREASED RISK; AMINO-ACID; CHILDREN; AUTOANTIBODIES; INSULIN;
D O I
10.2337/dc15-0101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Clinical type 1 diabetes is preceded by an asymptomatic phase that can be identified by serum islet autoantibodies. This perspective proposes that there is now sufficient evidence to allow a broader use of islet autoantibodies as biomarkers to diagnose type 1 diabetes that is already at an asymptomatic stage, so that attempts to prevent clinical hyperglycemia become a feature of disease management. Prediction would first, therefore, shift toward the use of genetic and other biomarkers to determine the likelihood that islet autoimmunity will develop in an infant, and second, toward metabolic assessment to stage and biomarkers to determine the rate of progression to hyperglycemia in children in whom islet autoimmunity is diagnosed. A case is presented for future comprehensive risk assessment that commences at birth and includes attempts to predict, stage, and prevent initiation and progression of the disease process at multiple stages. The biomarkers required achieving this level of sophistication and dissemination are discussed.
引用
收藏
页码:989 / 996
页数:8
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