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Prediction and prevention of type 1 diabetes: update on success of prediction and struggles at prevention

机译:1型糖尿病的预测和预防:预测成功的最新动态和预防方面的努力

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Type 1 diabetes mellitus (T1DM) is the archetypal example of a T cell-mediated autoimmune disease characterized by selective destruction of pancreatic cells. The pathogenic equation for T1DM presents a complex interrelation of genetic and environmental factors, most of which have yet to be identified. On the basis of observed familial aggregation of T1DM, it is certain that there is a decided heritable genetic susceptibility for developing T1DM. The well-known association of T1DM with certain human histocompatibility leukocyte antigen (HLA) alleles of the major histocompatibility complex (MHC) was a major step toward understanding the role of inheritance in T1DM. Type 1 diabetes is a polygenic disease with a small number of genes having large effects (e.g., HLA) and a large number of genes having small effects. Risk of T1DM progression is conferred by specific HLA DR/DQ alleles [e.g., DRB1*03-DQB1*0201 (DR3/DQ2) or DRB1*04-DQB1*0302 (DR4/DQ8)]. In addition, the HLA allele DQB1*0602 is associated with dominant protection from T1DM in multiple populations. A concordance rate lower than 100% between monozygotic twins indicates a potential involvement of environmental factors on disease development. The detection of at least two islet autoantibodies in the blood is virtually pre-diagnostic for T1DM. The majority of children who carry these biomarkers, regardless of whether they have an a priori family history of the disease, will develop insulin-requiring diabetes. Facilitating pre-diagnosis is the timing of seroconversion which is most pronounced in the first 2 yr of life. Unfortunately the significant progress in improving prediction of T1DM has not yet been paralleled by safe and efficacious intervention strategies aimed at preventing the disease. Herein we summarize the chequered history of prediction and prevention of T1DM, describing successes and failures alike, and thereafter examine future trends in the exciting, partially explored field of T1DM prevention.
机译:1型糖尿病(T1DM)是T细胞介导的自身免疫性疾病的典型例子,其特征是胰腺细胞的选择性破坏。 T1DM的致病方程表示遗传因素和环境因素之间存在复杂的相互关系,其中大多数尚未确定。根据观察到的T1DM家族聚集,可以肯定的是,对于T1DM的发展存在确定的遗传遗传易感性。 T1DM与主要组织相容性复合体(MHC)的某些人类组织相容性白细胞抗原(HLA)等位基因的众所周知的关联是迈向了解遗传在T1DM中的作用的重要一步。 1型糖尿病是一种多基因疾病,其具有少数具有较大影响的基因(例如,HLA)和大量具有较小影响的基因。特定的HLA DR / DQ等位基因[例如,DRB1 * 03-DQB1 * 0201(DR3 / DQ2)或DRB1 * 04-DQB1 * 0302(DR4 / DQ8)]赋予T1DM进展的风险。此外,HLA等位基因DQB1 * 0602与多个人群中T1DM的显性保护相关。单卵双胞胎之间的一致率低于100%,表明环境因素可能参与疾病发展。血液中至少两个胰岛自身抗体的检测实际上是T1DM的预诊断。携带这些生物标记物的大多数儿童,无论他们是否具有疾病的先验家族史,都会患上需要胰岛素的糖尿病。血清转化的时机很容易进行预诊断,这在生命的头两年中最为明显。不幸的是,改善T1DM预测的重大进展尚未与旨在预防该疾病的安全有效的干预策略相提并论。在这里,我们总结了T1DM预测和预防的方格历史,描述了成功与失败的相似之处,然后在T1DM预防的令人兴奋的,部分探索的领域中研究了未来的趋势。

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