HbA1c作为血清转化的TEDDY儿童中额外胰岛自身抗体和1型糖尿病的时间预测生物标志物。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2022-12-01 Epub Date: 2022-09-21 DOI:10.1111/pedi.13413
Falastin Salami, Roy Tamura, Lu You, Åke Lernmark, Helena Elding Larsson, Markus Lundgren, Jeffrey Krischer, Anette-Gabriele Ziegler, Jorma Toppari, Riitta Veijola, Marian Rewers, Michael J Haller, William Hagopian, Beena Akolkar, Carina Törn
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引用次数: 0

摘要

目的:糖化血红蛋白(HbA1c)水平的升高与1型糖尿病的发作有关,而1型糖尿病发作之前会出现一到几种针对胰岛β细胞自身抗原的自身抗体;胰岛素(IA)、谷氨酸脱羧酶(GAD)、胰岛抗原-2(IA-2)和锌转运蛋白8(ZnT8)。诊断为1型糖尿病的风险随着自身抗体数量的增加而增加。需要预测第二种或随后的自身抗体和1型糖尿病发展的生物标志物来预测疾病阶段并改进二级预防试验。本研究旨在调查参与青年糖尿病环境决定因素(TEDDY)研究的健康儿童的HbA1c是否可能预测从第一个自身抗体或1型糖尿病发展到随后的自身抗体或2型糖尿病。研究设计和方法:设计了一个联合模型来评估健康儿童从出生到15岁的纵向HbA1c水平与第一种(胰岛素或GAD自身抗体)到第二种、第二种到第三种、第三种到第四种自身抗体或1型糖尿病的发展之间的关系 年龄。结果:发现HbA1c水平升高与1型糖尿病的高风险相关(HR 1.82,95%CI[1.57-2.10],p 结论:总之,HbA1c升高是1型糖尿病发病的可靠时间预测指标。HbA1c从第一种自身抗体到第三种自身抗体的增加率增加以及HbA1c的降低预测了IA-2A的发展,这是新的发现,证明了HbA1c与自身抗体的出现之间的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HbA1c as a time predictive biomarker for an additional islet autoantibody and type 1 diabetes in seroconverted TEDDY children.

HbA1c as a time predictive biomarker for an additional islet autoantibody and type 1 diabetes in seroconverted TEDDY children.

Objective: Increased level of glycated hemoglobin (HbA1c) is associated with type 1 diabetes onset that in turn is preceded by one to several autoantibodies against the pancreatic islet beta cell autoantigens; insulin (IA), glutamic acid decarboxylase (GAD), islet antigen-2 (IA-2) and zinc transporter 8 (ZnT8). The risk for type 1 diabetes diagnosis increases by autoantibody number. Biomarkers predicting the development of a second or a subsequent autoantibody and type 1 diabetes are needed to predict disease stages and improve secondary prevention trials. This study aimed to investigate whether HbA1c possibly predicts the progression from first to a subsequent autoantibody or type 1 diabetes in healthy children participating in the Environmental Determinants of Diabetes in the Young (TEDDY) study.

Research design and methods: A joint model was designed to assess the association of longitudinal HbA1c levels with the development of first (insulin or GAD autoantibodies) to a second, second to third, third to fourth autoantibody or type 1 diabetes in healthy children prospectively followed from birth until 15 years of age.

Results: It was found that increased levels of HbA1c were associated with a higher risk of type 1 diabetes (HR 1.82, 95% CI [1.57-2.10], p < 0.001) regardless of first appearing autoantibody, autoantibody number or type. A decrease in HbA1c levels was associated with the development of IA-2A as a second autoantibody following GADA (HR 0.85, 95% CI [0.75, 0.97], p = 0.017) and a fourth autoantibody following GADA, IAA and ZnT8A (HR 0.90, 95% CI [0.82, 0.99], p = 0.036). HbA1c trajectory analyses showed a significant increase of HbA1c over time (p < 0.001) and that the increase is more rapid as the number of autoantibodies increased from one to three (p < 0.001).

Conclusion: In conclusion, increased HbA1c is a reliable time predictive marker for type 1 diabetes onset. The increased rate of increase of HbA1c from first to third autoantibody and the decrease in HbA1c predicting the development of IA-2A are novel findings proving the link between HbA1c and the appearance of autoantibodies.

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