Suppr超能文献

糖化血红蛋白 (HbA1c) 作为时间预测生物标志物,可预测 TEDDY 儿童血清转换后是否会出现额外的胰岛自身抗体和 1 型糖尿病。

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

机构信息

Department of Clinical Sciences, Lund University/CRC, Skåne University Hospital, Malmö, Sweden.

Health Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.

出版信息

Pediatr Diabetes. 2022 Dec;23(8):1586-1593. doi: 10.1111/pedi.13413. Epub 2022 Sep 21.

Abstract

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.

摘要

目的

糖化血红蛋白(HbA1c)水平升高与 1 型糖尿病发病有关,而 1 型糖尿病发病前会先出现一种或多种针对胰岛β细胞自身抗原的自身抗体,包括胰岛素(IA)、谷氨酸脱羧酶(GAD)、胰岛抗原-2(IA-2)和锌转运蛋白 8(ZnT8)。自身抗体数量的增加会增加 1 型糖尿病的诊断风险。需要有预测第二或后续自身抗体和 1 型糖尿病发展的生物标志物,以预测疾病阶段并改善二级预防试验。本研究旨在探讨 HbA1c 是否可能预测参加环境决定儿童糖尿病研究(TEDDY)的健康儿童从首次自身抗体到后续自身抗体或 1 型糖尿病的进展。

研究设计和方法

设计了一个联合模型,以评估 HbA1c 水平的纵向变化与健康儿童从出生到 15 岁期间首次(胰岛素或 GAD 自身抗体)到第二次、第二次到第三次、第三次到第四次自身抗体或 1 型糖尿病发展的相关性。

结果

研究发现,HbA1c 水平升高与 1 型糖尿病的风险增加相关(HR 1.82,95%CI [1.57-2.10],p<0.001),无论首次出现的自身抗体、自身抗体数量或类型如何。HbA1c 水平下降与 GADA 后出现 IA-2A 作为第二次自身抗体(HR 0.85,95%CI [0.75, 0.97],p=0.017)和 GADA、IAA 和 ZnT8A 后出现第四次自身抗体相关(HR 0.90,95%CI [0.82, 0.99],p=0.036)。HbA1c 轨迹分析显示 HbA1c 随时间显著升高(p<0.001),并且随着自身抗体数量从一个增加到三个,增加速度更快(p<0.001)。

结论

总之,HbA1c 升高是 1 型糖尿病发病的可靠时间预测标志物。从首次自身抗体到第三次自身抗体时 HbA1c 升高率的增加以及 HbA1c 下降预测 IA-2A 的出现,这些都是新的发现,证明了 HbA1c 与自身抗体出现之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d1/10087916/292d81b45293/PEDI-23-1586-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验