重新审视参加 TrialNet 口服胰岛素预防试验 (TN07) 的 HLA DR4-DQ8 参与者口服胰岛素延迟 1 型糖尿病 3 期的情况。

Diabetes care Pub Date : 2024-09-01 DOI:10.2337/dc24-0573
Lue Ping Zhao, George K Papadopoulos, Jay S Skyler, Hemang M Parikh, William W Kwok, George P Bondinas, Antonis K Moustakas, Ruihan Wang, Chul-Woo Pyo, Wyatt C Nelson, Daniel E Geraghty, Åke Lernmark
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引用次数: 0

摘要

目的探讨口服胰岛素是否能延缓携带HLA DR4-DQ8和/或IA-2自身抗体(IA-2As)水平升高的1型糖尿病(T1D)1/2期患者的3期发病:采用新一代靶向测序技术对TrialNet口服胰岛素预防试验(TN07)的546名参与者的8个HLA II类基因(DQA1、DQB1、DRB1、DRB3、DRB4、DRB5、DPA1和DPB1)进行基因分型。在分配治疗前,已测定了胰岛素(IAA)、GAD65(GADA)和 IA-2A 自身抗体的基线水平。TN07中的临床和人口统计学协变量被用于这项事后分析,通过Cox回归模型来量化口服胰岛素的预防效果:结果:口服胰岛素降低了IA-2A水平升高者的T1D发病频率(HR 0.62; P = 0.012),但对IA-2A水平较低者没有预防作用(HR 1.03; P = 0.91)。高IA-2A水平与HLA DR4-DQ8单倍型呈正相关(OR 1.63;P = 6.37 × 10-6),与含HLA DR7的DRB1*07:01-DRB4*01:01-DQA1*02:01-DQB1*02:02扩展单倍型呈负相关(OR 0.49;P = 0.037)。在DR4-DQ8携带者中,口服胰岛素可延缓T1D向3期发展(HR 0.59;P = 0.027),尤其是当参与者的IA-2A水平较高时(HR 0.50;P = 0.028):这些结果表明,存在一种以 HLA DR4-DQ8 和/或 IA-2A 水平升高为特征的 T1D 终末型;对于具有这种终末型的 1/2 期患者,口服胰岛素可延缓 T1D 的临床发病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral Insulin Delay of Stage 3 Type 1 Diabetes Revisited in HLA DR4-DQ8 Participants in the TrialNet Oral Insulin Prevention Trial (TN07).

Objective: To explore if oral insulin could delay onset of stage 3 type 1 diabetes (T1D) among patients with stage 1/2 who carry HLA DR4-DQ8 and/or have elevated levels of IA-2 autoantibodies (IA-2As).

Research and methods: Next-generation targeted sequencing technology was used to genotype eight HLA class II genes (DQA1, DQB1, DRB1, DRB3, DRB4, DRB5, DPA1, and DPB1) in 546 participants in the TrialNet oral insulin preventative trial (TN07). Baseline levels of autoantibodies against insulin (IAA), GAD65 (GADA), and IA-2A were determined prior to treatment assignment. Available clinical and demographic covariables from TN07 were used in this post hoc analysis with the Cox regression model to quantify the preventive efficacy of oral insulin.

Results: Oral insulin reduced the frequency of T1D onset among participants with elevated IA-2A levels (HR 0.62; P = 0.012) but had no preventive effect among those with low IA-2A levels (HR 1.03; P = 0.91). High IA-2A levels were positively associated with the HLA DR4-DQ8 haplotype (OR 1.63; P = 6.37 × 10-6) and negatively associated with the HLA DR7-containing DRB1*07:01-DRB4*01:01-DQA1*02:01-DQB1*02:02 extended haplotype (OR 0.49; P = 0.037). Among DR4-DQ8 carriers, oral insulin delayed the progression toward stage 3 T1D onset (HR 0.59; P = 0.027), especially if participants also had high IA-2A level (HR 0.50; P = 0.028).

Conclusions: These results suggest the presence of a T1D endotype characterized by HLA DR4-DQ8 and/or elevated IA-2A levels; for those patients with stage 1/2 disease with such an endotype, oral insulin delays the clinical T1D onset.

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