首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Association of adiponectin interleukin (IL)-1ra inducible protein 10 IL-6 and number of islet autoantibodies with progression patterns of type 1 diabetes the first year after diagnosis
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Association of adiponectin interleukin (IL)-1ra inducible protein 10 IL-6 and number of islet autoantibodies with progression patterns of type 1 diabetes the first year after diagnosis

机译:诊断后第一年脂联素白介素(IL)-1ra可诱导蛋白10IL-6和胰岛自身抗体数量与1型糖尿病进展模式的关系

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摘要

The progression of type 1 diabetes after diagnosis is poorly understood. Our aim was to assess the relation of disease progression of juvenile-onset type 1 diabetes, determined by preserved beta cell function the first year after diagnosis, with systemic cytokine concentrations and number of autoantibodies. Juvenile patients (n = 227) had a meal-stimulated C-peptide test 1 and 6 months after diagnosis. On the basis of the C-peptide course for the duration of 1–6 months, four progression groups were defined: patients with persistently low beta cell function (‘stable-low’), rapid progressers, slow progressers and remitters. Serum concentrations of adiponectin, interleukin (IL)-1ra, inducible protein 10 (IP-10), IL-6 and glutamic acid decarboxylase (GAD), IA-2A and islet-cell antibodies (ICA) were measured at 1, 6 and 12 months. We found that adiponectin concentrations at 1 month predicted disease progression at 6 months (P = 0·04). Patients with low adiponectin had a higher probability of becoming remitters than rapid progressers, odds ratio 3·1 (1·3–7·6). At 6 and 12 months, adiponectin differed significantly between the groups, with highest concentrations among stable-low and rapid progressers patients (P = 0·03 and P = 0·006). IL-1ra, IP-10 and IL-6 did not differ between the groups at any time-point. The number of autoantibodies differed significantly between the groups at 1 month (P = 0·04), where rapid progressers had the largest number. There was no difference between the groups in human leucocyte antigen-associated risk. We define progression patterns distinguishing patients diagnosed with low beta cell function from those with rapid decline, slow decline or actual increase in beta cell function, pointing to different mechanisms of disease progression. We find that adiponectin concentration at 1 month predicts, and at 6 and 12 months associates with, distinct progression patterns.
机译:诊断后对1型糖尿病的进展了解甚少。我们的目的是评估在诊断后第一年由保留的β细胞功能确定的少年1型糖尿病疾病进展与全身细胞因子浓度和自身抗体数量之间的关系。少年患者(n = 227)在诊断后1和6个月接受了膳食刺激的C肽测试。根据持续1到6个月的C肽疗程,定义了四个进展组:β细胞功能持续低下(“稳定-低”),进展迅速,进展缓慢和缓解的患者。分别在1,6和6分别测量血清脂联素,白介素(IL)-1ra,诱导蛋白10(IP-10),IL-6和谷氨酸脱羧酶(GAD),IA-2A和胰岛细胞抗体(ICA)的浓度。 12个月。我们发现,脂联素在1个月的浓度可以预测6个月时的疾病进展(P = 0·04)。脂联素低的患者比快速进展的患者更有可能成为缓解者,优势比为3·1(1·3-7·6)。在第6个月和第12个月时,两组之间的脂联素差异显着,在进展缓慢和进展较快的患者中浓度最高(P = 0·03和P = 0·006)。 IL-1ra,IP-10和IL-6在任何时间点之间均无差异。两组之间在1个月时自身抗体的数量差异显着(P = 0·04),其中快速进展者的数量最大。人类白细胞抗原相关风险的两组之间没有差异。我们定义了进展模式,将诊断为低β细胞功能的患者与快速下降,缓慢下降或β细胞功能实际增加的患者区分开来,指出了疾病进展的不同机制。我们发现脂联素浓度在1个月时可预测,在6个月和12个月时与不同的进展模式相关。

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