Institute of Diabetes Research, Helmholtz Munich, German Research Center for Environmental Health, Munich, Germany.
German Center for Diabetes Research (DZD), Munich, Germany.
Diabetologia. 2022 Dec;65(12):2121-2131. doi: 10.1007/s00125-022-05780-9. Epub 2022 Aug 27.
AIMS/HYPOTHESIS: The aim of this study was to develop strategies that identify children from the general population who have late-stage presymptomatic type 1 diabetes and may, therefore, benefit from immune intervention.
We tested children from Bavaria, Germany, aged 1.75-10 years, enrolled in the Fr1da public health screening programme for islet autoantibodies (n=154,462). OGTT and HbA were assessed in children with multiple islet autoantibodies for diagnosis of presymptomatic stage 1 (normoglycaemia) or stage 2 (dysglycaemia) type 1 diabetes. Cox proportional hazards and penalised logistic regression of autoantibody, genetic, metabolic and demographic information were used to develop a progression likelihood score to identify children with stage 1 type 1 diabetes who progressed to stage 3 (clinical) type 1 diabetes within 2 years.
Of 447 children with multiple islet autoantibodies, 364 (81.4%) were staged. Undiagnosed stage 3 type 1 diabetes, presymptomatic stage 2, and stage 1 type 1 diabetes were detected in 41 (0.027% of screened children), 30 (0.019%) and 293 (0.19%) children, respectively. The 2 year risk for progression to stage 3 type 1 diabetes was 48% (95% CI 34, 58) in children with stage 2 type 1 diabetes (annualised risk, 28%). HbA, islet antigen-2 autoantibody positivity and titre, and the 90 min OGTT value were predictors of progression in children with stage 1 type 1 diabetes. The derived progression likelihood score identified substages corresponding to ≤90th centile (stage 1a, n=258) and >90th centile (stage 1b, n=29; 0.019%) of stage 1 children with a 4.1% (95% CI 1.4, 6.7) and 46% (95% CI 21, 63) 2 year risk of progressing to stage 3 type 1 diabetes, respectively.
CONCLUSIONS/INTERPRETATION: Public health screening for islet autoantibodies found 0.027% of children to have undiagnosed clinical type 1 diabetes and 0.038% to have undiagnosed presymptomatic stage 2 or stage 1b type 1 diabetes, with 50% risk to develop clinical type 1 diabetes within 2 years.
目的/假设:本研究的目的是制定策略,以识别普通人群中处于晚期潜伏期 1 型糖尿病的儿童,这些儿童可能受益于免疫干预。
我们检测了来自德国巴伐利亚州的年龄在 1.75-10 岁之间的儿童,他们参加了 Fr1da 公共卫生筛查计划以检测胰岛自身抗体(n=154462)。在有多个人胰岛自身抗体的儿童中进行 OGTT 和 HbA 检测,以诊断潜伏期 1 期(血糖正常)或 2 期(血糖异常)1 型糖尿病。使用 Cox 比例风险和惩罚逻辑回归分析自身抗体、遗传、代谢和人口统计学信息,以制定进展可能性评分,以识别在 2 年内从潜伏期 1 期进展为临床 1 型糖尿病的儿童。
在 447 名有多个人胰岛自身抗体的儿童中,364 名(81.4%)被分期。在 41 名儿童(筛查儿童的 0.027%)中发现了未确诊的 3 期 1 型糖尿病、潜伏期 2 期和潜伏期 1 期 1 型糖尿病,分别为 30 名(0.019%)和 293 名(0.19%)儿童。在患有 2 型糖尿病的儿童中,2 年内进展为 3 期 1 型糖尿病的风险为 48%(95%CI 34,58)(年化风险为 28%)。HbA、胰岛抗原-2 自身抗体阳性和滴度以及 90 分钟 OGTT 值是预测儿童 1 型糖尿病进展的因素。所得到的进展可能性评分确定了与 ≤90 百分位(阶段 1a,n=258)和>90 百分位(阶段 1b,n=29;0.019%)相对应的亚期,患有阶段 1a 的儿童在 2 年内进展为 3 期 1 型糖尿病的风险分别为 4.1%(95%CI 1.4,6.7)和 46%(95%CI 21,63)。
结论/解释:对胰岛自身抗体的公共卫生筛查发现,0.027%的儿童患有未确诊的临床 1 型糖尿病,0.038%的儿童患有未确诊的潜伏期 2 期或 1b 期 1 型糖尿病,其中 50%的儿童在 2 年内会发展为临床 1 型糖尿病。