Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Pacific Northwest Research Institute, Seattle, WA, USA.
Diabetologia. 2020 Dec;63(12):2605-2615. doi: 10.1007/s00125-020-05276-4. Epub 2020 Oct 8.
AIMS/HYPOTHESIS: Diabetes diagnosed at <6 months of age is usually monogenic. However, 10-15% of affected infants do not have a pathogenic variant in one of the 26 known neonatal diabetes genes. We characterised infants diagnosed at <6 months of age without a pathogenic variant to assess whether polygenic type 1 diabetes could arise at early ages.
We studied 166 infants diagnosed with type 1 diabetes at <6 months of age in whom pathogenic variants in all 26 known genes had been excluded and compared them with infants with monogenic neonatal diabetes (n = 164) or children with type 1 diabetes diagnosed at 6-24 months of age (n = 152). We assessed the type 1 diabetes genetic risk score (T1D-GRS), islet autoantibodies, C-peptide and clinical features.
We found an excess of infants with high T1D-GRS: 38% (63/166) had a T1D-GRS >95th centile of healthy individuals, whereas 5% (8/166) would be expected if all were monogenic (p < 0.0001). Individuals with a high T1D-GRS had a similar rate of autoantibody positivity to that seen in individuals with type 1 diabetes diagnosed at 6-24 months of age (41% vs 58%, p = 0.2), and had markedly reduced C-peptide levels (median <3 pmol/l within 1 year of diagnosis), reflecting rapid loss of insulin secretion. These individuals also had reduced birthweights (median z score -0.89), which were lowest in those diagnosed with type 1 diabetes at <3 months of age (median z score -1.98).
CONCLUSIONS/INTERPRETATION: We provide strong evidence that type 1 diabetes can present before the age of 6 months based on individuals with this extremely early-onset diabetes subtype having the classic features of childhood type 1 diabetes: high genetic risk, autoimmunity and rapid beta cell loss. The early-onset association with reduced birthweight raises the possibility that for some individuals there was reduced insulin secretion in utero. Comprehensive genetic testing for all neonatal diabetes genes remains essential for all individuals diagnosed with diabetes at <6 months of age. Graphical abstract.
目的/假设:在 <6 个月大时被诊断出的糖尿病通常是单基因的。然而,10-15%的受影响婴儿在 26 种已知的新生儿糖尿病基因中没有致病性变异。我们对在 <6 个月大时被诊断为无致病性变异的婴儿进行了特征描述,以评估多基因 1 型糖尿病是否会在早期出现。
我们研究了 166 名在 <6 个月大时被诊断为 1 型糖尿病的婴儿,他们均排除了所有 26 种已知基因中的致病性变异,并将他们与单基因新生儿糖尿病(n=164)或在 6-24 个月大时被诊断为 1 型糖尿病的儿童(n=152)进行了比较。我们评估了 1 型糖尿病遗传风险评分(T1D-GRS)、胰岛自身抗体、C 肽和临床特征。
我们发现高 T1D-GRS 的婴儿过多:38%(63/166)的 T1D-GRS 高于健康个体的 95%分位数,而如果所有婴儿都是单基因的,则预期有 5%(8/166)(p<0.0001)。高 T1D-GRS 个体的自身抗体阳性率与在 6-24 个月大时被诊断为 1 型糖尿病的个体相似(41%比 58%,p=0.2),且 C 肽水平显著降低(<3 pmol/l,诊断后 1 年内中位数),提示胰岛素分泌迅速丧失。这些个体的出生体重也较低(中位数 z 评分-0.89),其中在 <3 个月大时被诊断为 1 型糖尿病的个体最低(中位数 z 评分-1.98)。
结论/解释:我们提供了强有力的证据,证明基于具有这种极早发糖尿病亚型的个体具有儿童 1 型糖尿病的典型特征,1 型糖尿病可在 <6 个月大时发病:高遗传风险、自身免疫和快速β细胞丢失。与出生体重降低的早期发病相关,提示对于一些个体,宫内胰岛素分泌减少。对所有新生儿糖尿病基因进行全面遗传检测仍然是所有在 <6 个月大时被诊断为糖尿病的个体的必要条件。
此译文仅供参考,具体译文以英文原文为准。