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A rising HbA1c does not carry the same predictive weight for type 1 diabetes in adults as it does in children. These findings were presented at the European Association for the Study of Diabetes Conference 2025. The study evaluated 6,085 islet-autoantibody-positive relatives, including 1,618 adults, tracking progression to clinical type 1 diabetes over 12 months.

Adults who progressed showed higher baseline HbA1c than children (36 mmol/mol versus 34 mmol/mol, p<0.001). Although higher HbA1c increased progression risk in both groups, adults needed elevated levels to reach comparable 12-month risk. For example, children with HbA1c at 39 mmol/mol faced a 39% progression risk, whereas adults required 45 mmol/mol to reach a similar 39% risk (p<0.001).

These results indicate that age-adjusted HbA1c thresholds may improve risk stratification and guide monitoring in adults at risk of type 1 diabetes. They also emphasize the need to consider age-related glycemic changes and potential type 2 diabetes overlap when interpreting HbA1c in at-risk adults.
 

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Key highlights
  • Adults had higher HbA1c than children at the time of autoantibody detection.
  • Children with HbA1c of 39 mmol/mol had the same 12-month progression risk as adults with 45 mmol/mol.
  • Age-adjusted HbA1c thresholds may improve risk prediction and management in autoantibody-positive individuals.
Source

Templeman E, Thomas N, Wherrett D, et al. Higher HbA$_{1c}$ thresholds are needed to predict type 1 diabetes progression in islet autoantibody-positive adults compared to children. Presented at: 61st EASD Annual Meeting of the European Association for the Study of Diabetes; September 15-19, 2025; Vienna, Austria. Diabetologia. 2025:22. https://link.springer.com/article/10.1007/s00125-025-06497-1#Sec4 

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Age Influences HbA1c Thresholds for Predicting Type 1 Diabetes in Autoantibody-Positive Individuals
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Adults with islet-autoantibody positivity require higher HbA1c thresholds than children to reach equivalent 12-month risk of progression to type 1 diabetes.

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