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Interindividual differences in hemoglobin glycation limit the accuracy of HbA1c as a universal glycemic marker. A study presented at the 51st Annual Conference of the International Society for Pediatric and Adolescent Diabetes (ISPAD) evaluated a CGM-independent adjusted HbA1c (aA1c) derived from the GA to HbA1c ratio as an alternative to the glucose management indicator (GMI).

The analysis included 803 individuals with T1DM with simultaneous measurement of HbA1c and GA. A GA-derived HbA1c served as the dependent variable. Multiple regression modeling incorporated age, body mass index percentile, HbA1c, GA/HbA1c ratio, and insulin dose (unit/kg). The predicted value from this model defined aA1c.

The resulting formulas were aA1c-NGSP = 0.71 × HbA1c + 1.96 × (GA/HbA1c) − 3.46 and aA1c-IFCC = 0.914 × HbA1c + 8.938 × (GA/HbA1c) − 54.3. Both estimates demonstrated strong correlation with GA-derived HbA1c (r = 0.998 for NGSP and r = 0.996 for IFCC; p < 0.0001).

These findings indicate that aA1c reliably adjusts for individual glycation variability without CGM and may support personalized assessment of glycation-related risk in T1DM.

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Key highlights
  • Adjusted hemoglobin A1c (aA1c) accounts for individual hemoglobin glycation variability without continuous glucose monitoring (CGM).
  • aA1c shows near-perfect correlation with glycated albumin (GA)-derived HbA1c in type 1 diabetes (T1DM).
  • The gap between measured HbA1c and aA1c may help identify glycation tendency and related complication risk.
Source

Mochizuki M, Amemiya S, Kobayashi K, et al. Proposal of adjusted HbA1c (aA1c) reflecting individual glycation variability using the GA/HbA1c ratio. Presented at: 51st Annual Conference of the International Society for Pediatric and Adolescent Diabetes; November 5–8, 2025; Montréal, Canada. Horm Res Paediatr. 2025;98(Suppl 4):1. doi:10.1159/000548269

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ISPAD Conference: Adjusted HbA1c Enables CGM-Independent Assessment of Glycation Variability in T1DM
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A glycated albumin–based index closely aligns with GA-derived HbA1c and may support individualized glycation risk evaluation

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