Key result
Elevated 1-hour glucose linked to ~52% lower β-cell function in HbA1c-defined prediabetes.
Why the study?
Does 1-hour postload plasma glucose identify distinct metabolic subgroups with differing β-cell function among adults with HbA1c-defined prediabetes and normal fasting/2-hour glucose?
Cross-Sectional (n=8,537)
No
Does 1-hour postload plasma glucose identify distinct metabolic subgroups with differing β-cell function among adults with HbA1c-defined prediabetes and normal fasting/2-hour glucose?
Effect estimate: β = -0.223 (95% CI -0.227 to -0.219)
Absolute Event Rate: 40.47% vs 85.19%
p-value: p=<0.001
A 1-hour postload glucose ≥8.6 mmol/L effectively identifies individuals with hidden β-cell dysfunction among those with prediabetes diagnosed solely by HbA1c, highlighting the utility of 1-hour glucose for risk stratification.
Background This study evaluated whether 1-hour postload glucose (1-h PG) identifies distinct metabolic subgroups with differing OGTT-derived β-cell function indices among Chinese adults with HbA1c-defined prediabetes and normal fasting and 2-hour glucose. Methods This cross-sectional study included 8,537 Chinese adults undergoing 75-g OGTT and HbA1c testing. Participants were stratified into four glycemic phenotypes based on HbA1c (≥5.7%) and OGTT criteria. Within the HbA1c+/OGTT− subgroup (n=922), individuals were further classified by 1-h PG (cutoff 8.6 mmol/L). β-cell function was assessed using the disposition index (DI). Linear mixed-effects models analyzed glucose and insulin dynamics. Results Among 3,800 individuals with prediabetes, 24.3% exhibited isolated HbA1c elevation (HbA1c+/OGTT−). Within this discordant subgroup, 51.8% had elevated 1-h PG (≥8.6 mmol/L). The 1-h PG+ subgroup demonstrated lower β-cell function (DI = 40.47), delayed glucose peaks (60 min), impaired early-phase insulin secretion, and greater overall glycaemic exposure, whereas the 1-h PG− subgroup exhibited preserved or enhanced β-cell function (DI = 85.19 vs. 75.56 in NGT, P < 0.001). Multivariable linear regression analysis demonstrated that 1-h PG remained significantly associated with β-cell function after adjustment for age, sex, and HbA1c. Conclusions Among individuals with HbA1c-defined prediabetes and normal Fasting and 2-Hour Glucose, 1-hour plasma glucose identifies subgroups with differing metabolic profiles and β-cell function. These findings highlight substantial metabolic heterogeneity within this population. However, given the cross-sectional design of the study, longitudinal investigations are required to determine whether these metabolic differences translate into differences in future diabetes risk and clinical outcomes. Trial registration Not applicable.
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Ouyang et al. (2026) conducted a cross-sectional in HbA1c-defined prediabetes and normal fasting and 2-hour glucose (n=8,537). 1-hour plasma glucose ≥8.6 mmol/L vs. 1-hour plasma glucose <8.6 mmol/L was evaluated on β-cell function (disposition index) (β = -0.223, 95% CI -0.227 to -0.219, p=<0.001). Elevated 1-hour plasma glucose (≥8.6 mmol/L) identified significantly lower β-cell function (disposition index 40.47 vs 85.19, p<0.001) in adults with HbA1c-defined prediabetes but normal OGTT.
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