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Updated: Oct 9, 2026

Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT)
Published on: January 7, 2018
Fasting proinsulin as a predictor of future glucose tolerance deterioration in Japanese adults
Nobuhiro Kajihara1,2, Tomonori Tsuyama1,3, Kazuki Fukuda2
1Center for Metabolic Regulation of Healthy Aging (CMHA), Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Aims/Introduction:
Proinsulin is associated with β-cell stress and has been linked to subsequent deterioration in glucose metabolism in Western populations, but its predictive value in Asian populations remains unclear. We investigated whether proinsulin is associated with future glucose tolerance deterioration in community-dwelling Japanese adults.
Materials And Methods:
Of 160 individuals who underwent a 75-g oral glucose tolerance test (OGTT) in 2020-2021, 88 completed a follow-up OGTT in 2024-2025. Fasting proinsulin concentrations were measured using stored baseline serum samples from 84 participants. Associations with glucose tolerance deterioration were examined using Firth's penalized logistic regression, and discriminatory performance was evaluated using receiver operating characteristic (ROC) analysis.
Results:
During the 4-year follow-up, glucose tolerance deteriorated in 16 participants. Fasting proinsulin concentrations were higher in progressors than in non-progressors (5.8 vs. 3.6 pmol/L; P = 0.009). Each 1-standard deviation increase in fasting proinsulin was associated with glucose tolerance deterioration (odds ratio 2.11, 95% confidence interval 1.31-3.72; P = 0.002). In exploratory ROC analysis, the area under the curve was 0.710, and a cutoff of 5.1 pmol/L yielded 68.8% sensitivity and 83.8% specificity. Participants with elevated fasting proinsulin (≥ 5.1 pmol/L) and a low disposition index (≤ 1.27) had the highest odds of deterioration.
Conclusions:
Fasting proinsulin may help identify Japanese adults at risk of future glucose tolerance deterioration, particularly when combined with indices of β-cell compensation.
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