Abstract 23: Predicting Glycemic Responses to Dietary Intake Among Non-diabetic Adults: an Evaluation of Modeling Approaches

S Suheng Yao (Boston University, Boston, Massachusetts, United States) V Vedika Srivastava (Boston University, Boston, Massachusetts, United States) B Bahar Bakhshi (Boston University School of Medicine, Dorchester, Massachusetts, United States) N Naznin Sultana (Boston University, Boston, Massachusetts, United States) H Honghuang Lin (Framingham Heart Study, National Heart, Lung, and Blood Institute, National Institutes of Health and Boston University, Framingham, MA, USA.) M Michael Cheney (Boston Medical Center, Jamaica Plain, Massachusetts, United States) N Nicola McKeown N Nicole Spartano (Boston University School of Medicine, Dorchester, Massachusetts, United States) M Maura Walker (Boston University School of Medicine, Dorchester, Massachusetts, United States) H Huimin Cheng

Abstract

Objective: To determine the features and models that improve the prediction of postprandial glucose response (PPGR) using continuous glucose monitoring (CGM) data. Method: We analyzed data from 860 Framingham Heart Study Third-Generation cohort participants without diabetes (with average age 60 years old, 59.8% women) who attended their fourth exam (2022-2025), wore a Dexcom G6 Pro CGM, and completed valid Automated Self-Administered 24 dietary recalls. A total of 3,402 valid meals, without eating occasions 2 hours before or after, were matched to CGM-derived PPGRs within a 2-hour postprandial window. We applied multiple predictive models, including Lasso, Linear Mixed Effect Model, Mixed Effect Random Forest (MERF), GPBoost, Generalized Additive Mixed Models (GAMM) and Supervised Autoencoder, to relate meal composition to two PPGR outcomes: incremental area under the curve (iAUC 120 , subtracting negative AUC from positive AUC) and relative glucose excursion. The baseline model included sex, age, BMI, HbA1c, and venous blood glucose, whereas fully adjusted models incorporated additional covariates including with CGM features, meal composition and context (for the specific meal and prior meals). Results: In fully adjusted models, the addition of CGM-derived variables (e.g. mean amplitude of glycemic excursions [MAGE], mean glucose over the 30 minutes prior to the meal [30mPreMeal glucose], and the change between 30mPreMeal glucose and glucose at meal time) and detailed dietary information (e.g., net carbohydrates, sugar and protein) significantly improved prediction over models using only demographic and clinical factors by at least 30% increase in R 2 . Based on the comparison of models’ results using Wilcoxon signed-rank test, we observed the highest model R 2 and strongest Pearson’s r (observed vs. predicted) with GPBoost models (iAUC 120 R 2 =57.91%, r=0.76; relative peak glucose excursion R 2 =47.57%, r=0.69). The Figure shows the top dietary predictors identified through feature importance analyses, which may inform actionable strategies to modulate glycemic response. Conclusion: Our integrative approach suggests that combining CGM-derived dynamics and dietary composition substantially enhances prediction of PPGR in real-world conditions. Optimizing such models could advance the use of CGM in the prevention and management of type 2 diabetes and related cardiometabolic disorders.

Article Details

Journal Circulation
Volume / Issue Vol. 153, Issue Suppl_1
Published March 24, 2026
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (10)

S

Suheng Yao

Boston University, Boston, Massachusetts, United States

V

Vedika Srivastava

Boston University, Boston, Massachusetts, United States

B

Bahar Bakhshi

Boston University School of Medicine, Dorchester, Massachusetts, United States

N

Naznin Sultana

Boston University, Boston, Massachusetts, United States

H

Honghuang Lin

Framingham Heart Study, National Heart, Lung, and Blood Institute, National Institutes of Health and Boston University, Framingham, MA, USA.

M

Michael Cheney

Boston Medical Center, Jamaica Plain, Massachusetts, United States

N

Nicola McKeown

N

Nicole Spartano

Boston University School of Medicine, Dorchester, Massachusetts, United States

M

Maura Walker

Boston University School of Medicine, Dorchester, Massachusetts, United States

H

Huimin Cheng