GlucoFM: A Dual-Stream Foundation Model for Continuous Glucose Monitoring
Zechen Li ⋅ Keerthana Natarajan ⋅ Weizhi Zhang ⋅ Simon Lee ⋅ Yuwei Zhang ⋅ Max Xu ⋅ Menglian Zhou ⋅ Zeinab Esmaeilpour ⋅ Flora Salim ⋅ Mark Malhotra ⋅ Lindsey Sunden ⋅ Shwetak Patel ⋅ Yuzhe Yang ⋅ Ahmed Metwally
Abstract
Continuous glucose monitoring (CGM) provides a dense window into metabolic physiology, yet existing generic time-series and CGM-specific foundation models typically learn from entangled glucose sequences without explicitly capturing the temporal structure of glycemic dynamics. We present GlucoFM, a lightweight CGM foundation model that aligns irregular recordings to a 24-hour chronological grid, preserves observation masks, and decomposes glucose dynamics into slow physiological state and transient event streams, capturing low-frequency glycemic baselines and short-term deviations that may reflect acute physiological responses or sensor artifacts. GlucoFM is pretrained on 109,066 hours of unlabeled CGM recordings from 477 subjects with two complementary objectives: masked contextual latent prediction over fused daily representations and temporal dynamics prediction over state and event streams. Across four diverse cohorts and seven clinical prediction tasks, GlucoFM achieves the strongest frozen linear-probing performance among evaluated baselines, improving average PR-AUC by 4.1 points over the best CGM-specific foundation model. Its gains are most pronounced on core metabolic outcomes, leading PR-AUC on all diabetes-risk and $\beta$-cell dysfunction tasks and on 3 of 4 insulin-resistance tasks. GlucoFM also achieves the best overall cross-dataset transfer performance among evaluated methods and strong few-shot adaptation, highlighting physiology-aware decomposition as an effective inductive bias for transferable CGM representation learning.
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