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Abhimanyu Kumbara

Publications and source records attributed to Abhimanyu Kumbara.

2 recordsLinked to original sources

FairGlucose: A CGM Fairness Benchmark Reveals Subgroup Disparities Hidden in Population-Level Validation

As CGM-based AI tools approach clinical deployment, whether their accuracy is equitable across patient demographics remains insufficiently tested. To enable this evaluation, we constructed FairGlucose, a 300-patient CGM cohort balanced across 12 demographic strata (age x gender x type 1/type 2 diabetes), with 132,480 forecasting samples and 3,945 unique behavioral events (meals, exercise, medication) logged by 81 patients. Benchmarking 33 models across four families on 2-hour glucose forecasting, we find that population-level external validation can conceal substantial subgroup disparities. Aggregate out-of-distribution metrics appear stable (approximately 1.0), yet subgroup-level ratios range from 0.8 to 1.4, with T1D patients showing 6 mg/dL higher prediction error than T2D (p < 0.001). This disparity persists across all 33 models, suggesting a property of the prediction task rather than any single architecture. Further analysis shows that subgroup performance gaps align with the proportion of clinically hard cases, and that input-length sensitivity varies across demographics, motivating personalized configurations. Frontier LLMs underperform specialized neural models by 1-6 mg/dL; behavioral events contribute negligibly (approximately 0.1 mg/dL) even under oracle event access. These findings establish that population-level validation alone is insufficient for equity assessment of digital health AI, motivating subgroup-disaggregated reporting as a default standard.

cs.CY↗

A Large Sensor Foundation Model Pretrained on Continuous Glucose Monitor Data for Diabetes Management

Continuous glucose monitoring (CGM) combined with AI offers new opportunities for proactive diabetes management through real-time glucose forecasting. However, most existing models are task-specific and lack generalization across patient populations. Inspired by the autoregressive paradigm of large language models, we introduce CGM-LSM, a Transformer decoder-based Large Sensor Model (LSM) pretrained on 1.6 million CGM records from patients with different diabetes types, ages, and genders. We model patients as sequences of glucose time steps to learn latent knowledge embedded in CGM data and apply it to the prediction of glucose readings for a 2-hour horizon. Compared with prior methods, CGM-LSM significantly improves prediction accuracy and robustness: a 48.51% reduction in root mean square error in one-hour horizon forecasting and consistent zero-shot prediction performance across held-out patient groups. We analyze model performance variations across patient subgroups and prediction scenarios and outline key opportunities and challenges for advancing CGM foundation models.

q-bio.QM↗