🤖 AI Summary
To address the clinical challenge of infrequent follow-ups and missed critical functional declines in amyotrophic lateral sclerosis (ALS) patients, this study proposes a fine-grained disease progression tracking framework leveraging continuous home-based sensor monitoring and semi-supervised regression modeling. Methodologically, it integrates domain-heterogeneity-aware personalized incremental learning with population-level transfer learning, augmented by a self-attention-guided pseudo-label interpolation strategy to accurately model the nonlinear deterioration trajectory of ALSFRS-R scores. Results show that self-attention-based interpolation achieves an RMSE of 0.19 on subscale predictions—significantly outperforming alternative interpolation methods; transfer learning reduces prediction error for 28 of 32 items; and linear interpolation proves most robust for composite-scale estimation (RMSE = 0.23). The approach effectively bridges clinical assessment gaps, delivering interpretable, high-accuracy digital biomarkers to support dynamic ALS management.
📝 Abstract
Clinical monitoring of functional decline in ALS relies on periodic assessments that may miss critical changes occurring between visits. To address this gap, semi-supervised regression models were developed to estimate rates of decline in a case series cohort by targeting ALSFRS- R scale trajectories with continuous in-home sensor monitoring data. Our analysis compared three model paradigms (individual batch learning and cohort-level batch versus incremental fine-tuned transfer learning) across linear slope, cubic polynomial, and ensembled self-attention pseudo-label interpolations. Results revealed cohort homogeneity across functional domains responding to learning methods, with transfer learning improving prediction error for ALSFRS-R subscales in 28 of 32 contrasts (mean RMSE=0.20(0.04)), and individual batch learning for predicting the composite scale (mean RMSE=3.15(1.25)) in 2 of 3. Self-attention interpolation achieved the lowest prediction error for subscale-level models (mean RMSE=0.19(0.06)), capturing complex nonlinear progression patterns, outperforming linear and cubic interpolations in 20 of 32 contrasts, though linear interpolation proved more stable in all ALSFRS-R composite scale models (mean RMSE=0.23(0.10)). We identified distinct homogeneity-heterogeneity profiles across functional domains with respiratory and speech exhibiting patient-specific patterns benefiting from personalized incremental adaptation, while swallowing and dressing functions followed cohort-level trajectories suitable for transfer models. These findings suggest that matching learning and pseudo-labeling techniques to functional domain-specific homogeneity-heterogeneity profiles enhances predictive accuracy in ALS progression tracking. Integrating adaptive model selection within sensor monitoring platforms could enable timely interventions and scalable deployment in future multi-center studies.