Program outcomes & validation

We continually evaluate our pipelines across imaging, diffusion, wearables, and clinician-facing deployment. This page summarizes quantitative readouts, cohort coverage, and the evidence trail that underpins Progressive AI.

Latent clustering outcomes

Cohort coverage

PPMI integration

Baseline-first harmonization of 4,775 patients across 388 features covering MDS-UPDRS, UPSIT, REM sleep behavior disorder, biospecimens, and genetics.

LRRK2 Consortium

2,958 participants inform genetic risk analyses and mechanism inference, highlighting the 1.89× elevated risk among G2019S carriers.

Wearable cohort

84 idiopathic Parkinson’s participants with synchronized CSFSAA labels, IMU-derived gait metrics, and comprehensive cognitive batteries.

Clinician pilots

ActionIntel and Free Motion prototypes evaluated with neurologists in weekly design reviews to pressure-test usability and interpretability.

Imaging classification performance

Automated SegFormer-based segmentation combined with DaT-SPECT features enables high-fidelity CSFSAA discrimination. Results below reflect cross-validated models trained on region-wise volumetrics and SBR-derived statistics.

MethodF1-scoreROC-AUC
Nearest Neighbors0.9600.900
Random Forest0.9500.858
Neural Network0.9500.843
Gaussian Process0.9440.837
Naive Bayes0.9350.907

Imaging alone yields AUC 0.70 ± 0.08; combining imaging with clinical and biologic features raises AUC to 0.93 ± 0.04.

Wearable-driven CSFSAA prediction

Histogram Gradient Boosting models trained on PPMI gait assessments quantify the contribution of each modality toward predicting CSFSAA status.

Feature GroupMean AUC ± SD
Gait & Arm Swing0.58 ± 0.16
Demographics0.81 ± 0.14
Clinical0.92 ± 0.07
All Modalities0.93 ± 0.07

SHAP analysis surfaces HVLT retention, Epworth Sleepiness Scale, and right-arm jerk amplitude as leading contributors.

Mechanism-inference highlights

  • Five motor phenotypes emerge from unsupervised clustering (Silhouette = 0.535), capturing differential striatal vulnerability.
  • 50.2% hyposmia prevalence and 37.5% REM sleep behavior disorder prevalence confirm early cholinergic and brainstem involvement.
  • Objective gait measures correlate with UPDRS-III severity (Spearman r = -0.301, p = 7.9×10⁻⁵, n = 166), grounding digital phenotyping in mechanism hypotheses.

Looking ahead

We are expanding evaluation to prospective, multi-site cohorts with emphasis on drift audits, fairness reporting, and regulatory documentation. Outcomes will be updated quarterly as we release new validation notes and open-source assets.