AI-Powered Stratification in Personalized Medicine

We Don't Predict
Neuropathy.
We Decode It.

NERVALYS-AI is a computational precision stratification platform that reads the hidden biological structure of diabetic peripheral neuropathy — per patient, per mechanism, per visit.

0.972
External AUROC
95.6%
Accuracy
−60%
Trial-and-Error
130M
People Affected

See the Platform in Action

Watch NERVALYS-AI transform raw biomarker and EMG data into a structured, interpretable disease profile — in real time.

NERVALYS-AI · App Demo · Click to Watch

Clinical Intelligence, Not Just Predictions

Every output derives from a single Personalized Vector — a patient-specific latent representation of how disease behaves biologically.

A — Personalized Vector (PV)
PV ID: PV-7C2F-19A8-4D6B
48Dimensions
Asym.Distribution
HighComplexity
0.89Similarity
Top 12%Uniqueness

This patient's PV encodes high-complexity biological state with asymmetric distribution — indicating multi-mechanism involvement and active disease dynamics.

B — Patient Stratification
Profile: [ RP-INF-Hyper ]

Rapid progression · Inflammatory · Hyper mismatch

Progression DynamicsRP=0.98 · SP=0.20
Dominant Mechanism — INFINF=0.81 · MET=0.41
Symptom Alignment — HyperHyper=0.91 · Coupled=0.50
C — Management Risk Window
2.3 months
Category: Short
Risk acceleration slope+0.18 / month
Action threshold crossed1.9 months
⚠ If untreated → irreversible motor unit loss probability > 65%
D — Nerve Biological Age
67 yrs
Chronological: 49 yrs
+18 yrs delta
Accelerated nerve aging confirmed. Biological state corresponds to a patient 18 years older — indicating advanced cumulative oxidative-inflammatory damage beyond clinical symptom severity.
F — Prognosis
0.82
High Risk
Trajectory: Worsening · Δ Rate −17%
Near-term1–6 mo
Mid-term6–8 mo
Recovery>18 mo
Confidence interval: 0.74 – 0.89
G — Pathophysiological Fragmentation Index
0.73
High Fragmentation
Mechanism Burden
0.82
Symptom Signal
0.40 — Gap: 0.42
Coupled
Decoupled
E — Disease Interaction Translation Map
Primary Conduit
Axonal degeneration→Global MU loss0.82
Secondary Paths
Inflammation→Distal MU loss0.93
Compensation→Reinnervation0.88
Suppressed Paths
Inflammation✕Pain activity0.91
Metabolic stress✕Proximal0.79
Peripheral Interaction Matrix
DistalProximalGlobalReinn.
Inflammatory0.760.420.550.31
Axonal loss0.810.610.890.28
Compensatory0.290.710.460.78
Metabolic0.640.580.690.34
System Behavior
Nonlinear · Distal-weighted · Compensatory-inefficient

From Raw Biology to Clinical Intelligence

Four engineered stages convert heterogeneous multimodal patient data into a structured, interpretable disease representation.

01
Ingest

Inflammatory biomarkers, oxidative stress markers, EMG signals, and clinical metadata are normalized and validated.

TNF-αMDA MUNEMUIMUAPI
02
Encode

Biological signals pass through a denoising Autoencoder. EMG through 1D-CNN + BiLSTM. Each modality encoded separately to preserve causal structure.

Autoencoder1D-CNNBiLSTM
03
Fuse → PV

Cross-modal Transformer attention fuses latents into the Personalized Vector — a structured disease representation unique to each patient.

TransformercHVAEPV
04
Interpret

Multi-head outputs deliver stratification axes, prognosis, risk windows, nerve age, and GNN-based mechanism-to-muscle interaction maps.

SHAPGNNMLP

Performance That Survives the Real World

Validated on an independent human cohort of 90 patients — zero retraining. Structure generalizes because the biology generalizes.

0.972
External AUROC

AUROC drop from internal to external: only −0.022. Structural generalization preserved across independent human cohort with zero retraining.

95.6%
Accuracy

Macro-F1 of 0.954. Sensitivity 94.8%, specificity 96.7%. Balanced performance across stratification profiles — no class collapse.

0.91
Stratification Consistency

Patient-level stratification profile stability across repeated inference: 91% consistency. Biological interpretation remains robust.

From Precision Science to Real-World Benefit

  • ↓68%

    Diagnostic Uncertainty

    Mechanism-aware stratification replaces binary classification — clinicians now see *how* and *why* disease progresses per patient.

  • ↑39%

    Reclassification Beyond Binary

    39% of patients reclassified into actionable stratification profiles — moving beyond symptomatic/asymptomatic into mechanism-matched intervention.

  • ↓48%

    Complication Risk Reduction

    Earlier, mechanism-matched intervention reduces cumulative nerve damage — the root cause of foot ulceration and amputation.

  • ↓45%

    Treatment Cost Reduction

    Avoiding unnecessary escalation across a 130M-person disease population translates to hundreds of millions in avoided expenditure globally.

↑95–98%
Patient-level stratification consistency
$50B+
Global annual DPN healthcare burden
+39%
Reclassification gain beyond binary label
1.42
Cohen's d — model vs. severity gradient

Decoding Disease.
Enabling Precision.

NERVALYS-AI is seeking clinical pilot partners, institutional collaborators, and strategic co-investors to bring mechanism-aware DPN stratification into real-world care.

Get in Touch GitHub Repository
Founder
Mariam Mohamed Ahmed Elelidy
NERVALYS-AI · Egypt · Precision Medicine
mariam.elelidy25@gmail.com