Modeling Disease-State Transitions Through Stochastic Delay Dynamics: A Computational Framework for Neurological Risk Stratification

This paper proposes a candidate mapping between a mathematically established delay-induced variance-divergence phenomenon (derived in a companion theoretical study of linear stochastic delay-differential equations) and longitudinal neurological biomarker trajectories. Rather than presenting validated clinical results, the paper specifies a falsification-oriented framework: an explicit scheme for estimating latent delay and feedback parameters from biomarker time series (e.g., p-tau217, NfL, structural MRI), a pre-specified definition of what would constitute a positive versus negative result, and a concrete validation protocol against established baselines (Cox proportional hazards, gradient-boosted trees) using public longitudinal cohorts such as ADNI, OASIS, or NACC. No patient-level data, clinical results, or diagnostic/prognostic claims are made in this paper; its contribution is a testable hypothesis and a pre-registerable study design intended to guide a future validation study.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-08-03
DOI
https://doi.org/10.5281/zenodo.21780274
Primary Topic
Multiple Sclerosis Research Studies
Type
preprint
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preprint

Modeling Disease-State Transitions Through Stochastic Delay Dynamics: A Computational Framework for Neurological Risk Stratification

Tanmay Srivastava
Zenodo (CERN European Organization for Nuclear Research)
Multiple Sclerosis Research Studies
preprint

Modeling Disease-State Transitions Through Stochastic Delay Dynamics: A Computational Framework for Neurological Risk Stratification

Tanmay Srivastava
preprint en

Abstract

This paper proposes a candidate mapping between a mathematically established delay-induced variance-divergence phenomenon (derived in a companion theoretical study of linear stochastic delay-differential equations) and longitudinal neurological biomarker trajectories. Rather than presenting validated clinical results, the paper specifies a falsification-oriented framework: an explicit scheme for estimating latent delay and feedback parameters from biomarker time series (e.g., p-tau217, NfL, structural MRI), a pre-specified definition of what would constitute a positive versus negative result, and a concrete validation protocol against established baselines (Cox proportional hazards, gradient-boosted trees) using public longitudinal cohorts such as ADNI, OASIS, or NACC. No patient-level data, clinical results, or diagnostic/prognostic claims are made in this paper; its contribution is a testable hypothesis and a pre-registerable study design intended to guide a future validation study.

Zenodo (CERN European Organization for Nuclear Research)
University of Georgia (US)
Multiple Sclerosis Research Studies
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