Intersystem Noise Coupling

A computational project investigating how stochastic interactions between body systems can produce emergent brain dynamics relevant to cognition and psychiatric disorders.
Signal Analysis
Instrumentation
Published

July 23, 2026

Overview

The Intersystem Noise Coupling project proposes that independent biological systems become functionally coupled through structured fluctuations in activity.

Instead of viewing neural networks as deterministic processors exchanging only explicit signals, INC suggests that communication also occurs through coordinated modulation of variability.

These fluctuations exhibit statistical structure capable of synchronizing distributed biological systems without requiring rigid connectivity.

Conceptual Framework

The human body consists of multiple interacting systems.

INC proposes, rather than relying exclusively on physical connectivity, systems may transiently coordinate through correlated stochastic dynamics.When variability becomes synchronized across multiple systems, information exchange becomes more efficient, allowing distributed networks to behave as integrated functional units.

Relationship to Existing Science

The framework draws inspiration from several established concepts

Neural Synchrony

Large-scale synchronisation of oscillatory activity has long been associated with attention, perception, and conscious awareness.

Critical Brain Dynamics

Many researchers argue that healthy brains operate near a critical state balancing stability and flexibility.Small fluctuations can propagate throughout the network, producing maximal computational efficiency.Structured noise coupling may represent one mechanism by which brains maintain this critical operating regime.

Predictive Processing

Predictive coding proposes that brains continuously minimise prediction error. INC suggests that variability itself may encode uncertainty, allowing prediction errors to propagate through dynamically coupled networks.

Complexity Theory

Complex adaptive systems frequently exhibit emergent behaviour through interactions among individually simple components.

Noise coupling provides a potential biological mechanism supporting emergence across neural systems.

Data & methods

  1. Signal extraction - RR intervals from ECG for the cardiac signal, accelerometer magnitude (√x²+y²+z²) for the locomotor signal, both resampled onto a shared 4 Hz grid so the two are directly comparable.

  2. Frequency-domain analysis - power spectral density of heart rate variability, split into low-frequency (0.04–0.15 Hz) and high-frequency (0.15–0.40 Hz) bands, with their ratio used as an index of sympathovagal balance.

  3. Cross-organ coherence - spectral coherence between the cardiac and locomotor signals, to identify which frequencies, if any, the two systems synchronize at.

  4. Coupled OU model fitting - the core model:

dX = θ_x(−X)dt + κ_xy·Y·dt + σ_x·dW_x    (cardiac)
dY = θ_y(−Y)dt + κ_yx·X·dt + σ_y·dW_y    (locomotor)

κ_xy and κ_yx capture directional coupling strength — locomotion→cardiac and cardiac→locomotion respectively — σ_x and σ_y the intrinsic noise level of each system, θ_x and θ_y how fast each reverts to its own baseline. Parameters are fit per subject by least-squares regression on the discretized derivatives.

  1. Transfer entropy - a model-free, information-theoretic check on the same question: how much knowing one system’s past reduces uncertainty about the other’s future, without assuming the linear relationship the OU model does.

  2. Windowed coupling - the same OU fit repeated across sliding windows within a single recording, to test whether coupling is a fixed trait or something that shifts over the course of a day.

Phase One: The Healthy Baseline

MMASH 24-hour continuous ECG and wrist-accelerometer recordings from 20 healthy, active adults, establishes what an undisturbed, healthy pair of systems looks like.

Population summary panels A through E for the MMASH cohort
Fig 1. Population overview across the 20-subject MMASH cohort.
Metric Value Interpretation
Mean LF/HF ratio 1.62 Slight sympathetic dominance, normal for an active cohort
Mean LF coherence ~0.000 Cardiac and locomotor systems are largely independent
Mean κ_xy (loco → cardiac) −0.00551 Movement mildly suppresses cardiac variability
Mean κ_yx (cardiac → loco) −0.00076 Cardiac activity barely influences movement
κ_xy vs. LF/HF correlation r = 0.436, p = 0.054 A trend, just short of conventional significance: more coupling tracks with more sympathetic activation
σ_cardiac range 0.13 – 0.80 Cardiac noise varies substantially between people
σ_locomotor range 0.31 – 0.39 Locomotor noise is remarkably consistent across people

The pattern in healthy people is near-independence, and the small coupling that does exist is negative, movement quiets cardiac variability, consistent with vagal withdrawal during physical activity.

OU model phase space showing coupled versus dissociated dynamics
Fig 2. Phase space of the fitted coupled OU model — near-independence is visible as dissociated, not synchronized, trajectories.

One subject stands apart from this pattern entirely, showing anomalously positive coupling on every metric, a single, consistent outlier rather than noise in the fit.

OU model phase space showing coupled versus dissociated dynamics
Fig 3. "Fig 3. Coupling strength ranked across all subjects (left), u15 stands apart from the rest of the cohort; sympathovagal correlation and per-subject noise levels shown alongside."

Phase Two: Testing It Under Stress

The healthy baseline is the control condition, not the finding. The actual test of the hypothesis is whether this near-independence signature holds up when a system is under genuine physiological strain, and that’s what MIMIC-IV is for. ICU waveform data (ECG-derived RR intervals and respiratory waveforms from critically ill patients) will run through the identical pipeline, asking whether intersystem coupling strengthens, reorganizes, or breaks down under critical illness