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Toward Personalized Neuroscience: Evaluating Individual-Level Information in Neural Mass Models
Carlotta B C Barkhau1,2, Clemens Pellengahr1, Zheng Wang3
1Institute for Translational Psychiatry, University of Münster, Münster, Germany.
Human Brain Mapping
|November 17, 2025
Summary
Neural mass models (NMMs) can simulate brain dynamics, but their parameters don't capture individual traits. Optimized models accurately replicate brain activity but fail to correlate with personal attributes like intelligence.
Area of Science:
- Neuroscience
- Computational Neuroscience
- Systems Neuroscience
Background:
- Macroscale brain modeling with neural mass models (NMMs) simulates whole-brain dynamics.
- Connectome-based NMMs enable personalized models but struggle with individual neural characteristics due to small sample sizes and computational limits.
Purpose of the Study:
- To develop and apply an efficient, algorithmically differentiable NMM for large-scale datasets.
- To investigate the capacity of NMM parameters to capture individual-specific neural characteristics and behavioral metrics.
Main Methods:
- Utilized a differentiable reduced Wong-Wang (RWW) model for efficient optimization.
- Applied the model to resting-state fMRI data from 1444 participants.
- Optimized models with varying parameter complexities (4, 658, 23,875) and assessed variance explanation in functional connectivity (FC).
Main Results:
- Optimized RWW models explained 4%, 19%, and 56% of empirical FC variance with increasing parameter complexity.
- Subject identification accuracy based on simulated FC improved from <1% to nearly 100% with increased complexity.
- Individual-level correlations between model parameters and attributes (age, gender, IQ) were minimal (effect sizes: η² ≤ 0.03, β ≤ 0.234).
Conclusions:
- Current RWW NMM implementations robustly replicate resting-state dynamics but lack granularity for individual behavioral metrics.
- A critical alignment problem exists: neural patterns and behavioral constructs may not map one-to-one.
- Future research requires more expressive models and multimodal data to bridge the gap between neural similarity and clinical personalization.

