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Simple brain activity statistics, spatial and temporal autocorrelation, explain complex network topology measures. These findings link neuroimaging complexity to underlying biological processes.

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Area of Science:

  • Neuroscience
  • Network Neuroscience
  • Computational Neuroscience

Background:

  • High-throughput neuroscience methods generate vast, complex data.
  • Understanding emergent phenomena from simpler statistics is a key challenge.

Purpose of the Study:

  • To investigate if low-dimensional statistics explain complex network topology measures in resting-state functional magnetic resonance imaging (rs-fMRI).
  • To determine the neurobiological underpinnings of network topology variations.

Main Methods:

  • Analysis of resting-state functional magnetic resonance imaging (rs-fMRI) data.
  • Application of complex topology measures from network neuroscience.
  • Generation of surrogate time series matched for spatial and temporal autocorrelation.

Main Results:

  • Spatial and temporal autocorrelation reliably explain numerous network topology measures.
  • Surrogate time series capture most individual and regional variation in topology measures.
  • Aging-related network topology changes are driven by spatial autocorrelation.
  • Serotonergic drugs induce topographic changes in temporal autocorrelation.

Conclusions:

  • Widely used complexity measures in network neuroscience can be reduced to simpler autocorrelation statistics.
  • This reductionistic approach offers a potential link between complex neuroimaging measures and neurobiology.