1 / 34

Physiology-based modeling and quantification of auditory evoked potentials

Physiology-based modeling and quantification of auditory evoked potentials. Cliff Kerr Complex Systems Group School of Physics, University of Sydney. Introduction. Aim: to develop a physiology-based method of evoked potential (EP) analysis, in order to: Provide a means to quantify EPs

linh
Télécharger la présentation

Physiology-based modeling and quantification of auditory evoked potentials

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Physiology-based modeling and quantification of auditory evoked potentials Cliff Kerr Complex Systems Group School of Physics, University of Sydney

  2. Introduction • Aim: to develop a physiology-based method of evoked potential (EP) analysis, in order to: • Provide a means to quantify EPs • Relate EP data to brain physiology • Implementation: biophysical modeling and deconvolution of EEG data

  3. Outline • What are evoked potentials? • Fitting: • Methods: theory, data, implementation • Results: group average waveforms • Application: arousal • Deconvolution: • Motivation • Theory • Results: synthetic and experimental data • Discussion and summary • Challenges and future directions

  4. EEG: EP: Time-locked averaging V(mV) V(mV) t(s) t(s) What are EPs? stimulus:

  5. Traditional analysis: scoring Standard Target N1 6.5 mV 112 ms P50 1.2 mV 56 ms N1 8.0 mV 120 ms N2 3.4 mV 224 ms P2 -8.0 mV 264 ms P3 -19.6 mV 320 ms

  6. Theory e Cortex i r Thalamus s Brain stem n

  7. Theory • Physiology-based continuum modeling: uses 11 vs. 1,000,000,000,000,000 connections • Five populations of neurons: • Sensory (excitatory; labeled n) • Cortical (excitatory & inhibitory; e & i) • Thalamic relay (excitatory; s) • Thalamic reticular (inhibitory; r) • Five neuronal loops: • cortical (Gee, Gei ) • thalamic (Gsrs) • thalamocortical (Gese , Gesre) e i r s n

  8. Theory • Model has 14 parameters: • 5 for neuronal coupling strength (Gee, Gei , Gese , Gesre , Gsrs ) • 4 for neuronal network properties (a, b, g, t0) • 5 for stimulus properties (tos, ts, ros, rs) • Most important parameters are the gains Gab (coupling strength between neuron populations) • Model describes conversion process (auditory stimulus → neuronal activity → scalp electrical field) using an analytic transfer function fe/fn:

  9. Theory • Direct impulse: • Cortical modulation: • Corticothalamic modulation: • Transfer function:

  10. Theory • Impulse: • Time-domain impulse response:

  11. Data • Sampled from 1527 normal subjects: • Aged 6-80 years • Equal numbers male & female • No neurological diseases, chemical dependencies, etc. • Stimulus: 1 tone/second for 6 minutes (280 standard tones, 80 target tones) • Used to produce group average standard and target EPs (generated using >100,000 single trials!)

  12. c2 P2 P1 Fitting 1) Initial parameters are chosen .

  13. 2) Gradient descent algorithm reduces c2 of fit c2 P2 P1 Fitting .

  14. 3) Process is repeated using different initialisations c2 P2 P1 Fitting

  15. Results • Excellent fits to standards (up to 400 ms)

  16. Results • Excellent fits to targets (up to 300 ms)

  17. Results • Possible changes in neuronal network properties:

  18. Results • Probable changes in neuronal coupling strengths:

  19. Results • Definite changes in stability parameters:

  20. 0 2 4 6 -5 μV 0.1 s Application: arousal • Same task (auditory oddball) • 43 subjects • Averaged over ten time intervals of 40 seconds each task duration (min)

  21. Application: arousal • Increased cortical activity → decreased acetylcholine?

  22. Deconvolution: motivation • In model, thalamocortical loop → N2 feature of targets • Could target response = standard response + delayed standard response?

  23. Deconvolution: motivation

  24. Theory • Assumption: responses are product of task-dynamic and task-invariant properties: • Fourier transform: • Take the ratio of the two: • Inverse Fourier transform to get the result:

  25. Theory • Direct deconvolution is uselessly noisy: • Hence, use Wiener deconvolution:

  26. Synthetic data

  27. Group average data

  28. Single-subject data

  29. Discussion and summary • Physiology-based EP fitting can be achieved • Offers significant advantages over traditional methods • Results tentatively suggest physiology underlying stimulus perception: • Increase in stability: required for a transient response • Arousal determined by thalamocortical activity: standards show increased inhibition, targets show increased excitation • Standards generated by ≈1 thalamocortical impulse, targets by ≈2

  30. Challenges • Fitting challenges • Degeneracy • Constraints • Testability • Deconvolution challenges • Noise and artifact • What are we looking for? • Physiological challenges • Only 1D information • What’s signal?

  31. Future directions • How does the brain change with age? Standard Target

  32. Future directions • Can our model account for depression?

  33. Future directions • Modeling the ERP “zoo” • modality • arousal • disease • drugs Visual: Somatosensory: Oddball: Quiet sleep: Bipolar: Radiculopathy: Carbonyl sulfide: Ecstasy:

  34. Acknowledgements Chris J. Rennie Peter A. Robinson Jonathon M. Clearwater Andrew H. Kemp Brain Resource Ltd.

More Related