Objective: To describe the underlying dynamical mechanisms of photosensitive epilepsy (PSE) and different photosensitivity types. Methods: This retrospective study included healthy controls (HC), non-PSE patients with epilepsy (PWE), and PSE patients. All participants were stimulated with flickering white light (1-60Hz) under 10-20 EEG monitoring. Results: We observed significantly higher occipital Photoparoxysmal response (PPR) power in PSE patients compared to HC for stimulation frequencies 10Hz-20Hz. This activity was highest in Type 4, which shows a type-specific variation of the PPR. However, the excitability of the visual cortex, investigated by the occipital transient (P100) and steady-state visual evoked potentials (ssVEP), remained unchanged in most PSE types compared to HC and to PWE. The ssVEP power only increased significantly in Type 4 compared to HC. Instead, PSE patients showed apparent differences in functional connectivity in the PPR band (3-4Hz) with hypoconnected centro-parietal regions and hyperconnected anterior and anterio-posterior areas compared to HC and PWE for stimulation frequencies 10Hz-20Hz. Conclusion: PSE is a network effect modulated by hyperconnected anterior and anterio-posterior regions, accompanied by a hyperexcitable visual cortex. Significance: We provide novel evidence that altered network dynamics in PSE patients are likely a prerequisite for the propagation of the PPR and type-specific responses.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study was supported by DRS Research Labs. L.T. L.I. and T.D. received support from the Swiss Epilepsy Foundation.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The Ethics Committee of Kantonale Ethikkommission Zurich gave ethical approval for this work
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
留言 (0)