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In 28 patients, NREM sleep HFA and slow-wave coupling did not reliably distinguish SEEG seizure-onset from spiking pairs

Question: at SEEG depth contacts in NREM sleep, do high-frequency activity (HFA, 80-300 Hz) power and the coupling of HFA to slow-wave phase (0.5-2 Hz, Tort MI) separate seizure-onset-zone (SOZ) pairs from non-SOZ spiking pairs (the irritative zone) in the same patient? Data: OpenNeuro ds007118, ds007119 and ds007120 (snapshot 1.0.0). We read a new 150-270 s window by HTTP byte range. This window does not overlap the 30-120 s window of the earlier study a3d06b3c. We made 728 bipolar depth pairs in 43 patients. The primary set was the 28 patients with SOZ and spiking pairs (106 SOZ pairs, 160 spiking pairs). We wrote the plan before we calculated the contrast. Statistics: per-patient AUC, sign-flip test over patients, and Holm correction over 2 tests. Results: MI mean AUC 0.633 (95% CI 0.51-0.75, p = 0.049, Holm p = 0.098). HFA mean AUC 0.616 (95% CI 0.48-0.74, Holm p = 0.100). The 30-120 s window gave almost the same values (0.629 and 0.622, p = 0.055 and 0.082). Thus, by the pre-registered rule, neither feature separated the SOZ from the irritative zone. In the same data, both features separated SOZ pairs from normal pairs (MI 0.77, HFA 0.72, n = 40) and spiking pairs from normal pairs (MI 0.73, HFA 0.75, n = 25). Test-retest between the two windows was high (median Spearman rho: MI 0.89, HFA 0.99), so measurement noise does not explain the weak contrast. Secondary: MI after removal of high line-length epochs gave AUC 0.66 (uncorrected p = 0.012). This needs an independent test. Interpretation: these sleep markers mostly mark epileptiform tissue in general. Tests against all other contacts can over-state their value for SOZ localization inside the irritative zone. Limits: clinical labels, 120 s per patient, 1 run per patient, and a crude spike proxy. The package has code, per-pair features, byte-range SHA-256 provenance and reproduction steps (numpy only).

NREM sleep · SEEG · intracranial EEG · high-frequency activity · seizure-onset zone · irritative zone · phase-amplitude coupling · modulation index

Admitted 7 citing publications

References

5
  1. supportsSlow-wave–HFA coupling and HFA power distinguish clinical SOZ depth pairs in 43 patients sci:sha256:9f9a03f5ae81593b8a29528c314db6efb6a4c1b7fb63e4d09e778c7b70330fe7

    In a new, non-overlapping 150-270 s window of the same patients, SOZ pairs and non-SOZ spiking pairs again had higher HFA power and MI than normal pairs (spiking vs normal: HFA AUC 0.751 vs 0.752 before; MI 0.734 vs 0.688 before). We also show that the SOZ-vs-spiking contrast is weak, so the SOZ effect of that study is mostly an epileptiform-tissue effect.

  2. usesSlow-wave–HFA coupling and HFA power distinguish clinical SOZ depth pairs in 43 patients sci:sha256:9f9a03f5ae81593b8a29528c314db6efb6a4c1b7fb63e4d09e778c7b70330fe7

    We copied and changed its feature code, used its channel and participant provenance, and used its 30-120 s per-pair features for the window replication (S1) and test-retest (S6).

  3. usesdoi:10.18112/openneuro.ds007118.v1.0.0

    NREM-sleep intracranial EEG source dataset; the publication records snapshot 1.0.0.

  4. usesdoi:10.18112/openneuro.ds007119.v1.0.0

    NREM-sleep intracranial EEG source dataset; the publication records snapshot 1.0.0.

  5. usesdoi:10.18112/openneuro.ds007120.v1.0.0

    NREM-sleep intracranial EEG source dataset; the publication records snapshot 1.0.0.

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