Stymulacja magnetyczna czaszki jako biologiczny wskaźnik w wczesnych fazach opracowywania nowych leków przeciwpadaczkowych: badanie randomizowane, podwójnie zaślepione, kontrolowane placebo u pacjentów z padaczką uogólnioną
Transcranial Magnetic Stimulation as a Translational Biomarker in Early-Phase Anti-Seizure Medication Development: A Randomized, Double-Blind, Placebo-Controlled Study in Generalized Epilepsy
W skrócie
Badanie pokazało, że stymulacja magnetyczna czaszki (TMS) może być przydatnym narzędziem do oceny działania nowych leków przeciwpadaczkowych na mózg. Lekarze testowali to narzędzie u pacjentów z padaczką otrzymujących lek lewetiracetam i stwierdzili, że mierzone parametry zmian aktywności mózgu reagują na dawkę leku w sposób, który można przewidzieć. Te pomiary mogą pomóc naukowcom szybciej sprawdzić, czy nowe leki przeciwpadaczkowe rzeczywiście działają, zanim będą testowane u większych grup pacjentów.
Oryginalny abstract (angielski)
One-third of epilepsy patients remain treatment-resistant, underscoring the need for novel anti-seizure medications (ASMs) and reliable biomarkers of central target engagement. Cortical hyperexcitability is a hallmark of epilepsy, making excitability a valuable pharmacodynamic biomarker for early-phase drug development supporting go/no-go decision making. Building upon prior transcranial magnetic stimulation (TMS) work in healthy participants, this study aimed to establish TMS-derived endpoints as translational biomarkers of ASM effects in patients. In a randomized, double-blind, placebo-controlled, two-way crossover design, patients with generalized epilepsy on levetiracetam (500 mg twice daily; n = 14) or valproic acid (≤1,000 mg/day; levetiracetam-naïve, n = 12) received a single oral dose of levetiracetam (2000 mg) or placebo. Participants were asked to refrain from their morning ASM dose to minimize background ASM levels while maintaining seizure protection. TMS combined with electromyography (EMG) and electroencephalography (EEG), and resting-state EEG were performed pre-dose, 1.5 h, and 3 h post-dose. Outcomes were analyzed using mixed-effects analysis of covariance or cluster-based permutation testing. Levetiracetam significantly reduced motor-evoked potential (MEP) amplitude, enhanced long-interval intracortical inhibition (LICI), and increased frontal gamma and beta power, with larger effect sizes in levetiracetam-naïve patients. These findings were further supported by linear concentration-response relationships for these endpoints. TMS-EEG revealed group-specific modulation: early TMS-evoked potential components (P30/N45) in levetiracetam patients vs. later components (N100/P180) in levetiracetam-naïve patients. These findings build upon prior results, demonstrating that TMS-based biomarkers are sensitive to levetiracetam's acute effects in epilepsy patients with MEP amplitude, LICI, and frontal beta/gamma power emerging as promising biomarkers, possible also for new ASM development.