Frontiers in Pharmacology (Jun 2021)

Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications

  • Stefan Wolking,
  • Stefan Wolking,
  • Ciarán Campbell,
  • Caragh Stapleton,
  • Mark McCormack,
  • Norman Delanty,
  • Norman Delanty,
  • Norman Delanty,
  • Chantal Depondt,
  • Michael R. Johnson,
  • Bobby P. C. Koeleman,
  • Roland Krause,
  • Wolfram S. Kunz,
  • Anthony G. Marson,
  • Anthony G. Marson,
  • Anthony G. Marson,
  • Josemir W. Sander,
  • Josemir W. Sander,
  • Josemir W. Sander,
  • Graeme J. Sills,
  • Pasquale Striano,
  • Pasquale Striano,
  • Federico Zara,
  • Federico Zara,
  • Sanjay M. Sisodiya,
  • Sanjay M. Sisodiya,
  • Gianpiero L. Cavalleri,
  • Gianpiero L. Cavalleri,
  • Gianpiero L. Cavalleri,
  • Holger Lerche,
  • EpiPGX Consortium

DOI
https://doi.org/10.3389/fphar.2021.688386
Journal volume & issue
Vol. 12

Abstract

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Objective: Resistance to anti-seizure medications (ASMs) presents a significant hurdle in the treatment of people with epilepsy. Genetic markers for resistance to individual ASMs could support clinicians to make better-informed choices for their patients. In this study, we aimed to elucidate whether the response to individual ASMs was associated with common genetic variation.Methods: A cohort of 3,649 individuals of European descent with epilepsy was deeply phenotyped and underwent single nucleotide polymorphism (SNP)-genotyping. We conducted genome-wide association analyses (GWASs) on responders to specific ASMs or groups of functionally related ASMs, using non-responders as controls. We performed a polygenic risk score (PRS) analyses based on risk variants for epilepsy and neuropsychiatric disorders and ASM resistance itself to delineate the polygenic burden of ASM-specific drug resistance.Results: We identified several potential regions of interest but did not detect genome-wide significant loci for ASM-specific response. We did not find polygenic risk for epilepsy, neuropsychiatric disorders, and drug-resistance associated with drug response to specific ASMs or mechanistically related groups of ASMs.Significance: This study could not ascertain the predictive value of common genetic variants for ASM responder status. The identified suggestive loci will need replication in future studies of a larger scale.

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