4.7 Article

Detection of Brain Somatic Mutations in Cerebrospinal Fluid from Refractory Epilepsy Patients

Journal

ANNALS OF NEUROLOGY
Volume 89, Issue 6, Pages 1248-1252

Publisher

WILEY
DOI: 10.1002/ana.26080

Keywords

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Funding

  1. European Research Council [682345]
  2. Investissements d'avenir [ANR18-RHUS-0005]
  3. National Research Foundation of Korea - Korean Ministry of Science and Information and Communication Technology (ICT) [2019R1A3B2066619, 2020R1A6A3A13076897]
  4. Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea [H15C3143]
  5. Suh Kyungbae Foundation
  6. Korea Health Promotion Institute [HI15C3143000020] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [2020R1A6A3A13076897] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. European Research Council (ERC) [682345] Funding Source: European Research Council (ERC)

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The study shows that brain mosaic mutations can be detected in cfDNA derived from cerebrospinal fluid, providing potential for detecting the mutant allele driving epilepsy in the future.
Brain mosaic mutations are a major cause of refractory focal epilepsies with cortical malformations such as focal cortical dysplasia, hemimegalencephaly, malformation of cortical development with oligodendroglial hyperplasia in epilepsy, and ganglioglioma. Here, we collected cerebrospinal fluid (CSF) during epilepsy surgery to search for somatic variants in cell-free DNA (cfDNA) using targeted droplet digital polymerase chain reaction. In 3 of 12 epileptic patients with known somatic mutations previously identified in brain tissue, we here provide evidence that brain mosaicism can be detected in the CSF-derived cfDNA. These findings suggest future opportunities for detecting the mutant allele driving epilepsy in CSF. ANN NEUROL 2021

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