AI Article Synopsis

  • Brain mosaic mutations contribute significantly to severe focal epilepsies linked to various cortical malformations.
  • Researchers collected cerebrospinal fluid (CSF) during surgery to identify somatic variants in cell-free DNA (cfDNA) using a specialized testing method.
  • Evidence showed that in 3 out of 12 patients with known brain mutations, these mutations could also be detected in cfDNA from CSF, indicating a new potential way to diagnose the causes of epilepsy.

Article Abstract

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;89:1248-1252.

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Source
http://dx.doi.org/10.1002/ana.26080DOI Listing

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