Somatic <i>SLC35A2</i> mosaicism correlates with clinical findings in epilepsy brain tissue
Katherine E. Miller, Daniel C. Koboldt, Kathleen M. Schieffer, Tracy A. Bedrosian, Erin Crist, Adrienne Sheline, Kristen Leraas, Vincent Magrini, Huachun Zhong, Patrick M. Brennan, Jocelyn Bush, James Fitch, Natalie Bir, Anthony R. Miller, Catherine E. Cottrell, Jeffrey R. Leonard, Jonathan Pindrik, Jerome Rusin, Summit Shah, Peter White, Richard K. Wilson, Elaine R. Mardis, Christopher R. Pierson, Adam P. Ostendorf
Abstract
<h3>Objective</h3> Many genetic studies of intractable epilepsy in pediatric patients primarily focus on inherited, constitutional genetic deficiencies identified in patient blood. Recently, studies have revealed somatic mosaicism associated with epilepsy in which genetic variants are present only in a subset of brain cells. We hypothesize that tissue-specific, somatic mosaicism represents an important genetic etiology in epilepsy and aim to discover somatic alterations in epilepsy-affected brain tissue. <h3>Methods</h3> We have pursued a research study to identify brain somatic mosaicism, using next-generation sequencing (NGS) technologies, in patients with treatment refractory epilepsy who have undergone surgical resection of affected brain tissue. <h3>Results</h3> We used an integrated combination of NGS techniques and conventional approaches (radiology, histopathology, and electrophysiology) to comprehensively characterize multiple brain regions from a single patient with intractable epilepsy. We present a 3-year-old male patient with West syndrome and intractable tonic seizures in whom we identified a pathogenic frameshift somatic variant in <i>SLC35A2</i>, present at a range of variant allele fractions (4.2%–19.5%) in 12 different brain tissues detected by targeted sequencing. The proportion of the <i>SLC35A2</i> variant correlated with severity and location of neurophysiology and neuroimaging abnormalities for each tissue. <h3>Conclusions</h3> Our findings support the importance of tissue-based sequencing and highlight a correlation in our patient between <i>SLC35A2</i> variant allele fractions and the severity of epileptogenic phenotypes in different brain tissues obtained from a grid-based resection of clinically defined epileptogenic regions.