Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia
Galea, B. G.; Reid, J.; Gooley, S.; Witkowski, T.; Lane, T.; Macdonald, S.; Green, T. E.; Ye, Z.; Adikari, T.; Bulluss, K.; Mullen, S. A.; Bennett, C. A.; Forster, B.; Bradshaw, G.; Lin, W.; De Silva, W.; Ramirez, R. B.; Khoshkhoo, S.; Gupta, S.; Krivanek, M.; Menezes, M.; Kothur, K.; Gill, D.; Pope, K.; Gillies, G.; Coleman, M.; Lee, W.-S.; Stephenson, S. M.; Maixner, W.; Harvey, A. S.; Macdonald-Laurs, E.; Howell, K. B.; D'Arcy, C.; Lockhart, P. J.; Leventer, R. J.; Kalnins, R. M.; Clark, J.; Bennett, M. F.; Bahlo, M.; Scheffer, I. E.; Perucca, P.; Berkovic, S. F.; Hildebrand, M. S.
Show abstract
Focal cortical dysplasias (FCDs) are malformations of cortical development associated with drug-resistant focal epilepsy. We analysed surgical tissue from 28 consecutive cases recruited from adult and pediatric epilepsy surgery programs. We performed high-depth sequencing of lesional tissue, validated somatic variants using droplet digital PCR, and investigated genotype-phenotype correlations. A pathogenic or likely pathogenic variant was detected in 71% (n=20/28) of cases. Of these, six cases with FCDIIa or FCDIIb had germline variants in NPRL3 (n=4) or DEPDC5 (n=2). Somatic variants were identified in 50% (n=14/28) of cases. The genetic yield for FCDIIb was 85% of cases having a pathogenic mTOR pathway variant detected (n=12/14), and for FCDIIa 66% (n=6/9). This was achieved through high depth sequencing approaches that allowed detection of somatic variants with very low (down to 0.4%) variant allele fractions (VAFs). No pathogenic variants were detected in 3 cases with FCDI. 70% (n=18/26) of the cases with [≥]12 months follow up experienced a favourable seizure outcome (Engel 1-2) following surgery. Of note, n=10 patients required repeat surgery to resect residual dysplasia. Determining a genetic diagnosis reveals aetiology and paves the way to precision therapies that may benefit those with FCD who do not respond to current treaments.
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