Austin Health

Title
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study.
Publication Date
2022
Author(s)
Wagstyl, Konrad
Whitaker, Kirstie
Raznahan, Armin
Seidlitz, Jakob
Vértes, Petra E
Foldes, Stephen
Humphreys, Zachary
Hu, Wenhan
Mo, Jiajie
Likeman, Marcus
Davies, Shirin
Lenge, Matteo
Cohen, Nathan T
Tang, Yingying
Wang, Shan
Ripart, Mathilde
Chari, Aswin
Tisdall, Martin
Bargallo, Nuria
Conde-Blanco, Estefanía
Pariente, Jose Carlos
Pascual-Diaz, Saül
Delgado-Martínez, Ignacio
Pérez-Enríquez, Carmen
Lagorio, Ilaria
Abela, Eugenio
Mullatti, Nandini
O'Muircheartaigh, Jonathan
Vecchiato, Katy
Liu, Yawu
Caligiuri, Maria
Sinclair, Ben
Vivash, Lucy
Willard, Anna
Kandasamy, Jothy
McLellan, Ailsa
Sokol, Drahoslav
Semmelroch, Mira K H G
Kloster, Ane
Opheim, Giske
Yasuda, Clarissa
Zhang, Kai
Hamandi, Khalid
Barba, Carmen
Guerrini, Renzo
Gaillard, William Davis
You, Xiaozhen
Wang, Irene
González-Ortiz, Sofía
Severino, Mariasavina
Striano, Pasquale
Tortora, Domenico
Kalviainen, Reetta
Gambardella, Antonio
Labate, Angelo
Desmond, Patricia
Lui, Elaine
O'Brien, Terry
Shetty, Jay
Jackson, Graeme D
Duncan, John S
Winston, Gavin P
Pinborg, Lars
Cendes, Fernando
Cross, Judith Helen
Baldeweg, Torsten
Adler, Sophie
Subject
MRI
drug-resistant epilepsy
focal cortical dysplasia
lesions
neurosurgery
Type of document
Journal Article
OrcId
0000-0003-3439-5808
0000-0002-1410-3487
0000-0001-5813-0308
0000-0002-6238-2644
0000-0003-0053-147X
0000-0001-7436-987X
0000-0002-2109-0426
0000-0002-1516-0838
0000-0001-5445-5842
0000-0002-7272-7079
0000-0001-5709-0033
0000-0002-3829-5217
0000-0002-6065-1476
0000-0001-7384-3074
0000-0002-8827-7324
0000-0001-9336-9568
0000-0002-5724-1679
DOI
10.1111/epi.17130
Abstract
Drug-resistant focal epilepsy is often caused by focal cortical dysplasias (FCDs). The distribution of these lesions across the cerebral cortex and the impact of lesion location on clinical presentation and surgical outcome are largely unknown. We created a neuroimaging cohort of patients with individually mapped FCDs to determine factors associated with lesion location and predictors of postsurgical outcome. The MELD (Multi-centre Epilepsy Lesion Detection) project collated a retrospective cohort of 580 patients with epilepsy attributed to FCD from 20 epilepsy centers worldwide. Magnetic resonance imaging-based maps of individual FCDs with accompanying demographic, clinical, and surgical information were collected. We mapped the distribution of FCDs, examined for associations between clinical factors and lesion location, and developed a predictive model of postsurgical seizure freedom. FCDs were nonuniformly distributed, concentrating in the superior frontal sulcus, frontal pole, and temporal pole. Epilepsy onset was typically before the age of 10 years. Earlier epilepsy onset was associated with lesions in primary sensory areas, whereas later epilepsy onset was associated with lesions in association cortices. Lesions in temporal and occipital lobes tended to be larger than frontal lobe lesions. Seizure freedom rates varied with FCD location, from around 30% in visual, motor, and premotor areas to 75% in superior temporal and frontal gyri. The predictive model of postsurgical seizure freedom had a positive predictive value of 70% and negative predictive value of 61%. FCD location is an important determinant of its size, the age at epilepsy onset, and the likelihood of seizure freedom postsurgery. Our atlas of lesion locations can be used to guide the radiological search for subtle lesions in individual patients. Our atlas of regional seizure freedom rates and associated predictive model can be used to estimate individual likelihoods of postsurgical seizure freedom. Data-driven atlases and predictive models are essential for evidence-based, precision medicine and risk counseling in epilepsy.
Link
Citation
Epilepsia 2022; 63(1): 61-74
Jornal Title
Epilepsia

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