Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study

Kerestes, Rebecca, Perry, Andrew, Vivash, Lucy, O'Brien, Terence J., Alvim, Marina K. M., Arienzo, Donatello, Aventurato, Ítalo K., Ballerini, Alice, Baltazar, Gabriel F., Bargalló, Núria, Bender, Benjamin, Brioschi, Ricardo, Bürkle, Eva, Caligiuri, Maria Eugenia, Cendes, Fernando, de Tisi, Jane, Duncan, John S., Engel, Jerome P., Foley, Sonya ORCID: https://orcid.org/0000-0002-8390-2709, Fortunato, Francesco, Gambardella, Antonio, Giacomini, Thea, Guerrini, Renzo, Hall, Gerard, Hamandi, Khalid, Ives‐Deliperi, Victoria, João, Rafael B., Keller, Simon S., Kleiser, Benedict, Labate, Angelo, Lenge, Matteo, Marotta, Cassandra, Martin, Pascal, Mascalchi, Mario, Meletti, Stefano, Owens‐Walton, Conor, Parodi, Costanza B., Pascual‐Diaz, Saül, Powell, David, Rao, Jun, Rebsamen, Michael, Reiter, Johannes, Riva, Antonella, Rüber, Theodor, Rummel, Christian, Scheffler, Freda, Severino, Mariasavina, Silva, Lucas S., Staba, Richard J., Stein, Dan J., Striano, Pasquale, Taylor, Peter N., Thomopoulos, Sophia I., Thompson, Paul M., Tortora, Domenico, Vaudano, Anna Elisabetta, Weber, Bernd, Wiest, Roland, Winston, Gavin P., Yasuda, Clarissa L., Zheng, Hong, McDonald, Carrie R., Sisodiya, Sanjay M. and Harding, Ian H. 2024. Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study. Epilepsia 65 (4) , pp. 1072-1091. 10.1111/epi.17881

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Abstract

Objective: The intricate neuroanatomical structure of the cerebellum is of longstanding interest in epilepsy, but has been poorly characterized within the current corticocentric models of this disease. We quantified cross‐sectional regional cerebellar lobule volumes using structural magnetic resonance imaging in 1602 adults with epilepsy and 1022 healthy controls across 22 sites from the global ENIGMA‐Epilepsy working group. Methods: A state‐of‐the‐art deep learning‐based approach was employed that parcellates the cerebellum into 28 neuroanatomical subregions. Linear mixed models compared total and regional cerebellar volume in (1) all epilepsies, (2) temporal lobe epilepsy with hippocampal sclerosis (TLE‐HS), (3) nonlesional temporal lobe epilepsy, (4) genetic generalized epilepsy, and (5) extratemporal focal epilepsy (ETLE). Relationships were examined for cerebellar volume versus age at seizure onset, duration of epilepsy, phenytoin treatment, and cerebral cortical thickness. Results: Across all epilepsies, reduced total cerebellar volume was observed (d = .42). Maximum volume loss was observed in the corpus medullare (dmax = .49) and posterior lobe gray matter regions, including bilateral lobules VIIB (dmax = .47), crus I/II (dmax = .39), VIIIA (dmax = .45), and VIIIB (dmax = .40). Earlier age at seizure onset ( η ρ max 2 $$ \eta {\mathit{\mathsf{\rho}}}_{\mathsf{max}}^{\mathsf{2}} $$ = .05) and longer epilepsy duration ( η ρ max 2 $$ \eta {\mathit{\mathsf{\rho}}}_{\mathsf{max}}^{\mathsf{2}} $$ = .06) correlated with reduced volume in these regions. Findings were most pronounced in TLE‐HS and ETLE, with distinct neuroanatomical profiles observed in the posterior lobe. Phenytoin treatment was associated with reduced posterior lobe volume. Cerebellum volume correlated with cerebral cortical thinning more strongly in the epilepsy cohort than in controls. Significance: We provide robust evidence of deep cerebellar and posterior lobe subregional gray matter volume loss in patients with chronic epilepsy. Volume loss was maximal for posterior subregions implicated in nonmotor functions, relative to motor regions of both the anterior and posterior lobe. Associations between cerebral and cerebellar changes, and variability of neuroanatomical profiles across epilepsy syndromes argue for more precise incorporation of cerebellar subregional damage into neurobiological models of epilepsy.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Psychology Cardiff University Brain Research Imaging Centre (CUBRIC)
Additional Information:	License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/
Publisher:	Wiley
ISSN:	0013-9580
Funders:	Swiss National Science Foundation, São Paulo Research Foundation, National Health and Medical Research Council, Conselho Nacional de Pesquisa, NIHR UCL/UCLH Biomedical Research Centre, Tuscany Region for Health, Health and Care Research Wales, Medical Research Council, University of Tübingen, Italian Ministry of Health, Swiss League Against Epilepsy, NIH, Christina Louise George Trust, MNESYS, UKRI Future Leaders Fellowship, FASEP, Epilepsy Society
Date of First Compliant Deposit:	29 February 2024
Date of Acceptance:	3 January 2024
Last Modified:	14 May 2024 10:56
URI:	https://orca.cardiff.ac.uk/id/eprint/166662

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