Rare coding variants in genes encoding GABA_A receptors in genetic generalised epilepsies: an exome-based case-control study

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May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline et al (show 88 more authors) , Niturad, Cristina E, Knaus, Julia, De Kovel, Carolien, Toliat, Mohamad, Polvi, Anne, Iacomino, Michele, Guerrero-Lopez, Rosa, Baulac, Stephanie, Marini, Carla, Thiele, Holger, Altmueller, Janine, Jabbari, Kamel, Ruppert, Ann-Kathrin, Jurkowski, Wiktor, Lal, Dennis, Rusconi, Raffaella, Cestele, Sandrine, Terragni, Benedetta, Coombs, Ian D, Reid, Christopher A, Striano, Pasquale, Caglayan, Hande, Siren, Auli, Everett, Kate, Moller, Rikke S, Hjalgrim, Helle, Muhle, Hiltrud, Helbig, Ingo, Kunz, Wolfram S, Weber, Yvonne G, Weckhuysen, Sarah, De Jonghe, Peter, Sisodiya, Sanjay M, Nabbout, Rima, Franceschetti, Silvana, Coppola, Antonietta, Vari, Maria S, Trenite, Dorothee Kasteleijn-Nolst, Baykan, Betul, Ozbek, Ugur, Bebek, Nerses, Klein, Karl M, Rosenow, Felix, Nguyen, Dang K, Dubeau, Francois, Carmant, Lionel, Lortie, Anne, Desbiens, Richard, Clement, Jean-Francois, Cieuta-Walti, Cecile, Sills, Graeme J ORCID: 0000-0002-3389-8713, Auce, Pauls, Francis, Ben ORCID: 0000-0002-2130-5976, Johnson, Michael R, Marson, Anthony G ORCID: 0000-0002-6861-8806, Berghuis, Bianca, Sander, Josemir W, Avbersek, Andreja, McCormack, Mark, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Krenn, Martin, Zimprich, Fritz, Peter, Sarah, Nikanorova, Marina, Kraaij, Robert, van Rooij, Jeroen, Balling, Rudi, Ikram, M Arfan, Uitterlinden, Andre G, Avanzini, Giuliano, Schorge, Stephanie, Petrou, Steven, Mantegazza, Massimo, Sander, Thomas, LeGuern, Eric, Serratosa, Jose M, Koeleman, Bobby PC, Palotie, Aarno, Lehesjoki, Anna-Elina, Nothnagel, Michael, Nuernberg, Peter, Maljevic, Snezana, Zara, Federico, Cossette, Patrick, Krause, Roland and Lerche, Holger (2018) Rare coding variants in genes encoding GABA_A receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). pp. 699-708.

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Abstract

<h4>Background</h4>Genetic generalised epilepsy is the most common type of inherited epilepsy. Despite a high concordance rate of 80% in monozygotic twins, the genetic background is still poorly understood. We aimed to investigate the burden of rare genetic variants in genetic generalised epilepsy.<h4>Methods</h4>For this exome-based case-control study, we used three different genetic generalised epilepsy case cohorts and three independent control cohorts, all of European descent. Cases included in the study were clinically evaluated for genetic generalised epilepsy. Whole-exome sequencing was done for the discovery case cohort, a validation case cohort, and two independent control cohorts. The replication case cohort underwent targeted next-generation sequencing of the 19 known genes encoding subunits of GABA_A receptors and was compared to the respective GABA_A receptor variants of a third independent control cohort. Functional investigations were done with automated two-microelectrode voltage clamping in Xenopus laevis oocytes.<h4>Findings</h4>Statistical comparison of 152 familial index cases with genetic generalised epilepsy in the discovery cohort to 549 ethnically matched controls suggested an enrichment of rare missense (Nonsyn) variants in the ensemble of 19 genes encoding GABA_A receptors in cases (odds ratio [OR] 2·40 [95% CI 1·41-4·10]; p_Nonsyn=0·0014, adjusted p_Nonsyn=0·019). Enrichment for these genes was validated in a whole-exome sequencing cohort of 357 sporadic and familial genetic generalised epilepsy cases and 1485 independent controls (OR 1·46 [95% CI 1·05-2·03]; p_Nonsyn=0·0081, adjusted p_Nonsyn=0·016). Comparison of genes encoding GABA_A receptors in the independent replication cohort of 583 familial and sporadic genetic generalised epilepsy index cases, based on candidate-gene panel sequencing, with a third independent control cohort of 635 controls confirmed the overall enrichment of rare missense variants for 15 GABA_A receptor genes in cases compared with controls (OR 1·46 [95% CI 1·02-2·08]; p_Nonsyn=0·013, adjusted p_Nonsyn=0·027). Functional studies for two selected genes (GABRB2 and GABRA5) showed significant loss-of-function effects with reduced current amplitudes in four of seven tested variants compared with wild-type receptors.<h4>Interpretation</h4>Functionally relevant variants in genes encoding GABA_A receptor subunits constitute a significant risk factor for genetic generalised epilepsy. Examination of the role of specific gene groups and pathways can disentangle the complex genetic architecture of genetic generalised epilepsy.<h4>Funding</h4>EuroEPINOMICS (European Science Foundation through national funding organisations), Epicure and EpiPGX (Sixth Framework Programme and Seventh Framework Programme of the European Commission), Research Unit FOR2715 (German Research Foundation and Luxembourg National Research Fund).

Item Type:	Article
Additional Information:	publisher: Elsevier articletitle: Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study journaltitle: The Lancet Neurology articlelink: https://doi.org/10.1016/S1474-4422(18)30215-1 associatedlink: https://doi.org/10.1016/S1474-4422(18)30252-7 content_type: article copyright: © 2018 Elsevier Ltd. All rights reserved.
Uncontrolled Keywords:	Epicure Consortium, EuroEPINOMICS CoGIE Consortium, EpiPGX Consortium, Humans, Epilepsy, Generalized, Genetic Predisposition to Disease, Receptors, GABA-A, Case-Control Studies, Cohort Studies, Models, Molecular, International Cooperation, Adolescent, Adult, Aged, Aged, 80 and over, Middle Aged, Child, Child, Preschool, Infant, Infant, Newborn, Family Health, Europe, Female, Male, Genetic Variation, Young Adult, Exome Sequencing
Depositing User:	Symplectic Admin
Date Deposited:	31 Jul 2018 07:45
Last Modified:	05 Oct 2023 21:53
DOI:	10.1016/S1474-4422(18)30215-1
Related URLs:	Author Publisher
URI:	https://livrepository.liverpool.ac.uk/id/eprint/3024398