Polygenic burden in focal and generalized epilepsies

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http://hdl.handle.net/10138/309535

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Epi25 Consortium , Leu , C , Stevelink , R , Palotie , A , Daly , M J & Lehesjoki , A-E 2019 , ' Polygenic burden in focal and generalized epilepsies ' , Brain : a journal of neurology , vol. 142 , pp. 3473-3481 . https://doi.org/10.1093/brain/awz292

Title: Polygenic burden in focal and generalized epilepsies
Author: Epi25 Consortium; Leu, Costin; Stevelink, Remi; Palotie, Aarno; Daly, Mark J.; Lehesjoki, Anna-Elina
Contributor: University of Helsinki, Centre of Excellence in Complex Disease Genetics
University of Helsinki, Institute for Molecular Medicine Finland
University of Helsinki, Department of Medical and Clinical Genetics
Date: 2019-11
Language: eng
Number of pages: 9
Belongs to series: Brain : a journal of neurology
ISSN: 0006-8950
URI: http://hdl.handle.net/10138/309535
Abstract: Rare genetic variants can cause epilepsy, and genetic testing has been widely adopted for severe, paediatric-onset epilepsies. The phenotypic consequences of common genetic risk burden for epilepsies and their potential future clinical applications have not yet been determined. Using polygenic risk scores (PRS) from a European-ancestry genome-wide association study in generalized and focal epilepsy, we quantified common genetic burden in patients with generalized epilepsy (GE-PRS) or focal epilepsy (FE-PRS) from two independent non-Finnish European cohorts (Epi25 Consortium, n = 5705; Cleveland Clinic Epilepsy Center, n = 620; both compared to 20 435 controls). One Finnish-ancestry population isolate (Finnish-ancestry Epi25, n = 449; compared to 1559 controls), two European-ancestry biobanks (UK Biobank, n = 383 656; Vanderbilt biorepository, n = 49 494), and one Japanese-ancestry biobank (BioBank Japan, n = 168 680) were used for additional replications. Across 8386 patients with epilepsy and 622 212 population controls, we found and replicated significantly higher GE-PRS in patients with generalized epilepsy of European-ancestry compared to patients with focal epilepsy (Epi25: P = 1.64 x 10(-15); Cleveland: P = 2.85 x 10(-4); Finnish-ancestry Epi25: P = 1.80 x 10(-4)) or population controls (Epi25: P = 2.35 x 10(-70); Cleveland: P = 1.43 x 10(-7); Finnish-ancestry Epi25: P = 3.11 x 10(-4); UK Biobank and Vanderbilt biorepository meta-analysis: P = 7.99 x 10(-4)). FE-PRS were significantly higher in patients with focal epilepsy compared to controls in the non-Finnish, non-biobank cohorts (Epi25: P = 5.74 x 10(-19); Cleveland: P = 1.69 x 10(-6)). European ancestry-derived PRS did not predict generalized epilepsy or focal epilepsy in Japanese-ancestry individuals. Finally, we observed a significant 4.6-fold and a 4.5-fold enrichment of patients with generalized epilepsy compared to controls in the top 0.5% highest GE-PRS of the two non-Finnish European cohorts (Epi25: P = 2.60 x 10(-15); Cleveland: P = 1.39 x 10(-2)). We conclude that common variant risk associated with epilepsy is significantly enriched in multiple cohorts of patients with epilepsy compared to controls-in particular for generalized epilepsy. As sample sizes and PRS accuracy continue to increase with further common variant discovery, PRS could complement established clinical biomarkers and augment genetic testing for patient classification, comorbidity research, and potentially targeted treatment.
Subject: epilepsy
genetics
genetic generalized epilepsy
common variant risk
GENOME-WIDE ASSOCIATION
SEIZURE RECURRENCE
RISK PREDICTION
1ST SEIZURE
METAANALYSIS
POPULATION
FEATURES
HISTORY
BIOBANK
SCORES
3112 Neurosciences
3124 Neurology and psychiatry
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