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Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.

Authors :
Skotte L
Fadista J
Bybjerg-Grauholm J
Appadurai V
Hildebrand MS
Hansen TF
Banasik K
Grove J
Albiñana C
Geller F
Bjurström CF
Vilhjálmsson BJ
Coleman M
Damiano JA
Burgess R
Scheffer IE
Pedersen OBV
Erikstrup C
Westergaard D
Nielsen KR
Sørensen E
Bruun MT
Liu X
Hjalgrim H
Pers TH
Mortensen PB
Mors O
Nordentoft M
Dreier JW
Børglum AD
Christensen J
Hougaard DM
Buil A
Hviid A
Melbye M
Ullum H
Berkovic SF
Werge T
Feenstra B
Source :
Brain : a journal of neurology [Brain] 2022 Apr 18; Vol. 145 (2), pp. 555-568.
Publication Year :
2022

Abstract

Febrile seizures represent the most common type of pathological brain activity in young children and are influenced by genetic, environmental and developmental factors. In a minority of cases, febrile seizures precede later development of epilepsy. We conducted a genome-wide association study of febrile seizures in 7635 cases and 83 966 controls identifying and replicating seven new loci, all with P < 5 × 10-10. Variants at two loci were functionally related to altered expression of the fever response genes PTGER3 and IL10, and four other loci harboured genes (BSN, ERC2, GABRG2, HERC1) influencing neuronal excitability by regulating neurotransmitter release and binding, vesicular transport or membrane trafficking at the synapse. Four previously reported loci (SCN1A, SCN2A, ANO3 and 12q21.33) were all confirmed. Collectively, the seven novel and four previously reported loci explained 2.8% of the variance in liability to febrile seizures, and the single nucleotide polymorphism heritability based on all common autosomal single nucleotide polymorphisms was 10.8%. GABRG2, SCN1A and SCN2A are well-established epilepsy genes and, overall, we found positive genetic correlations with epilepsies (rg = 0.39, P = 1.68 × 10-4). Further, we found that higher polygenic risk scores for febrile seizures were associated with epilepsy and with history of hospital admission for febrile seizures. Finally, we found that polygenic risk of febrile seizures was lower in febrile seizure patients with neuropsychiatric disease compared to febrile seizure patients in a general population sample. In conclusion, this largest genetic investigation of febrile seizures to date implicates central fever response genes as well as genes affecting neuronal excitability, including several known epilepsy genes. Further functional and genetic studies based on these findings will provide important insights into the complex pathophysiological processes of seizures with and without fever.<br /> (© The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain.)

Details

Language :
English
ISSN :
1460-2156
Volume :
145
Issue :
2
Database :
MEDLINE
Journal :
Brain : a journal of neurology
Publication Type :
Academic Journal
Accession number :
35022648
Full Text :
https://doi.org/10.1093/brain/awab260