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GWAS Study

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

Skotte L, Fadista J, Bybjerg-Grauholm J et al.

35022648 PubMed ID
GWAS Study Type
91601 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SL
Skotte L
FJ
Fadista J
BJ
Bybjerg-Grauholm J
AV
Appadurai V
HM
Hildebrand MS
HT
Hansen TF
BK
Banasik K
GJ
Grove J
AC
Albiñana C
GF
Geller F
BC
Bjurström CF
VB
Vilhjálmsson BJ
CM
Coleman M
DJ
Damiano JA
BR
Burgess R
SI
Scheffer IE
PO
Pedersen OBV
EC
Erikstrup C
WD
Westergaard D
NK
Nielsen KR
SE
Sørensen E
BM
Bruun MT
LX
Liu X
HH
Hjalgrim H
PT
Pers TH
MP
Mortensen PB
MO
Mors O
NM
Nordentoft M
DJ
Dreier JW
BA
Børglum AD
CJ
Christensen J
HD
Hougaard DM
BA
Buil A
HA
Hviid A
MM
Melbye M
UH
Ullum H
BS
Berkovic SF
WT
Werge T
FB
Feenstra B
Chapter II

Abstract

Summary of the research findings

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.

4,502 Danish ancestry cases, 51,049 Danish ancestry controls

Chapter III

Study Statistics

Key metrics and study information

91601
Total Participants
GWAS
Study Type
Yes
Replicated
3,133 European ancestry cases, 32,917 European ancestry controls
Replication Participants
European
Ancestry
Australia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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