Abstract
Elevated impulsivity is a key component of attention-deficit hyperactivity disorder (ADHD), bipolar disorder and juvenile myoclonic epilepsy (JME). We performed a genome-wide association, colocalization, polygenic risk score, and pathway analysis of impulsivity in JME (n = 381).
Results were followed up with functional characterisation using a drosophila model. We identified genome-wide associated SNPs at 8q13.3 (P = 7.5 x 10-9) and 10p11.21 (P = 3.6 x 10-8).
The 8q13.3 locus colocalizes with SLCO5A1 expression quantitative trait loci in cerebral cortex (P = 9.5 x 10-3). SLCO5A1 codes for an organic anion transporter and upregulates synapse assembly/organisation genes.
Pathway analysis demonstrates 12.7-fold enrichment for presynaptic membrane assembly genes (P = 0.0005) and 14.3-fold enrichment for presynaptic organisation genes (P = 0.0005) including NLGN1 and PTPRD. RNAi knockdown of Oatp30B, the Drosophila polypeptide with the highest homology to SLCO5A1, causes over-reactive startling behaviour (P = 8.7 x 10-3) and increased seizure-like events (P = 6.8 x 10-7).
Polygenic risk score for ADHD genetically correlates with impulsivity scores in JME (P = 1.60 x 10-3). SLCO5A1 loss-of-function represents an impulsivity and seizure mechanism.
Synaptic assembly genes may inform the aetiology of impulsivity in health and disease.