Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Dashti HS., Jones SE., Wood AR., Lane JM., van Hees VT., Wang H., Rhodes JA., Song Y., Patel K., Anderson SG., Beaumont RN., Bechtold DA., Bowden J., Cade BE., Garaulet M., Kyle SD., Little MA., Loudon AS., Luik AI., Scheer FAJL., Spiegelhalder K., Tyrrell J., Gottlieb DJ., Tiemeier H., Ray DW., Purcell SM., Frayling TM., Redline S., Lawlor DA., Rutter MK., Weedon MN., Saxena R.
© 2019, The Author(s). Sleep is an essential state of decreased activity and alertness but molecular factors regulating sleep duration remain unknown. Through genome-wide association analysis in 446,118 adults of European ancestry from the UK Biobank, we identify 78 loci for self-reported habitual sleep duration (p < 5 × 10 −8 ; 43 loci at p < 6 × 10 −9 ). Replication is observed for PAX8, VRK2, and FBXL12/UBL5/PIN1 loci in the CHARGE study (n = 47,180; p < 6.3 × 10 −4 ), and 55 signals show sign-concordant effects. The 78 loci further associate with accelerometer-derived sleep duration, daytime inactivity, sleep efficiency and number of sleep bouts in secondary analysis (n = 85,499). Loci are enriched for pathways including striatum and subpallium development, mechanosensory response, dopamine binding, synaptic neurotransmission and plasticity, among others. Genetic correlation indicates shared links with anthropometric, cognitive, metabolic, and psychiatric traits and two-sample Mendelian randomization highlights a bidirectional causal link with schizophrenia. This work provides insights into the genetic basis for inter-individual variation in sleep duration implicating multiple biological pathways.