Lixia Dong, Hanliang Wei, Tingting Wu, Junxing Dong, Tengteng Fan, Weifeng Mi, Sanwang Wang
The prevalence of sleep disorders has been rising over recent decades. Sleep disorders are frequently associated with disruptions in resting-state functional brain networks. Despite these associations, the direction and genetic basis of the relationships between brain functional networks and sleep disorders remain unclear. Utilizing bidirectional two-sample Mendelian randomization (MR), we examined bidirectional associations between 191 resting-state functional magnetic resonance imaging (rsfMRI) phenotypes (n = 34,691 individuals) and 8 sleep disorder phenotypes (N = 307,843-410,385 individuals). Forward MR identified 14 rsfMRI traits that showed significant associations with sleep disorder phenotypes. Notably, the inverse variance-weighted method showed that increased amplitude in the precuneus or occipital regions within the default mode or central executive network was associated with 13.2% higher odds of sleep disorders (combined; odds ratio = 1.132, 95% confidence interval: 1.064-1.204, P = 8.30 × 10-5). In addition, reverse MR identified 6 sleep disorder phenotypes with significant associations involving 18 rsfMRI traits. For example, higher genetic liability to sleep disorders (combined) was associated with a 14.2% lower strength of functional connectivity between precentral, frontal, or supplementary motor and frontal networks (odds ratio = 0.858, 95% confidence interval: 0.795-0.927, P = 9.62 × 10-5). This study identified 32 bidirectional MR associations between sleep disorders and brain functional networks, providing candidate neural circuits for future mechanistic and interventional studies of sleep disorders.