Background
Epidemiological evidence relating sleep disorders to end-stage renal disease (ESRD) has been obscure. The present study is sought to examine sleep characteristics and ESRD.
Methods
For this analysis, we selected genetic instruments for sleep traits from published genome-wide association studies (GWAS). As instrumental variables, independent genetic variations linked with seven sleep-related features (sleep duration, getting up in the morning, daytime napping, chronotype of morning/evening person, sleeplessness/insomnia, snoring, and daytime dozing) were chosen. A two-sample Mendelian randomization (TSMR) study was conducted to assess the causal relationship between sleep traits and ESRD (N = 16405). The reverse MR analysis subsequently determined the causal relationship between ESRD and sleep traits. The causal effects were estimated using inverse variance weighted, MR-Egger, weighted median. To conduct sensitivity studies, Cochran's Q test, MR-Egger intercept test, MR-PRESSO, leave-one-out analysis, and funnel plot were used. To study the potential mediators, risk factor analyses were undertaken further.
Results
Genetically predicted sleeplessness/ insomnia was associated with an increased risk of ESRD(OR = 6.11, 95%CI 1.00-37.3, P = 0.049). Genetic liability to getting up in the morning easily (OR = 0.23, 95%CI 0.063–0.85; P = 0.0278) and non-snoring (OR 4.76E-02, 95%CI 2.29E-03-0.985, P = 0.0488) reduced the risk for ESRD.
Conclusion
The present TSMR reveals possible causal correlations between genetic susceptibility to several sleep traits and the risk of ESRD.