Subject(s)
Depression , Dyssomnias , Inflammatory Bowel Diseases , Interleukin-33 , Humans , Depression/blood , Depression/etiology , Depression/genetics , Depression/metabolism , Inflammatory Bowel Diseases/blood , Inflammatory Bowel Diseases/complications , Inflammatory Bowel Diseases/genetics , Inflammatory Bowel Diseases/metabolism , Interleukin-33/blood , Interleukin-33/genetics , Interleukin-33/metabolism , Sleep/genetics , Sleep/physiology , Sleep Quality , Dyssomnias/blood , Dyssomnias/etiology , Dyssomnias/genetics , Dyssomnias/metabolismABSTRACT
Background: Sleep disturbance is an outcome of multiple factors including environmental and genetic influences. Job stress, a complex environmental factor, likely affects sleep quality, significantly reducing the quality of life of workers. Additionally, FK506 binding protein 51 (FKBP5) may be a pathogenic factor for sleep disturbance as it regulates hypothalamic-pituitary-adrenal (HPA) axis activity, where HPA axis has been found to be involved in the regulation mechanism of sleep and stress response. Objectives: The main aim of this study was to investigate the association between job stress and FKBP5 gene polymorphism as well as their interaction with sleep disturbance in Chinese workers; to date, these relationships have not been explored. Methods: This is a cross-sectional study. A total of 675 railway workers (53.8% male) completed a short Effort-Reward Imbalance questionnaire and the Pittsburgh Sleep Quality Index. The SNaPshot single nucleotide polymorphism (SNP) assay was carried out by screening for FKBP5 SNPs in every participant. Generalized multifactor dimensionality reduction (GMDR) was used to identify the strongest G×E interaction combination. Results: The findings showed that job stress was significantly associated with sleep disturbance; specifically, scores on the PSQI subscales (sleep disturbance, sleep medication, and daytime dysfunction) exhibited significant differences between the two job stress groups (X2 = 18.10, p = 0.01). Additionally, the FKBP5 SNP rs1360780-TT (adjusted odds ratio [AOR] = 4.98, 95% confidence interval [CI] = 2.80-8.84) and rs3800373-CC genotype (AOR = 2.06, CI = 1.10-3.86) were associated with an increased risk of sleep disturbance. Job stress and rs1360780 and rs3800373 variants showed a high-dimensional interaction with sleep disturbance as determined by the GMDR model. Conclusion: The FKBP5 gene may increase susceptibility to job stress and result in sleep disturbance, especially in the presence of negative work-related events. These findings contribute to the field of sleep disturbance prevention and treatment.
Subject(s)
Dyssomnias , Occupational Stress , Tacrolimus Binding Proteins , Female , Humans , Male , Cross-Sectional Studies , Hypothalamo-Hypophyseal System/metabolism , Occupational Stress/genetics , Pituitary-Adrenal System/metabolism , Polymorphism, Single Nucleotide/genetics , Quality of Life , Tacrolimus Binding Proteins/genetics , Dyssomnias/geneticsABSTRACT
Disruptions of normal circadian rhythms and sleep cycles are consequences of aging and can profoundly affect health. Accumulating evidence indicates that circadian and sleep disturbances, which have long been considered symptoms of many neurodegenerative conditions, may actually drive pathogenesis early in the course of these diseases. In this Review, we explore potential cellular and molecular mechanisms linking circadian dysfunction and sleep loss to neurodegenerative diseases, with a focus on Alzheimer's disease. We examine the interplay between central and peripheral circadian rhythms, circadian clock gene function, and sleep in maintaining brain homeostasis, and discuss therapeutic implications. The circadian clock and sleep can influence a number of key processes involved in neurodegeneration, suggesting that these systems might be manipulated to promote healthy brain aging.
Subject(s)
Alzheimer Disease/physiopathology , Circadian Clocks/genetics , Circadian Rhythm/genetics , Sleep , Aging , Alzheimer Disease/genetics , Animals , Brain/physiology , Dyssomnias/genetics , Dyssomnias/physiopathology , Humans , Mice , Suprachiasmatic Nucleus/physiopathologyABSTRACT
Usual sleep duration is a heritable trait correlated with psychiatric morbidity, cardiometabolic disease and mortality, although little is known about the genetic variants influencing this trait. A genome-wide association study (GWAS) of usual sleep duration was conducted using 18 population-based cohorts totaling 47 180 individuals of European ancestry. Genome-wide significant association was identified at two loci. The strongest is located on chromosome 2, in an intergenic region 35- to 80-kb upstream from the thyroid-specific transcription factor PAX8 (lowest P=1.1 × 10(-9)). This finding was replicated in an African-American sample of 4771 individuals (lowest P=9.3 × 10(-4)). The strongest combined association was at rs1823125 (P=1.5 × 10(-10), minor allele frequency 0.26 in the discovery sample, 0.12 in the replication sample), with each copy of the minor allele associated with a sleep duration 3.1 min longer per night. The alleles associated with longer sleep duration were associated in previous GWAS with a more favorable metabolic profile and a lower risk of attention deficit hyperactivity disorder. Understanding the mechanisms underlying these associations may help elucidate biological mechanisms influencing sleep duration and its association with psychiatric, metabolic and cardiovascular disease.
Subject(s)
Dyssomnias/genetics , Sleep/genetics , Adult , Black or African American/genetics , Aged , Female , Genetic Association Studies , Genome-Wide Association Study , Humans , Male , Middle Aged , Polymorphism, Single Nucleotide , Self Report , White People/geneticsABSTRACT
OBJECTIVE: To estimate genetic and environmental influences on parasomnias and dyssomnias and their association in 8-year-olds. DESIGN: Parents of twins completed the Children's Sleep Habits Questionnaire. SETTING: Families were primarily tested at the Institute of Psychiatry, London, England. PARTICIPANTS: A total of 300 pairs of 8-year-old twins and their parents participated in the study. MAIN OUTCOME MEASURES: Sleep difficulties in children. RESULTS: Individual differences in parasomnias and dyssomnias were largely explained by genes (accounting for 50% and 71% of the variances, respectively). The rest of the variances were mainly due to nonshared environmental influences. A moderate association was found between parasomnias and dyssomnias (r = 0.42), which was mainly accounted for by genetic influences (87%). The genetic correlation between parasomnias and dyssomnias was moderate (r = 0.61). In contrast, the nonshared environmental correlation was small (r = 0.10). CONCLUSIONS: The decomposition of the association between parasomnias and dyssomnias suggests that there may be different manifestations of shared underlying genetic risks for sleep problems partly dependent on nonshared environmental influence.