Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank
Autor: | Max A. Little, Richa Saxena, Simon G. Anderson, Andrew S. I. Loudon, Shubhroz Gill, Debbie A Lawlor, Richard Emsley, Martin K. Rutter, Irma Vlasac, David A. Bechtold, Jacqueline M. Lane, David W. Ray, Simon D. Kyle, Susan Redline, Frank A.J.L. Scheer, Annemarie I. Luik, William G Dixon |
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Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
Adult
Male 0301 basic medicine Candidate gene Science Circadian clock General Physics and Astronomy Genome-wide association study Biology Article White People General Biochemistry Genetics and Molecular Biology Cohort Studies 03 medical and health sciences 0302 clinical medicine Mendelian randomization medicine Humans Circadian rhythm Aged 030304 developmental biology Genetics 0303 health sciences Multidisciplinary Genome Human Chronotype Cognition General Chemistry Middle Aged medicine.disease Biobank United Kingdom Educational attainment Circadian Rhythm 3. Good health 030104 developmental biology Genetic Loci Schizophrenia Evolutionary biology Female 030217 neurology & neurosurgery Genome-Wide Association Study |
Zdroj: | Nature Communications, Vol 7, Iss 1, Pp 1-10 (2016) Lane, J M, Vlasac, I, Anderson, S G, Kyle, S D, Dixon, W G, Bechtold, D A, Gill, S, Little, M A, Luik, A, Loudon, A, Emsley, R, Scheer, F A J L, Lawlor, D A, Redline, S, Ray, D W, Rutter, M K & Saxena, R 2016, ' Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank ', Nature Communications, vol. 7, 10889 . https://doi.org/10.1038/ncomms10889 Nature Communications |
ISSN: | 2041-1723 |
Popis: | Our sleep timing preference, or chronotype, is a manifestation of our internal biological clock. Variation in chronotype has been linked to sleep disorders, cognitive and physical performance, and chronic disease. Here we perform a genome-wide association study of self-reported chronotype within the UK Biobank cohort (n=100,420). We identify 12 new genetic loci that implicate known components of the circadian clock machinery and point to previously unstudied genetic variants and candidate genes that might modulate core circadian rhythms or light-sensing pathways. Pathway analyses highlight central nervous and ocular systems and fear-response-related processes. Genetic correlation analysis suggests chronotype shares underlying genetic pathways with schizophrenia, educational attainment and possibly BMI. Further, Mendelian randomization suggests that evening chronotype relates to higher educational attainment. These results not only expand our knowledge of the circadian system in humans but also expose the influence of circadian characteristics over human health and life-history variables such as educational attainment. Here, Richa Saxena and colleagues perform a genome-wide association study (GWAS) of self-reported morningness/eveningness preference in the UKBiobank cohort, and identify new genetic loci that contribute to a person's chronotype. |
Databáze: | OpenAIRE |
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