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Genetic variants affect diurnal glucose levels throughout the day.
Sinnott-Armstrong, Nasa; Strausz, Satu; Urpa, Lea; Abner, Erik; Valliere, Jesse; Palta, Priit; Dashti, Hassan S; Daly, Mark; Pritchard, Jonathan K; Saxena, Richa; Jones, Samuel E; Ollila, Hanna M.
Afiliação
  • Sinnott-Armstrong N; Herbold Computational Biology Program, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Strausz S; Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki, Helsinki, Finland.
  • Urpa L; Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki, Helsinki, Finland.
  • Abner E; Department of Genetics, Stanford University, CA, USA.
  • Valliere J; Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki, Helsinki, Finland.
  • Palta P; Broad Institute of Harvard and MIT and Center of Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Dashti HS; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Pritchard JK; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
  • Saxena R; Broad Institute of Harvard and MIT and Center of Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Jones SE; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Ollila HM; Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki, Helsinki, Finland.
bioRxiv ; 2024 Jul 23.
Article em En | MEDLINE | ID: mdl-39091879
ABSTRACT
Circadian rhythms not only coordinate the timing of wake and sleep but also regulate homeostasis within the body, including glucose metabolism. However, the genetic variants that contribute to temporal control of glucose levels have not been previously examined. Using data from 420,000 individuals from the UK Biobank and replicating our findings in 100,000 individuals from the Estonian Biobank, we show that diurnal serum glucose is under genetic control. We discover a robust temporal association of glucose levels at the Melatonin receptor 1B (MTNR1B) (rs10830963, P = 1e-22) and a canonical circadian pacemaker gene Cryptochrome 2 (CRY2) loci (rs12419690, P = 1e-16). Furthermore, we show that sleep modulates serum glucose levels and the genetic variants have a separate mechanism of diurnal control. Finally, we show that these variants independently modulate risk of type 2 diabetes. Our findings, together with earlier genetic and epidemiological evidence, show a clear connection between sleep and metabolism and highlight variation at MTNR1B and CRY2 as temporal regulators for glucose levels.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article