RT Journal Article T1 Circadian clock gene variants and their link with chronotype, chrononutrition, sleeping patterns and obesity in the European prospective investigation into cancer and nutrition (EPIC) study. A1 Molina-Montes, Esther A1 Rodriguez-Barranco, Miguel A1 Ching-Lopez, Ana A1 Artacho, Reyes A1 Huerta, Jose Maria A1 Amiano, Pilar A1 Lasheras, Cristina A1 Moreno-Iribas, Conchi A1 Jimenez-Zabala, Ana A1 Chirlaque, Maria-Dolores A1 Barricarte, Aurelio A1 Lujan-Barroso, Leila A1 Agudo, Antonio A1 Jakszyn, Paula A1 Quiros, Jose Ramon A1 Sanchez-Perez, Maria-Jose K1 Anthropometry K1 Chronobiology K1 Circadian clock K1 Diet habits K1 Genetic association analyses K1 Genetics K1 Obesity AB The circadian clock is involved in the control of daily rhythms and is related to the individual's chronotype, i.e., the morningness-eveneningness preference. Knowledge is limited on the relationship between circadian genes, chronotype, sleeping patterns, chronutrition and obesity. The aim was to explore these associations within the EPIC-Spain cohort study. There were 3183 subjects with information on twelve genetic variants of six genes (PER1, PER2, PER3, CRY1, NR1D1, CLOCK). Their association was evaluated with: chronotype and sleeping duration/quality (assessed by questionnaires), chrononutrition (number of meals and timing of intake assessed by a diet history), and also anthropometric measures of obesity at early and late adulthood (in two points in time), such as weight and waist circumference (assessed by physical measurements). Multivariable logistic and linear regression as well as additive genetic models were applied. Odds ratios (ORs), β coefficients, and p-values corrected for multiple comparisons were estimated. Genetic risk scores (GRS) were built to test gene-outcome associations further. At nominal significance level, the variant rs2735611 (PER1 gene) was associated with a 11.6% decrease in long-term weight gain (per-allele β = -0.12), whereas three CLOCK gene variants (rs12649507, rs3749474 and rs4864548), were associated with a ∼20% decrease in waist circumference gain (per-allele β ∼ -0.19). These and other associations with body measures did not hold after multiple testing correction, except waist-to-hip ratio and rs1801260, rs2070062 and rs4580704 (CLOCK gene). Associations with chrononutrition variables, chronotype and sleep duration/quality failed to reach statistical significance. Conversely, a weighted GRS was associated with the evening/late chronotype and with all other outcomes (p  Genetic variants of some circadian clock genes could explain the link between genetic susceptibility to the individual's chronotype and obesity risk. PB Elsevier BV YR 2022 FD 2022-07-16 LK http://hdl.handle.net/10668/22116 UL http://hdl.handle.net/10668/22116 LA en NO Molina-Montes E, Rodríguez-Barranco M, Ching-López A, Artacho R, Huerta JM, Amiano P, et al. Circadian clock gene variants and their link with chronotype, chrononutrition, sleeping patterns and obesity in the European prospective investigation into cancer and nutrition (EPIC) study. Clin Nutr. 2022 Sep;41(9):1977-1990. NO The authors are thankful to the study participants of the EPICSpain chronodiet study. We also acknowledge the collaboration ofBiobank Network of the Region of Murcia, BIOBANC-MUR, registered on the Registro Nacional de Biobancos with registrationnumber B.0000859. BIOBANC-MUR is supported by the “Institutode Salud Carlos III" (project PT20/00109), by “Instituto Murciano deInvestigacion Biosanitaria Virgen de la Arrixaca, IMIB ” and by“Consejeria de Salud de la Comunidad Autonoma de la Regi on de Murcia". Also, we acknowledge the Basque Biobank, which belongsto the Basque Government, Department of Health, with registrationnumber B.0000140, and the BIOBANCO del Principado de Asturiaswith registration number B.0000827. The genotyping was performed at the Spanish National Cancer Research Centre, in theHumanGenotyping lab, a member of CeGen, PRB3 and is supportedby grant PT17/0019, of the PE IþDþi 2013e2016, funded by ISCIIIand ERDF. DS RISalud RD Apr 11, 2025