dc.contributor.author
Dimopoulou, Olympia
dc.contributor.author
Fuller, Harriett
dc.contributor.author
Richmond, Rebecca C.
dc.contributor.author
Bouras, Emmanouil
dc.contributor.author
Hayes, Bryony
dc.contributor.author
Dimou, Niki
dc.contributor.author
Murphy, Neil
dc.contributor.author
Brenner, Hermann
dc.contributor.author
Gsur, Andrea
dc.contributor.author
Le Marchand, Loïc
dc.contributor.author
Moreno Aguado, Víctor
dc.contributor.author
Pai, Rish K.
dc.contributor.author
Phipps, Amanda I.
dc.contributor.author
Um, Caroline Y.
dc.contributor.author
Duijnhoven, Franzel J. B. van
dc.contributor.author
Vodicka, Pavel
dc.contributor.author
Martin, Richard M.
dc.contributor.author
Platz, Elizabeth A.
dc.contributor.author
Gunter, Marc J.
dc.contributor.author
Peters, Ulrike
dc.contributor.author
Lewis, Sarah J.
dc.contributor.author
Cao, Yin
dc.contributor.author
Tsilidis, Konstantinos K.
dc.date.issued
2025-06-25T09:37:41Z
dc.date.issued
2025-06-25T09:37:41Z
dc.date.issued
2025-04-18
dc.date.issued
2025-06-19T14:24:16Z
dc.identifier
https://hdl.handle.net/2445/221727
dc.description.abstract
A potential association of endogenous circadian rhythm disruption with risk of cancer development has been suggested, however, epidemiological evidence for the association of sleep traits with colorectal cancer (CRC) is limited and often contradictory. Here we investigated whether genetically predicted chronotype, insomnia and sleep duration are associated with CRC risk in males, females and overall and according to CRC anatomical subsites using Mendelian randomization (MR). The two-sample inverse variance weighted (IVW) method was applied using summary-level data in up to 58,221 CRC cases and 67,694 controls and genome-wide association data of genetic variants for self-reported sleep traits. Secondary analyses using alternative instruments and sensitivity analyses assessing potential violations of MR assumptions were conducted. Genetically predicted morning preference was associated with 13% lower risk of CRC in men (ORIVW = 0.87, 95% CI = 0.78, 0.97, P = 0.01), but not in women or in both sexes combined. Tau his association remained consistent in some, but not all, sensitivity analyses and was very similar for colon and rectal cancer. There was no evidence of an association for any other sleep trait. Overall, this study provides little to no evidence of an association between genetically predicted sleep traits and CRC risk.
dc.format
application/pdf
dc.publisher
Springer Science and Business Media LLC
dc.relation
Reproducció del document publicat a: https://doi.org/10.1038/s41598-024-83693-w
dc.relation
Scientific Reports, 2025, vol. 15
dc.relation
https://doi.org/10.1038/s41598-024-83693-w
dc.rights
cc-by (c) Dimopoulou et al., 2024
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Càncer colorectal
dc.subject
Colorectal cancer
dc.subject
Carcinogenesis
dc.title
Mendelian randomization study of sleep traits and risk of colorectal cancer
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion