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dc.contributor.authorStocks, Tanjaen_US
dc.contributor.authorBjørge, Toneen_US
dc.contributor.authorUlmer, Hannoen_US
dc.contributor.authorManjer, Jonasen_US
dc.contributor.authorHäggström, Christelen_US
dc.contributor.authorNagel, Gabrieleen_US
dc.contributor.authorEngeland, Andersen_US
dc.contributor.authorJohansen, Dortheen_US
dc.contributor.authorHallmans, Göranen_US
dc.contributor.authorSelmer, Randien_US
dc.contributor.authorConcin, Hansen_US
dc.contributor.authorTretli, Steinaren_US
dc.contributor.authorJonsson, Håkanen_US
dc.contributor.authorStattin, Pären_US
dc.date.accessioned2016-03-08T13:20:28Z
dc.date.available2016-03-08T13:20:28Z
dc.date.issued2015
dc.PublishedInternational Journal of Epidemiology 2015, 44(4):1353-1363eng
dc.identifier.issn0300-5771
dc.identifier.urihttps://hdl.handle.net/1956/11467
dc.description.abstractBackground: There are few data on the joint influence of metabolic factors on risk of separate cancers. Methods: We analysed data on body mass index, blood pressure and plasma levels of glucose, total cholesterol and triglycerides from seven European cohorts comprising 564 596 men and women with a mean age of 44 years. We weighted those factors equally into a standardized metabolic risk score [MRS, mean = 0, standard deviation (SD) = 1], with an individual’s level indicated as SDs from the sex- and cohort-specific means. Cancer hazard ratios were calculated by Cox regression with age as timescale and with relevant adjustments including smoking status. All statistical tests were two-sided. Results: During a mean follow-up of 12 years, 21 593 men and 14 348 women were diagnosed with cancer. MRS was linearly and positively associated with incident cancer in total and at sites (P < 0.05). In men, risk per SD MRS was increased by 43% (95% confidence interval: 27–61) for renal cell cancer, 43% (16–76) for liver cancer, 29% (20–38) for colon cancer, 27% (5–54) for oesophageal cancer, 20% (9–31) for rectal cancer, 19% (4–37) for leukaemias, 15% (1–30) for oral cancer and 10% (2–19) for bladder cancer. In women, risk increases per SD MRS were 56% (42–70) for endometrial cancer, 53% (29–81) for pancreatic cancer, 40% (16–67) for renal cell cancer, 27% (9–47) for cervical cancer and 17% (3–32) for rectal cancer. Conclusion: This largest study to date on the joint influence of metabolic factors on risk of separate cancers showed increased risks for several cancers, in particular renal cell and liver cancer in men and endometrial and pancreatic cancer in women.en_US
dc.language.isoengeng
dc.publisherOxford University Presseng
dc.relation.urihttp://ije.oxfordjournals.org/content/early/2015/02/03/ije.dyv001.full.pdf+html
dc.rightsAttribution CC BY-NCeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/eng
dc.subjectcohort studieseng
dc.subjectmetabolic syndrome xeng
dc.subjectneoplasmseng
dc.titleMetabolic risk score and cancer risk: pooled analysis of seven cohortsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2015-09-22T08:36:21Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2015 The Authors
dc.identifier.doihttps://doi.org/10.1093/ije/dyv001
dc.identifier.cristin1266314


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