dc.contributor.author | Lu, Yunxia | |
dc.contributor.author | Ness-Jensen, Eivind | |
dc.contributor.author | Hveem, Kristian | |
dc.contributor.author | Martling, Anna | |
dc.date.accessioned | 2018-02-08T16:45:48Z | |
dc.date.available | 2018-02-08T16:45:48Z | |
dc.date.created | 2015-11-06T06:30:39Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | American Journal of Epidemiology. 2015, 182 (10), 883-893. | nb_NO |
dc.identifier.issn | 0002-9262 | |
dc.identifier.uri | http://hdl.handle.net/11250/2483625 | |
dc.description.abstract | Whether different definitions of metabolic syndrome (MetS) are differently associated with colorectal adenocarcinoma (CA) by anatomical location is unclear. A population-based cohort study, the Cohort of Norway (CONOR) Study, was conducted in Norway from 1995 to 2010. Anthropometric measurements, blood samples, and lifestyle data were collected at recruitment. CAs were identified through linkage to the Norwegian Cancer Register. A composite index of MetS as defined by the International Diabetes Federation (IDF) or/and the National Cholesterol Education Program's Adult Treatment Panel III (ATP III) and single components of MetS, including anthropometric factors, blood pressure, lipids, triglycerides, and glucose, were analyzed. Cox proportional hazards regression was performed to estimate hazard ratios and 95% confidence intervals. Significant associations between single MetS components and CA, except for reduced high-density lipoprotein cholesterol and nonfasting glucose levels, were observed. MetS defined by 2 criteria separately showed a similar association with CA in general, and MetS defined by both the IDF and ATP III showed consistent results. Stronger associations were observed in the proximal colon among men (IDF: hazard ratio (HR) = 1.51, 95% confidence interval (CI): 1.24, 1.84; ATP III: HR = 1.40, 95% CI: 1.15, 1.70) and in the rectum among women (IDF: HR = 1.42, 95% CI: 1.07, 1.89; ATP III: HR = 1.43, 95% CI: 1.08, 1.90). | nb_NO |
dc.language.iso | eng | nb_NO |
dc.publisher | Oxford University Press | nb_NO |
dc.relation.uri | http://aje.oxfordjournals.org/content/182/10/883.full.pdf+html | |
dc.title | Metabolic predispositions and increased risk of colorectal adenocarcinoma by anatomical location: a large population-based cohort study in Norway | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | nb_NO |
dc.description.version | acceptedVersion | nb_NO |
dc.source.pagenumber | 883-893 | nb_NO |
dc.source.volume | 182 | nb_NO |
dc.source.journal | American Journal of Epidemiology | nb_NO |
dc.source.issue | 10 | nb_NO |
dc.identifier.doi | 10.1093/aje/kwv141 | |
dc.identifier.cristin | 1286730 | |
dc.description.localcode | © The Author 2015. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health. All rights reserved. This is a pre-copyedited, author-produced version of the article accepted for publication following peer review. The version of record is available online at: http://dx.doi.org/10.1093/aje/kwv141. | nb_NO |
cristin.unitcode | 194,65,20,15 | |
cristin.unitcode | 194,65,20,0 | |
cristin.unitname | Helseundersøkelsen i Nord-Trøndelag | |
cristin.unitname | Institutt for samfunnsmedisin og sykepleie | |
cristin.ispublished | true | |
cristin.fulltext | postprint | |
cristin.qualitycode | 2 | |