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Adipokines and inflammation markers and risk of differentiated thyroid carcinoma:the EPIC study
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Dossus_et_al-2018-International_Journal_of_Cancer.pdf | Published version | 678.23 kB | Adobe PDF | View/Open |
Title: | Adipokines and inflammation markers and risk of differentiated thyroid carcinoma:the EPIC study |
Authors: | Dossus, L Franceschi, S Biessy, C Navionis, A-S Travis, R Weiderpass, E Scalbert, A Romieu, I Tjonneland, A Olsen, A Overvad, K Boutron-Ruault, M-C Bonnet, F Fournier, A Fortner, R Kaaks, R Aleksandrova, K Trichopoulou, A La Vecchia, C Peppa, E Tumino, R Panico, S Palli, D Agnoli, C Vineis, P Bueno-de-Mesquita, B Peeters, PH Skeie, G Zamora-Ros, R Chirlaque, M-D Ardanaz, E Sanchez, M-J Quiros, JR Dorronsoro, M Sandstrom, M Nilsson, LM Schmidt, JA Khaw, K-T Tsilidis, K Aune, D Riboli, E Rinaldi, S |
Item Type: | Journal Article |
Abstract: | Other than the influence of ionizing radiation and benign thyroid disease, little is known about the risk factors for differentiated thyroid cancer (TC) which is an increasing common cancer worldwide. Consistent evidence shows that body mass is positively associated with TC risk. As excess weight is a state of chronic inflammation, we investigated the relationship between concentrations of leptin, adiponectin, C-reactive protein, interleukin (IL)-6, IL-10 and tumor necrosis factor (TNF)-α and the risk of TC. A case-control study was nested within the European Prospective Investigation into Cancer and Nutrition (EPIC) study and included 475 first primary incident TC cases (399 women and 76 men) and 1,016 matched cancer-free cohort participants. Biomarkers were measured in serum samples using validated and highly sensitive commercially available immunoassays. Odds ratios (ORs) of TC by levels of each biomarker were estimated using conditional logistic regression models, adjusting for BMI and alcohol consumption. Adiponectin was inversely associated with TC risk among women (ORT3vs.T1 = 0.69, 95% CI: 0.49–0.98, Ptrend = 0.04) but not among men (ORT3vs.T1 = 1.36, 95% CI: 0.67–2.76, Ptrend = 0.37). Increasing levels of IL-10 were positively associated with TC risk in both genders and significantly so in women (ORT3vs.T1 = 1.59, 95% CI: 1.13–2.25, Ptrend = 0.01) but not in men (ORT3vs.T1 = 1.78, 95% CI: 0.80–3.98, Ptrend = 0.17). Leptin, CRP, IL-6 and TNF-α were not associated with TC risk in either gender. These results indicate a positive association of TC risk with IL-10 and a negative association with adiponectin that is probably restricted to women. Inflammation may play a role in TC in combination with or independently of excess weight. |
Issue Date: | 20-Dec-2017 |
Date of Acceptance: | 6-Nov-2017 |
URI: | http://hdl.handle.net/10044/1/53106 |
DOI: | https://dx.doi.org/10.1002/ijc.31172 |
ISSN: | 0020-7136 |
Publisher: | Wiley |
Start Page: | 1332 |
End Page: | 1342 |
Journal / Book Title: | International Journal of Cancer |
Volume: | 142 |
Issue: | 7 |
Copyright Statement: | © 2017 International Agency for Research on Cancer (IARC/WHO); licensed by UICC This is an open access article distributed under the terms of the Creative Commons Attribution IGO License IARC's preferred IGO license is the non-commercial: https://creativecommons.org/licenses/by-nc/3.0/igo/legalcode which permits non-commercial unrestricted use, distribution and reproduction in any medium, provided that the original work is properly cited. In any reproduction of this article there should not be any suggestion that IARC/WHO or the article endorse any specific organization or products. The use of the IARC/WHO logo is not permitted. This notice should be preserved along with the article's URL. |
Sponsor/Funder: | Institut National du Cancer |
Funder's Grant Number: | NIL |
Keywords: | Science & Technology Life Sciences & Biomedicine Oncology thyroid cancer inflammation cytokine adipokine prospective cohort C-REACTIVE PROTEIN PLASMA ADIPONECTIN CONCENTRATIONS ENDOMETRIAL CANCER-RISK ADIPOSE-TISSUE BREAST-CANCER CIRCULATING ADIPONECTIN GENE POLYMORPHISM POOLED ANALYSIS INTERLEUKIN-10 BIOMARKERS 1112 Oncology And Carcinogenesis Oncology & Carcinogenesis |
Publication Status: | Published |
Appears in Collections: | School of Public Health |