TY - JOUR
T1 - Dietary intake of acrylamide and epithelial ovarian cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort.
AU - Obón-Santacana, Mireia
AU - Peeters, Petra H
AU - Freisling, Heinz
AU - Dossus, Laure
AU - Clavel-Chapelon, Francoise
AU - Baglietto, Laura
AU - Schock, Helena
AU - Fortner, Renée T
AU - Boeing, Heiner
AU - Tjonneland, Anne
AU - Olsen, Anja
AU - Overvad, Kim
AU - Menéndez, Virginia
AU - Sanchez, Maria-Jose
AU - Larranaga, Nerea
AU - Huerta Castaño, José María
AU - Barricarte, Aurelio
AU - Khaw, Kay-Tee
AU - Wareham, Nick
AU - Travis, Ruth C
AU - Merritt, Melissa A
AU - Trichopoulou, Antonia
AU - Trichopoulos, Dimitrios
AU - Orfanos, Philippos
AU - Masala, Giovanna
AU - Sieri, Sabina
AU - Tumino, Rosario
AU - Vineis, Paolo
AU - Mattiello, Amalia
AU - Bueno-de-Mesquita, H Bas
AU - Onland-Moret, N Charlotte
AU - Wirfält, Elisabet
AU - Stocks, Tanja
AU - Idahl, Annika
AU - Lundin, Eva
AU - Skeie, Guri
AU - Gram, Inger T
AU - Weiderpass, Elisabete
AU - Riboli, Elio
AU - Duell, Eric J
PY - 2015
Y1 - 2015
N2 - Acrylamide, classified in 1994 by IARC as 'probably carcinogenic' to humans, was discovered in 2002 in some heat-treated, carbohydrate-rich foods. The association between dietary acrylamide intake and epithelial ovarian cancer risk (EOC) has been previously studied in one case-control and three prospective cohort studies which obtained inconsistent results, and could not further examine histological subtypes other than serous EOC. The present study was carried out in the European Prospective Investigation into Cancer and Nutrition (EPIC) sub-cohort of women (n=325,006). Multivariate Cox proportional hazards models were used to assess the association between questionnaire-based acrylamide intake and EOC risk. Acrylamide was energy-adjusted using the residual method, and was evaluated both as a continuous variable (per 10µg/day) and in quintiles; when subgroups by histological EOC subtypes were analyzed, acrylamide intake was evaluated in quartiles. During a mean follow-up of 11 years, 1,191 incident EOC cases were diagnosed. At baseline, the median acrylamide intake in EPIC was 21.3 μg/day. No associations, and no evidence for a dose-response were observed between energy-adjusted acrylamide intake and EOC risk (HR10µg/day:1.02, 95%CI:0.96-1.09; HRQ5vsQ1:0.97, 95%CI:0.76-1.23). No differences were seen when invasive EOC subtypes (582 serous, 118 endometrioid, and 79 mucinous tumors) were analyzed separately. This study did not provide evidence that acrylamide intake, based on food intake questionnaires, was associated with risk for EOC in EPIC. Additional studies with more reliable estimates of exposure based on biomarkers may be needed.
AB - Acrylamide, classified in 1994 by IARC as 'probably carcinogenic' to humans, was discovered in 2002 in some heat-treated, carbohydrate-rich foods. The association between dietary acrylamide intake and epithelial ovarian cancer risk (EOC) has been previously studied in one case-control and three prospective cohort studies which obtained inconsistent results, and could not further examine histological subtypes other than serous EOC. The present study was carried out in the European Prospective Investigation into Cancer and Nutrition (EPIC) sub-cohort of women (n=325,006). Multivariate Cox proportional hazards models were used to assess the association between questionnaire-based acrylamide intake and EOC risk. Acrylamide was energy-adjusted using the residual method, and was evaluated both as a continuous variable (per 10µg/day) and in quintiles; when subgroups by histological EOC subtypes were analyzed, acrylamide intake was evaluated in quartiles. During a mean follow-up of 11 years, 1,191 incident EOC cases were diagnosed. At baseline, the median acrylamide intake in EPIC was 21.3 μg/day. No associations, and no evidence for a dose-response were observed between energy-adjusted acrylamide intake and EOC risk (HR10µg/day:1.02, 95%CI:0.96-1.09; HRQ5vsQ1:0.97, 95%CI:0.76-1.23). No differences were seen when invasive EOC subtypes (582 serous, 118 endometrioid, and 79 mucinous tumors) were analyzed separately. This study did not provide evidence that acrylamide intake, based on food intake questionnaires, was associated with risk for EOC in EPIC. Additional studies with more reliable estimates of exposure based on biomarkers may be needed.
U2 - 10.1158/1055-9965.EPI-14-0636
DO - 10.1158/1055-9965.EPI-14-0636
M3 - Article
C2 - 25300475
SN - 1538-7755
VL - 24
SP - 291
EP - 297
JO - Cancer Epidemiology Biomarkers & Prevention
JF - Cancer Epidemiology Biomarkers & Prevention
IS - 1
ER -