TY - JOUR
T1 - Pre-diagnostic circulating insulin-like growth factor-I and bladder cancer risk in the European Prospective Investigation into Cancer and Nutrition
AU - Lin, Crystal
AU - Travis, Ruth C.
AU - Appleby, Paul N.
AU - Tipper, Sarah
AU - Weiderpass, Elisabete
AU - Chang-Claude, Jenny
AU - Gram, Inger T.
AU - Kaaks, Rudolf
AU - Kiemeney, Lambertus A.
AU - Ljungberg, Börje
AU - Tumino, Rosario
AU - Tjønneland, Anne
AU - Roswall, Nina
AU - Overvad, Kim
AU - Boutron-Ruault, Marie Christine
AU - Manciniveri, Francesca Romana
AU - Severi, Gianluca
AU - Trichopoulou, Antonia
AU - Masala, Giovanna
AU - Sacerdote, Carlotta
AU - Agnoli, Claudia
AU - Panico, Salvatore
AU - Bueno-de-Mesquita, Bas
AU - Peeters, Petra H.
AU - Salamanca-Fernández, Elena
AU - Chirlaque, Maria Dolores
AU - Ardanaz, Eva
AU - Dorronsoro, Miren
AU - Menéndez, Virginia
AU - Luján-Barroso, Leila
AU - Liedberg, Fredrik
AU - Freisling, Heinz
AU - Gunter, Marc
AU - Aune, Dagfinn
AU - Cross, Amanda J.
AU - Riboli, Elio
AU - Key, Timothy J.
AU - Perez-Cornago, Aurora
N1 - Publisher Copyright:
© 2018 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
PY - 2018/11/15
Y1 - 2018/11/15
N2 - Previous in vitro and case–control studies have found an association between the insulin-like growth factor (IGF)-axis and bladder cancer risk. Circulating concentrations of IGF-I have also been found to be associated with an increased risk of several cancer types; however, the relationship between pre-diagnostic circulating IGF-I concentrations and bladder cancer has never been studied prospectively. We investigated the association of pre-diagnostic plasma concentrations of IGF-I with risk of overall bladder cancer and urothelial cell carcinoma (UCC) in a case–control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. A total of 843 men and women diagnosed with bladder cancer between 1992 and 2005 were matched with 843 controls by recruitment centre, sex, age at recruitment, date of blood collection, duration of follow-up, time of day and fasting status at blood collection using an incidence density sampling protocol. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using conditional logistic regression with adjustment for smoking status. No association was found between pre-diagnostic circulating IGF-I concentration and overall bladder cancer risk (adjusted OR for highest versus lowest fourth: 0.91, 95% CI: 0.66–1.24, p trend = 0.40) or UCC (n of cases = 776; 0.91, 0.65–1.26, p trend = 0.40). There was no significant evidence of heterogeneity in the association of IGF-I with bladder cancer risk by tumour aggressiveness, sex, smoking status, or by time between blood collection and diagnosis (p heterogeneity > 0.05 for all). This first prospective study indicates no evidence of an association between plasma IGF-I concentrations and bladder cancer risk.
AB - Previous in vitro and case–control studies have found an association between the insulin-like growth factor (IGF)-axis and bladder cancer risk. Circulating concentrations of IGF-I have also been found to be associated with an increased risk of several cancer types; however, the relationship between pre-diagnostic circulating IGF-I concentrations and bladder cancer has never been studied prospectively. We investigated the association of pre-diagnostic plasma concentrations of IGF-I with risk of overall bladder cancer and urothelial cell carcinoma (UCC) in a case–control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. A total of 843 men and women diagnosed with bladder cancer between 1992 and 2005 were matched with 843 controls by recruitment centre, sex, age at recruitment, date of blood collection, duration of follow-up, time of day and fasting status at blood collection using an incidence density sampling protocol. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using conditional logistic regression with adjustment for smoking status. No association was found between pre-diagnostic circulating IGF-I concentration and overall bladder cancer risk (adjusted OR for highest versus lowest fourth: 0.91, 95% CI: 0.66–1.24, p trend = 0.40) or UCC (n of cases = 776; 0.91, 0.65–1.26, p trend = 0.40). There was no significant evidence of heterogeneity in the association of IGF-I with bladder cancer risk by tumour aggressiveness, sex, smoking status, or by time between blood collection and diagnosis (p heterogeneity > 0.05 for all). This first prospective study indicates no evidence of an association between plasma IGF-I concentrations and bladder cancer risk.
KW - EPIC cohort
KW - IGF-I
KW - bladder cancer
KW - prospective
KW - urothelial cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85053382965&partnerID=8YFLogxK
U2 - 10.1002/ijc.31650
DO - 10.1002/ijc.31650
M3 - Article
C2 - 29971779
AN - SCOPUS:85053382965
SN - 0020-7136
VL - 143
SP - 2351
EP - 2358
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 10
ER -