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dc.contributor.authorNair-Shalliker Ven_AU
dc.contributor.authorYap Sen_AU
dc.contributor.authorNunez Cen_AU
dc.contributor.authorEgger Sen_AU
dc.contributor.authorRodger Jen_AU
dc.contributor.authorPatel Men_AU
dc.contributor.authorO'Connell DLen_AU
dc.contributor.authorSitas Fen_AU
dc.contributor.authorArmstrong BKen_AU
dc.contributor.authorSmith DPen_AU
dc.date.issued2017en
dc.identifier.urihttps://hdl.handle.net/2123/30901
dc.description.abstractProstate cancer (PC) is the most common non-cutaneous cancer in men worldwide. The relationships between PC and possible risk factors for PC cases (n = 1,181) and male controls (n = 875) from the New South Wales (NSW) Cancer, Lifestyle and Evaluation of Risk Study (CLEAR) were examined in this study. The associations between PC risk and paternal history of PC, body mass index (BMI), medical conditions, sexual behaviour, balding pattern and puberty, after adjusting for age, income, region of birth, place of residence, and PSA testing, were examined. Adjusted risk of PC was higher for men with a paternal history of PC (OR = 2.31; 95%CI: 1.70-3.14), personal history of prostatitis (OR = 2.30; 95%CI: 1.44-3.70), benign prostatic hyperplasia (OR = 2.29; 95%CI: 1.79-2.93), being overweight (vs. normal; OR = 1.24; 95%CI: 0.99-1.55) or obese (vs. normal; OR = 1.44; 95%CI: 1.09-1.89), having reported more than seven sexual partners in a lifetime (vs. < 3 partners; OR = 2.00; 95%CI: 1.49-2.68), and having reported more than 5 orgasms a month prior to PC diagnosis (vs. ≤3 orgasms; OR = 1.59; 95%CI: 1.18-2.15). PC risk was lower for men whose timing of puberty was later than their peers (vs. same as peers; OR = 0.75; 95%CI: 0.59-0.97), and a smaller risk reduction of was observed in men whose timing of puberty was earlier than their peers (vs. same as peers; OR = 0.85; 95%CI: 0.61-1.17). No associations were found between PC risk and vertex balding, erectile function, acne, circumcision, vasectomy, asthma or diabetes. These results support a role for adult body size, sexual activity, and adolescent sexual development in PC development.en_AU
dc.publisherInternational Journal of Canceren_AU
dc.subject.otherEtiology - Interactions of Genes and/or Genetic Polymorphisms with Exogenous and/or Endogenous Factorsen_AU
dc.subject.otherCancer Type - Prostate Canceren_AU
dc.titleAdult body size, sexual history and adolescent sexual development, may predict risk of developing prostate cancer: Results from the New South Wales Lifestyle and Evaluation of Risk Study (CLEAR).en_AU
dc.typeArticleen_AU
dc.identifier.doi10.1002/ijc.30471
dc.relation.otherDPS was supported by a National Health and Medical Research Council Training Fellowship (APP1016598)en_AU


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