Supplemental selenium may decrease ovarian cancer risk in African-American women

Academic Article

Abstract

  • © 2017 American Society for Nutrition. Background: To our knowledge, no previous study has evaluated the associations of antioxidant intake with the risk of ovarian cancer in African-American women, who are known to have high mortality from the disease. Objective: We sought to evaluate these associations among 406 ovarian cancer cases and 632 age- and site-matched controls of African-American descent recruited from AACES (African American Cancer Epidemiology Study), a populationbased, case-control study in 11 geographical areas within the United States. Methods: Multivariable logistic regression models were used to estimate ORs and 95% CIs adjusted for a wide range of potentially confounding factors, including age, region, education, parity, oral contraceptive use, menopause, tubal ligation, family history, body mass index (BMI), smoking status, total energy, and physical activity. Results: Women with the highest intakes of supplemental selenium (≥ 20 mg/d) had an ;30% lower risk of ovarian cancer than those with no supplemental intake (OR: 0.67; 95% CI: 0.46, 0.97; P-trend = 0.035). This inverse association was stronger in current smokers (OR: 0.13; 95% CI: 0.04, 0.46; P-trend = 0.001). There was no association with dietary selenium. The associations with carotenoid intakes were weak and nonsignificant (P = 0.07-0.60). We observed no association with dietary or supplemental intake of vitamin C or vitamin E. There were no appreciable differences in results between serous and nonserous tumors. Conclusions: These findings provide the first insights, to our knowledge, into the potential association between antioxidants and ovarian cancer in African-American women, indicating potential inverse associations with supplemental selenium.
  • Published In

    Digital Object Identifier (doi)

    Author List

  • Terry PD; Qin B; Camacho F; Moorman PG; Alberg AJ; Barnholtz-Sloan JS; Bondy M; Cote ML; Funkhouser E; Guertin KA
  • Start Page

  • 621
  • End Page

  • 627
  • Volume

  • 147
  • Issue

  • 4