4.7 Article

Adolescent animal product intake in relation to later prostate cancer risk and mortality in the NIH-AARP Diet and Health Study

Journal

BRITISH JOURNAL OF CANCER
Volume 125, Issue 8, Pages 1158-1167

Publisher

SPRINGERNATURE
DOI: 10.1038/s41416-021-01463-1

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Funding

  1. Barnes-Jewish Hospital Foundation
  2. Alvin J. Siteman Cancer Center
  3. Institute for Clinical and Translational Sciences

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The study found suggestive inverse trends between adolescent unprocessed beef intake and total, advanced, and fatal prostate cancer (PCa), suggesting a potential association with reduced risk and mortality from PCa. However, no consistent patterns of association were observed for other animal products by PCa outcome. Further studies with more early-life exposure information are needed to better understand this relationship.
Background Adolescent intake of animal products has been proposed to contribute to prostate cancer (PCa) development because of its potentially carcinogenic constituents and influence on hormone levels during adolescence. Methods We used data from 159,482 participants in the NIH-AARP Diet and Health Study to investigate associations for recalled adolescent intake of red meat (unprocessed beef and processed red meat), poultry, egg, canned tuna, animal fat and animal protein at ages 12-13 years with subsequent PCa risk and mortality over 14 years of follow-up. Cox proportional hazard regression was used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs) of total (n = 17,349), advanced (n = 2,297) and fatal (n = 804) PCa. Results Suggestive inverse trends were observed for adolescent unprocessed beef intake with risks of total, advanced and fatal PCa (multivariable-adjusted P-trends = 0.01, 0.02 and 0.04, respectively). No consistent patterns of association were observed for other animal products by PCa outcome. Conclusion We found evidence to suggest that adolescent unprocessed beef intake, or possibly a correlate of beef intake, such as early-life socioeconomic status, may be associated with reduced risk and mortality from PCa. Additional studies with further early-life exposure information are warranted to better understand this association.

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