The dose-effect relationship between 'unopposed' oestrogens and endometrial mitotic rate: Its central role in explaining and predicting endometrial cancer risk
1988

Unopposed Oestrogens and Endometrial Cancer Risk

publication Evidence: moderate

Author Information

Author(s): T.J.A. Key, M.C. Pike

Primary Institution: Imperial Cancer Research Fund's Epidemiology Unit, Radcliffe Infirmary, Oxford, UK

Hypothesis

The unopposed oestrogen hypothesis suggests that endometrial cancer risk increases with exposure to oestrogen not opposed by progestagen.

Conclusion

The study concludes that both short-term and long-term use of oestrogens can significantly affect endometrial cancer risk.

Supporting Evidence

  • Short-term use of combination-type oral contraceptives can reduce endometrial cancer risk by about 60%.
  • Five years of unopposed oestrogen replacement therapy can increase lifetime risk of endometrial cancer by at least 90%.
  • Obesity is associated with increased endometrial cancer risk due to progesterone deficiency.

Takeaway

If women take oestrogen without progesterone, it can increase their chances of getting endometrial cancer. But using a combination of both can help protect them.

Methodology

The study analyzed the mitotic rate of endometrial cells in relation to oestrogen levels and examined epidemiological data on hormone therapy and obesity.

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