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Plasma prolactin and prostate cancer risk: A prospective study
P Stattin1, S Rinaldi, U H Stenman
1Department of Urology and Andrology, Umeå University Hospital, Umeå, Sweden. par.stattin@urologi.umu.se
International Journal of Cancer
|April 6, 2001
Summary
This study found no link between high prolactin levels and increased prostate cancer risk. Elevated circulating prolactin is not associated with prostate cancer development.
Area of Science:
- Endocrinology
- Oncology
- Urology
Background:
- Prolactin, a pituitary hormone, stimulates prostate growth in experimental models.
- Prolactin receptors are found in human prostate tissue, including pre-cancerous lesions, suggesting a potential role in prostate cancer.
- Previous research indicates a possible association between prolactin and prostate cancer development.
Purpose of the Study:
- To investigate the hypothesis that elevated circulating prolactin levels are associated with an increased risk of prostate cancer.
- To determine if prolactin plays a role in the development of prostate cancer.
Main Methods:
- A case-control study was conducted within the Northern Sweden Health and Disease Cohort.
- Plasma samples from 144 men diagnosed with prostate cancer and 289 matched controls were analyzed for prolactin levels.
- Statistical analyses, including univariate regression and adjustments for covariates like testosterone and IGFs, were performed.
Main Results:
- No significant association was found between plasma prolactin levels and prostate cancer risk in univariate analysis.
- Odds ratios for prostate cancer across increasing quartiles of prolactin were consistently close to 1.0.
- Adjusting for height, weight, testosterone, sex hormone-binding globulin, IGF-I, and IGF-binding protein-3 did not alter the risk estimates.
Conclusions:
- Elevated circulating prolactin levels are not related to an increased risk of prostate cancer.
- High circulating prolactin is not associated with the development of prostate cancer.
- The findings do not support a role for prolactin in prostate cancer etiology.