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The Journal of Clinical Endocrinology & Metabolism Vol. 86, No. 3 1341-1345
Copyright © 2001 by The Endocrine Society


Original Studies

Leptin Is Associated with Increased Prostate Cancer Risk: A Nested Case-Referent Study1

Pär Stattin, Stefan Söderberg, Göran Hallmans, Annika Bylund, Rudolf Kaaks, Ulf-Håkan Stenman, Anders Bergh and Tommy Olsson

Departments of Urology and Andrology (P.S.), Public Health and Clinical Medicine (S.S., G.H., T.O.), Geriatric Medicine (A.By.), and Pathology (A.Be.), Umeå University Hospital, SE-901 85 Umeå, Sweden; International Agency for Research on Cancer (R.K.), F-69372 Lyon, France; and Department of Clinical Chemistry (U.-H.S.), Helsinki University Central Hospital, SF-00290 Helsinki, Finland

Address correspondence and requests for reprints to: Dr. Stefan Söderberg, Department of Medicine, Umeå University Hospital, SE-901 85 Umeå, Sweden. E-mail: stefan.soderberg{at}medicin.umu.se

A Western lifestyle has been implicated in the pathogenesis of prostate cancer. However, no clear association between obesity and prostate cancer has been shown. Leptin may stimulate prostate growth and angiogenesis, and receptors for leptin are present in the prostate. Leptin may, thus, be associated with increased risk of prostate cancer.

One hundred forty-nine men with prostate cancer were identified (together with 298 matched referents) who, before diagnosis, had participated in population-based health surveys in Northern Sweden. Blood pressure, body mass index, and use of tobacco were recorded. Leptin, insulin, insulin-like growth factor I (IGF-I), IGF-I-binding proteins 1–3, testosterone, and sex hormone-binding globulin were analyzed in stored samples. Their influences on prostate cancer were estimated by conditional logistic regression analysis. Prostate cancer specimens were investigated for immunoreactivity for the leptin receptor.

Relative risk (95% confidence intervals) estimates of prostate cancer over the quintiles of leptin were 1.0, 2.1 (1.1–4.1), 2.6 (1.4–4.8), 1.4 (0.7–2.7), and 1.6 (0.8–3.2). Adjustments for metabolic variables, testosterone, and IGF-I and its binding proteins did not attenuate this increased risk. Immunoreactivity for the leptin receptor was detected in normal, high-grade prostatic intraepithelial neoplasia lesions and malignant prostatic epithelium.

Moderately elevated plasma leptin concentrations are associated with later development of prostate cancer. This may be due to direct effects of leptin on prostatic intraepithelial neoplasia lesions, or to indirect actions through other mechanisms. A critical fat mass related to an interior milieu favorable for prostate cancer development seems to exist, because intermediate but not high leptin levels are related to prostate cancer risk.




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