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dc.contributor.authorTivesten, Å
dc.contributor.authorPinthus, J
dc.contributor.authorClarke, Noel W
dc.contributor.authorDuivenvoorden, W
dc.contributor.authorNilsson, J
dc.date.accessioned2016-01-06T10:49:22Zen
dc.date.available2016-01-06T10:49:22Zen
dc.date.issued2015-11en
dc.identifier.citationCardiovascular risk with androgen deprivation therapy for prostate cancer: Potential mechanisms. 2015, 33 (11):464-75 Urol Oncolen
dc.identifier.issn1873-2496en
dc.identifier.pmid26141678en
dc.identifier.doi10.1016/j.urolonc.2015.05.030en
dc.identifier.urihttp://hdl.handle.net/10541/592965en
dc.description.abstractAndrogen deprivation therapy (ADT) is frequently used for the treatment of advanced prostate cancer. ADT is associated with numerous side effects related to its mode of action, namely the suppression of testosterone to castrate levels. Recently, several large retrospective studies have also reported an increased risk of diabetes and cardiovascular disease in men receiving ADT, although these risks have not been confirmed by prospective randomized trials. We review the literature to consider the risk of cardiovascular disease with different forms of ADT and examine in detail potential mechanisms by which any such risk could be mediated. Mechanisms discussed include the metabolic syndrome resulting from low testosterone level and the potential roles of testosterone flare, gonadotropin-releasing hormone receptors outside the pituitary gland, and altered levels of follicle-stimulating hormone. Finally, the clinical implications for men prescribed ADT for the treatment of advanced prostate cancer are considered.
dc.language.isoenen
dc.rightsArchived with thanks to Urologic oncologyen
dc.titleCardiovascular risk with androgen deprivation therapy for prostate cancer: Potential mechanisms.en
dc.typeArticleen
dc.contributor.departmentWallenberg Laboratory for Cardiovascular and Metabolic Research, Sahlgrenska University Hospital, Göteborg, Sweden.en
dc.identifier.journalUrologic Oncologyen
html.description.abstractAndrogen deprivation therapy (ADT) is frequently used for the treatment of advanced prostate cancer. ADT is associated with numerous side effects related to its mode of action, namely the suppression of testosterone to castrate levels. Recently, several large retrospective studies have also reported an increased risk of diabetes and cardiovascular disease in men receiving ADT, although these risks have not been confirmed by prospective randomized trials. We review the literature to consider the risk of cardiovascular disease with different forms of ADT and examine in detail potential mechanisms by which any such risk could be mediated. Mechanisms discussed include the metabolic syndrome resulting from low testosterone level and the potential roles of testosterone flare, gonadotropin-releasing hormone receptors outside the pituitary gland, and altered levels of follicle-stimulating hormone. Finally, the clinical implications for men prescribed ADT for the treatment of advanced prostate cancer are considered.


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