Zusammenfassung
Die Hormonersatztherapie (HRT) ist zur Behandlung klimakterischer Symptome etabliert. Es konnte allerdings gezeigt werden, dass die HRT zu einem Mammakarzinomrisiko führt. Deshalb sind Substanzen von Interesse, die eine Behandlung klimakterischer Symptome zulassen, ohne mit einem erhöhten Mammakarzinomrisiko behaftet zu sein. Hier spielen insbesondere die selektiven Östrogenrezeptormodulatoren (SERMs) sowie die gewebeselektiven Regulatoren der Östrogenaktivität (STEARs) eine Rolle. Die Wirkungsweise von Tibolon als dem wichtigsten Vertreter der STEARs wird dargestellt. Im Vergleich zum Placebo bzw. zur herkömmlichen HRT führt Tibolon zu einer signifikanten Reduktion bzw. zu einer gleichwertigen Verminderung vegetativer Beschwerden. Tibolon zeigt einen günstigen Einfluss auf die Vita sexualis. Im Gegensatz zur HRT zeigt es keine Stimulation der Proliferationsrate des Brustdrüsengewebes. Durch Stimulation der Östrogenrezeptorexpression im Knochen und eine Verminderung der Knochenresorption bewirkt es eine Zunahme der Knochendichte. Aufgrund fehlender Stimulation des Endometriums kann Tibolon auch ohne Gestagenzusatz bei Frauen mit intaktem Uterus eingesetzt werden.
Abstract
Hormone replacement therapy (HRT) has been shown to significantly reduce postmenopausal symptoms. However, it has been shown that women under HRT are at increased risk for the development of breast cancer. Thus, drugs which effectively treat postmenopausal symptoms without affecting breast tissue are of interest. Two classes of drugs have been investigated extensively: selective estrogen receptor modulators (SERMs) and selective tissue estrogenic activity regulators (STEARs). Tibolone is the most renowned member of the STEAR family and its effects on climacteric symptoms are discussed. It has been shown that tibolone effectively reduces climacteric symptoms without stimulating proliferation of breast or endometrial tissue. Due to its estrogenic effects on the bone tibolone increases bone density. Because it does not stimulate the endometrium, tibolone can be administered, also without added gestagens, to women with an intact uterus.
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Keck, C., Tempfer, C. Einfluss von Tibolon auf das Brustdrüsengewebe. Gynäkologische Endokrinologie 2, 153–158 (2004). https://doi.org/10.1007/s10304-004-0068-3
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DOI: https://doi.org/10.1007/s10304-004-0068-3
Schlüsselwörter
- Hormonersatztherapie
- Selektive Östrogenrezeptormodulatoren (SERMs)
- STEARs
- Klimakterisches Syndrom
- Tibolon