Deficiency in androgens and upregulation of insulin-like growth factor-1 are involved in high bone turnover in men receiving androgen deprivation therapy for prostate cancer

Abstract Objective This study was performed to elucidate the mechanism of high bone turnover during androgen deprivation therapy (ADT) in terms of osteogenic endocrine activity by testosterone, adrenal androgens, and insulin-like growth factor-1 (IGF-I), and to identify markers reflecting the bone m...

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Veröffentlicht in:Growth hormone & IGF research 2012-06, Vol.22 (3), p.122-128
Hauptverfasser: Ishizaki, Fumio, Hara, Noboru, Takizawa, Itsuhiro, Nishiyama, Tsutomu, Isahaya, Etsuko, Kawasaki, Takashi, Takahashi, Kota
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Sprache:eng
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Zusammenfassung:Abstract Objective This study was performed to elucidate the mechanism of high bone turnover during androgen deprivation therapy (ADT) in terms of osteogenic endocrine activity by testosterone, adrenal androgens, and insulin-like growth factor-1 (IGF-I), and to identify markers reflecting the bone mineral density (BMD) during ADT. Design BMD and samples of blood and urine were studied before and after 6 months of ADT in 70 patients with localized prostate cancer. Results Before ADT, serum free-testosterone, dehydroepiandrosterone sulfate (DHEA-S), androstenedione, and IGF-I levels were correlated with BMD (rs = 0.344, p = 0.004; rs = 0.264, p = 0.027; rs = 0.329, p = 0.005; rs = 0.300, p = 0.012, respectively). The serum IGF-I level was independently correlated with the pretreatment BMD (Multivariate p = 0.001). These relationships disappeared after ADT (p = 0.519, 0.316, 0.116, and 0.597, respectively). After ADT, serum levels of free-testosterone decreased (7.9 to 0.2 pg/mL), and DHEA-S and androstenedione were also reduced (3.6 to 2.3 μmol/L and 5.6 to 2.9 nmol/L, respectively) (p < 0.001 in all). In contrast, IGF-I levels were elevated after ADT by 11.6% (19.9 to 22.3 nmol/L, p < 0.001). Delta-values of IGF-I (post- minus pretreatment levels, mean: + 2.2, ranged between − 7.1 and + 15.3) were inversely correlated with the pretreatment (rs = − 0.333 p = 0.005) and post-treatment (rs = − 0.408, p = 0.001) BMD. After ADT, the serum IGF-I level was closely correlated with the serum level of the bone formation marker bone-specific alkaline phosphatase (BAP) (rs = 0.328, p = 0.006), and delta-IGF-I and delta-BAP showed a close positive correlation (rs = 0.388, p = 0.001). The post-treatment BMD was correlated only with the urine deoxypyridinoline (DPD) concentration (rs = − 0.302, p = 0.024) among the bone formation/resorption markers including serum/urine N-telopeptide. Conclusions Serum IGF-I levels increased during ADT in men with a low BMD. Coupled with reduced androgen levels, elevated IGF-I levels, which were positively correlated with BAP during ADT, possibly explain the mechanism of ADT-related high bone turnover. The increase of IGF-I is more prominent in men whose BMD is already low at the baseline, and urine DPD might be a marker that reflects BMD during ADT.
ISSN:1096-6374
1532-2238
DOI:10.1016/j.ghir.2012.04.003