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首页> 外文期刊>The Professional Medical Journal >Early changes in bone metabolism and serum sex hormones in androgen deprivation therapy
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Early changes in bone metabolism and serum sex hormones in androgen deprivation therapy

机译:雄激素剥夺治疗中骨代谢和血清性激素的早期变化

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Background: Androgen deprivation therapy (ADT) with luteinizing hormone releasing hormone agonists (LHRHa) is a major treatment modality for prostate cancer (PC), particularly advanced disease. LHRHa induced hypogonadism promotes bone loss, leading to osteoporosis and heightened fracture risk. Most previous studies on skeletal impact of LHRHa employed bone mineral density (BMD) testing. Serum bone-specific alkaline phosphatase (BSAP), an established bone biomarker, is reflective of changes in skeletal metabolism which precede BMD changes. In postmenopausal women, serum BSAP has been associated with fracture risk irrespective of BMD. Setting: Charing Cross Hospital, London, United Kingdom. Methods: We assessed early changes in serum BSAP levels of patients with non-metastatic PC (n=9) undergoing LHRHa therapy. Serum testosterone and estradiol concentrations were also measured. Samples were taken at baseline before the start of treatment and three months afterward. Comparisons were made with blood samples taken at similar time points for age- matched controls without PC (n=9). Results: No significant difference in BSAP levels was seen between groups (p=0.242). Testosterone and estradiol levels were significantly reduced following treatment (p=0.000). No correlation was observed between serum BSAP and serum testosterone (R=0.187, p=0.276) or serum estradiol (R=0.055, p=0.75). Conclusions: Changes in serum BSAP levels may not be evident as early as 3 months following ADT with LHRHa. The study was limited by the small sample size and use of serum BSAP only which is one of the many bone markers. A larger study using multiple bone markers is warranted to determine early effects of LHRHa treatment on bone metabolism.
机译:背景:促黄体激素释放激素激动剂(LHRHa)的雄激素剥夺疗法(ADT)是前列腺癌(PC)特别是晚期疾病的主要治疗方式。 LHRHa诱发的性腺功能低下会促进骨质流失,导致骨质疏松和骨折风险增加。先前有关LHRHa骨骼影响的研究大多采用骨矿物质密度(BMD)测试。血清骨特异性碱性磷酸酶(BSAP)是一种已建立的骨生物标志物,反映了BMD变化之前骨骼代谢的变化。在绝经后妇女中,无论BMD为何,血清BSAP均与骨折风险相关。地点:英国伦敦查令十字医院。方法:我们评估了接受LHRHa治疗的非转移性PC(n = 9)患者血清BSAP水平的早期变化。还测量了血清睾丸激素和雌二醇的浓度。在治疗开始之前和之后三个月在基线采集样品。对于年龄相似的无PC对照,在相似的时间点对血液样本进行了比较(n = 9)。结果:各组之间BSAP水平无显着差异(p = 0.242)。治疗后睾丸激素和雌二醇水平显着降低(p = 0.000)。血清BSAP与血清睾丸激素(R = 0.187,p = 0.276)或血清雌二醇(R = 0.055,p = 0.75)之间没有相关性。结论:早在LHRHa的ADT后3个月,血清BSAP水平的变化可能并不明显。这项研究受到样本量小和仅使用血清BSAP的限制,血清BSAP是众多骨标志物之一。有必要使用多种骨标记物进行较大的研究以确定LHRHa治疗对骨代谢的早期影响。

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