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Androgens and osteoporosis

机译:雄激素和骨质疏松

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Purpose of review The review is timely given recent advances regarding mechanisms of androgen action on bone cells and in humans. Osteoporosis in men is an important public health problem. An improved understanding of the role of androgens in the pathophysiology of bone loss will lead to new treatments. Recent findings Androgen receptors are present in most bone cells. Testosterone acts on bone both directly via the androgen receptor and indirectly, following aromatization, via the oestrogen receptor. During skeletal modelling, ERalpha is critical for longitudinal bone growth. For periostea! growth and bone expansion, androgen receptor activation has a positive effect, whereas ERalpha activation is inhibitory. During skeletal remodelling, both receptor pathways generate similar and additive effects on bone. Androgen deficiency is a common secondary cause of osteoporosis in men and should be treated with testosterone, particularly in symptomatic men. However, lack of efficacy data for testosterone in osteoporosis means it is less useful as a first-line treatment in men with age-related declines in testosterone and osteoporosis, when other agents such as bisphosphonates and parathyroid hormone are effective. Summary Randomized, placebo-controlled trials of testosterone therapy in men with age-related declines in testosterone and osteoporosis are needed, and should carefully evaluate potential risks, as well as its efficacy in reducing fractures and other health benefits.
机译:审查的目的鉴于有关雄激素作用于骨细胞和人类的机制的最新进展,该审查是及时的。男性的骨质疏松是重要的公共卫生问题。对雄激素在骨丢失的病理生理学中的作用的进一步了解将导致新的治疗方法。最新发现大多数骨骼细胞中都存在雄激素受体。睾丸激素不仅直接通过雄激素受体作用于骨骼,而且在芳香化后通过雌激素受体间接作用于骨骼。在骨骼建模期间,ERalpha对于纵向骨骼生长至关重要。对于柿子!生长和骨骼扩张,雄激素受体激活具有积极作用,而ERalpha激活具有抑制作用。在骨骼重塑过程中,两种受体途径都会对骨骼产生相似和累加的作用。雄激素缺乏症是男性骨质疏松症的常见继发原因,应使用睾丸激素治疗,尤其是在有症状的男性中。然而,缺乏骨质疏松症中睾丸激素的功效数据,这意味着当其他药物(如双膦酸盐和甲状旁腺激素)有效时,睾丸激素和骨质疏松症年龄相关性下降的男性作为一线治疗的用处不大。总结需要对年龄相关的睾丸激素和骨质疏松症年龄下降的男性进行随机,安慰剂对照的睾丸激素治疗试验,并且应仔细评估其潜在风险以及其减少骨折和其他健康益处的功效。

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