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Update: Update on Bone Anabolics in Osteoporosis Treatment: Rationale Current Status and Perspectives

机译:更新:骨质疏松症治疗中骨合成代谢的更新:理论基础当前状况和观点

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摘要

Osteoporosis is defined as low bone mineral density associated with skeletal fractures secondary to minimal or no trauma, most often involving the spine, the hip, and the forearm. The decrease in bone mineral density is the consequence of an unbalanced bone remodeling process, with higher bone resorption than bone formation. Osteoporosis affects predominantly postmenopausal women, but also older men. This chronic disease represents a considerable medical and socioeconomic burden for modern societies. The therapeutic options for the treatment of osteoporosis have so far comprised mostly antiresorptive drugs, in particular bisphosphonates and more recently denosumab, but also calcitonin and, for women, estrogens or selective estrogen receptor modulators. These drugs have limitations, however, in particular the fact that they lead to a low turnover state where bone formation decreases with the decrease in bone-remodeling activity. In this review, we discuss the alternative class of osteoporosis drugs, i.e. bone anabolics, their biology, and the perspectives they offer for our therapeutic armamentarium. We focus on the two main osteoanabolic pathways identified as of today: PTH, the only anabolic drug currently on the market; and activation of canonical Wnt signaling through inhibition of the endogenous inhibitors sclerostin and dickkopf1. Each approach is based on a different molecular mechanism, but most recent evidence suggests that these two pathways may actually converge, at least in part. Whereas recombinant human PTH treatment is being revisited with different formulations and attempts to regulate endogenous PTH secretion via the calcium-sensing receptor, antibodies to sclerostin and dickkopf1 are currently in clinical trials and may prove to be even more efficient at increasing bone mass, possibly independent of bone turnover. Each of these anabolic approaches has its own limitations and safety issues, but the prospects of effective anabolic therapy for osteoporosis are indeed bright.
机译:骨质疏松症的定义是骨矿物质密度低,继发于轻度或无外伤的骨骼骨折,最常累及脊柱,臀部和前臂。骨矿物质密度的降低是骨重塑过程不平衡的结果,与骨形成相比,骨吸收更高。骨质疏松症主要影响绝经后的女性,但也影响老年男性。对于现代社会来说,这种慢性疾病代表着相当大的医学和社会经济负担。迄今为止,用于治疗骨质疏松症的治疗选择主要包括抗吸收药,特别是双膦酸盐和最近的地诺单抗,还包括降钙素,对于女性而言,还包括雌激素或选择性雌激素受体调节剂。然而,这些药物具有局限性,特别是它们导致低周转状态的事实,其中骨形成随着骨重塑活性的降低而减少。在这篇综述中,我们讨论了骨质疏松药物的替代类别,即骨合成代谢药物,它们的生物学以及它们为我们的治疗性武器库提供的​​观点。我们将重点关注截至目前已确定的两种主要的骨代谢途径:PTH,目前市场上唯一的合成代谢药物;通过抑制内源性抑制剂硬化蛋白和dickkopf1激活和激活经典Wnt信号。每种方法都基于不同的分子机制,但是最新证据表明这两种途径可能至少部分地会聚。尽管重组人PTH的治疗正在以不同的配方进行重新尝试,并试图通过钙敏感受体调节内源性PTH的分泌,但是针对硬化蛋白和dickkopf1的抗体目前正在临床试验中,并且可能被证明在增加骨量方面更为有效,可能是独立的骨转换。这些合成代谢方法中的每一种都有其自身的局限性和安全性问题,但是有效的合成代谢治疗骨质疏松症的前景确实是光明的。

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