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1970 年至 2018 年骨质疏松症的研究进展。

Advances in osteoporosis from 1970 to 2018.

机构信息

Department of Endocrinology, Creighton University, Omaha, NE.

出版信息

Menopause. 2018 Dec;25(12):1403-1417. doi: 10.1097/GME.0000000000001263.

DOI:10.1097/GME.0000000000001263
PMID:30489459
Abstract

In 1970, there were no drugs under study for osteoporosis. Estrogen was used, but little was known about the correct dose for preventing bone loss. At that time, fractures were not even recognized as a disease, but regarded as part of normal aging. From 1970 to this year (2018), there have been extensive advances in the osteoporosis field ranging from fracture epidemiology to the remarkable invention of bone density measurements. There have been major advances in therapeutic options available for patients for prevention and treatment of osteoporosis. In parallel, the advances in the laboratory helped elucidate the process of bone remodeling, not only at the macroscopic level but also at the cellular level. This led to rapid advances in translational research from cellular biology to new therapies exemplified by the development of monoclonal antibodies for osteoporosis. Further understanding of the signaling pathways in bone cells will lead to new small molecules made for osteoporosis treatment, perhaps causing less adverse events. University-based research throughout the world has been a leader in most of these advances, and Pharma support for phase 1 to 4 studies helped bring these discoveries to patients. In the osteoporosis field alone, one sees the tremendous value of grant support for university research by National funding agencies such as the National Institute of Health in this country and similar agencies in other countries. There are clinical challenges that have to be solved with long-term compliance with osteoporosis medication if we want to reduce fracture incidence in the long term.

摘要

1970 年,没有研究骨质疏松症的药物。当时使用了雌激素,但对于预防骨质流失的正确剂量知之甚少。当时,骨折甚至不被认为是一种疾病,而是被视为正常衰老的一部分。从 1970 年到今年(2018 年),骨质疏松症领域取得了广泛的进展,从骨折流行病学到骨密度测量的显著发明。为预防和治疗骨质疏松症,患者的治疗选择有了重大进展。与此同时,实验室的进展有助于阐明骨重建过程,不仅在宏观水平上,而且在细胞水平上。这导致了从细胞生物学到新疗法的转化研究的快速进展,以开发用于骨质疏松症的单克隆抗体为例。进一步了解骨细胞中的信号通路将为骨质疏松症治疗带来新的小分子药物,也许会减少不良反应事件。世界各地的大学研究在这些进展中处于领先地位,制药公司为 1 期至 4 期研究提供的支持帮助将这些发现带给了患者。仅在骨质疏松症领域,人们就看到了国家资助机构(如美国国立卫生研究院)为大学研究提供资助的巨大价值,以及其他国家的类似机构。如果我们要长期降低骨折发生率,就必须解决长期服用骨质疏松症药物的依从性问题。

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