Advances in osteoporosis from 1970 to 2018

被引:13
作者
Gallagher, J. Christopher [1 ]
机构
[1] Creighton Univ, Dept Endocrinol, 2400 Burt St,Criss Bldg,Suite 281, Omaha, NE 68131 USA
来源
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY | 2018年 / 25卷 / 12期
关键词
Bone density; Bone remodeling; Clinical trials; Osteoporosis; BONE-MINERAL DENSITY; PARATHYROID-HORMONE FRAGMENT; DUAL-PHOTON-ABSORPTIOMETRY; VERTEBRAL FRACTURE RISK; POSTMENOPAUSAL WOMEN; OSTEOCLAST DIFFERENTIATION; SALMON-CALCITONIN; RANDOMIZED-TRIAL; TRABECULAR BONE; DOUBLE-BLIND;
D O I
10.1097/GME.0000000000001263
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
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.
引用
收藏
页码:1403 / 1417
页数:15
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