4.3 Review

Medical treatment of osteoporosis

期刊

CLIMACTERIC
卷 25, 期 1, 页码 43-49

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/13697137.2021.1951697

关键词

Abaloparatide; anabolic agents; antiresorptives; bisphosphonates; denosumab; fractures; osteoporosis; romosozumab; selective estrogen receptor modulators; teriparatide

资金

  1. Theramex Healthcare Spain S.L.U.

向作者/读者索取更多资源

Osteoporosis is a common chronic condition that increases the risk of fractures. Lifestyle changes, calcium and vitamin D3 supplementation, as well as the use of appropriate medications, such as antiresorptives and anabolic agents, can help reduce this risk and improve bone health.
Osteoporosis is a common chronic condition that markedly increases the risk of fractures. Osteoporotic-related fractures increase morbidity and mortality and impair quality of life. Therefore, a correct approach for fracture prevention seems mandatory. Lifestyle changes should be recommended to all patients, including weight reduction if patients are obese/overweight, increasing physical activity and avoiding alcohol consumption and smoking. Additionally, calcium and vitamin D3 should be prescribed until the vitamin D deficit is resolved. Osteoporosis treatment options mainly include antiresorptives (i.e. estrogens, selective estrogen receptor modulators, bisphosphonates, denosumab) and anabolic agents (i.e. teriparatide, abaloparatide, romosozumab). Although presenting differences in efficacy and side effects, they have all been shown to increase bone mineral density (BMD) and to reduce osteoporotic-related fractures. Monotherapy with antiresorptive agents, particularly oral bisphosphonates, should be considered routinely as the first option for treatment of postmenopausal women. However, in the case of side effects, therapeutic failure or the need for long-term use, anabolic agents may be considered. In high-risk patients, anabolic agents may be considered as an initial therapeutic option. The combination of antiresorptive and anabolic agents may be useful to increase BMD compared with monotherapy, but more information is warranted to determine the effects on fracture risk.

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