Anabolic treatment for osteoporosis: teriparatide

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Effects of teriparatide versus alendronate for treatment of postmenopausal osteoporosis

OBJECTIVES Osteoporosis remains a clinical challenge. Teriparatide is an anabolic drug and alendronate is an antiresorptive agent; both are used in the treatment of osteoporosis. Comprehensive reviews investigating the comparative safety and efficacy of teriparatide versus alendronate are scarce. Therefore, we conducted a systematic review and meta-analysis of randomized controlled trials (RCTs...

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[Teriparatide--new value in osteoporosis treatment: treatment guidelines].

Osteoporosis has become global health issue due to the longer life-cycle and increased percentage of older people in population. The great improvement was done in the treatment of postmenopausal osteoporosis. By the mechanism of action, drugs for osteoporosis treatment are antiresorptives and osteoanabolics. Teriparatide is an osteoanabolic drug that stimulates bone turnover and building of a n...

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Appropriate use of anabolic treatment for severe osteoporosis.

Osteoporotic fractures remain a major public health problem for their correlated morbidity and mortality. The primary aim of therapy must be the prevention of the first fragility fracture and avoiding subsequent fractures in patients who already have an existing fracture. There are evidences from randomized controlled trials (RCTs) about the efficacy of antiresorptives, such as bisphosphonates ...

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Teriparatide: Its Use in the Treatment of Osteoporosis

The prevalence of osteoporosis is likely to rise with the increase in life expectancy of an ageing population. Current first line therapies for the treatment of osteoporosis are predominantly anti-resorptive. Teriparatide is a first in class, anabolic agent with a unique mechanism that results in increased bone formation. Daily subcutaneous injection for 6–24 months was effective in reducing ve...

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ژورنال

عنوان ژورنال: Clinical Cases in Mineral and Bone Metabolism

سال: 2017

ISSN: 1971-3266

DOI: 10.11138/ccmbm/2017.14.1.173