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Teriparatide can treat steroid-induced osteoporosis

December 2, 2009  |  Posted in  Steroids Blog

Teriparatide can treat steroid-induced osteoporosisTeriparatide, a synthetic form of the human parathyroid hormone, can prove its worth when it comes to effectively treating glucocorticoid-induced osteoporosis (OP), as per a recent study.

The involved researchers remarked that patients with glucocorticoid-induced OP and treated with teriparatide for a period of 36 months tend to experience fewer new vertebral fractures and increased BMD (bone mineral density) than patients being treated with alendronate.

The study findings were published in the November issue of Arthritis & Rheumatism, a journal of the American College of Rheumatology (ACR).

From News-Medical.Net:

Glucocorticoids are steroid hormones that are naturally produced in the body or synthetically created compounds (drugs) used to reduce inflammation. These steroid drugs are used to control inflammation in patients with such autoimmune diseases as rheumatoid arthritis, systemic lupus erythematosus, and Crohn’s disease as well as inflammatory conditions such as asthma. Glucocorticoid-induced osteoporosis occurs when patients taking steroid medications such as prednisone, prednisolone, dexamethasone, and cortisone exhibit reduced bone mass and bone strength.

This 36-month, randomized, double-blind, controlled trial, led by Kenneth Saag, M.D., from the University of Alabama, was conducted at 76 centers located in 13 countries. A total of 428 patients between the ages of 22-89 with confirmed OP who had received greater than 5 mg/day of prednisone or equivalent for more than 3 months preceding screening were included. Research measures included changes in lumbar spine and hip bone, BMD, changes in bone biomarkers, fracture incidence, and safety.

It was remarked by Kenneth Saag, M.D., from the University of Alabama, that the requirement of therapies for mitigating this side-effect of steroid use and enhancements of bone mass on a substantial basis is vital.

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