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Clinical Utilization of Salmon Calcitonin in the Treatment of Osteoporosis

Rationale, Supportive Data, and Considerations for the Future

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Osteoporosis

Part of the book series: Contemporary Endocrinology ((COE))

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Abstract

Calcitonin, a physiologic endogenous inhibitor of bone resorption, decreases osteoclast formation (1,2),osteoclast attachment (2,3),and bone resorption in organ culture and in animal models (1,4,5). Thus there is a rationale for treatment with calcitonin, and specifically salmon calcitonin (S-CT), of diseases associated with increased bone resorption, such as osteoporosis. The last twenty years has witnessed an accumulation of clinical trials with S-CT providing supportive data for such a clinical indication. Also, the ongoing development of newer preparations of S-CT (an oral formulation), and the applicability of S-CT for newer indications (for pain, for hip fracture, etc.) via new clinical trials promises continued usage of this therapeutic agent for the future management of osteoporosis.

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Chesnut, C.H., Azria, M. (2003). Clinical Utilization of Salmon Calcitonin in the Treatment of Osteoporosis. In: Orwoll, E.S., Bliziotes, M. (eds) Osteoporosis. Contemporary Endocrinology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-278-4_21

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  • DOI: https://doi.org/10.1007/978-1-59259-278-4_21

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61737-260-5

  • Online ISBN: 978-1-59259-278-4

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