Calcitonin
Overview
A 32-amino acid peptide hormone naturally produced by parafollicular C-cells of the thyroid gland. Calcitonin inhibits osteoclast-mediated bone resorption by binding to calcitonin receptors on osteoclasts, reducing their activity and number.
Mechanism of Action
Salmon calcitonin is approximately 40-50 times more potent than human calcitonin and has a longer half-life, making it the preferred therapeutic form.
Research Summary & Key Findings
FDA-approved for postmenopausal osteoporosis, Paget's disease, and hypercalcemia. PROOF trial demonstrated 33% reduction in vertebral fractures with nasal calcitonin 200 IU daily. Has analgesic properties for acute vertebral compression fractures independent of its anti-resorptive effects. Use has declined due to availability of more potent anti-resorptive agents and a small signal of increased malignancy risk with long-term use.
Clinical Status
Calcitonin has received FDA approval and is available for clinical use under appropriate medical supervision. Consult a qualified healthcare provider for prescribing information.
Administration Routes
References
Primary literature
- PubMed — "Calcitonin"
Peer-reviewed literature indexed by the National Library of Medicine.
- ClinicalTrials.gov — "Calcitonin"
Registered interventional and observational studies, including status and phase.
- PubChem — "Calcitonin"
Chemical structure, molecular properties, and bioactivity data.
Study-level citations for this compound are being verified against the primary sources before publication. The database queries above return the current indexed literature in the meantime.
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