Literature DB >> 14529539

Calcitonin for osteoporosis and bone pain.

N M Mehta1, A Malootian, J P Gilligan.   

Abstract

Calcitonin has been approved for the treatment of osteoporosis and other diseases involving accelerated bone turnover for approximately 25 years. The most commonly studied and prescribed form is salmon calcitonin, which has a greater efficacy in clinical use. A wealth of well-controlled clinical studies have demonstrated that calcitonin preserves or increases bone mineral density (BMD) and reduces the risk of vertebral fractures in osteoporosis. Recent studies have indicated that while a low BMD is correlated with an increase in fracture risk, increases in BMD alone do not explain the antifracture efficacy of antiresorptive therapies such as calcitonin. Therapies that moderately increase BMD may reduce fracture risk by reducing the rate of bone turnover and maintaining the integrity of the trabecular architecture, resulting in the preservation of bone strength and quality in osteoporotic patients. An advantage of calcitonin that is not shared by other antiresorptive therapies is its direct analgesic effect on bone pain. Calcitonin has been demonstrated to be clinically useful in improving pain, not only from the acute vertebral fractures of osteoporosis, but also in Paget's disease, bone malignancies, and other sources of musculoskeletal pain. Drugs containing calcitonin may be approved for additional indications in the near future, and as more convenient routes of administration such as the oral route become available, the demand for the calcitonin peptide is expected to increase.

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Year:  2003        PMID: 14529539     DOI: 10.2174/1381612033453622

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  15 in total

Review 1.  Osteoporotic fractures in older adults.

Authors:  Cathleen S Colón-Emeric; Kenneth G Saag
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2.  Rational design of aggregation-resistant bioactive peptides: reengineering human calcitonin.

Authors:  Susan B Fowler; Stephen Poon; Roman Muff; Fabrizio Chiti; Christopher M Dobson; Jesús Zurdo
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-08       Impact factor: 11.205

Review 3.  Amyloidogenesis of natively unfolded proteins.

Authors:  Vladimir N Uversky
Journal:  Curr Alzheimer Res       Date:  2008-06       Impact factor: 3.498

4.  Chimeric glutathione S-transferases containing inserts of kininogen peptides: potential novel protein therapeutics.

Authors:  Amber A Bentley; Sergei M Merkulov; Yi Peng; Rita Rozmarynowycz; Xiaoping Qi; Marianne Pusztai-Carey; William C Merrick; Vivien C Yee; Keith R McCrae; Anton A Komar
Journal:  J Biol Chem       Date:  2012-05-10       Impact factor: 5.157

Review 5.  Calcitonin for treating acute and chronic pain of recent and remote osteoporotic vertebral compression fractures: a systematic review and meta-analysis.

Authors:  J A Knopp-Sihota; C V Newburn-Cook; J Homik; G G Cummings; D Voaklander
Journal:  Osteoporos Int       Date:  2011-06-10       Impact factor: 4.507

Review 6.  Vitamin C, Pain and Opioid Use Disorder.

Authors:  Erica Zelfand
Journal:  Integr Med (Encinitas)       Date:  2020-06

Review 7.  Osteoporosis prevention and therapy: preserving and building strength through bone quality.

Authors:  M Kleerekoper
Journal:  Osteoporos Int       Date:  2006-08-15       Impact factor: 4.507

8.  Early effect of nasal salmon calcitonin on the bone marker Crosslaps.

Authors:  Demet Ofluoglu; Evrim Karadag-Saygi; Cuneyt Canbulat; Osman Hakan Gunduz; Evren Kul-Panza; Gulseren Akyuz
Journal:  Rheumatol Int       Date:  2005-05-05       Impact factor: 2.631

Review 9.  Osteoporosis in paediatric patients with spina bifida.

Authors:  Humberto Marreiros; Humberto Filipe Marreiros; Clara Loff; Eulalia Calado
Journal:  J Spinal Cord Med       Date:  2012-01       Impact factor: 1.985

10.  The effects of calcitonin on post-orthodontic relapse in rats.

Authors:  Hussein Abid Ali Muhsin Alnajar; Dheaa H Al Groosh
Journal:  Clin Exp Dent Res       Date:  2020-12-09
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