Literature DB >> 9074843

Alendronate. A review of its pharmacological properties and therapeutic efficacy in postmenopausal osteoporosis.

W Jeal1, L B Barradell, D McTavish.   

Abstract

Alendronate is an aminobisphosphonate which appears to attenuate, rather than completely inhibiting bone turnover, by suppressing the activity of osteoclasts. Clinical trials have established that 10 mg/day orally administered alendronate is the optimum dosage. Despite its poor bioavailability after oral administration, alendronate is highly effective at preventing bone loss associated with the absence of endogenous estrogen. A sustained increase in bone mass was observed during alendronate therapy without accelerated loss after withdrawal of the drug. Increased bone mass was associated with a reduction in the risk and rate of occurrence of vertebral fractures. A recent study demonstrated a 47% reduction in the risk of developing new radiographic vertebral fractures over 3 years in women with low bone mass and pre-existing vertebral fractures. There have been few direct comparisons in clinical trials. However, when compared with calcium or low dosages of salmon calcitonin (salcatonin) therapy in women with postmenopausal osteoporosis, alendronate induced a sustained increase in bone mass during therapy that was not seen with the comparator. In clinical trials alendronate was generally well tolerated when taken as recommended. Adverse events tended to be transient and usually associated with the upper gastrointestinal tract; the most common events included abdominal pain, nausea, dyspepsia, constipation and diarrhoea, which are also common with other bisphosphonates. Of potential concern are the small number of reports of patients developing oesophageal ulceration; however, this adverse event was attributed to noncompliance with the manufacturer's recommendations for administration of the drug. In addition, alendronate has not been associated with osteomalacia. Studies are still required to establish the long term efficacy of alendronate, particularly with regard to other available therapies. Although estrogen replacement therapy is generally considered the treatment of choice for the management of postmenopausal osteoporosis, many women are unable or unwilling to receive estrogens on a long term basis. Thus, alendronate, with its demonstrated beneficial effects and its good tolerability profile (when taken as recommended), is a promising alternative treatment option for the management of postmenopausal osteoporosis.

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Year:  1997        PMID: 9074843     DOI: 10.2165/00003495-199753030-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  54 in total

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Journal:  J Chromatogr       Date:  1990-12-14

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Journal:  Drugs Aging       Date:  1991 Sep-Oct       Impact factor: 3.923

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6.  Comparison of new biochemical markers of bone turnover in late postmenopausal osteoporotic women in response to alendronate treatment.

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Journal:  J Clin Endocrinol Metab       Date:  1994-12       Impact factor: 5.958

Review 7.  Esophagitis associated with the use of alendronate.

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Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

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Journal:  J Pharmacol Exp Ther       Date:  1993-11       Impact factor: 4.030

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Journal:  J Bone Miner Res       Date:  1994-11       Impact factor: 6.741

10.  Long-term effects of a treatment course with oral alendronate of postmenopausal osteoporosis.

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Journal:  J Bone Miner Res       Date:  1994-11       Impact factor: 6.741

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  14 in total

1.  New insights into human farnesyl pyrophosphate synthase inhibition by second-generation bisphosphonate drugs.

Authors:  D Fernández; R Ramis; J Ortega-Castro; R Casasnovas; B Vilanova; J Frau
Journal:  J Comput Aided Mol Des       Date:  2017-06-19       Impact factor: 3.686

Review 2.  Alendronate: an update of its use in osteoporosis.

Authors:  M Sharpe; S Noble; C M Spencer
Journal:  Drugs       Date:  2001       Impact factor: 9.546

3.  Bisphosphonates and tetracycline: experimental models for their evaluation in calcium-related disorders.

Authors:  H Cohen; V Solomon; I S Alferiev; E Breuer; A Ornoy; N Patlas; N Eidelman; G Hägele; G Golomb
Journal:  Pharm Res       Date:  1998-04       Impact factor: 4.200

Review 4.  Current Treatments and New Developments in the Management of Glucocorticoid-induced Osteoporosis.

Authors:  Hennie G Raterman; Irene E M Bultink; Willem F Lems
Journal:  Drugs       Date:  2019-07       Impact factor: 9.546

Review 5.  Clodronate: a review of its use in breast cancer.

Authors:  M Hurst; S Noble
Journal:  Drugs Aging       Date:  1999-08       Impact factor: 3.923

Review 6.  Raloxifene: a review of its use in postmenopausal osteoporosis.

Authors:  D Clemett; C M Spencer
Journal:  Drugs       Date:  2000-08       Impact factor: 9.546

7.  The Local Effect of Alendronate with Intra-alveolar Collagen Sponges on Post Extraction Alveolar ridge Resorption: A Clinical Trial.

Authors:  Avishek De Sarkar; Nikhil Singhvi; Jayaprasad N Shetty; T Ramakrishna; Omkar Shetye; Mueedul Islam; Hari Keerthy
Journal:  J Maxillofac Oral Surg       Date:  2014-10-07

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Authors:  G Lehmann; G Hein; G Wolf
Journal:  Z Rheumatol       Date:  2006-09       Impact factor: 1.372

Review 9.  The clinical and cost considerations of bisphosphonates in preventing bone complications in patients with metastatic breast cancer or multiple myeloma.

Authors:  E V McCloskey; J F Guest; J A Kanis
Journal:  Drugs       Date:  2001       Impact factor: 9.546

10.  Safety profile of raloxifene as used in general practice in England: results of a prescription-event monitoring study.

Authors:  Deborah Layton; Andrea Clarke; Lynda V Wilton; Saad A W Shakir
Journal:  Osteoporos Int       Date:  2004-08-07       Impact factor: 4.507

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