File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1007/s002230001142
- Scopus: eid_2-s2.0-0033796017
- PMID: 11000341
- WOS: WOS:000089360200002
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: The efficacy and tolerability of alendronate in postmenopausal osteoporotic Chinese women: A randomized placebo-controlled study
Title | The efficacy and tolerability of alendronate in postmenopausal osteoporotic Chinese women: A randomized placebo-controlled study |
---|---|
Authors | |
Keywords | Alendronate Asian women BMD Osteoporosis |
Issue Date | 2000 |
Publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00223 |
Citation | Calcified Tissue International, 2000, v. 67 n. 4, p. 286-290 How to Cite? |
Abstract | Osteoporosis is a growing health problem in Asian women and it is expected that half of the world's hip fractures will occur in Asia in 50 years' time. As the use of hormonal replacement therapy (HRT) is extremely low in postmenopausal Asian women, nonhormonal agents will be more acceptable for the treatment and prevention of osteoporosis. The efficacy, tolerability, and acceptability of alendronate, an amino-bisphosphonate, for Asian women was evaluated in 70 osteoporotic southern Chinese women in a prospective, randomized, double-blind study. The subjects were randomized to receive either alendronate 10 mg daily or placebo, plus calcium supplementation 500 mg daily. The baseline L 1-4 and hip bone mineral density (BMD) were similar between both groups. At the end of 1 year, there was an increase of 5.8% in the lumbar spine BMD and 3.4% at the total hip with alendronate treatment when compared with baseline values (P < 0.001). Alendronate treatment for 1 year resulted in significant improvement in BMD at all sites measured when compared with placebo. There was also marked reduction in serum alkaline phosphatase (ALP) and urinary n-telopeptide (NTx) in the alendronate group when compared with the placebo group (ALP 25% versus 2%, NTx 75% versus 14%, both P < 0.005). The changes in ALP and NTx at 6 and 12 months correlated with the change in BMD at all sites measured at 1 year (P all <0.05). Alendronate was well tolerated and accepted, although two cases of gastric ulcer were reported. We conclude that alendronate is an effective and well-accepted agent for the treatment of osteoporosis in Asian women. |
Persistent Identifier | http://hdl.handle.net/10722/162379 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 1.016 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kung, AWC | en_US |
dc.contributor.author | Yeung, SSC | en_US |
dc.contributor.author | Chu, LW | en_US |
dc.date.accessioned | 2012-09-05T05:19:24Z | - |
dc.date.available | 2012-09-05T05:19:24Z | - |
dc.date.issued | 2000 | en_US |
dc.identifier.citation | Calcified Tissue International, 2000, v. 67 n. 4, p. 286-290 | en_US |
dc.identifier.issn | 0171-967X | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162379 | - |
dc.description.abstract | Osteoporosis is a growing health problem in Asian women and it is expected that half of the world's hip fractures will occur in Asia in 50 years' time. As the use of hormonal replacement therapy (HRT) is extremely low in postmenopausal Asian women, nonhormonal agents will be more acceptable for the treatment and prevention of osteoporosis. The efficacy, tolerability, and acceptability of alendronate, an amino-bisphosphonate, for Asian women was evaluated in 70 osteoporotic southern Chinese women in a prospective, randomized, double-blind study. The subjects were randomized to receive either alendronate 10 mg daily or placebo, plus calcium supplementation 500 mg daily. The baseline L 1-4 and hip bone mineral density (BMD) were similar between both groups. At the end of 1 year, there was an increase of 5.8% in the lumbar spine BMD and 3.4% at the total hip with alendronate treatment when compared with baseline values (P < 0.001). Alendronate treatment for 1 year resulted in significant improvement in BMD at all sites measured when compared with placebo. There was also marked reduction in serum alkaline phosphatase (ALP) and urinary n-telopeptide (NTx) in the alendronate group when compared with the placebo group (ALP 25% versus 2%, NTx 75% versus 14%, both P < 0.005). The changes in ALP and NTx at 6 and 12 months correlated with the change in BMD at all sites measured at 1 year (P all <0.05). Alendronate was well tolerated and accepted, although two cases of gastric ulcer were reported. We conclude that alendronate is an effective and well-accepted agent for the treatment of osteoporosis in Asian women. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00223 | en_US |
dc.relation.ispartof | Calcified Tissue International | en_US |
dc.subject | Alendronate | - |
dc.subject | Asian women | - |
dc.subject | BMD | - |
dc.subject | Osteoporosis | - |
dc.subject.mesh | Absorptiometry, Photon | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Alendronate - Therapeutic Use | en_US |
dc.subject.mesh | Alkaline Phosphatase - Blood | en_US |
dc.subject.mesh | Asian Continental Ancestry Group | en_US |
dc.subject.mesh | Bone Density - Drug Effects | en_US |
dc.subject.mesh | China - Epidemiology | en_US |
dc.subject.mesh | Collagen - Urine | en_US |
dc.subject.mesh | Collagen Type I | en_US |
dc.subject.mesh | Double-Blind Method | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Femur | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Lumbar Vertebrae | en_US |
dc.subject.mesh | Osteoporosis, Postmenopausal - Drug Therapy - Ethnology - Metabolism | en_US |
dc.subject.mesh | Pelvic Bones | en_US |
dc.subject.mesh | Peptides - Urine | en_US |
dc.subject.mesh | Placebos | en_US |
dc.subject.mesh | Prospective Studies | en_US |
dc.title | The efficacy and tolerability of alendronate in postmenopausal osteoporotic Chinese women: A randomized placebo-controlled study | en_US |
dc.type | Article | en_US |
dc.identifier.email | Kung, AWC:awckung@hku.hk | en_US |
dc.identifier.authority | Kung, AWC=rp00368 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s002230001142 | en_US |
dc.identifier.pmid | 11000341 | - |
dc.identifier.scopus | eid_2-s2.0-0033796017 | en_US |
dc.identifier.hkuros | 57616 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0033796017&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 67 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 286 | en_US |
dc.identifier.epage | 290 | en_US |
dc.identifier.isi | WOS:000089360200002 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Kung, AWC=7102322339 | en_US |
dc.identifier.scopusauthorid | Yeung, SSC=7102767673 | en_US |
dc.identifier.scopusauthorid | Chu, LW=7202236665 | en_US |
dc.identifier.issnl | 0171-967X | - |