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Effect of etidronate on urinary calcium / creatinin ratio in postmenopausal women: A prospective, randomized, placebo controlled study

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dc.contributor.author Küçük, Şenol
dc.contributor.author Gökdeniz, Remzi
dc.contributor.author Atmaca, Ruşen
dc.contributor.author Uryan, İsmail
dc.contributor.author Buhur, Ali
dc.contributor.author Taşkın, Ömür
dc.date.accessioned 2020-09-18T12:10:19Z
dc.date.available 2020-09-18T12:10:19Z
dc.date.issued 1999
dc.identifier.citation KÜÇÜK Ş,GÖKDENİZ R,ATMACA R,URYAN İ,BUHUR A,TAŞKIN Ö (1999). Effect of etidronate on urinary calcium / creatinin ratio in postmenopausal women: A prospective, randomized, placebo controlled study. Turkish Journal of Medical Sciences, 29(6), 683 - 687. en_US
dc.identifier.uri https://app.trdizin.gov.tr/publication/paper/detail/T1RJNE5EUT0
dc.identifier.uri http://hdl.handle.net/11616/18074
dc.description Yıl: 1999Cilt: 29Sayı: 6ISSN: 1300-0144 / 1303-6165Sayfa Aralığı: 683 - 687Metin Dili:İngilizce en_US
dc.description.abstract Abstract: There are both histomorphometric and nonhistomorphometric studies confirming that etidronate reduces bone resorption. In this study, we have examined urinary Calcium/Creatinine ratio (uCA/Cr) as a biochemical marker of bone turnover to show the effectiveness of etidronate and whether it could be used as a follow-up parameter of treatment. Eighty-one postmenopausal women aged 40 to 65 included into the study to investigate the effects of etidronate on uCa/Cr in a prospective, randomised, placebo controlled clinical trial. All necessary criteria matched 81 women were divided into 3 groups at random, each group consisted of 27 patients. Prior to treatment, uCa/Cr was calculated from all subjects 3 hours after drinking 1 liter of water in the morning. Twenty seven (33.3%) women were randomised to oral doses of etidronate (400 mg/day for two weeks followed by drug free period of 10 weeks), twenty seven women to etidronate (400 mg/day for two weeks) plus calcium (1000 mg/day) for the following 10 weeks and twenty seven women to placebo (Fe, 50 mg/day) for 12 weeks. After 12 weeks of treatment, uCa/Cr declined significantly in the etidronate group from 0.118±0.064 to 0.053±0.021, in etidronate+calcium group from 0.08±0.03 to 0.06±0.015 ((p=0.004) and (p=0.005), respectively). In the placebo group no significant change was observed (p=0.03). In conclusion, etidronate is effective in postmenopausal women and the effectiveness of treatment may be followed up by measuring uCa/Cr which is a simple and cheap parameter of determining the effectivensess of etidronate in prevention of osteoporosis. However, since there are contradictory findings concerning uCa/Cr exist, larger clinical and prospective studies should be carried out. en_US
dc.language.iso tur en_US
dc.publisher Turkish Journal of Medical Sciences en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Effect of etidronate on urinary calcium / creatinin ratio in postmenopausal women: A prospective, randomized, placebo controlled study en_US
dc.type article en_US
dc.relation.journal Turkish Journal of Medical Sciences en_US
dc.contributor.department İnönü Üniversitesi en_US


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