Effectiveness of alendronate and etidronate in the treatment of osteoporosis in men : a prospective observational study
The prevalence of osteoporosis in men is higher than previously assumed; consequently, numerous therapies are being investigated to treat these patients. The Canadian Database of Osteoporosis and Osteopenia patients (CANDOO) was analyzed to examine changes in bone mineral density (BMD) in consecutiv...
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creator | OLSZYNSKI, W. P DAVISON, K. S PETRIE, A GOLDSMITH, C. H ADACHI, J. D IOANNIDIS, G BROWN, J. P HANLEY, D. A JOSSE, R. G MURRAY, T. M PAPAIOANNOU, A SEBALDT, R. J TENENHOUSE, A. M |
description | The prevalence of osteoporosis in men is higher than previously assumed; consequently, numerous therapies are being investigated to treat these patients. The Canadian Database of Osteoporosis and Osteopenia patients (CANDOO) was analyzed to examine changes in bone mineral density (BMD) in consecutively seen osteoporotic men administered alendronate, etidronate or no bone-active drugs (control) over 1 year. A total of 244 men attending six Canadian osteoporosis clinics were included in the study (42 alendronate, 102 etidronate and 100 control). Multiple imputation was used to model missing data to provide a more robust statistical model. The imputed datasets (five) were analyzed using multivariable linear regression to determine differences between groups in the percent change of lumbar spine (LS) and femoral neck (FN) BMD from baseline to 1 year. Differences in the percent change in BMD from baseline were most notable at the LS in favor of alendronate (4.3%; 95% CI: 2.1, 6.6 ) and etidronate (2.1%; 95% CI: 0.3, 4.0) therapy when compared with controls. At the LS, alendronate therapy led to significantly greater (2.2%; 95% CI: 0.2, 4.2) gains in BMD as compared to etidronate therapy. Compared to controls, there were no significant differences in FN BMD with alendronate (2.1%; 95% CI: -0.4, 4.7) or etidronate therapy (0.9%; 95% CI: -1.1, 2.8), nor were there significant differences between bisphosphonate groups (1.3%; 95% CI: -1.1, 3.6, in favor of alendronate). While both alendronate and etidronate significantly increased LS BMD in osteoporotic men after 1 year in real-world settings, alendronate therapy resulted in significantly superior gains in LS BMD. The effect of these two bisphosphonates on fractures and FN BMD in osteoporotic men is likely positive, but requires further study. |
doi_str_mv | 10.1007/s00198-005-1965-6 |
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P ; DAVISON, K. S ; PETRIE, A ; GOLDSMITH, C. H ; ADACHI, J. D ; IOANNIDIS, G ; BROWN, J. P ; HANLEY, D. A ; JOSSE, R. G ; MURRAY, T. M ; PAPAIOANNOU, A ; SEBALDT, R. J ; TENENHOUSE, A. M</creator><creatorcontrib>OLSZYNSKI, W. P ; DAVISON, K. S ; PETRIE, A ; GOLDSMITH, C. H ; ADACHI, J. D ; IOANNIDIS, G ; BROWN, J. P ; HANLEY, D. A ; JOSSE, R. G ; MURRAY, T. M ; PAPAIOANNOU, A ; SEBALDT, R. J ; TENENHOUSE, A. M</creatorcontrib><description>The prevalence of osteoporosis in men is higher than previously assumed; consequently, numerous therapies are being investigated to treat these patients. The Canadian Database of Osteoporosis and Osteopenia patients (CANDOO) was analyzed to examine changes in bone mineral density (BMD) in consecutively seen osteoporotic men administered alendronate, etidronate or no bone-active drugs (control) over 1 year. A total of 244 men attending six Canadian osteoporosis clinics were included in the study (42 alendronate, 102 etidronate and 100 control). Multiple imputation was used to model missing data to provide a more robust statistical model. The imputed datasets (five) were analyzed using multivariable linear regression to determine differences between groups in the percent change of lumbar spine (LS) and femoral neck (FN) BMD from baseline to 1 year. Differences in the percent change in BMD from baseline were most notable at the LS in favor of alendronate (4.3%; 95% CI: 2.1, 6.6 ) and etidronate (2.1%; 95% CI: 0.3, 4.0) therapy when compared with controls. At the LS, alendronate therapy led to significantly greater (2.2%; 95% CI: 0.2, 4.2) gains in BMD as compared to etidronate therapy. Compared to controls, there were no significant differences in FN BMD with alendronate (2.1%; 95% CI: -0.4, 4.7) or etidronate therapy (0.9%; 95% CI: -1.1, 2.8), nor were there significant differences between bisphosphonate groups (1.3%; 95% CI: -1.1, 3.6, in favor of alendronate). While both alendronate and etidronate significantly increased LS BMD in osteoporotic men after 1 year in real-world settings, alendronate therapy resulted in significantly superior gains in LS BMD. The effect of these two bisphosphonates on fractures and FN BMD in osteoporotic men is likely positive, but requires further study.</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-005-1965-6</identifier><identifier>PMID: 15997420</identifier><language>eng</language><publisher>London: Springer</publisher><subject>Alendronate - therapeutic use ; Biological and medical sciences ; Body Height - physiology ; Body Weight - physiology ; Bone Density - physiology ; Bone Density Conservation Agents - therapeutic use ; Bones, joints and connective tissue. Antiinflammatory agents ; Diseases of the osteoarticular system ; Etidronic Acid - therapeutic use ; Femur Neck - physiopathology ; Fractures, Bone - etiology ; Fractures, Bone - physiopathology ; Humans ; Life Style ; Lumbar Vertebrae - physiopathology ; Male ; Medical sciences ; Middle Aged ; Osteoporosis - drug therapy ; Osteoporosis - physiopathology ; Osteoporosis. Osteomalacia. Paget disease ; Pharmacology. Drug treatments ; Prospective Studies ; Regression Analysis ; Treatment Outcome</subject><ispartof>Osteoporosis international, 2006-02, Vol.17 (2), p.217-224</ispartof><rights>2006 INIST-CNRS</rights><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-42544a3e7a7b465ef78d2cab9ae11d5d12311ab6de6c3c235ac8a869f76be2693</citedby><cites>FETCH-LOGICAL-c422t-42544a3e7a7b465ef78d2cab9ae11d5d12311ab6de6c3c235ac8a869f76be2693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17453302$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15997420$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OLSZYNSKI, W. P</creatorcontrib><creatorcontrib>DAVISON, K. S</creatorcontrib><creatorcontrib>PETRIE, A</creatorcontrib><creatorcontrib>GOLDSMITH, C. H</creatorcontrib><creatorcontrib>ADACHI, J. D</creatorcontrib><creatorcontrib>IOANNIDIS, G</creatorcontrib><creatorcontrib>BROWN, J. P</creatorcontrib><creatorcontrib>HANLEY, D. A</creatorcontrib><creatorcontrib>JOSSE, R. G</creatorcontrib><creatorcontrib>MURRAY, T. M</creatorcontrib><creatorcontrib>PAPAIOANNOU, A</creatorcontrib><creatorcontrib>SEBALDT, R. J</creatorcontrib><creatorcontrib>TENENHOUSE, A. M</creatorcontrib><title>Effectiveness of alendronate and etidronate in the treatment of osteoporosis in men : a prospective observational study</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><description>The prevalence of osteoporosis in men is higher than previously assumed; consequently, numerous therapies are being investigated to treat these patients. The Canadian Database of Osteoporosis and Osteopenia patients (CANDOO) was analyzed to examine changes in bone mineral density (BMD) in consecutively seen osteoporotic men administered alendronate, etidronate or no bone-active drugs (control) over 1 year. A total of 244 men attending six Canadian osteoporosis clinics were included in the study (42 alendronate, 102 etidronate and 100 control). Multiple imputation was used to model missing data to provide a more robust statistical model. The imputed datasets (five) were analyzed using multivariable linear regression to determine differences between groups in the percent change of lumbar spine (LS) and femoral neck (FN) BMD from baseline to 1 year. Differences in the percent change in BMD from baseline were most notable at the LS in favor of alendronate (4.3%; 95% CI: 2.1, 6.6 ) and etidronate (2.1%; 95% CI: 0.3, 4.0) therapy when compared with controls. At the LS, alendronate therapy led to significantly greater (2.2%; 95% CI: 0.2, 4.2) gains in BMD as compared to etidronate therapy. Compared to controls, there were no significant differences in FN BMD with alendronate (2.1%; 95% CI: -0.4, 4.7) or etidronate therapy (0.9%; 95% CI: -1.1, 2.8), nor were there significant differences between bisphosphonate groups (1.3%; 95% CI: -1.1, 3.6, in favor of alendronate). While both alendronate and etidronate significantly increased LS BMD in osteoporotic men after 1 year in real-world settings, alendronate therapy resulted in significantly superior gains in LS BMD. The effect of these two bisphosphonates on fractures and FN BMD in osteoporotic men is likely positive, but requires further study.</description><subject>Alendronate - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Body Height - physiology</subject><subject>Body Weight - physiology</subject><subject>Bone Density - physiology</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Bones, joints and connective tissue. Antiinflammatory agents</subject><subject>Diseases of the osteoarticular system</subject><subject>Etidronic Acid - therapeutic use</subject><subject>Femur Neck - physiopathology</subject><subject>Fractures, Bone - etiology</subject><subject>Fractures, Bone - physiopathology</subject><subject>Humans</subject><subject>Life Style</subject><subject>Lumbar Vertebrae - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Osteoporosis - drug therapy</subject><subject>Osteoporosis - physiopathology</subject><subject>Osteoporosis. Osteomalacia. Paget disease</subject><subject>Pharmacology. 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S ; PETRIE, A ; GOLDSMITH, C. H ; ADACHI, J. D ; IOANNIDIS, G ; BROWN, J. P ; HANLEY, D. A ; JOSSE, R. G ; MURRAY, T. M ; PAPAIOANNOU, A ; SEBALDT, R. J ; TENENHOUSE, A. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-42544a3e7a7b465ef78d2cab9ae11d5d12311ab6de6c3c235ac8a869f76be2693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Alendronate - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Body Height - physiology</topic><topic>Body Weight - physiology</topic><topic>Bone Density - physiology</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Bones, joints and connective tissue. Antiinflammatory agents</topic><topic>Diseases of the osteoarticular system</topic><topic>Etidronic Acid - therapeutic use</topic><topic>Femur Neck - physiopathology</topic><topic>Fractures, Bone - etiology</topic><topic>Fractures, Bone - physiopathology</topic><topic>Humans</topic><topic>Life Style</topic><topic>Lumbar Vertebrae - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Osteoporosis - drug therapy</topic><topic>Osteoporosis - physiopathology</topic><topic>Osteoporosis. Osteomalacia. Paget disease</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Regression Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OLSZYNSKI, W. P</creatorcontrib><creatorcontrib>DAVISON, K. S</creatorcontrib><creatorcontrib>PETRIE, A</creatorcontrib><creatorcontrib>GOLDSMITH, C. 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P</au><au>DAVISON, K. S</au><au>PETRIE, A</au><au>GOLDSMITH, C. H</au><au>ADACHI, J. D</au><au>IOANNIDIS, G</au><au>BROWN, J. P</au><au>HANLEY, D. A</au><au>JOSSE, R. G</au><au>MURRAY, T. M</au><au>PAPAIOANNOU, A</au><au>SEBALDT, R. J</au><au>TENENHOUSE, A. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effectiveness of alendronate and etidronate in the treatment of osteoporosis in men : a prospective observational study</atitle><jtitle>Osteoporosis international</jtitle><addtitle>Osteoporos Int</addtitle><date>2006-02-01</date><risdate>2006</risdate><volume>17</volume><issue>2</issue><spage>217</spage><epage>224</epage><pages>217-224</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>The prevalence of osteoporosis in men is higher than previously assumed; consequently, numerous therapies are being investigated to treat these patients. The Canadian Database of Osteoporosis and Osteopenia patients (CANDOO) was analyzed to examine changes in bone mineral density (BMD) in consecutively seen osteoporotic men administered alendronate, etidronate or no bone-active drugs (control) over 1 year. A total of 244 men attending six Canadian osteoporosis clinics were included in the study (42 alendronate, 102 etidronate and 100 control). Multiple imputation was used to model missing data to provide a more robust statistical model. The imputed datasets (five) were analyzed using multivariable linear regression to determine differences between groups in the percent change of lumbar spine (LS) and femoral neck (FN) BMD from baseline to 1 year. Differences in the percent change in BMD from baseline were most notable at the LS in favor of alendronate (4.3%; 95% CI: 2.1, 6.6 ) and etidronate (2.1%; 95% CI: 0.3, 4.0) therapy when compared with controls. At the LS, alendronate therapy led to significantly greater (2.2%; 95% CI: 0.2, 4.2) gains in BMD as compared to etidronate therapy. Compared to controls, there were no significant differences in FN BMD with alendronate (2.1%; 95% CI: -0.4, 4.7) or etidronate therapy (0.9%; 95% CI: -1.1, 2.8), nor were there significant differences between bisphosphonate groups (1.3%; 95% CI: -1.1, 3.6, in favor of alendronate). While both alendronate and etidronate significantly increased LS BMD in osteoporotic men after 1 year in real-world settings, alendronate therapy resulted in significantly superior gains in LS BMD. The effect of these two bisphosphonates on fractures and FN BMD in osteoporotic men is likely positive, but requires further study.</abstract><cop>London</cop><pub>Springer</pub><pmid>15997420</pmid><doi>10.1007/s00198-005-1965-6</doi><tpages>8</tpages></addata></record> |
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subjects | Alendronate - therapeutic use Biological and medical sciences Body Height - physiology Body Weight - physiology Bone Density - physiology Bone Density Conservation Agents - therapeutic use Bones, joints and connective tissue. Antiinflammatory agents Diseases of the osteoarticular system Etidronic Acid - therapeutic use Femur Neck - physiopathology Fractures, Bone - etiology Fractures, Bone - physiopathology Humans Life Style Lumbar Vertebrae - physiopathology Male Medical sciences Middle Aged Osteoporosis - drug therapy Osteoporosis - physiopathology Osteoporosis. Osteomalacia. Paget disease Pharmacology. Drug treatments Prospective Studies Regression Analysis Treatment Outcome |
title | Effectiveness of alendronate and etidronate in the treatment of osteoporosis in men : a prospective observational study |
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