Publication:
A Pooled Analysis of Fall Incidence From Placebo-Controlled Trials of Denosumab

dc.contributor.authorPojchong Chotiyarnwongen_US
dc.contributor.authorEugene McCloskeyen_US
dc.contributor.authorRichard Eastellen_US
dc.contributor.authorMichael R. McClungen_US
dc.contributor.authorEvelien Gielenen_US
dc.contributor.authorJohn Gostageen_US
dc.contributor.authorMichele McDermotten_US
dc.contributor.authorArkadi Chinesen_US
dc.contributor.authorShuang Huangen_US
dc.contributor.authorSteven R. Cummingsen_US
dc.contributor.otherKU Leuven– University Hospital Leuvenen_US
dc.contributor.otherUniversity of California, San Franciscoen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherOregon Osteoporosis Centeren_US
dc.contributor.otherUniversity of Sheffielden_US
dc.contributor.otherAmgen Incorporateden_US
dc.date.accessioned2020-05-05T05:58:16Z
dc.date.available2020-05-05T05:58:16Z
dc.date.issued2020-01-01en_US
dc.description.abstract© 2020 The Authors. Journal of Bone and Mineral Research published by American Society for Bone and Mineral Research. Recent studies suggest that the RANK/RANKL system impacts muscle function and/or mass. In the pivotal placebo-controlled fracture trial of the RANKL inhibitor denosumab in women with postmenopausal osteoporosis, treatment was associated with a lower incidence of non-fracture-related falls (p = 0.02). This ad hoc exploratory analysis pooled data from five placebo-controlled trials of denosumab to determine consistency across trials, if any, of the reduction of fall incidence. The analysis included trials in women with postmenopausal osteoporosis and low bone mass, men with osteoporosis, women receiving adjuvant aromatase inhibitors for breast cancer, and men receiving androgen deprivation therapy for prostate cancer. The analysis was stratified by trial, and only included data from the placebo-controlled period of each trial. A time-to-event analysis of first fall and exposure-adjusted subject incidence rates of falls were analyzed. Falls were reported and captured as adverse events. The analysis comprised 10,036 individuals; 5030 received denosumab 60 mg subcutaneously once every 6 months for 12 to 36 months and 5006 received placebo. Kaplan–Meier estimates showed an occurrence of falls in 6.5% of subjects in the placebo group compared with 5.2% of subjects in the denosumab group (hazard ratio = 0.79; 95% confidence interval 0.66–0.93; p = 0.0061). Heterogeneity in study designs did not permit overall assessment of association with fracture outcomes. In conclusion, denosumab may reduce the risk of falls in addition to its established fracture risk reduction by reducing bone resorption and increasing bone mass. These observations require further exploration and confirmation in studies with muscle function or falls as the primary outcome. © 2020 The Authors. Journal of Bone and Mineral Research published by American Society for Bone and Mineral Research.en_US
dc.identifier.citationJournal of Bone and Mineral Research. (2020)en_US
dc.identifier.doi10.1002/jbmr.3972en_US
dc.identifier.issn15234681en_US
dc.identifier.issn08840431en_US
dc.identifier.other2-s2.0-85082840462en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/54690
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082840462&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleA Pooled Analysis of Fall Incidence From Placebo-Controlled Trials of Denosumaben_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082840462&origin=inwarden_US

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