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Influence of age on the efficacy of pharmacologic treatments on fracture risk reduction and increases in BMD: RCT results from the FNIH-ASBMR-SABRE project.
Schini, Marian; Vilaca, Tatiane; Vittinghoff, Eric; Lui, Li-Yung; Ewing, Susan K; Thompson, Austin R; Bauer, Douglas C; Bouxsein, Mary L; Black, Dennis M; Eastell, Richard.
Afiliação
  • Schini M; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, S10 2TN, United Kingdom.
  • Vilaca T; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, S10 2TN, United Kingdom.
  • Vittinghoff E; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA 94158, United States.
  • Lui LY; California Pacific Medical Center Research Institute, San Francisco, CA 94158, United States.
  • Ewing SK; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA 94158, United States.
  • Thompson AR; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA 94158, United States.
  • Bauer DC; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA 94158, United States.
  • Bouxsein ML; Department of Medicine, University of California, San Francisco, CA 94158, United States.
  • Black DM; Department of Orthopedic Surgery, Harvard Medical School, Center for Advanced Orthopedic Studies, Beth Israel Deaconess Medical Center, Boston, MA 02215330, United States.
  • Eastell R; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA 94158, United States.
J Bone Miner Res ; 39(5): 544-550, 2024 May 24.
Article em En | MEDLINE | ID: mdl-38501786
ABSTRACT
There is a common belief that antiosteoporosis medications are less effective in older adults. This study used data from randomized controlled trials (RCTs) to determine whether the anti-fracture efficacy of treatments and their effects on BMD differ in people ≥70 compared to those <70 yr. We used individual patient data from 23 RCTs of osteoporosis medications collected as part of the FNIH-ASBMR SABRE project. We assessed the following fractures radiographic vertebral, non-vertebral, hip, all clinical, and all fractures. We used Cox proportional hazard regression to estimate treatment effect for clinical fracture outcomes, logistic regression for the radiographic vertebral fracture outcome, and linear regression to estimate treatment effect on 24-mo change in hip and spine BMD in each age subgroup. The analysis included 123 164 (99% female) participants; 43% being ≥70 yr. Treatment with anti-osteoporosis drugs significantly and similarly reduced fractures in both subgroups (eg, odds ratio [OR] = 0.47 and 0.51 for vertebral fractures in those below and above 70 yr, interaction P = .19; hazard ratio [HR] for all fractures 0.72 vs 0.70, interaction P = .20). Results were similar when limited to bisphosphonate trials with the exception of hip fracture risk reduction which was somewhat greater in those <70 (HR = 0.44) vs ≥70 (HR = 0.79) yr (interaction P = .02). Allocation to anti-osteoporotic drugs resulted in significantly greater increases in hip and spine BMD at 24 mo in those ≥70 compared to those <70 yr. In summary, anti-osteoporotic medications similarly reduced the risk of fractures regardless of age, and the few small differences in fracture risk reduction by age were of uncertain clinical significance.
Medications used for osteoporosis maybe are less effective in older adults. This study used data from clinical trials to determine whether these medications work equally well in reducing the risk of fractures in people ≥70 compared to those <70 yr. The analysis included 123 164 participants with data from 23 trials. Treatment with anti-osteoporosis drugs significantly reduced fractures in both groups in a similar way. The BMD increased more in the older group.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Densidade Óssea Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Bone Miner Res Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Densidade Óssea Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Bone Miner Res Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido