Table 2.
Study | Year | Design | Country | Population | Sex and mean age | Intervention | Control | Outcome | Follow-up duration |
---|---|---|---|---|---|---|---|---|---|
Bonnet et al.20) | 2019 | Single-blind RCT | Geneva, Switzerland | Post-menopausal osteoporotic women | Females only | Denosumab (n=18) | n=20 | BMD-LS, ALM, handgrip strength | 2.9 yr (range, 2.2–3.7 yr) |
Mean age: Denosumab 64.9±1.5 yr, control 65.7±0.9 yr | BPs: alendronate (n=8), zoledronate (n=12) | ||||||||
Miedany et al.21) | 2021 | Single-blind RCT | Egypt | Patients with osteoporosis | Male and female | Denosumab (n=135) | n=136 | Hip and spine BMD, calcium, vitamin D, FRAX, TUG, handgrip strength, gait speed | 5 yr |
Mean ages: NA | BPs: oral alendronate 70 mg once weekly, zoledronate once yearly 5 mg iv | ||||||||
Rupp et al.22) | 2022 | Retrospective cohort | Germany | Patients with osteopenia and osteoporosis | Male (n=8) and female (n=52) in both groups | Denosumab (n=60) | n=60 | 25(OH)D3 level, femoral and spinal BMD, handgrip strength, CRT force | 17.6±9 mo (range, 8–59 mo) |
Mean age: Denosumab 68.9±9.2 yr, control 68.0±7.6 yr | BPs: alendronate 70 mg once weekly oral, ibandronate 3 mg intravenously every 3 months | ||||||||
Phu et al.23) | 2019 | Cohort | Melbourne, Australia | Older adults ≥65 yr with history or risk of falls and/or fractures | Male and female | Denosumab + vitamin D (n=51) | n=28 | Gait speed, TUG, FSST, SPPB score, ABC | 6 mo |
Mean age: NA | Zoledronic acid + vitamin D |
RCT, randomized controlled trial; BPs, bisphosphonates; BMD, bone mineral density; ALM, appendicular lean mass; iv, intravenous; FRAX, Fracture Risk Assessment Tool; TUG, timed up and go; CRT, chair raising test; FSST, four square step test; SPPB, Short Physical Performance Battery; ABC, Activity-specific Balance Confidence Scale.