Scinovex
article Open AccessTop 1% cited

Effects of Oral Ibandronate Administered Daily or Intermittently on Fracture Risk in Postmenopausal Osteoporosis

Journal of Bone and Mineral Research · 2004 · Vol. 19(8) · pp. 1241–1249
Charles H. ChesnutArne SkagClaus ChristiansenRobert R. ReckerJ. A. StakkestadArne HøisethDieter FelsenbergHermann HussJennifer GilbrideRalph C. SchimmerPierre D. Delmasfor the Oral Ibandronate Osteoporosis Vertebral Fracture Trial in North America and Europe (BONE)

Abstract

After 3 years, the rate of new vertebral fractures was significantly reduced in patients receiving oral daily (4.7%) and intermittent ibandronate (4.9%), relative to placebo (9.6%). Thus, daily and intermittent oral ibandronate significantly reduced the risk of new morphometric vertebral fractures by 62% (p = 0.0001) and 50% (p = 0.0006), respectively, versus placebo. Both treatment groups also produced a statistically significant relative risk reduction in clinical vertebral fractures (49% and 48% for daily and intermittent ibandronate, respectively). Significant and progressive increases in lumbar spine (6.5%, 5.7%, and 1.3% for daily ibandronate, intermittent ibandronate, and placebo, respectively, at 3 years) and hip BMD, normalization of bone turnover, and significantly less height loss than in the placebo group were also observed for both ibandronate regimens. The overall population was at low risk for osteoporotic fractures. Consequently, the incidence of nonvertebral fractures was similar between the ibandronate and placebo groups after 3 years (9.1%, 8.9%, and 8.2% in the daily, intermittent, and placebo groups, respectively; difference between arms not significant). However, findings from a posthoc analysis showed that the daily regimen reduces the risk of nonvertebral fractures (69%; p = 0.012) in a higher-risk subgroup (femoral neck BMD T score < -3.0). In addition, oral ibandronate was well tolerated. Oral ibandronate, whether administered daily or intermittently with an extended between-dose interval of >2 months, is highly effective in reducing the incidence of osteoporotic fractures in postmenopausal women. This is the first time that significant fracture efficacy has been prospectively shown with an intermittently administered bisphosphonate in the overall study population of a randomized, controlled clinical trial. Thus, oral ibandronate holds promise as an effective and convenient alternative to current bisphosphonate therapies.

Bone health and osteoporosis researchBone health and treatmentsBone and Joint DiseasesMedicinePlaceboOsteoporosisBisphosphonateRelative riskDosingInternal medicineConfidence intervalUrologySurgery

MeSH terms

Ibandronic AcidAgedBody HeightBone and BonesDiphosphonatesDouble-Blind MethodFemaleFemurHumansLumbar VertebraeMiddle AgedPelvic BonesProspective StudiesRisk FactorsBone Density

Funding

  • F. Hoffmann-La Roche
Citations
1,220
FWCI
69.19
field-weighted impact
References
45
Percentile
100%
vs. same field & year
Citations per year
References
Noninvasive assessment of bone mineral and structure: State of the art
Journal of Bone and Mineral Research · 1996 · 942 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.