Journal of Clinical Densitometry
Volume 13, Issue 2 , Pages 181-189, April 2010

The Utility of Changes in Serum Levels of C-Terminal Telopeptide of Type I Collagen in Predicting Patient Response to Oral Monthly Ibandronate Therapy

Portions of this work have been presented at the following meetings: 7th European Congress on Clinical and Economic Aspects of Osteoporosis and Osteoarthritis, Porto, Portugal, March 28–31, 2007; 16th Annual Meeting & Clinical Congress, American Association of Clinical Endocrinologists, Seattle, WA, USA, April 11–15, 2007; 7th International Symposium on Osteoporosis, National Osteoporosis Foundation, Washington, DC, USA, April 18–22, 2007.

  • Marc C. Hochberg

      Affiliations

    • Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
    • Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
    • Corresponding Author InformationAddress correspondence to: Marc C. Hochberg, MD, MPH, Division of Rheumatology & Clinical Immunology, Department of Medicine, University of Maryland School of Medicine, 10 S. Pine Street, MSTF 8-34, Baltimore, MD 21201.
  • ,
  • Stuart L. Silverman

      Affiliations

    • Cedars-Sinai/UCLA and OMC Clinical Research Center, Beverly Hills, CA, USA
  • ,
  • Charles E. Barr

      Affiliations

    • Roche, Nutley, NJ, USA
  • ,
  • Paul D. Miller

      Affiliations

    • Colorado Center for Bone Research, Lakewood, CO, USA

Received 6 May 2009; received in revised form 1 October 2009; accepted 10 January 2010. published online 29 March 2010.

Abstract 

Bone turnover markers may provide a more rapid indication of patient response to osteoporosis treatment than bone mineral density (BMD) measurements. This post hoc analysis of data from the MOBILE (Monthly Oral iBandronate In LadiEs) study assessed the relationship between increases in BMD at 12mo from baseline after starting ibandronate treatment and changes in bone resorption marker serum C-terminal telopeptide of type I collagen (sCTX) from baseline at 3 and 6mo. MOBILE enrolled postmenopausal women aged 55–80yr with mean lumbar spine (LS) BMD T-score of −2.5 to −5.0. This analysis included women who received 150-mg monthly oral ibandronate (n=323). A high proportion of women were classified as BMD responders after 1yr (BMD increase was ≥0%, i.e., 74–91% depending on skeletal site; BMD increase was ≥3%, i.e., 34–67%). Women with larger decreases in sCTX were more likely to be BMD responders. The percent increase in LS BMD at 12mo was significantly associated with the percent decrease in sCTX at 3mo from baseline (Pearson correlation coefficient: −0.19, p=0.0016). In linear regression models, percent decrease in sCTX at 3mo from baseline was a significant predictor of 1-yr LS BMD response (R2=0.61, p=0.0007). These data suggest that 3-mo changes in sCTX levels are associated with 1-yr LS BMD increases in postmenopausal women treated with once-monthly oral ibandronate.

Key Words: Bisphosphonates, bone densitometry, bone turnover markers, ibandronate, osteoporosis

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 Funding sources: This research was funded by Roche.

 Conflicts of interest. Dr. Hochberg has served as a consultant for Amgen, Eli Lilly, Merck, Novartis, Procter & Gamble, Roche, and Wyeth. Dr. Silverman has received grants or research support from Lilly, Merck, Novartis, Procter & Gamble, Roche, and Wyeth. and has acted as a consultant or speaker for Amgen, Lilly, GlaxoSmithKline, and Merck. Dr. Barr is an employee of Roche. Dr. Miller has received scientific grants from Procter & Gamble, sanofi-aventis, Roche, Eli Lilly, Merck, Novartis, and Amgen. He has served on speaker boards, advisory boards or as a consultant for Procter & Gamble, sanofi-aventis, Merck, Eli Lilly, Amgen, NPS, Novartis, Roche, and GlaxoSmithKline.

PII: S1094-6950(10)00008-9

doi:10.1016/j.jocd.2010.01.007

Journal of Clinical Densitometry
Volume 13, Issue 2 , Pages 181-189, April 2010