4.5 Article

Bone quality of the newest bone formed after two years of teriparatide therapy in patients who were previously treatment-na⟨ve or on long-term alendronate therapy

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 25, Issue 12, Pages 2709-2719

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-014-2814-2

Keywords

Alendronate; Bone material properties; Collagen cross-links; Mineral maturity/crystallinity; Raman microspectroscopy; Teriparatide

Funding

  1. Eli Lilly Co
  2. Austrian workers compensation board
  3. Wiener Gebietskrankenkasse (WGKK), Viennese insurance funds

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The results of the present study, involving analysis of biopsies from patients who received teriparatide for 2 years and were previously either treatment-na < ve or on long-term alendronate therapy, suggest that prior alendronate use does not blunt the favorable effects of teriparatide on bone quality. Examine the effect of 2 years of teriparatide (TPTD) treatment on mineral and organic matrix properties of the newest formed bone in patients who were previously treatment-na < ve (TN) or on long-term alendronate (ALN) therapy. Raman and Fourier transform infrared microspectroscopic analyses were used to determine the mineral/matrix (M/M) ratio, the relative proteoglycan (PG) content, and the mineral maturity/crystallinity (MMC; determined by three methods: carbonate content, full width at half height of the v (1) PO4 band [FWHH], and wavelength at maxima of the v (1) PO4 band), as well as collagen maturity (ratio of pyridinoline/divalent cross-links), in paired iliac crest biopsies at trabecular, endosteal, and osteonal surfaces of newly formed bone in postmenopausal osteoporotic women who were previously either TN (n = 16) or receiving long-term ALN treatment (n = 24). Trabecular M/M ratio increased and matrix content decreased significantly in the ALN pretreated group. Collagen maturity decreased in both patient groups. Endosteal M/M ratio increased significantly in the TN group. Trabecular M/M ratio was higher at endpoint in the ALN pretreated group than in the TN group. Overall, no changes from baseline were observed in PG content, except that PG content was higher in the ALN pretreated group than in the TN group at endosteal surfaces at endpoint. The ability of TPTD treatment to reduce MMC in both patient groups and at the different bone surfaces depended on the measurement tool (relative carbonate content or wavelength at maxima of the v (1) PO4 band). None of the changes in MMC were different between the two patient groups. The results suggest some favorable impact of TPTD on bone mineral and organic matrix properties of in situ forming bone in terms of increased initial mineralization and decreased MMC and collagen maturity. Moreover, prior long-term ALN administration may have only limited influence on these properties in bone newly formed after 2 years of TPTD treatment.

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