A Longitudinal Study of Skeletal Histomorphometry at 6 and 24 Months Across Four Bone Envelopes in Postmenopausal Women With Osteoporosis Receiving Teriparatide or Zoledronic Acid in the SHOTZ Trial

Author:

Dempster David W1,Zhou Hua1,Recker Robert R2,Brown Jacques P3,Bolognese Michael A4,Recknor Christopher P5,Kendler David L6,Lewiecki E Michael7,Hanley David A8,Rao Sudhaker D9,Miller Paul D10,Woodson Grattan C11,Lindsay Robert1,Binkley Neil12,Alam Jahangir13,Ruff Valerie A13,Gallagher Eileen R14,Taylor Kathleen A13

Affiliation:

1. Regional Bone CenterHelen Hayes HospitalWest HaverstrawNYUSA

2. School of MedicineCreighton UniversityOmahaNEUSA

3. CHU de Québec (CHUL) Research CentreLaval UniversityQuebec CityCanada

4. Bethesda Health ResearchBethesdaMDUSA

5. United Osteoporosis CentersGainesvilleGAUSA

6. Prohealth Clinical ResearchVancouverBritish ColumbiaCanada

7. New Mexico Clinical Research & Osteoporosis CenterAlbuquerqueNMUSA

8. Department of MedicineUniversity of CalgaryCalgaryAlbertaCanada

9. Bone & Mineral Research LaboratoryDetroitMIUSA

10. Colorado Center for Bone ResearchLakewoodCOUSA

11. Atlanta Research CenterAtlantaGAUSA

12. University of WisconsinMadisonWIUSA

13. Lilly USA, LLCIndianapolisINUSA

14. inVentiv Health ClinicalPrincetonNJUSA

Abstract

ABSTRACT Previously, we reported the effects of teriparatide (TPTD) and zoledronic acid (ZOL) on bone formation based on biochemical markers and bone histomorphometry of the cancellous envelope at month 6 in postmenopausal women with osteoporosis who participated in the 12-month primary Skeletal Histomorphometry in Subjects on Teriparatide or Zoledronic Acid Therapy (SHOTZ) study. Patients were eligible to enter a 12-month extension on their original treatment regimen: TPTD 20 μg/day (s.c. injection) or ZOL 5 mg/year (i.v. infusion). A second biopsy was performed at month 24. Here we report longitudinal changes between and within each treatment group in the cancellous, endocortical, intracortical, and periosteal bone envelopes in patients with evaluable biopsies at months 6 and 24 (paired data set: TPTD, n = 10; ZOL, n = 9). Between-group differences are also reported in the larger set of patients with evaluable biopsies at month 6 (TPTD, n = 28; ZOL, n = 30). Data from the cancellous envelope at month 6 or month 24 provided a reference to compare differences across envelopes within each treatment group. The 24-month results extend our earlier report that TPTD and ZOL possess different tissue-level mechanisms of action. Moreover, these differences persisted for at least 2 years in all four bone envelopes. Few longitudinal differences were observed within or across bone envelopes in ZOL-treated patients, suggesting that the low bone formation indices at month 6 persisted to month 24. Conversely, the magnitude of the effect of TPTD on bone formation varied across individual envelopes: median values for mineralizing surface (MS/BS) and bone formation rate (BFR/BS) at month 6 were approximately 3-fold to 5-fold higher in the endocortical and intracortical envelopes compared to the cancellous envelope. Although MS/BS and BFR/BS declined in these envelopes at month 24, median values continued to exceed, or were not significantly different from, those in the cancellous envelope. This study demonstrates for the first time that bone formation indices are higher with TPTD treatment than with ZOL in all four bone envelopes and the difference persists for at least 2 years. Moreover, the magnitude of the effect of TPTD in cortical bone remains robust at 24 months. © 2016 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research (ASBMR).

Publisher

Oxford University Press (OUP)

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