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Bone Mineral and Organic Properties in Postmenopausal Women Treated With Denosumab for Up to 10 years.
Farlay, Delphine; Rizzo, Sébastien; Dempster, David W; Huang, Shuang; Chines, Arkadi; Brown, Jacques P; Boivin, Georges.
Afiliación
  • Farlay D; INSERM, UMR 1033, University of Lyon, Université Claude Bernard Lyon 1, Lyon, France.
  • Rizzo S; INSERM, UMR 1033, University of Lyon, Université Claude Bernard Lyon 1, Lyon, France.
  • Dempster DW; Department of Pathology and Cell Biology, Columbia University, New York, NY, USA.
  • Huang S; Regional Bone Center, Helen Hayes Hospital, West Haverstraw, NY, USA.
  • Chines A; Clinical Development, Amgen Inc., Thousand Oaks, CA, USA.
  • Brown JP; Clinical Development, Amgen Inc., Thousand Oaks, CA, USA.
  • Boivin G; CHU de Quebec Research Centre, Laval University, Quebec City, Canada.
J Bone Miner Res ; 37(5): 856-864, 2022 05.
Article en En | MEDLINE | ID: mdl-35249242
ABSTRACT
In postmenopausal women with osteoporosis, denosumab (DMAb) therapy through 10 years resulted in significantly higher degree of mineralization of bone, with a subsequent increase from years 2-3 to year 5 and no further difference between years 5 and 10. Our aim was to assess the variables reflecting the quality of bone mineral and organic matrix (Fourier transform infrared microspectroscopy), and the microhardness of bone (Vickers microindentation). Cross-sectional assessments were performed in blinded fashion on iliac bone biopsies from osteoporotic women (72 from FREEDOM trial, 49 from FREEDOM Extension trial), separately in cortical and cancellous compartments. After 2-3 years of DMAb, mineral/matrix ratio and microhardness of cortical bone were significantly higher compared with placebo, whereas mineral maturity, mineral crystallinity, mineral carbonation, and collagen maturity were not different in both bone compartments. Through 5 years of DMAb, mineral carbonation was significantly lower and mineral/matrix ratio, mineral maturity, and crystallinity were significantly higher versus 2-3 years and were not different between 5 and 10 years, with the exception of mineral maturity in cancellous bone. These data support a transition of mineral to more mature crystals (within physiological range) and the completeness of secondary mineralization within 5 years of DMAb treatment. Microhardness in cortical and cancellous compartments was significantly lower at 5 years of DMAb versus 2-3 years and was not different from years 5 to 10. The lower microhardness at years 5 and 10 is likely the result of maturation of the organic matrix in a persistently low state of bone remodeling over 5 and 10 years. © 2022 American Society for Bone and Mineral Research (ASBMR).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoporosis Posmenopáusica / Conservadores de la Densidad Ósea Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoporosis Posmenopáusica / Conservadores de la Densidad Ósea Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2022 Tipo del documento: Article País de afiliación: Francia
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