Farlay Delphine, Rizzo Sébastien, Dempster David W, Huang Shuang, Chines Arkadi, Brown Jacques P, Boivin Georges
INSERM, UMR 1033, University of Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Department of Pathology and Cell Biology, Columbia University, New York, NY, USA.
J Bone Miner Res. 2022 May;37(5):856-864. doi: 10.1002/jbmr.4538. Epub 2022 Mar 24.
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).
在患有骨质疏松症的绝经后女性中,地诺单抗(DMAb)治疗10年导致骨矿化程度显著更高,在第2至3年到第5年有随后的增加,而第5年和第10年之间没有进一步差异。我们的目的是评估反映骨矿物质和有机基质质量的变量(傅里叶变换红外显微光谱法)以及骨的显微硬度(维氏显微压痕法)。对来自骨质疏松症女性的髂骨活检样本(72例来自FREEDOM试验,49例来自FREEDOM扩展试验)进行横断面评估,分别在皮质骨和松质骨区域以盲法进行。在使用DMAb 2至3年后,与安慰剂相比,皮质骨的矿物质/基质比率和显微硬度显著更高,而在两个骨区域中,矿物质成熟度、矿物质结晶度、矿物质碳酸化和胶原蛋白成熟度没有差异。在使用DMAb 5年后,与2至3年相比,矿物质碳酸化显著更低,矿物质/基质比率、矿物质成熟度和结晶度显著更高,并且第5年和第10年之间没有差异,但松质骨中的矿物质成熟度除外。这些数据支持矿物质向更成熟晶体的转变(在生理范围内)以及在DMAb治疗5年内二级矿化的完整性。与2至3年相比,在使用DMAb 5年时,皮质骨和松质骨区域的显微硬度显著更低,并且第5年到第10年没有差异。第5年和第10年较低的显微硬度可能是由于在5年和10年期间骨重塑持续处于低状态下有机基质成熟的结果。© 2022美国骨与矿物质研究学会(ASBMR)