Cosman Felicia, Hans Didier, Shevroja Enisa, Wang Yamei, Mitlak Bruce
Columbia University, New York, New York, USA.
Interdisciplinary Center of Bone Diseases, Lausanne University Hospital and Lausanne University, Lausanne, Switzerland.
J Bone Miner Res. 2023 Apr;38(4):464-470. doi: 10.1002/jbmr.4764. Epub 2023 Feb 12.
Although bone mineral density (BMD) is a predictor of fracture, many fractures occur in women with T-scores > -2.5. Bone microarchitecture, assessed by trabecular bone score (TBS), predicts fracture risk independent of BMD. We evaluated whether abaloparatide improves TBS and whether TBS trends were associated with vertebral fracture risk reduction. Women with osteoporosis randomized to abaloparatide or placebo for 18 months (ACTIVE), followed by alendronate for 24 months (ACTIVExtend), with evaluable TBS, were included in this post hoc analysis (N = 911). TBS was calculated from spine BMD scans using an algorithm adjusted for tissue thickness (TBS ) at baseline, 6, 18, and 43 months. Mean increments in TBS from baseline within and between treatment groups, proportion of women with TBS increments above least significant change (LSC) and proportion with degraded TBS (<1.027) were calculated. Risk estimates for vertebral fracture were compared using binary logistic regressions adjusted for baseline age and spine BMD. At baseline, 42% had degraded TBS . Mean TBS increased 4% after 18 months abaloparatide (p < 0.001) and was unchanged with placebo. After 2 subsequent years of alendronate, the total cumulative TBS increase was 4.4% with abaloparatide/alendronate and 1.7% with placebo/alendronate (group difference, p < 0.001). At 43 months, the proportion of women with degraded TBS had declined to 21% with abaloparatide/alendronate and 37% with placebo/alendronate (p < 0.05). An increase in TBS ≥ LSC was observed in 50% of abaloparatide-treated women at 18 months and was associated with decreased odds (odds ratio [OR]; 95% confidence interval [CI]) of vertebral fracture (0.19; 95% CI, 0.04-0.80, 6 months; 0.30; 95% CI, 0.11-0.79, 43 months). In conclusion, abaloparatide increased TBS rapidly and progressively over 18 months and increments were maintained over 2 years with alendronate. TBS increase was associated with vertebral fracture risk reduction. Microarchitectural improvement may be one mechanism by which abaloparatide strengthens vertebral bone. © 2023 Radius Health, Inc and The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
尽管骨密度(BMD)是骨折的一个预测指标,但许多骨折发生在T值> -2.5的女性中。通过小梁骨评分(TBS)评估的骨微结构可独立于BMD预测骨折风险。我们评估了阿巴洛肽是否能改善TBS,以及TBS的变化趋势是否与椎体骨折风险降低相关。将患有骨质疏松症的女性随机分为阿巴洛肽组或安慰剂组,治疗18个月(ACTIVE研究),随后给予阿仑膦酸钠治疗24个月(ACTIVExtend研究),对具有可评估TBS的患者进行本次事后分析(N = 911)。使用针对组织厚度进行调整的算法(TBS ),在基线、6个月、18个月和43个月时从脊柱BMD扫描计算TBS。计算治疗组内和组间TBS相对于基线的平均增量、TBS增量高于最小显著变化(LSC)的女性比例以及TBS降低(<1.027)的女性比例。使用针对基线年龄和脊柱BMD进行调整的二元逻辑回归比较椎体骨折的风险估计值。在基线时,42%的患者TBS降低。阿巴洛肽治疗18个月后,TBS平均增加4%(p <0.001),而安慰剂组无变化。在随后两年的阿仑膦酸钠治疗后,阿巴洛肽/阿仑膦酸钠组TBS的总累积增加为4.4%,安慰剂/阿仑膦酸钠组为1.7%(组间差异,p <0.001)。在43个月时,阿巴洛肽/阿仑膦酸钠组TBS降低的女性比例降至21%,安慰剂/阿仑膦酸钠组为37%(p <0.05)。在18个月时,50%接受阿巴洛肽治疗的女性TBS增加≥LSC,这与椎体骨折几率降低相关(优势比[OR];95%置信区间[CI])(0.19;95% CI,0.04 - 0.80,6个月;0.30;95% CI,0.11 - 0.79,43个月)。总之,阿巴洛肽在18个月内迅速且逐渐增加TBS,并且在随后2年的阿仑膦酸钠治疗中增量得以维持。TBS增加与椎体骨折风险降低相关。微结构改善可能是阿巴洛肽强化椎体骨的一种机制。© 2023 Radius Health公司及作者。《骨与矿物质研究杂志》由Wiley Periodicals LLC代表美国骨与矿物质研究学会(ASBMR)出版。