Ferrari Serge, Betah Donald, Feldman Robert G, Langdahl Bente L, Oates Mary, Timoshanko Jen, Wang Zhenxun, Dhaliwal Ruban
Geneva University Hospital, Geneva 1211, Switzerland.
Amgen Inc., Thousand Oaks, CA 91320, USA.
J Clin Endocrinol Metab. 2025 Jan 24. doi: 10.1210/clinem/dgae862.
Trabecular bone score (TBS), a gray-level texture index derived from lumbar spine (LS) dual-energy x-ray absorptiometry (DXA) scans, is decreased in patients with diabetes and is associated with increased fracture risk, independent of areal bone mineral density (aBMD), but potentially influenced by abdominal fat tissue.
Evaluate effect of romosozumab (210 mg monthly) for 12 months followed by alendronate (70 mg weekly) for 24 months vs alendronate alone (70 mg weekly) for 36 months on LS aBMD and TBS in women with type 2 diabetes (T2D) enrolled in the ARCH study.
This post hoc analysis included women from ARCH who had T2D at baseline and LS DXA scans at baseline and ≥1 postbaseline visit (romosozumab-to-alendronate, n = 165; alendronate-to-alendronate, n = 195). aBMD and TBS (determined by an updated tissue thickness-adjusted TBS algorithm [TBSTT]) were assessed on LS DXA scans at baseline and ≥1 postbaseline visit (months 12, 24, and 36).
Romosozumab led to significantly greater gains in LS aBMD and TBSTT at month 12 vs alendronate, and the greater gains with romosozumab were maintained after transition to alendronate and persisted significantly at months 24 and 36 vs alendronate alone. TBSTT percentage changes weakly correlated to LS aBMD percentage changes from baseline to month 36 (romosozumab-to-alendronate, R2 = 0.1493; alendronate-to-alendronate, R2 = 0.0429).
In postmenopausal women with osteoporosis and T2D, 12 months of romosozumab followed by 24 months of alendronate vs alendronate alone significantly improved LS aBMD and TBSTT (independently of abdominal fat) and to a greater extent. Hence, romosozumab may improve bone strength in patients with T2D.
ClinicalTrials.gov-NCT01631214.
小梁骨评分(TBS)是一种从腰椎双能X线吸收测定(DXA)扫描中得出的灰度纹理指数,在糖尿病患者中降低,且与骨折风险增加相关,独立于骨面积密度(aBMD),但可能受腹部脂肪组织影响。
在ARCH研究中,评估12个月每月一次注射罗莫单抗(210毫克)随后24个月每周一次服用阿仑膦酸钠(70毫克)与单独36个月每周一次服用阿仑膦酸钠(70毫克)对2型糖尿病(T2D)女性腰椎aBMD和TBS的影响。
这项事后分析纳入了ARCH研究中基线时患有T2D且基线时有腰椎DXA扫描以及≥1次基线后访视的女性(罗莫单抗转阿仑膦酸钠组,n = 165;阿仑膦酸钠转阿仑膦酸钠组,n = 195)。在基线以及≥1次基线后访视(第12、24和36个月)时通过腰椎DXA扫描评估aBMD和TBS(由更新的组织厚度调整TBS算法[TBSTT]确定)。
与阿仑膦酸钠相比,罗莫单抗在第12个月时使腰椎aBMD和TBSTT有显著更大的增加,在转换为阿仑膦酸钠后,罗莫单抗的更大增加得以维持,并且在第24和36个月时与单独使用阿仑膦酸钠相比仍显著持续。从基线到第36个月,TBSTT百分比变化与腰椎aBMD百分比变化弱相关(罗莫单抗转阿仑膦酸钠组,R2 = 0.1493;阿仑膦酸钠转阿仑膦酸钠组,R2 = 0.0429)。
在患有骨质疏松症和T2D的绝经后女性中,12个月的罗莫单抗随后24个月的阿仑膦酸钠与单独使用阿仑膦酸钠相比,显著改善了腰椎aBMD和TBSTT(独立于腹部脂肪)且改善程度更大。因此,罗莫单抗可能改善T2D患者的骨强度。
ClinicalTrials.gov - NCT01631214。