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  4. Administration of romosozumab improves vertebral trabecular and cortical bone as assessed with quantitative computed tomography and finite element analysis
 
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Administration of romosozumab improves vertebral trabecular and cortical bone as assessed with quantitative computed tomography and finite element analysis

Publikationstyp
Journal Article
Date Issued
2015-07-29
Sprache
English
Author(s)
Graeff, Christian  
Campbell, Graeme Michael  
Peña, Jaime Andrés  
Borggrefe, Jan  
Padhi, Desmond  
Kaufman, Allegra  
Chang, Sung  
Libanati, Cesar  
Glüer, Claus Christian  
Institut
Biomechanik M-3  
TORE-URI
http://hdl.handle.net/11420/9406
Journal
Bone  
Volume
81
Start Page
364
End Page
369
Citation
Bone 81: 364-369 (2015-12-01)
Publisher DOI
10.1016/j.bone.2015.07.036
Scopus ID
2-s2.0-84939477240
PubMed ID
26232375
Publisher
Elsevier Science
Romosozumab inhibits sclerostin, thereby increasing bone formation and decreasing bone resorption. This dual effect of romosozumab leads to rapid and substantial increases in areal bone mineral density (aBMD) as measured by dual-energy X-ray absorptiometry (DXA). In a phase 1b, randomized, double-blind, placebo-controlled study, romosozumab or placebo was administered to 32 women and 16 men with low aBMD for 3. months, with a further 3-month follow-up: women received six doses of 1 or 2. mg/kg every 2. weeks (Q2W) or three doses of 2 or 3. mg/kg every 4. weeks (Q4W); men received 1. mg/kg Q2W or 3. mg/kg Q4W. Quantitative computed tomography (QCT) scans at lumbar (L1-2) vertebrae and high-resolution QCT (HR-QCT) scans at thoracic vertebra (T12) were analyzed in a subset of subjects at baseline, month 3, and month 6. The QCT subset included 24 romosozumab and 9 placebo subjects and the HR-QCT subset included 11 romosozumab and 3 placebo subjects. The analyses pooled the romosozumab doses. Linear finite element modeling of bone stiffness was performed. Compared with placebo, the romosozumab group showed improvements at month 3 for trabecular BMD by QCT and HR-QCT, HR-QCT trabecular bone volume fraction (BV/TV) and separation, density-weighted cortical thickness, and QCT stiffness (all p<. 0.05). At month 6, improvements from baseline were observed in QCT trabecular BMD and stiffness, and in HR-QCT BMD, trabecular BV/TV and separation, density-weighted cortical thickness, and stiffness in the romosozumab group (all p<. 0.05 compared with placebo). The mean (SE) increase in HR-QCT stiffness with romosozumab from baseline was 26.9%. ±. 6.8% and 35.0%. ±. 6.8% at months 3 and 6, respectively; subjects administered placebo had changes of -. 2.7%. ±. 13.4% and -. 6.4%. ±. 13.4%, respectively. In conclusion, romosozumab administered for 3. months resulted in rapid and large improvements in trabecular and cortical bone mass and structure as well as whole bone stiffness, which continued 3. months after the last romosozumab dose.
Subjects
Bone mineral density
Bone quantitative computed tomography
Romosozumab
Sclerostin
DDC Class
570: Biowissenschaften, Biologie
600: Technik
610: Medizin
More Funding Information
This study was funded by Amgen Inc. (contract no. 200704274 ) and UCB Pharma .
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