Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, USA.
Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
J Bone Miner Res. 2019 Dec;34(12):2301-2310. doi: 10.1002/jbmr.3858. Epub 2019 Nov 7.
Sclerostin antibody (Scl-Ab) is an anabolic bone agent that has been shown to increase bone mass in clinical trials of adult diseases of low bone mass, such as osteoporosis and osteogenesis imperfecta (OI). Its use to decrease bone fragility in pediatric OI has shown efficacy in several growing mouse models, suggesting translational potential to pediatric disorders of low bone mass. However, the effects of pharmacologic inhibition of sclerostin during periods of rapid growth and development have not yet been described with respect to the cranium, where lifelong deficiency of functioning sclerostin leads to patterns of excessive bone growth, cranial compression, and facial palsy. In the present study, we undertook dimensional and volumetric measurements in the skulls of growing Brtl/+ OI mice treated with Scl-Ab to examine whether therapy-induced phenotypic changes were similar to those observed clinically in patients with sclerosteosis or Van Buchem disorder. Mice treated between 3 and 14 weeks of age with high doses of Scl-Ab show significant calvarial thickening capable of rescuing OI-induced deficiencies in skull thickness. Other changes in cranial morphology, such as lengths and distances between anatomic landmarks, intracranial volume, and suture interdigitation, showed minimal effects of Scl-Ab when compared with growth-induced differences over the treatment duration. Treatment-induced narrowing of foramina was limited to sites of vascular but not neural passage, suggesting patterns of local regulation. Together, these findings reveal a site specificity of Scl-Ab action in the calvaria with no measurable cranial nerve impingement or brainstem compression. This differentiation from the observed outcomes of lifelong sclerostin deficiency complements reports of Scl-Ab treatment efficacy at other skeletal sites with the prospect of minimal cranial secondary complications. © 2019 American Society for Bone and Mineral Research. © 2019 American Society for Bone and Mineral Research.
骨硬化蛋白抗体(Scl-Ab)是一种促合成代谢的骨制剂,临床试验已证明其可增加骨质疏松症和成骨不全症(OI)等低骨量成人疾病的骨量。在几种生长中的小鼠模型中,使用 Scl-Ab 降低小儿 OI 的骨脆性已显示出疗效,这表明其具有向小儿低骨量疾病转化的潜力。然而,在快速生长和发育期间,骨硬化蛋白的药理抑制作用对颅骨的影响尚未得到描述,在颅骨中,终生缺乏功能正常的骨硬化蛋白会导致过度骨生长、颅骨压迫和面瘫的模式。在本研究中,我们对接受 Scl-Ab 治疗的生长中的 Brtl/+OI 小鼠颅骨进行了尺寸和体积测量,以检查治疗引起的表型变化是否与临床中观察到的硬骨化症或范布吕根疾病患者相似。在 3 至 14 周龄时用高剂量 Scl-Ab 治疗的小鼠表现出明显的颅骨增厚,能够挽救 OI 引起的颅骨厚度不足。颅骨形态的其他变化,如解剖标志之间的长度和距离、颅内体积和骨缝交织,与治疗期间的生长诱导差异相比,Scl-Ab 的影响最小。治疗引起的孔狭窄仅限于血管而不是神经通过的部位,表明存在局部调节模式。这些发现共同揭示了 Scl-Ab 在颅骨中的作用具有部位特异性,没有可测量的颅神经压迫或脑干压迫。这与终生骨硬化蛋白缺乏所观察到的结果不同,补充了 Scl-Ab 在其他骨骼部位治疗效果的报告,具有最小的颅部继发性并发症的前景。 © 2019 美国骨矿研究协会。 © 2019 美国骨矿研究协会。