Department of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Lottestr. 59, 22529, Hamburg, Germany.
Department of Orthopedics, University Medical Center Hamburg-Eppendorf, Martinistraße 52, 20246, Hamburg, Germany.
Calcif Tissue Int. 2018 Nov;103(5):512-521. doi: 10.1007/s00223-018-0447-8. Epub 2018 Jun 26.
Diagnosis and management of adult individuals with low bone mass and increased bone fragility before the age of 50 can be challenging. A number of these patients are diagnosed with mild osteogenesis imperfecta (OI) through detection of COL1A1 or COL1A2 mutations; however, a clinical differentiation from early-onset osteoporosis (EOOP) may be difficult. The purpose of this study was to determine the bone microstructural differences between mild OI and EOOP patients. 29 patients showed mutations in COL1A1 or COL1A2 and were classified as OI. Skeletal assessment included dual-energy X-ray absorptiometry (DXA), high-resolution peripheral quantitative computed tomography (HR-pQCT), and bone turnover serum analyses. Bone microstructure of 21/29 OI patients was assessed and compared to 23 age- and sex-matched patients clinically classified EOOP but without mutations in the known disease genes as well as to 20 healthy controls. In the OI patients, we did not observe an age-dependent decrease in DXA Z-scores. HR-pQCT revealed a significant reduction in volumetric BMD and microstructural parameters in the distal radius and tibia in both the OI and EOOP cohorts compared to the healthy controls. When comparing the bone microstructure of OI patients with the EOOP cohort, significant differences were found in terms of bone geometry in the radius, while no significant changes were detected in all other HR-pQCT parameters at the radius and tibia. Taken together, adult mild OI patients demonstrate a predominantly high bone turnover trabecular bone loss syndrome that shows minor microstructural differences compared to EOOP without mutation detection.
50 岁以下低骨量和高骨脆性的成人个体的诊断和管理具有挑战性。这些患者中的许多人通过检测 COL1A1 或 COL1A2 突变被诊断为轻度成骨不全症(OI);然而,与早发性骨质疏松症(EOOP)进行临床区分可能很困难。本研究旨在确定轻度 OI 和 EOOP 患者之间的骨微观结构差异。29 名患者在 COL1A1 或 COL1A2 中显示突变,并被归类为 OI。骨骼评估包括双能 X 射线吸收法(DXA)、高分辨率外周定量计算机断层扫描(HR-pQCT)和骨转换血清分析。评估了 29 名 OI 患者中的 21 名的骨微观结构,并将其与 21 名年龄和性别匹配的临床分类为 EOOP 但无已知疾病基因突变的患者以及 20 名健康对照者进行比较。在 OI 患者中,我们没有观察到 DXA Z 分数随年龄的下降。HR-pQCT 显示,与健康对照组相比,远端桡骨和胫骨的体积 BMD 和微观结构参数在 OI 和 EOOP 两组中均显著降低。当比较 OI 患者与 EOOP 队列的骨微观结构时,在桡骨的骨几何形状方面发现了显著差异,而在桡骨和胫骨的所有其他 HR-pQCT 参数方面均未发现显著变化。总之,成人轻度 OI 患者表现出主要的高骨转换小梁骨丢失综合征,与未检测到突变的 EOOP 相比,其微观结构差异较小。