Hung V W Y, Zhu T Y, Cheung W-H, Fong T-N, Yu F W P, Hung L-K, Leung K-S, Cheng J C Y, Lam T-P, Qin L
Bone Quality and Health Centre, Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Joint ACC-CUHK Space Medicine Center on Health Maintenance of Musculoskeletal System (Shenzhen Base of ACC-CUHK State Key Lab of Basic and Applied Space Medicine), The Chinese University Shenzhen Research Institute, Shenzhen, China.
Osteoporos Int. 2015 Jun;26(6):1691-703. doi: 10.1007/s00198-015-3045-x. Epub 2015 Jan 28.
In a cohort of 393 Chinese women, by using high-resolution peripheral quantitative computed tomography (HR-pQCT), we found that significant cortical bone loss occurred after midlife. Prominent increase in cortical porosity began at the fifth decade but reached a plateau before the sixth decade. Trabecular bone loss was already evident in young adulthood and continued throughout life.
This study aimed to investigate age-related differences in volumetric bone mineral density (vBMD), microarchitecture, and estimated bone strength at peripheral skeleton in Chinese female population.
In a cross-sectional cohort of 393 Chinese women aged 20-90 years, we obtained vBMD, microarchtecture, and micro-finite element-derived bone strength at distal radius and tibia using HR-pQCT.
The largest predictive age-related difference was found for cortical porosity (Ct.Po) which showed over four-fold and two-fold differences at distal radius and tibia, respectively, over the adulthood. At both sites, cortical bone area, vBMD, and thickness showed significant quadratic association with age with significant decrease beginning after midlife. Change of Ct.Po became more prominent between age of 50 and 57 (0.26 %/year at distal radius, 0.54 %/year at distal tibia, both p ≤ 0.001) but thereafter, reached a plateau (0.015 and 0.028 %/year, both p > 0.05). In contrast, trabecular vBMD and microarchitecture showed linear association with age with significant deterioration observed throughout adulthood. Estimated age of peak was around age of 20 for trabecular vBMD and microarchitecture and Ct.Po and age of 40 for cortical vBMD and microarchitecture. Estimated stiffness and failure load peaked at mid-30s at the distal radius and at age 20 at distal tibia.
Age-related differences in vBMD and microarchitecture in Chinese women differed by bone compartments. Significant cortical bone loss occurred after midlife. Prominent increase in Ct.Po began at the fifth decade but appeared to be arrested before the sixth decade. Loss of trabecular bone was already evident in young adulthood and continued throughout life.
在一个由393名中国女性组成的队列中,通过使用高分辨率外周定量计算机断层扫描(HR-pQCT),我们发现中年后出现了显著的皮质骨丢失。皮质孔隙率在第五个十年开始显著增加,但在第六个十年之前达到平稳状态。小梁骨丢失在成年早期就已明显,并持续终生。
本研究旨在调查中国女性人群外周骨骼的骨体积密度(vBMD)、微结构和估计骨强度的年龄相关差异。
在一个由393名年龄在20至90岁的中国女性组成的横断面队列中,我们使用HR-pQCT获得了桡骨远端和胫骨的vBMD、微结构以及微有限元衍生的骨强度。
发现皮质孔隙率(Ct.Po)与年龄的预测差异最大,在成年期,桡骨远端和胫骨的该指标差异分别超过四倍和两倍。在两个部位,皮质骨面积、vBMD和厚度与年龄呈显著的二次关联,中年后开始显著下降。Ct.Po的变化在50至57岁之间变得更加显著(桡骨远端为0.26%/年,胫骨远端为0.54%/年,p均≤0.001),但此后达到平稳状态(分别为0.015%/年和0.028%/年,p均>0.05)。相比之下,小梁vBMD和微结构与年龄呈线性关联,在整个成年期均观察到显著恶化。小梁vBMD和微结构以及Ct.Po的峰值估计年龄约为20岁,皮质vBMD和微结构的峰值估计年龄为40岁。估计的刚度和破坏载荷在桡骨远端35岁左右达到峰值,在胫骨远端20岁时达到峰值。
中国女性vBMD和微结构的年龄相关差异因骨分区而异。中年后出现显著的皮质骨丢失。Ct.Po在第五个十年开始显著增加,但在第六个十年之前似乎停止。小梁骨丢失在成年早期就已明显,并持续终生。