Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Alfred Hospital, Monash University, Melbourne VIC 3004, Australia.
Rheumatology (Oxford). 2011 Mar;50(3):563-8. doi: 10.1093/rheumatology/keq341. Epub 2010 Nov 16.
Although there is a well-established sex difference in the prevalence and severity of OA, the mechanism for this is not clear. The aim of this study was to examine the potential role of BMD and BMC in explaining gender differences in knee cartilage volume.
A total of 153 subjects aged 25-60 years, 81% female, were recruited. MRI was performed of the dominant knee. Cartilage volume was measured using validated methods. Total body BMD and content was measured using DXA.
Total body BMC and BMD was significantly associated with medial cartilage volume in both sexes. However, the associations were stronger in men for BMC (B = 0.52; 95% CI 0.21, 0.83; P for difference = 0.001) and BMD (B = 2242; 95% CI 443, 4041; P for difference = 0.05). Similar results were obtained in the lateral tibial compartment. No significant association was obtained between total body BMD and BMC and patella cartilage volume in either men or women.
In this relatively healthy population, we found a positive relationship between total body BMD and BMC and tibial cartilage volume in the medial and lateral compartments. These relationships were stronger in men than women. Thus, the results of this study may provide some insight into the sex differences in knee cartilage volume, which may in turn facilitate our understanding of the pathogenesis of OA.
尽管 OA 的患病率和严重程度存在明确的性别差异,但其机制尚不清楚。本研究旨在探讨骨密度(BMD)和骨矿物质含量(BMC)在解释膝关节软骨体积性别差异方面的潜在作用。
共招募了 153 名年龄在 25-60 岁之间的受试者,其中 81%为女性。对优势膝关节进行 MRI 检查。使用经过验证的方法测量软骨体积。使用 DXA 测量全身 BMC 和 BMD。
全身 BMC 和 BMD 与两性的内侧软骨体积均显著相关。然而,对于 BMC(B=0.52;95%CI 0.21,0.83;差异 P 值=0.001)和 BMD(B=2242;95%CI 443,4041;差异 P 值=0.05),男性的相关性更强。在外侧胫骨间室也得到了类似的结果。男性和女性的全身 BMD 和 BMC 与髌骨软骨体积之间均无显著相关性。
在这个相对健康的人群中,我们发现全身 BMC 和 BMD 与内侧和外侧胫骨间室的胫骨软骨体积之间存在正相关关系。这些关系在男性中比女性更强。因此,本研究的结果可能为膝关节软骨体积的性别差异提供一些见解,从而有助于我们理解 OA 的发病机制。