Office of Surveillance and Epidemiology, US Food and Drug Administration, Silver Spring, MD, USA.
Department of Biostatistics, University of Washington, Seattle, WA, USA.
J Bone Miner Res. 2018 Feb;33(2):221-228. doi: 10.1002/jbmr.3301. Epub 2017 Nov 6.
Several in vitro and animal studies have showed that inflammatory markers play a role in bone remodeling and pathogenesis of osteoporosis. Additionally, some human longitudinal studies showed suggestive associations between elevated inflammatory markers and increased risk of nontraumatic fractures. We examined several inflammatory markers and multiple fracture types in a single study of older individuals with extensive follow-up. We assessed the association of four inflammatory markers with the risk of incident hip fractures among 5265 participants of the Cardiovascular Health Study (CHS) and a composite endpoint of incident fractures of the hip, pelvis, humerus, or proximal forearm in 4477 participants. Among CHS participants followed between 1992 and 2009, we observed 480 incident hip fractures during a median follow-up of 11 years. In the composite fracture analysis cohort of 4477 participants, we observed 711 fractures during a median follow-up of 7 years. Adjusted hazard ratios (HRs) and 95% confidence intervals (CIs) for hip fracture associated with doubling of IL-6 were HR 1.15 (95% CI, 1.02 to 1.30) overall and HR 1.17 (95% CI, 1.01 to 1.35) in women. We also observed a positive association between each unit increase in white blood cell (WBC) count and risk of hip fracture: HR 1.04 (95% CI, 1.01 to 1.06) overall and HR 1.06 (95% CI, 0.95 to 1.20) in women. We observed no significant associations between any of the four inflammatory markers and a composite fracture endpoint. Our findings suggest that chronic inflammatory and immune processes may be related to higher rates of incident hip fractures. © 2017 American Society for Bone and Mineral Research.
几项体外和动物研究表明,炎症标志物在骨重塑和骨质疏松症发病机制中起作用。此外,一些人类纵向研究表明,炎症标志物升高与非外伤性骨折风险增加之间存在提示性关联。我们在一项对老年人的单一研究中检查了几种炎症标志物和多种骨折类型,并进行了广泛的随访。我们评估了四项炎症标志物与心血管健康研究(CHS)中 5265 名参与者的髋部骨折发生率风险之间的关联,以及 4477 名参与者中髋部、骨盆、肱骨或近端前臂骨折的复合终点事件。在 CHS 参与者中,我们观察到在中位数为 11 年的随访期间发生了 480 例髋部骨折。在 4477 名参与者的复合骨折分析队列中,我们观察到在中位数为 7 年的随访期间发生了 711 例骨折。与白细胞介素 6(IL-6)翻倍相关的髋部骨折的调整后的危险比(HR)和 95%置信区间(CI)为 HR 1.15(95%CI,1.02 至 1.30)总体和 HR 1.17(95%CI,1.01 至 1.35)在女性中。我们还观察到白细胞(WBC)计数每增加一个单位与髋部骨折风险之间存在正相关:HR 1.04(95%CI,1.01 至 1.06)总体和 HR 1.06(95%CI,0.95 至 1.20)在女性中。我们没有观察到这四个炎症标志物中的任何一个与复合骨折终点之间存在显著关联。我们的研究结果表明,慢性炎症和免疫过程可能与更高的髋部骨折发生率有关。© 2017 美国骨骼与矿物质研究协会。