MRC Lifecourse Epidemiology Unit, Southampton General Hospital, University of Southampton, Southampton, SO16 6YD, UK.
MRC-ARUK Centre for Musculoskeletal Ageing Research, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Calcif Tissue Int. 2018 Mar;102(3):287-295. doi: 10.1007/s00223-017-0354-4. Epub 2017 Nov 3.
We investigated the longitudinal relationships between inflammation markers and the following outcomes in a UK cohort study: appendicular lean mass (ALM); walking speed; level and change in grip strength; and sarcopenia defined by the European Working Group on Sarcopenia in Older People. Analyses were based on 336 community-dwelling older men and women (aged 59-70 years) who participated in the Hertfordshire Cohort Study (HCS). Inflammation markers were ascertained at baseline using enzyme-linked immunosorbent assay techniques and Bio-Plex Pro Assays. Grip strength was measured at baseline and follow-up [median follow-up time: 10.8 years (inter-quartile range 10.2-11.6)] and change in grip strength was ascertained using a residual change approach. At follow-up, ALM was ascertained using dual-energy X-ray absorptiometry, customary walking speed was measured and sarcopenia status was ascertained. Gender-adjusted linear and Poisson regression was used to examine the associations between inflammation markers and outcomes with and without adjustment for anthropometric and lifestyle factors. Higher C-reactive protein was associated (p < 0.04) with lower grip strength and accelerated decline in grip strength from baseline to follow-up. Higher cortisol was associated with lower ALM (p < 0.05). Higher interleukin-8 (IL-8) was associated with lower ALM (p < 0.05) and increased risk of sarcopenia [fully-adjusted relative risk per SD increase in IL-8: 1.37 (95% CI 1.10, 1.71), p = 0.005]. All associations were robust in fully-adjusted analyses. Inflammation markers were associated with measures of muscle mass, strength and function in HCS. Further work is required to replicate these associations and to delineate the underlying mechanisms.
四肢瘦体重(ALM);步行速度;握力水平和变化;以及欧洲老年人肌少症工作组定义的肌少症。分析基于 336 名居住在社区的老年男女(年龄 59-70 岁),他们参加了赫特福德郡队列研究(HCS)。在基线时使用酶联免疫吸附测定技术和 Bio-Plex Pro 测定法确定炎症标志物。基线和随访时测量握力[中位随访时间:10.8 年(四分位距 10.2-11.6)],并使用残差变化法确定握力变化。随访时,使用双能 X 射线吸收法确定 ALM,测量常规步行速度,并确定肌少症状态。性别调整的线性和泊松回归用于检查炎症标志物与未调整和调整了人体测量学和生活方式因素后的结果之间的关联。较高的 C 反应蛋白与较低的握力和从基线到随访的握力加速下降相关(p < 0.04)。较高的皮质醇与较低的 ALM 相关(p < 0.05)。较高的白细胞介素-8(IL-8)与较低的 ALM 相关(p < 0.05)和肌少症的风险增加[每增加一个标准差的 IL-8 ,完全调整后的相对风险:1.37(95%CI 1.10,1.71),p = 0.005]。所有关联在完全调整分析中均具有稳健性。炎症标志物与 HCS 中肌肉质量、力量和功能的测量结果相关。需要进一步的工作来复制这些关联并阐明潜在的机制。