Relationships Between Markers of Inflammation and Muscle Mass, Strength and Function: Findings from the Hertfordshire Cohort Study

被引:0
作者
L. D. Westbury
N. R. Fuggle
H. E. Syddall
N. A. Duggal
S. C. Shaw
K. Maslin
E. M. Dennison
J. M. Lord
C. Cooper
机构
[1] University of Southampton,MRC Lifecourse Epidemiology Unit, Southampton General Hospital
[2] University of Birmingham,MRC
[3] Victoria University of Wellington,ARUK Centre for Musculoskeletal Ageing Research, Institute of Inflammation and Ageing
[4] University of Southampton and University Hospital Southampton NHS Foundation Trust,NIHR Southampton Biomedical Research Centre
[5] University of Oxford,NIHR Musculoskeletal Biomedical Research Unit
来源
Calcified Tissue International | 2018年 / 102卷
关键词
Inflammation; Muscle; Sarcopenia; Strength; Adipokine; Interleukin;
D O I
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学科分类号
摘要
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.
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页码:287 / 295
页数:8
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