Sedentary Time and Markers of Chronic Low-Grade Inflammation in a High Risk Population

被引:152
作者
Henson, Joseph [1 ,2 ]
Yates, Thomas [1 ,2 ]
Edwardson, Charlotte L. [1 ,2 ]
Khunti, Kamlesh [1 ,2 ]
Talbot, Duncan [3 ]
Gray, Laura J. [4 ]
Leigh, Thomas M. [5 ]
Carter, Patrice [1 ,2 ]
Davies, Melanie J. [1 ,2 ]
机构
[1] Natl Inst Hlth Res NIHR Leicester Loughborough Di, Leicester, Leics, England
[2] Univ Leicester, Diabet Res Ctr, Coll Med Biol Sci & Psychol, Leicester, Leics, England
[3] Unilever Discover, Sharnbrook, Beds, England
[4] Univ Leicester, Dept Hlth Sci, Leicester, Leics, England
[5] Leicester Gen Hosp, Leicester Diabet Ctr, Univ Hosp Leicester, Leicester LE5 4PW, Leics, England
关键词
C-REACTIVE PROTEIN; ACTIVITY ENERGY-EXPENDITURE; RANDOMIZED CONTROLLED-TRIAL; PHYSICAL-ACTIVITY; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; SKELETAL-MUSCLE; GLUCOSE REGULATION; DIABETES-MELLITUS; IMMUNE-SYSTEM;
D O I
10.1371/journal.pone.0078350
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Sedentary behaviour has been identified as a distinct risk factor for several health outcomes. Nevertheless, little research has been conducted into the underlying mechanisms driving these observations. This study aimed to investigate the association of objectively measured sedentary time and breaks in sedentary time with markers of chronic low-grade inflammation and adiposity in a population at a high risk of type 2 diabetes mellitus. Methods: This study reports data from an ongoing diabetes prevention programme conducted in Leicestershire, UK. High risk individuals were recruited from 10 primary care practices. Sedentary time (<25counts per 15s) was measured using Actigraph GT3X accelerometers (15s epochs). A break was considered as any interruption in sedentary time (>= 25counts per 15s). Biochemical outcomes included interleukin-6 (IL-6), C-reactive protein (CRP), leptin, adiponectin and leptin: adiponectin ratio (LAR). A sensitivity analysis investigated whether results were affected by removing participants with a CRP level >10 mg/L, as this can be indicative of acute inflammation. Results: 558 participants (age = 63.6 +/- 7.7years; male = 64.7%) had complete adipokine and accelerometer data. Following adjustment for various confounders, sedentary time was detrimentally associated with CRP (beta = 0.176 +/- 0.057, p = 0.002), IL-6 (beta = 0.24260.056, p = <0.001), leptin (beta = 0.146 +/- 0.043, p = <0.001) and LAR (beta = 0.208 +/- 0.052, p = <0.001). Associations were attenuated after further adjustment for moderate-to-vigorous physical activity (MVPA) with only IL-6 (beta = 0.231 +/- 0.073, p = 0.002) remaining significant; this result was unaffected after further adjustment for body mass index and glycosylated haemoglobin (HbA(1c)). Similarly, breaks in sedentary time were significantly inversely associated with IL-6 (beta = -0.094 +/- 0.047, p = 0.045) and leptin (beta = 20.075 +/- 0.037, p = 0.039); however, these associations were attenuated after adjustment for accelerometer derived variables. Excluding individuals with a CRP level >10 mg/L consistently attenuated the significant associations across all markers of inflammation. Conclusion: These novel findings from a high risk population recruited through primary care suggest that sedentary behaviour may influence markers associated with inflammation, independent of MVPA, glycaemia and adiposity.
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