Knaeps Sara, Lefevre Johan, Wijtzes Anne, Charlier Ruben, Mertens Evelien, Bourgois Jan G
Physical Activity, Sports and Health Research Group, Department of Kinesiology, KU Leuven, Leuven, Belgium.
Department of Movement and Sports Sciences, Ghent University, Ghent, Belgium.
PLoS One. 2016 Jul 27;11(7):e0160166. doi: 10.1371/journal.pone.0160166. eCollection 2016.
We aimed to study the independent associations of sedentary time (ST), moderate-to-vigorous physical activity (MVPA), and objectively measured cardiorespiratory fitness (CRF) with clustered cardio-metabolic risk and its individual components (waist circumference, fasting glucose, HDL-cholesterol, triglycerides and blood pressure). We also investigated whether any associations between MVPA or ST and clustered cardio-metabolic risk were mediated by CRF. MVPA, ST, CRF and individual cardio-metabolic components were measured in a population-based sample of 341 adults (age 53.8 ± 8.9 years; 61% men) between 2012 and 2014. MVPA and ST were measured with the SenseWear pro 3 Armband and CRF was measured with a maximal exercise test. Multiple linear regression models and the product of coefficients method were used to examine independent associations and mediation effects, respectively. Results showed that low MVPA and low CRF were associated with a higher clustered cardio-metabolic risk (β = -0.26 and β = -0.43, both p<0.001, respectively). CRF explained 73% of the variance in the association between MVPA and clustered cardio-metabolic risk and attenuated this association to non-significance. After mutual adjustment for MVPA and ST, CRF was the most important risk factor for a higher clustered cardio-metabolic risk (β = -0.39, p<0.001). In conclusion, because of the mediating role of CRF, lifestyle-interventions need to be feasible yet challenging enough to lead to increases in CRF to improve someone's cardio-metabolic health.
我们旨在研究久坐时间(ST)、中度至剧烈身体活动(MVPA)以及客观测量的心肺适能(CRF)与聚集性心血管代谢风险及其个体组分(腰围、空腹血糖、高密度脂蛋白胆固醇、甘油三酯和血压)之间的独立关联。我们还研究了MVPA或ST与聚集性心血管代谢风险之间的任何关联是否由CRF介导。在2012年至2014年间,对341名成年人(年龄53.8±8.9岁;61%为男性)的基于人群的样本进行了MVPA、ST、CRF和个体心血管代谢组分的测量。MVPA和ST使用SenseWear pro 3臂带进行测量,CRF通过最大运动试验进行测量。分别使用多元线性回归模型和系数乘积法来检验独立关联和中介效应。结果显示,低MVPA和低CRF与较高的聚集性心血管代谢风险相关(β = -0.26和β = -0.43,p均<0.001)。CRF解释了MVPA与聚集性心血管代谢风险之间关联中73%的方差,并使这种关联减弱至无显著性。在对MVPA和ST进行相互调整后,CRF是较高聚集性心血管代谢风险的最重要危险因素(β = -0.39,p<0.001)。总之,由于CRF的中介作用,生活方式干预需要切实可行且具有足够挑战性,以促使CRF升高,从而改善个体的心血管代谢健康。