Howard Bethany J, Hurtig-Wennlöf Anita, Olsson Lovisa A, Nilsson Torbjörn K, Dunstan David W, Wennberg Patrik
Baker IDI Heart and Diabetes Institute, Melbourne, Australia.
School of Public Health & Preventive Medicine, Monash University, Melbourne, Australia.
PLoS One. 2016 Sep 22;11(9):e0163409. doi: 10.1371/journal.pone.0163409. eCollection 2016.
Too much sitting is linked with an increased risk of cardiovascular disease and mortality. The mediating mechanisms for these associations are largely unknown, however dysregulated fibrinolysis have emerged as a possible contributor.
We examined the associations of self-reported overall sitting time and physical activity with fibrinolytic and other novel cardio-metabolic biomarkers in older adults.
Data was analysed for 364 participants (74±7 yrs) of the Active Seniors group (retired, living independently in their own homes). Linear regression analyses examined associations of categories of categories of sitting time (≤3, 3-6, >6 hrs/day) and overall physical activity (Low, Moderate and High) with biomarkers in serum or plasma, adjusting for age, gender and smoking (with further adjustment for either overall physical activity or sitting time and BMI in secondary analyses).
Compared to sitting ≤ 3 hrs/day, sitting >6 hrs/day was associated with higher tissue plasminogen activator (tPA) and tissue plasminogen activator/plasminogen activator inhibitor-1 complex (tPA-PAI-1 complex). These associations were not independent of overall physical activity or BMI. Compared to those in the high physical activity, low physical activity was associated with a higher BMI, high-sensitivity C-reactive protein (hs-CRP) and tPA-PAI-1 complex levels. Only the associations of BMI and hs-CRP were independent of sitting time.
These findings provide preliminary cross-sectional evidence for the relationships of sitting time with fibrinolytic markers in older adults. They also reinforce the importance of regular physical activity for cardio-metabolic health.
久坐与心血管疾病风险增加及死亡率上升有关。然而,这些关联的中介机制很大程度上尚不清楚,不过纤维蛋白溶解功能失调已成为一个可能的因素。
我们研究了老年人自我报告的总久坐时间和身体活动与纤维蛋白溶解及其他新型心脏代谢生物标志物之间的关联。
对活跃老年人组(退休,独立居住在家)的364名参与者(74±7岁)的数据进行了分析。线性回归分析检验了久坐时间类别(≤3、3 - 6、>6小时/天)和总体身体活动(低、中、高)与血清或血浆中生物标志物的关联,并对年龄、性别和吸烟情况进行了调整(在二次分析中进一步对总体身体活动或久坐时间及体重指数进行了调整)。
与每天久坐≤3小时相比,每天久坐>6小时与更高的组织型纤溶酶原激活剂(tPA)和组织型纤溶酶原激活剂/纤溶酶原激活剂抑制剂-1复合物(tPA - PAI - 1复合物)相关。这些关联并非独立于总体身体活动或体重指数。与高身体活动者相比,低身体活动者的体重指数、高敏C反应蛋白(hs - CRP)和tPA - PAI - 1复合物水平更高。只有体重指数和hs - CRP的关联独立于久坐时间。
这些发现为老年人久坐时间与纤维蛋白溶解标志物之间的关系提供了初步的横断面证据。它们还强化了规律身体活动对心脏代谢健康的重要性。