Department of Exercise Sciences, 237 SFH, Brigham Young University, Provo, UT 84602, USA.
Prev Med. 2017 Jul;100:145-151. doi: 10.1016/j.ypmed.2017.04.027. Epub 2017 Apr 24.
The principal objective was to determine the extent to which physical activity (PA) accounts for differences in leukocyte telomere length (LTL) in a large random sample of U.S. adults. Another purpose was to assess the extent to which multiple demographic and lifestyle covariates affect the relationship between PA and LTL. A total of 5823 adults from the National Health and Nutrition Examination Survey (NHANES 1999-2002) were studied cross-sectionally. Employing the quantitative polymerase chain reaction method, LTL was compared to standard reference DNA. PA was indexed using MET-minutes using self-reported frequency, intensity, and duration of participation in 62 physical activities. Covariates were controlled statistically. Telomeres were 15.6 base pairs shorter for each year of chronological age (F=723.2, P<0.0001). PA was inversely related to LTL after adjusting for all the covariates (F=8.3, P=0.0004). Telomere base pair differences between adults with High activity and those in the Sedentary, Low, and Moderate groups were 140, 137, and 111, respectively. Adults with High activity were estimated to have a biologic aging advantage of 9years (140 base pairs÷15.6) over Sedentary adults. The difference in cell aging between those with High and Low activity was also significant, 8.8years, as was the difference between those with High and Moderate PA (7.1years). Overall, PA was significantly and meaningfully associated with telomere length in U.S. men and women. Evidently, adults who participate in high levels of PA tend to have longer telomeres, accounting for years of reduced cellular aging compared to their more sedentary counterparts.
主要目的是确定身体活动(PA)在很大的美国成年人随机样本中对白细胞端粒长度(LTL)差异的解释程度。另一个目的是评估多种人口统计学和生活方式协变量对 PA 与 LTL 之间关系的影响程度。共有 5823 名来自国家健康和营养检查调查(NHANES 1999-2002)的成年人进行了横断面研究。采用定量聚合酶链反应方法,将 LTL 与标准参考 DNA 进行比较。PA 使用自我报告的频率、强度和参与 62 项体力活动的持续时间,通过 MET 分钟进行索引。协变量通过统计学进行控制。端粒每增加一年的年龄就会缩短 15.6 个碱基对(F=723.2,P<0.0001)。在调整所有协变量后,PA 与 LTL 呈负相关(F=8.3,P=0.0004)。与久坐、低活动和中活动组相比,高活动组成年人的端粒碱基对差异分别为 140、137 和 111。高活动组成年人的生物老化优势估计为 9 岁(140 个碱基对÷15.6),高于久坐组成年人。高活动组和低活动组之间的细胞衰老差异也很显著,为 8.8 岁,高活动组和中活动组之间的差异为 7.1 岁。总的来说,PA 与美国男性和女性的端粒长度有显著而有意义的关联。显然,与更久坐的同龄人相比,参与高水平 PA 的成年人往往拥有更长的端粒,这意味着他们的细胞衰老减少了数年。