UGC Medicina Física y Rehabilitación, Hospital de Neurotraumatología y Rehabilitación, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Instituto de Investigación Biosanitaria ibs.GRANADA, Avda. de Madrid, 15, Granada, 18012, Spain.
Int J Behav Nutr Phys Act. 2023 Jun 15;20(1):72. doi: 10.1186/s12966-023-01471-9.
While there is evidence that physical activity, sedentary behaviour (SB) and sleep may all be associated with modified levels of inflammatory markers in adolescents and children, associations with one movement behaviour have not always been adjusted for other movement behaviours, and few studies have considered all movement behaviours in the 24-hour day as an exposure.
The aim of the study was to explore how longitudinal reallocations of time between moderate-to-vigorous physical activity (MVPA), light physical activity (LPA), SB and sleep are associated with changes in inflammatory markers in children and adolescents.
A total of 296 children/adolescents participated in a prospective cohort study with a 3-year follow-up. MVPA, LPA and SB were assessed by accelerometers. Sleep duration was assessed using the Health Behavior in School-aged Children questionnaire. Longitudinal compositional regression models were used to explore how reallocations of time between movement behaviours are associated with changes in inflammatory markers.
Reallocations of time from SB to sleep were associated with increases in C3 levels (difference for 60 min/d reallocation [d] = 5.29 mg/dl; 95% confidence interval [CI] = 0.28, 10.29) and TNF-α (d = 1.81 mg/dl; 95% CI = 0.79, 15.41) levels. Reallocations from LPA to sleep were also associated with increases in C3 levels (d = 8.10 mg/dl; 95% CI = 0.79, 15.41). Reallocations from LPA to any of the remaining time-use components were associated with increases in C4 levels (d ranging from 2.54 to 3.63 mg/dl; p < 0.05), while any reallocation of time away from MVPA was associated with unfavourable changes in leptin (d ranging from 3088.44 to 3448.07 pg/ml; p < 0.05).
Reallocations of time between 24-h movement behaviours are prospectively associated with some inflammatory markers. Reallocating time away from LPA appears to be most consistently unfavourably associated with inflammatory markers. Given that higher levels of inflammation during childhood and adolescence are associated with an increased risk of chronic diseases in adulthood, children and adolescents should be encouraged to maintain or increase the level of LPA to preserve a healthy immune system.
虽然有证据表明,体力活动、久坐行为(SB)和睡眠都可能与青少年和儿童炎症标志物水平的改变有关,但与一种运动行为的关联并不总是调整其他运动行为,而且很少有研究将 24 小时内的所有运动行为作为暴露因素进行考虑。
本研究旨在探讨青少年中,中等到剧烈体力活动(MVPA)、低强度体力活动(LPA)、SB 和睡眠之间的时间重新分配如何与炎症标志物的变化相关。
共有 296 名儿童/青少年参加了一项为期 3 年的前瞻性队列研究。MVPA、LPA 和 SB 通过加速度计进行评估。睡眠时长通过《青少年健康行为问卷》进行评估。采用纵向组合回归模型来探索运动行为之间的时间重新分配与炎症标志物变化之间的关系。
将 SB 时间重新分配到睡眠中与 C3 水平的升高相关(60 分钟/天重新分配的差异[d]为 5.29mg/dl;95%置信区间[CI]为 0.28,10.29)和 TNF-α 水平的升高(d=1.81mg/dl;95%CI为 0.79,15.41)。将 LPA 时间重新分配到睡眠中也与 C3 水平的升高相关(d=8.10mg/dl;95%CI为 0.79,15.41)。将 LPA 时间重新分配到任何其他时间利用组成部分都会导致 C4 水平的升高(d 范围为 2.54 至 3.63mg/dl;p<0.05),而任何从 MVPA 中重新分配时间的行为都会导致瘦素的不利变化(d 范围为 3088.44 至 3448.07pg/ml;p<0.05)。
24 小时运动行为之间的时间重新分配与某些炎症标志物呈前瞻性相关。将时间从 LPA 中重新分配似乎与炎症标志物最不一致地呈不利相关。鉴于儿童和青少年时期较高的炎症水平与成年后慢性疾病风险增加有关,应鼓励儿童和青少年保持或增加 LPA 水平,以维持健康的免疫系统。