老年人的身体活动碎片化和功能衰退:来自国家健康和老龄化趋势研究的发现。

Nicholas R Lamoureux,Joey M Saavedra,Brian Downer,Jennifer A Schrack,Amal A Wanigatunga
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引用次数: 0

摘要

背景:体力活动碎片化与老年人身体功能差有关,但体力活动碎片化的变化与并发和未来身体功能变化之间的关系尚不清楚,这一信息对指导临床决策很重要。因此,我们在一个具有全国代表性的老年人样本中描述了这种关系。方法数据来自国家健康和老龄化趋势研究的一个子集。活动碎片被定义为从活动到久坐转变的概率,使用腕带活动记录仪捕获,而功能使用短物理性能电池(SPPB)评估。使用多变量逻辑回归评估体力活动碎片化与SPPB纵向下降之间的关系。结果共纳入年龄≥70岁的参与者531人,其中女性55.4%。在基线SPPB≤6的患者中,基线活动碎片化程度越高,总体上基线功能越低,未来1年功能下降(调整OR: 1.32; 95% CI: 1.01-1.72)。1年的碎片化增加与SPPB同时下降的可能性增加相关,特别是在基线SPPB = 7-10的患者中(OR: 2.21; 95% CI: 1.17-4.17)。活动碎片化的1年变化与次年SPPB的下降无关。结论:身体活动碎片化可能代表了一种数字生物标志物,而不是身体功能变化的先决条件,这突出了加速度计在识别可能受益于早期干预的高危表型方面的潜在效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physical activity fragmentation and functional decline among older adults: Findings from the National Health and Aging Trends Study.
BACKGROUND Physical activity fragmentation is associated with poor physical function in older adulthood, but the relationship between changes in physical activity fragmentation with concurrent and future changes in physical function are unclear, and this information is important for guiding clinical decision making. We therefore characterized this relationship in a nationally representative sample of older adults. METHODS Data were drawn from a subset of the National Health and Aging Trends Study. Activity fragmentation was defined as the probability of transitioning from an active to a sedentary bout, captured using wrist-worn actigraphy, while function was assessed using the Short Physical Performance Battery (SPPB). The association between physical activity fragmentation with any instance of longitudinal decline in SPPB was evaluated using multivariable logistic regression. RESULTS The sample included 531 participants aged ≥70 years (55.4% female). Among those with baseline SPPB ≤ 6, higher baseline activity fragmentation was associated with lower baseline function overall, and with a 1-year future decline in function (adjusted OR: 1.32; 95% CI: 1.01-1.72 per 10% higher baseline fragmentation). A 1-year increase in fragmentation was associated with a greater likelihood of experiencing a concurrent decline in SPPB, particularly among those with baseline SPPB = 7-10 (OR: 2.21; 95% CI: 1.17-4.17). The 1-year change in activity fragmentation was not associated with declines in SPPB the following year. CONCLUSIONS Physical activity fragmentation may represent a digital biomarker, rather than an antecedent, of changes in physical function, highlighting the potential utility of accelerometry for identifying at-risk phenotypes likely to benefit from early interventions.
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