Department of Psychology, University of Denver, Denver, CO, USA.
Department of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, USA.
Int J Obes (Lond). 2020 Mar;44(3):646-655. doi: 10.1038/s41366-019-0447-4. Epub 2019 Sep 2.
BACKGROUND/OBJECTIVES: Associations between overweight and altered stress biology have been reported cross-sectionally during childhood, but it is unclear whether overweight precedes altered stress biology or if altered stress biology predicts greater likelihood of overweight over time. The current longitudinal study investigates associations between overweight/obesity, salivary alpha amylase and cortisol morning intercept, diurnal slope, and reactivity to social stress in a cohort of low-income children during preschool and middle childhood.
SUBJECTS/METHODS: Children were recruited through Head Start and were observed and followed into middle childhood (N = 257; M = 8.0 years). Height and weight were measured at both time points. Saliva samples were collected across the day and in response to a social challenge at both ages for alpha amylase and cortisol determination.
Cross-lagged panel analyses indicated that overweight/obesity at preschool predicted lower morning alpha amylase (β = -0.18, 95% CI: -0.34, -0.03; p = 0.023), lower morning cortisol (β = -0.22, 95% CI: -0.38, -0.06; p = 0.006), lower sAA diurnal slope (β = -0.18, 95% CI: -0.34, -0.03; p = 0.021), and lower cortisol stress reactivity (β = -0.19, 95% CI: -0.35, -0.02; p = 0.031) in middle childhood. Lower alpha amylase reactivity at preschool was the only biological factor that predicted higher likelihood of overweight/obesity at middle childhood (β = -0.20, 95% CI: -0.38, -0.01; p = 0.035).
These findings suggest that overweight/obesity may be driving changes in stress biology across early-to-middle childhood, particularly in downregulation of morning levels of stress hormones, diurnal sAA slope, and cortisol reactivity to stress, rather than stress biology driving overweight/obesity.
背景/目的:超重与应激生物学改变之间的关联已在儿童时期被横断面研究报道,但目前尚不清楚超重是否先于应激生物学改变,或者应激生物学改变是否预测超重的可能性随时间增加。本纵向研究调查了低收入儿童队列中,超重/肥胖与唾液 α-淀粉酶和皮质醇晨间截距、日间斜率以及对社会应激反应之间的关联,该队列的儿童在学前和整个儿童期都接受了观察和随访。
受试者/方法:通过 Head Start 招募儿童,在两个时间点测量身高和体重。在两个年龄阶段,均通过日间唾液样本采集和社会挑战应激反应来测定 α-淀粉酶和皮质醇。
交叉滞后面板分析表明,学前超重/肥胖预测了儿童在整个儿童期的较低晨间 α-淀粉酶(β=-0.18,95%置信区间:-0.34,-0.03;p=0.023)、较低晨间皮质醇(β=-0.22,95%置信区间:-0.38,-0.06;p=0.006)、较低日间唾液 α-淀粉酶斜率(β=-0.18,95%置信区间:-0.34,-0.03;p=0.021)和较低皮质醇应激反应性(β=-0.19,95%置信区间:-0.35,-0.02;p=0.031)。学前较低的 α-淀粉酶反应性是唯一预测儿童整个儿童期超重/肥胖可能性较高的生物学因素(β=-0.20,95%置信区间:-0.38,-0.01;p=0.035)。
这些发现表明,超重/肥胖可能导致整个儿童期早期至中期的应激生物学变化,特别是应激激素晨间水平、日间唾液 α-淀粉酶斜率和皮质醇对压力的反应性下调,而不是应激生物学导致超重/肥胖。