Berry Nathaniel T, Anderson Travis, Rhea Christopher K, Wideman Laurie
Department of Kinesiology, University of North Carolina at Greensboro, Greensboro, NC 27412, USA.
Ellmer College of Health Sciences, Old Dominion University, Norfolk, VA 23529, USA.
Sports (Basel). 2025 Apr 9;13(4):112. doi: 10.3390/sports13040112.
Cortisol is an important marker of hypothalamic-pituitary-adrenal function and follows robust circadian and diurnal rhythms. However, biomarker sampling protocols can be labor-intensive and cost-prohibitive.
Explore analytical approaches that can handle differing biological sampling frequencies to maximize these data in more detailed and time-dependent analyses.
Healthy adult males [N = 8; 26.1 (±3.1) years; 176.4 (±8.6) cm; 73.1 (±12.0) kg)] completed two 24 h admissions: one at rest and one including a high-intensity exercise session on the cycle ergometer. Serum and salivary cortisol were sampled every 60 and 120 min, respectively. Six alternative sampling profiles were defined by downsampling from the observed data and creating two intermittent sampling profiles. A polynomial (1-6 degrees) validation process was performed, and interpolation was conducted to match the observed data. Model fit and performance were assessed using the coefficient of determination (R) and the root mean square error (RMSE), as well as an examination of the equivalence, via two one-sided t-tests (TOST), of 24 h cortisol output between the observed and interpolated data.
Mean serum cortisol output was higher than salivary cortisol ( < 0.001), and no effect was observed for condition ( = 0.61). Second- and third-degree polynomial regressions were determined to be the optimal models for fitting salivary. TOST tests determined that serum data and estimated 24 h output from these models (with interpolation) provided statistically similar estimates to the observed data ( < 0.05).
Second- and third-degree polynomial fits of salivary and serum cortisol provide a reasonable means for interpolation without introducing bias into estimates of 24 h output. This allows researchers to sample biomarkers at biologically relevant frequencies and subsequently match necessary sampling frequencies during the data processing stage of various machine learning workflows.
皮质醇是下丘脑 - 垂体 - 肾上腺功能的重要标志物,遵循强烈的昼夜节律。然而,生物标志物采样方案可能 labor-intensive 且成本高昂。
探索能够处理不同生物采样频率的分析方法,以便在更详细和依赖时间的分析中最大化利用这些数据。
健康成年男性[N = 8;26.1(±3.1)岁;176.4(±8.6)厘米;73.1(±12.0)千克]完成两次24小时住院观察:一次是静息状态,一次包括在自行车测力计上进行高强度运动。分别每60分钟和120分钟采集血清和唾液皮质醇样本。通过从观察数据中进行下采样并创建两个间歇采样剖面来定义六个替代采样剖面。进行了多项式(1 - 6次)验证过程,并进行插值以匹配观察数据。使用决定系数(R)和均方根误差(RMSE)评估模型拟合和性能,以及通过两次单侧t检验(TOST)检查观察数据和插值数据之间24小时皮质醇输出的等效性。
血清皮质醇平均输出高于唾液皮质醇(<0.001),且未观察到状态影响(= 0.61)。二次和三次多项式回归被确定为拟合唾液的最佳模型。TOST检验确定血清数据和这些模型(通过插值)估计的24小时输出与观察数据提供了统计学上相似的估计(<0.05)。
唾液和血清皮质醇的二次和三次多项式拟合为插值提供了合理方法,且不会在24小时输出估计中引入偏差。这使研究人员能够在生物学相关频率下采样生物标志物,并随后在各种机器学习工作流程的数据处理阶段匹配必要的采样频率。