Faghih Rose T, Dahleh Munther A, Adler Gail K, Klerman Elizabeth B, Brown Emery N
IEEE Trans Biomed Eng. 2015 Oct;62(10):2379-88. doi: 10.1109/TBME.2015.2427745. Epub 2015 Apr 29.
Pulsatile release of cortisol from the adrenal glands is governed by pulsatile release of adrenocorticotropic hormone (ACTH) from the anterior pituitary. In return, cortisol has a negative feedback effect on ACTH release. Simultaneous recording of ACTH and cortisol is not typical, and determining the number, timing, and amplitudes of pulsatile events from simultaneously recorded data is challenging because of several factors: 1) stimulator ACTH pulse activity, 2) kinematics of ACTH and cortisol, 3) the sampling interval, and 4) the measurement error. We model ACTH and cortisol secretion simultaneously using a linear differential equations model with Gaussian errors and sparse pulsatile events as inputs to the model. We propose a novel framework for recovering pulses and parameters underlying the interactions between ACTH and cortisol. We recover the timing and amplitudes of pulses using compressed sensing and employ generalized cross validation for determining the number of pulses. We analyze serum ACTH and cortisol levels sampled at 10-min intervals over 24 h from ten healthy women. We recover physiologically plausible timing and amplitudes for these pulses and model the feedback effect of cortisol. We recover 15 to 18 pulses over 24 h, which is highly consistent with the results of another cortisol data analysis approach. Modeling the interactions between ACTH and cortisol allows for accurate quantification of pulsatile events, and normal and pathological states. This could lay the basis for a more physiologically-based approach for administering cortisol therapeutically. The proposed approach can be adapted to deconvolve other pairs of hormones with similar interactions.
肾上腺皮质醇的脉冲式释放受垂体前叶促肾上腺皮质激素(ACTH)脉冲式释放的调控。反过来,皮质醇对ACTH的释放具有负反馈作用。同时记录ACTH和皮质醇的情况并不常见,而且从同时记录的数据中确定脉冲事件的数量、时间和幅度具有挑战性,原因如下:1)刺激物ACTH脉冲活动;2)ACTH和皮质醇的运动学;3)采样间隔;4)测量误差。我们使用具有高斯误差和稀疏脉冲事件作为模型输入的线性微分方程模型,同时对ACTH和皮质醇的分泌进行建模。我们提出了一个新颖的框架,用于恢复ACTH与皮质醇相互作用背后的脉冲和参数。我们使用压缩感知来恢复脉冲的时间和幅度,并采用广义交叉验证来确定脉冲的数量。我们分析了10名健康女性在24小时内每隔10分钟采集的血清ACTH和皮质醇水平。我们恢复了这些脉冲在生理上合理的时间和幅度,并对皮质醇的反馈作用进行了建模。我们在24小时内恢复了15至18个脉冲,这与另一种皮质醇数据分析方法的结果高度一致。对ACTH和皮质醇之间的相互作用进行建模,有助于准确量化脉冲事件以及正常和病理状态。这可能为基于生理学的皮质醇治疗给药方法奠定基础。所提出的方法可用于对具有类似相互作用的其他激素对进行去卷积分析。