Veldhuis J D, Johnson M L
Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville 22908.
Methods Enzymol. 1992;210:539-75. doi: 10.1016/0076-6879(92)10028-c.
Deconvolution analysis of hormone data poses special problems in view of the sparse, noisy, and short data series typically available for analysis; the unknown true nature of the underlying secretory event; and potentially large variations in dissipation or clearance kinetics in different settings. Consequently, deconvolution techniques, which concern themselves with the estimation of hormone secretion and/or clearance based on serial circulating hormone concentration measurements, face a particular challenge. Ideal features of deconvolution algorithms are summarized in Table IV. Specific deconvolution techniques available to analyze hormone data include both waveform-defined procedures and waveform-independent algorithms. These approaches should be viewed as complementary rather than antagonistic. All deconvolution techniques are subject to individual limitations and specific strengths. Independently of the method employed, error propagation is necessary so as to define the statistical uncertainty intrinsic to the estimate of secretion and clearance. Such calculations of experimental uncertainty should include error inherent in the sample collection, processing, and assay as well as error in the kinetic constants and/or anticipated departures of the biological process from the algebraic structure of the convolution formulation. Moreover, more complex convolution statements will be required to describe the full range of behavior of hormone data in a systems view. The applications of such newer convolution methods as well as currently available techniques include model synthesis, model testing, and analysis of the interactions among multiple pulse generators.
鉴于用于分析的激素数据序列通常稀疏、有噪声且较短,潜在分泌事件的真实性质未知,以及在不同情况下激素消散或清除动力学可能存在较大差异,对激素数据进行去卷积分析存在特殊问题。因此,基于连续循环激素浓度测量来估计激素分泌和/或清除的去卷积技术面临着特殊挑战。表IV总结了去卷积算法的理想特征。可用于分析激素数据的特定去卷积技术包括波形定义程序和与波形无关的算法。这些方法应被视为互补而非对立的。所有去卷积技术都有各自的局限性和特定优势。无论采用何种方法,都需要进行误差传播,以确定分泌和清除估计中固有的统计不确定性。这种实验不确定性的计算应包括样本采集、处理和测定中固有的误差,以及动力学常数中的误差和/或生物过程与卷积公式代数结构预期偏差。此外,从系统角度描述激素数据的完整行为范围将需要更复杂的卷积表述。此类更新的卷积方法以及现有技术的应用包括模型合成、模型测试以及多个脉冲发生器之间相互作用的分析。