DeLean A, Munson P J, Rodbard D
Am J Physiol. 1978 Aug;235(2):E97-102. doi: 10.1152/ajpendo.1978.235.2.E97.
Physiological and pharmacological studies of hormones, drugs, and neurotransmitters often generate families of sigmoidal dose-response curves. Optimally efficient data analysis should involve simultaneous description of all curves, rather than fitting each one individually. We have developed a general computerized method to describe the dose-response curves in terms of basal and maximal responses, ED50, and curve shape or steepness. This facile method permits rigorous statistical analysis, provides a basis for pooling of information from separate experiments, and allows one to test which characteristics are shared by various curves.
对激素、药物和神经递质的生理学及药理学研究常常会产生一系列S形剂量反应曲线。最优效率的数据分析应涉及对所有曲线的同时描述,而非单独拟合每条曲线。我们已开发出一种通用的计算机化方法,用于根据基础反应和最大反应、半数有效剂量(ED50)以及曲线形状或斜率来描述剂量反应曲线。这种简便的方法允许进行严格的统计分析,为整合来自不同实验的信息提供了基础,还能让人检验各种曲线所共有的特征。