Horner R D, Samsa G
Center for Health Services Research in Primary Care, VA Medical Center, Durham, NC 27705.
J Clin Epidemiol. 1992 Oct;45(10):1071-80. doi: 10.1016/0895-4356(92)90147-f.
This study explores the conditions under which Sartwell's incubation period model may be appropriate for identifying a primary time period of etiologic risk for chronic diseases with uncertain etiology. The investigation begins with a description of the evolution of the application of Sartwell's model from infectious to chronic diseases. The model's underlying assumptions and some concerns about its use in the chronic disease context are specified. These concerns are addressed by data simulations and analyses of empirical data from the Connecticut Tumor Registry and the Radiation Effects Research Foundation. The results indicate that the distribution of age at diagnosis (i.e. onset) for chronic diseases is not necessarily lognormal. However, the representativeness of age distribution of the case series can affect the distribution's form; hence, it is important to determine the extent of "missing" cases, particularly those lost through truncation. Moreover, a lognormal age distribution may occur with both prenatal and age-related postnatal exposures. These findings suggest that only under certain conditions will Sartwell's model be useful in the study of chronic diseases of uncertain etiology, and indicate some caveats for interpretation of the results.
本研究探讨了在何种条件下,萨特韦尔的潜伏期模型可能适用于确定病因不明的慢性病的主要病因风险时间段。调查首先描述了萨特韦尔模型从传染病应用到慢性病应用的演变过程。明确了该模型的基本假设以及对其在慢性病背景下应用的一些担忧。通过数据模拟以及对康涅狄格肿瘤登记处和辐射效应研究基金会的实证数据进行分析,解决了这些担忧。结果表明,慢性病诊断(即发病)时的年龄分布不一定呈对数正态分布。然而,病例系列年龄分布的代表性会影响分布形式;因此,确定“缺失”病例的程度很重要,特别是那些因截断而丢失的病例。此外,产前和与年龄相关的产后暴露都可能出现对数正态年龄分布。这些发现表明,只有在某些条件下,萨特韦尔模型才会在病因不明的慢性病研究中有用,并指出了结果解释中的一些注意事项。