Rogerson Peter A
Department of Geography, Wilkeson Hall, University at Buffalo, Buffalo, NY 14261, USA.
Stat Med. 2006 Mar 15;25(5):811-23. doi: 10.1002/sim.2426.
In this paper, I develop new approaches for the detection of spatial clustering in case-control data. One method is based upon drawing Thiessen polygons around each control. It is unnecessary to actually draw or compute the boundaries of the polygons; it is sufficient to count, for each control, the number of cases that are closer to that control than to any other control. A second method is similar to the Cuzick-Edwards method, which is based on counts of cases that are among the k-nearest neighbours of cases, but is instead based upon the number of cases within a specified distance of cases. These first two methods are global methods in the sense that they provide a single statistic that measures the degree of spatial clustering. The third method suggests a local statistic, for tests of the null hypothesis of no spatial clustering around a prespecified focus. The method is based upon the cumulative chi2 test, which is typically used to test whether cases are more prevalent than expected around a prespecified location. This is also extended to the case where all observational locations are considered as potential cluster locations and multiple testing is carried out. Each of the new methods is illustrated using data on childhood leukaemia and lymphoma cases in North Humberside.
在本文中,我开发了用于检测病例对照数据中空间聚集性的新方法。一种方法是基于围绕每个对照绘制泰森多边形。实际上并不需要绘制或计算多边形的边界;对于每个对照,只需计算比其他任何对照更靠近该对照的病例数量即可。第二种方法类似于基于病例的k近邻中病例计数的Cuzick-Edwards方法,但它是基于病例指定距离内的病例数量。前两种方法是全局方法,因为它们提供了一个单一统计量来衡量空间聚集程度。第三种方法提出了一种局部统计量,用于检验围绕预先指定焦点不存在空间聚集的零假设。该方法基于累积卡方检验,通常用于检验在预先指定位置周围病例是否比预期更普遍。这也扩展到将所有观测位置视为潜在聚集位置并进行多次检验的情况。使用北亨伯赛德儿童白血病和淋巴瘤病例的数据对每种新方法进行了说明。