Lange K
Am J Hum Genet. 1986 May;38(5):681-7.
In current genetic counseling practice, a single risk estimate is often quoted to a family rather than a range of risks. Such point estimates are predicated on knowing basic parameters like recombination fractions exactly when, in fact, there may be considerable uncertainty about them. Using the large sample theory of statistics, it is possible to derive approximate risk intervals that incorporate known statistical imprecision. The necessary theory will be briefly discussed and illustrated by an application to family counseling for Duchenne muscular dystrophy in the presence of two flanking markers. Some of the problems of the theory will be mentioned. These include lack of adequate sample size to justify the conclusions of large sample theory, pronounced nonlinearity in the risk function, and failure to take into proper account genetic interference. Except in trivial cases, sophisticated computer software is needed to carry out the computations of risk intervals.
在当前的遗传咨询实践中,通常向一个家庭提供的是单一风险估计值,而非一系列风险值。这种点估计是基于精确知晓诸如重组率等基本参数,但实际上,这些参数可能存在相当大的不确定性。运用统计学的大样本理论,可以推导出纳入已知统计不精确性的近似风险区间。将简要讨论必要的理论,并通过在存在两个侧翼标记的情况下对杜兴氏肌营养不良症家庭咨询的应用进行说明。还将提及该理论存在的一些问题。这些问题包括样本量不足无法证明大样本理论的结论合理、风险函数存在明显的非线性以及未能适当考虑遗传干扰。除了一些简单情况外,需要复杂的计算机软件来进行风险区间的计算。