Stewart J, Debray Q, Caillard V
Am J Hum Genet. 1980 Jan;32(1):55-63.
Simulated pedigrees of schizophrenia generally show a clear peak in their likelihood surface corresponding to analysis by the genetic models, which served as the basis for the simulation. The likelihood surface obtained with real data permits determination of the allelic frequency and the selection of an optimal one-locus, two-locus, and four-locus model. These three models have certain features in common, notably, a relatively high frequency of the allele predisposing to schizophrenia (about 20%) and a relatively low index of genetic determination (23%--34%). However, direct likelihood comparisons do not permit distinctions between the one-locus, two-locus, and four-locus models. The most likely interpretation of this finding is that the etiology of schizophrenia is heterogeneous or even nongenetic. However, a simple model with a single completely recessive locus and incomplete penetrance in the homozygote also produces a flat likelihood surface closely resembling that obtained with the real data. With reservation, this single-locus model may be put forward as a potentially useful working hypothesis.
精神分裂症的模拟系谱通常在其似然面上呈现出一个明显的峰值,该峰值对应于作为模拟基础的遗传模型分析。通过实际数据获得的似然面允许确定等位基因频率,并选择最优的单基因座、双基因座和四基因座模型。这三种模型有一些共同特征,特别是,易患精神分裂症的等位基因频率相对较高(约20%),遗传决定指数相对较低(23% - 34%)。然而,直接的似然比较无法区分单基因座、双基因座和四基因座模型。对这一发现最可能的解释是,精神分裂症的病因是异质性的,甚至是非遗传性的。然而,一个具有单一完全隐性基因座且纯合子中存在不完全外显率的简单模型也会产生一个与实际数据获得的似然面非常相似的平坦似然面。有所保留地说,这个单基因座模型可以作为一个潜在有用的工作假设提出来。