Hashimoto T, Ohtaki M, Kamada N, Yamamoto H, Munaka M
Research Institute for Nuclear Medicine and Biology, Hiroshima University, Japan.
Environ Health Perspect. 1990 Jul;87:135-41. doi: 10.1289/ehp.9087135.
Relationships among additional chromosome abnormalities in chronic myelocytic leukemia (CML) with translocation 9;22 [Philadelphia chromosome (Ph1)-positive CML] were analyzed by log-linear models on 709 karyotypes reported in the literature. Additional abnormalities, such as the gain of chromosome 8 (+8), gain of Philadelphia chromosome (+Ph1), isochromosome of the long arm (q) of chromosome 17 [i(17q)], and the gain of chromosome 19 (+19), were frequently observed. A four-way 2 x 2 x 2 x 2 contingency table was considered with respect to the appearance of these four abnormalities, then the hierarchical log-linear models having at least four main effects were fitted to the observed contingency table. Akaike's information criteria of the models reflected the fitness of the model very well. Parameter estimates of the interaction terms indicated that the combinations of two abnormalities, '+8 and +19', '+Ph1 and +19', and '+8 and i(17q)' were positively associated, while '+Ph1 and i(17q)', and '+19 and i(17q)' were negatively associated. Based on the results of the data analysis, an inference was made on the route of karyotypic evolution in Ph1-positive CML; it statistically supports the hypothesis presented by Heim and Mitelman.
运用对数线性模型,对文献报道的709例慢性髓细胞白血病(CML)伴有9;22易位[费城染色体(Ph1)阳性CML]的核型中其他染色体异常之间的关系进行了分析。经常观察到其他异常情况,如8号染色体三体(+8)、费城染色体三体(+Ph1)、17号染色体长臂等臂染色体[i(17q)]以及19号染色体三体(+19)。针对这四种异常情况的出现构建了一个4×2×2×2的列联表,然后将至少具有四个主效应的分层对数线性模型应用于观察到的列联表。模型的赤池信息准则很好地反映了模型的拟合优度。交互项的参数估计表明,两种异常情况的组合,即“+8和+19”、“+Ph1和+19”以及“+8和i(17q)”呈正相关,而“+Ph1和i(17q)”以及“+19和i(17q)”呈负相关。基于数据分析结果,对Ph1阳性CML的核型进化途径进行了推断;它在统计学上支持了海姆和米特尔曼提出的假说。