Statistical design and analysis of mutation studies in transgenic mice

We have been working on identifying sources of variability in data from transgenic mouse mutation assays in order to develop appropriate statistical methods and designs for routine studies. Data from our lab and elsewhere point to the presence of significant animal‐to‐animal variability, which must be taken into account in statistical hypothesis tests. Here, the usual Cochran‐Armitage (CA) test for trend in mutant frequencies, which takes the transgene as the experimental unit, and a generalized Cochran‐Armitage test (GCA), which takes the animal as the experimental unit, are contrasted in computer simulations that help to quantify the differences between these statistical tests. The simulations report the statistical power of each test to detect treatment group differences, and their type I error rates. We find in general that the GCA test performs poorly compared to the CA test when it is appropriate to take the transgene as the experimental unit, and the study also uses a small number of animals. However, the CA test performs poorly in small group‐size studies when the animal is the appropriate experimental unit. Extensions of the computer simulations allow for identification of cost‐effective experimental designs. The results emphasize that the benefits of using additional animals in these mutation studies can be realized without substantial increases in costs. Here we illustrate the methods for liver studies in our lab. These methods can be used to derive optimal experimental designs for any combination of spontaneous mutant frequency and animal‐to‐animal variability. © 1995 Wiley‐Liss, Inc.

[1]  J. Vijg,et al.  High somatic mutation frequencies in a LacZ transgene integrated on the mouse X-chromosome. , 1991, Mutation research.

[2]  P. Armitage Tests for Linear Trends in Proportions and Frequencies , 1955 .

[3]  J M Nam,et al.  A simple approximation for calculating sample sizes for detecting linear trend in proportions. , 1987, Biometrics.

[4]  B. Margolin,et al.  Sources of variability in data from a lacl transgenic mouse mutation assay , 1994, Environmental and molecular mutagenesis.

[5]  M Lefkopoulou,et al.  Global tests for multiple binary outcomes. , 1993, Biometrics.

[6]  C. Schlatter,et al.  Mutations in liver DNA of lacI transgenic mice (Big Blue) following subchronic exposure to 2-acetylaminofluorene. , 1993, Mutation research.

[7]  D. Gunz,et al.  Can nongenotoxic carcinogens be detected with the lacl transgenic mouse mutation assay? , 1993, Environmental and molecular mutagenesis.

[8]  D L Putman,et al.  Spectra of spontaneous and mutagen-induced mutations in the lacI gene in transgenic mice. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[9]  J Vijg,et al.  Efficient rescue of integrated shuttle vectors from transgenic mice: a model for studying mutations in vivo. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. T. Macgregor,et al.  Induction of hepatic mutations in lacI transgenic mice. , 1993, Mutagenesis.

[11]  N. Gorelick,et al.  Overview of the workshops on statistical analysis of mutation data from transgenic mice , 1994, Environmental and molecular mutagenesis.

[12]  N. Gorelick,et al.  Statistical tests of significance in transgenic mutation assays: Considerations on the experimental unit , 1994, Environmental and molecular mutagenesis.

[13]  J. Short,et al.  Transgenic systems for in vivo mutation analysis. , 1993, Mutation research.

[14]  J. Short,et al.  Analysis of spontaneous and induced mutations in transgenic mice using a lambda ZAP/lacl shuttle vector , 1991, Environmental and molecular mutagenesis.

[15]  Haseman Jk,et al.  Analysis of dichotomous response data from certain toxicological experiments. , 1979 .

[16]  John J. Gart,et al.  On the Robustness of Combined Tests for Trends in Proportions , 1980 .

[17]  L. Ryan,et al.  The Analysis of Multiple Correlated Binary Outcomes: Application to Rodent Teratology Experiments , 1989 .

[18]  W. G. Cochran Some Methods for Strengthening the Common χ 2 Tests , 1954 .

[19]  J. A. Bond,et al.  Determination of mutagenicity in tissues of transgenic mice following exposure to 1,3-butadiene and N-ethyl-N-nitrosourea. , 1992, Toxicology and applied pharmacology.

[20]  J. Short,et al.  The use of shuttle vectors for mutation analysis in transgenic mice and rats. , 1994, Mutation research.