|The GLM Procedure|
Analysis of covariance combines some of the features of both regression and analysis of variance. Typically, a continuous variable (the covariate) is introduced into the model of an analysis-of-variance experiment.
Data in the following example are selected from a larger experiment on the use of drugs in the treatment of leprosy (Snedecor and Cochran; 1967, p. 422).
Variables in the study are as follows:
two antibiotics (A and D) and a control (F)
a pretreatment score of leprosy bacilli
a posttreatment score of leprosy bacilli
Ten patients are selected for each treatment (Drug), and six sites on each patient are measured for leprosy bacilli.
The covariate (a pretreatment score) is included in the model for increased precision in determining the effect of drug treatments on the posttreatment count of bacilli.
data DrugTest; input Drug $ PreTreatment PostTreatment @@; datalines; A 11 6 A 8 0 A 5 2 A 14 8 A 19 11 A 6 4 A 10 13 A 6 1 A 11 8 A 3 0 D 6 0 D 6 2 D 7 3 D 8 1 D 18 18 D 8 4 D 19 14 D 8 9 D 5 1 D 15 9 F 16 13 F 13 10 F 11 18 F 9 5 F 21 23 F 16 12 F 12 5 F 12 16 F 7 1 F 12 20 ;
proc glm data=DrugTest; class Drug; model PostTreatment = Drug PreTreatment / solution; lsmeans Drug / stderr pdiff cov out=adjmeans; run;
proc print data=adjmeans; run;
|Class Level Information|
|Drug||3||A D F|
|Source||DF||Sum of Squares||Mean Square||F Value||Pr > F|
This model assumes that the slopes relating posttreatment scores to pretreatment scores are parallel for all drugs. You can check this assumption by including the class-by-covariate interaction, Drug*PreTreatment, in the model and examining the ANOVA test for the significance of this effect. This extra test is omitted in this example, but it is insignificant, justifying the equal-slopes assumption.
In Output 39.4.3, the Type I SS for Drug (293.6) gives the between-drug sums of squares that are obtained for the analysis-of-variance model PostTreatment=Drug. This measures the difference between arithmetic means of posttreatment scores for different drugs, disregarding the covariate. The Type III SS for Drug (68.5537) gives the Drug sum of squares adjusted for the covariate. This measures the differences between Drug LS-means, controlling for the covariate. The Type I test is highly significant (), but the Type III test is not. This indicates that, while there is a statistically significant difference between the arithmetic drug means, this difference is reduced to below the level of background noise when you take the pretreatment scores into account. From the table of parameter estimates, you can derive the least squares predictive formula model for estimating posttreatment score based on pretreatment score and drug:
|Source||DF||Type I SS||Mean Square||F Value||Pr > F|
|Source||DF||Type III SS||Mean Square||F Value||Pr > F|
Output 39.4.4 displays the LS-means, which are, in a sense, the means adjusted for the covariate. The STDERR option in the LSMEANS statement causes the standard error of the LS-means and the probability of getting a larger value under the hypothesis to be included in this table as well. Specifying the PDIFF option causes all probability values for the hypothesis to be displayed, where the indexes and are numbered treatment levels.
|Drug||PostTreatment LSMEAN||Standard Error||Pr > |t|||LSMEAN Number|
|Least Squares Means for effect Drug
Pr > |t| for H0: LSMean(i)=LSMean(j)
Dependent Variable: PostTreatment
The new graphical features of PROC GLM enable you to visualize the fitted analysis of covariance model. The following statements enable the graphics by specifying the ODS GRAPHICS statement and then fit an analysis-of-covariance model with LS-means for Drug.
ods graphics on; proc glm data=DrugTest plot=meanplot(cl); class Drug; model PostTreatment = Drug PreTreatment; lsmeans Drug / pdiff; run; ods graphics off;
With graphics enabled, the GLM procedure output includes an analysis-of-covariance plot, as in Output 39.4.6. The LSMEANS statement produces a plot of the LS-means; the SAS statements previously shown use the PLOTS=MEANPLOT(CL) option to add confidence limits for the individual LS-means, shown in Output 39.4.7. If you also specify the PDIFF option in the LSMEANS statement, the output also includes a plot appropriate for the type of LS-mean differences computed. In this case, the default is to compare all LS-means with each other pairwise, so the plot is a "diffogram" or "mean-mean scatter plot" (Hsu 1996), as in Output 39.4.8. For general information about ODS Graphics, see Chapter 21, Statistical Graphics Using ODS. For specific information about the graphics available in the GLM procedure, see the section ODS Graphics.
The analysis of covariance plot Output 39.4.6 makes it clear that the control (drug F) has higher posttreatment scores across the range of pretreatment scores, while the fitted models for the two antibiotics (drugs A and D) nearly coincide. Similarly, while the diffogram Output 39.4.7 indicates that none of the LS-mean differences are significant at the 5% level, the difference between the LS-means for the two antibiotics is much closer to zero than the differences between either one and the control.