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There's a lot about collinearity with respect to continuous predictors but not so much that I can find on categorical predictors. I have data of this type illustrated below.

The first factor is a genetic variable (allele count), the second factor is a disease category. Clearly the genes precede the disease and are a factor in showing symptoms that lead to a diagnosis. However, a regular analysis using type II or III sums of squares, as would be commonly done in psych with SPSS, misses the effect. A type I sums of squares analysis picks it up, when the appropriate order is entered because it is order dependent. Further, there are likely to be extra components to the disease process which are not related to the gene that are not well identified with type II or III, see anova(lm1) below vs lm2 or Anova.

Example data:

set.seed(69)
iv1 <- sample(c(0,1,2), 150, replace=T)
iv2 <- round(iv1 + rnorm(150, 0, 1), 0)
iv2 <- ifelse(iv2<0, 0, iv2)
iv2 <- ifelse(iv2>2, 2, iv2)
dv  <- iv2 + rnorm(150, 0, 2)
iv2 <- factor(iv2, labels=c("a", "b", "c"))
df1 <- data.frame(dv, iv1, iv2)

library(car)
chisq.test(table(iv1, iv2))          # quick gene & disease relations
lm1 <- lm(dv~iv1*iv2, df1);    lm2 <- lm(dv~iv2*iv1, df1)
anova(lm1);                    anova(lm2)
Anova(lm1, type="II");         Anova(lm2, type="II")
  1. lm1 with type I SS to me seems the appropriate way to analyse the data given the background theory. Is my assumption correct?
  2. I'm used to explicitly manipulated orthogonal designs, where these problems don't usually pop up. Is it difficult to convince reviewers that this is the best process (assuming point 1 is correct) in the context of an SPSS centric field?
  3. And what to report in the stats section? Any extra analysis, or comments that should go in?
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  • $\begingroup$ It is surprising to hear that somebody using SPSS knows only Type III or II SS. And you sound like that. $\endgroup$ – ttnphns Nov 9 '11 at 11:51
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    $\begingroup$ Well, I used to have the same knowledge gap I'm referring to in my question. It seems to be more a reflection of people's interests, knowledge and how they get introduced to the software rather than the software itself. But default options play a large part as well with the default type III option being used in SPSS. $\endgroup$ – Matt Albrecht Nov 9 '11 at 16:17
  • $\begingroup$ You seem to be saying that you have a way to enter 2 predictors in a specific order using SPSS's anova procedure (unianova?). I only know of a way to specify order by switching to the regression procedure. How do you accomplish this? $\endgroup$ – rolando2 Jan 14 '12 at 5:49
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Collinearity between factors is quite complicated. The classical example is the one you get when you group and dummy-encode the three continuous variables 'age', 'period' and 'year'. It is analysed in:

The coefficients you get, after removing four (not three) references are only identified up to an unknown linear trend. This can be analysed because the collinearity arises from a known collinearity in the source variables (age+year=period).

Some work has also been done on spurious collinearity between two factors. It has been analysed in:

The upshot is that collinearity among categorical variables means that the dataset must be split into disconnected parts, with a reference level in each component. Estimated coefficients from different components can not be compared directly.

For more complicated collinearities between three or more factors, the situation is complicated. There do exist procedures for finding estimable functions, i.e. linear combinations of the coefficients which are interpretable, e.g. in:

  • "On the connectivity of row-column designs" by Godolphin and Godolphin in Utilitas Mathematica (60) pp 51-65

But to my knowledge no general silver-bullet for handling such collinearities in an intuitive way exists.

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After having a chat with some of the stats people around the place. It seems this kind of question may not be the most correct question to answer. Using ANOVA (or similar methods) to investigate genetic and diagnostic interactions on neuropsychological measures when they are highly correlated is a difficult question. I've been pointed instead to examine the structure of the data with structural equation modelling.

This answer will get updated as I learn more about SEM.

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