At 05:42 AM 6/12/2009, Lindsay Banin wrote:
Hi there,

I am looking to compare nonlinear mixed effects models that have different nonlinear functions (different types of growth curve)embedded. Most of the literature I can find focuses on comparing nested models with likelihood ratios and AIC. Is there a way to compare model fits when models are not nested, i.e. when the nonlinear functions are not the same?

Transform back into original units, if necessary, and compare distributions of and statistics of residuals from fitted values in original units.

This is not a significance-test, but instead a measure of the better approximation to the observed model.

Types of measures: 1) rms residual, 2) max absolute residual, 3) mean absolute residual.

In my opinion, models should be chosen based on the principles of causality (theory), degree of approximation and parsimony. None of these involve significance testing.

Choosing models based upon significance testing (which merely identifies whether or not the experiment is large enough to distinguish an effect clearly) amounts to admitting intellectually that you have no subject matter expertise, and you must therefore fall back on the crumbs of significance testing to get glimmers of understanding of what's going on. (Much like stepwise regression techniques.)

As an example, suppose you have two models, one with 5 parameters and one with only 1. The rms residual error for the two models are 0.50 and 0.53 respectively. You have a very large study, and all 4 additional parameters are significant at p = 0.01 or less. What should you do? What I would do is select the 1 parameter study as my baseline model. It will be easy to interpret physically, will generalize to other studies much better (stable), and is almost identical in degree of approximation as the 5 parameter model. I would be excited that a one parameter model could do this. The fact that the other 4 parameters have detectable effects at a very low level is not important for modeling the study, but may conceivably have some special significance on their own for future investigations.

So not being able to do significance testing on non-nested models is not that big a loss, in my opinion. Such tests encourage wrong thinking, in my opinion.

What I've expressed as an opinion here (which I am sure some will disagree with) is similar to the philosophy of choosing the number of principal components to use, or number of latent factors in factor analysis. What investigation do people ever do on the small eigenvalue principal components, even if their contributions are "statistically significant"?

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Robert A. LaBudde, PhD, PAS, Dpl. ACAFS  e-mail: r...@lcfltd.com
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