Hi Fiona;

You didn’t state this, but I am assuming that you have looked at plots of 
partial residuals of each parameter with respect to each covariate and have 
determined whether a pattern exists which would help you decide whether a given 
covariate is worth including in the model? Also, I would assume that you’ve 
considered the ultimate purpose of the model , and have a pre-specified notion 
of which covariates you would like to test, based on some biological/medical 
rationale? My point being, you should not rely on p-values to select covariates 
– doing so will give you the situation you have just described: a large, 
overly-complex model.

Regardless of the technical details, if you can’t see a pattern in the residual 
plots with regard to a given covariate, it is unlikely to provide any 
meaningful reduction in the residual error of your parameter model.

Michael Fossler, Pharm. D., Ph. D., F.C.P.
Senior Director
Clinical Pharmacology Modeling and Simulation
RD Projects Clinical Platforms & Sciences

GSK
Upper Merion West
King of Prussia, PA
Email   [email protected]<mailto:[email protected]>
Tel       +1 610 270 4797
Cell       443-350-1194

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[cid:[email protected]]

From: [email protected] [mailto:[email protected]] On 
Behalf Of Fiona Vanobberghen
Sent: Thursday, February 26, 2015 5:01 AM
To: [email protected]
Subject: [NMusers] Covariate modelling question

I posted this message a few days ago but it doesn't seem to have been sent to 
the list - so I'm resending without the example output.
Best wishes
Fiona

--
Dear all

I am attempting to do some covariate modelling, using the scm wizard in Pirana. 
I have seen some results which I wasn't expecting and would be grateful if 
anyone could shed any light on it for me.

Initially, I used a forward inclusion p value of 0.1 and a backward elimination 
p value of 0.05. This resulted in quite a complex (implausible) model (we do 
have a reasonably large dataset), and I decided to be more stringent, using 
p<0.05 for inclusion (and the same p>0.05 for elimination at the last step). As 
a shortcut, I could see from the output from the first attempt (with p<0.1) 
what I expected the final model to look like if I were to run it again with 
p<0.05, ie where the process would truncate. Just to double check (and verify 
that nothing would be eliminated at the last step), I re-ran the scm wizard 
with the more stringent p<0.05. And the results are not what I expected... 
Below I have pasted the output for the first few forward steps from each 
attempt. The results are essentially the same up until the third step, although 
we see some small differences in the OFV creeping in from the second step. 
However, at the fourth step, the results are completely different. This isn't 
what I was expecting, based on my understanding of the model selection process. 
Is this a known behaviour? Has anyone experienced this problem and/or know why 
these differences might occur? I'd be grateful for any advice.

Many thanks in advance for your help.

Best wishes
Fiona

--
Fiona Vanobberghen (née Ewings), PhD
Swiss Tropical and Public Health Institute
Socinstrasse 57, 4051, Basel, Switzerland
Tel: +41 61 284 87 41

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