Hi Armin,
Alternatively you could use premutation statistics. You could shuffle
your subjects between groups randomly under the Null hypothesis of no
differences between groups and each time claculating the lme model. I am
not sure, but if you do it at each time point of your repetition at each
draw, then you could remember the greates F value for your F-value
distribution. This could control the multiple comparison problem. Then
after let's say 1000 draws you have a F value distribution under the
Null hypothesis and you could determine your critical F value from that
distribution.
Hope that helps,
Stephan
Armin wrote:
Hi
I constructed a mixed-effects model from longitudinal repeated
measurements of lab values in 22 patients seperated into two groups
with the groups as fixed effect using lme. I thought about using the
jackknife procedure, i. e., removing any one subject and calculating
the fixed effect, to assess the stability of the fixed effect and
thereby validate the model. I suppose this has been done in the
following study:
http://content.nejm.org/cgi/content/full/357/19/1903
(this may be restricted access, sorry)
Is such an approach feasible?
Also in the article results are confirmed by comparing the mixed model
with a fitted least-squares regression. I understand that this can be
achieved with lmlist, but only for for models without an additional
fixed effect!?
Are there any other good approaches to validate a mixed-effects model
that will be accepted in medical peer review?
--
*Stephan Moratti, PhD/
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