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Re: Interpretation of 'interquartile effects' in summary.lrm

To: "Inman, Brant A. M.D." <Inman.Brant@mayo.edu>
Subject: Re: Interpretation of 'interquartile effects' in summary.lrm
From: Stephen D.Weigand <weigand.stephen@charter.net>
Date: Tue, 28 Nov 2006 00:21:21 -0600
Cc: s-news@lists.biostat.wustl.edu
In-reply-to: <456BBFD6.7010203@vanderbilt.edu>
References: <6021CA6EF4C8374084D4F5A141F1CBBB6648DE@msgebe23.mfad.mfroot.org> <456BBFD6.7010203@vanderbilt.edu>

On Nov 27, 2006, at 10:49 PM, Frank E Harrell Jr wrote:

Inman, Brant A. M.D. wrote:
S-experts: I am using the Design and Hmisc libraries to fit a logistic regression model in a manner similar to that given below (note that this model may
not make sense, I just use it to demonstrate my question):


[...]

ddist <- datadist(pbc)
options(datadist='ddist')
fit <- lrm(edema ~ age + alb + ascites + hepmeg, data=pbc)
--------------------------
Since my goal is to extract the odds ratios from this model, I have
tried two different methods: the obvious method of exponentiation of the
regression coefficients and using the summary.Design function.
--------------------------
exp(fit$coef)
summary(fit)
--------------------------
The problem that I have is with the "summary(fit)" output, namely that
its odds ratios are different from those of "exp(fit$coef)".  From the
documentation that is provided by the function's author, I surmise that the reason the odds ratios for the continuous variables are different is
that the function calculates the odds ratios using "inter-quartile
effects".  I have not previously encountered this method of computing
odds ratios and would appreciate any advice from the experts regarding
the reasons for using the inter-quartile method for calculating the odds ratios rather than the usual method. Which method should be reported in
a paper and is there evidence/publications to support this choice?

Please see my book Regression Modeling Strategies which details the reasons for this and for not doing exp(coef). A one-unit change is not meaningful for many of the variables we see in biomedical research.

Frank

Brant Inman
Mayo Clinic


--
Frank E Harrell Jr   Professor and Chair           School of Medicine
Department of Biostatistics Vanderbilt University

Brant,

My additional comments:

For continuous variables that are found to be approximately linear in the logit (perhaps only due to limited power to detect non-linearity), I report an odds ratio based on a difference that is easy to understand or clinically
meaningful: e.g., a 10-year difference in age, or a 0.5 cm difference in
lesion size.

If it's hard to come up with a meaningful difference, if I've transformed a variable, or if it enters into the model non-linearly, then I follow the above reference and report an odds ratio based on Q3 vs. Q1 since a k-unit change in the variable does not have the same effect across the distribution of values.

I've had some success explaining the use of Q3 vs. Q1 as "comparing a person with a typical above-average value to one with a typical below-average value".

The one drawback to the Q3 vs. Q1 approach is that a careless reviewer may think you've cut the variable into quartiles, fit the model, and reported ORs based on this. So a few sentences justifying Q3 vs. Q1 ORs may be worth including in your
report.

Hope this helps,

Stephen Weigand
Rochester, Minnesota, USA


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