Dear all,

log-transformation has also some practical value. It adds stability to the 
parameter estimation process when the observations cover a wide range. I 
just had an example running with data from a phase I dose ranging study . 
The doses increased during the execution of the study over a 50-fold 
range.  With fairly complete profiles I had concentrations which differed 
up to 500-fold. I fit the data on the linear scale and then 
log-transformed. Only with the log-transformed data was I able to fit a 
full BLOCK(5) OMEGA matrix. Rounding error terminations were diminished. 
The VPC was much easier as I had no negative predictions.

These are all just practical observations, and I cannot give you an 
eloquent statistical explanation (Leonid may). But I will log-transform my 
concentration data in the future, especially when they cover a wide range. 
Thanks also to Mats for pointing that out in his workshop.

Joachim

__________________________________________
Joachim GREVEL, Ph.D.
Merck Serono S.A. - Genève
Human Pharmacology
1202 Geneva
Tel: +41.22.414.4751
Fax: +41.22.414.3059
Email: [email protected]





Leonid Gibiansky <[email protected]> 
Sent by: [email protected]
03/26/2009 11:52 PM

To
"Elassaiss - Schaap, J. \(Jeroen\)" <[email protected]>
cc
[email protected]
Subject
Re: [NMusers] Log transformation of concentration






Jeroen,

I think that the goal of modeling is to recover (predict) the underlying 
quantity (concentration, pd effect, whatever we are modeling). Our 
assumptions about the model (error model, in particular) help us (if 
they are correct) to recover those quantities. So there is no such thing 
as "prediction mode": we should always predict the underlying quantity. 
If the "true" error model is additive or proportional, then, given 1000 
observations at the same true-concentration level, true concentration is 
equal to the mean of those observations. If the "true" error model is 
exponential, then, given the same 1000 observations, concentration is 
equal to the geometric mean of the observations. If the true model is 
exponential but we fit an additive model, then the fit is biased 
(relative to the true value), and vice versa. Investigation of the data 
should allow (in theory, given sufficient amount of data) to recover the 
true model, including the true error model. Log-transformation is just 
the trick that allows to implement the exponential error model in nonmem.

Thanks
Leonid

--------------------------------------
Leonid Gibiansky, Ph.D.
President, QuantPharm LLC
web:    www.quantpharm.com
e-mail: LGibiansky at quantpharm.com
tel:    (301) 767 5566




Elassaiss - Schaap, J. (Jeroen) wrote:
> Dear Chenguang,
> 
> There is one difference that could be added to the excellent explanation 

> by Leonid; this has been previously brought forward by Mats in another 
> thread (Calculation of AUC) this week. When log-transforming on both 
> sides (TBS) your model will predict the median (geometric mean) rather 
> than the average of your data on the normal scale. This only will be 
> noticable when the residual error is large, see the values provided by 
> Mats. This effect does not depend on between-subject variability, i.e. 
> it also holds for single-subject models.
> 
> So while the log-transformation does not change the meaning of the 
> parameters, it will change the prediction 'mode' from average to median.
> 
> Best regards,
> Jeroen
> 
> 
> *Jeroen Elassaiss-Schaap, PhD*
> Modeling & Simulation Expert
> Pharmacokinetics, Pharmacodynamics & Pharmacometrics (P3)
> Early Clinical Research and Experimental Medicine
> Schering-Plough Research Institute
> T: +31 41266 9320
> 
> 
> 
> ------------------------------------------------------------------------
> *From:* [email protected] 
> [mailto:[email protected]] *On Behalf Of *Chenguang Wang
> *Sent:* Thursday, 26 March, 2009 14:40
> *To:* Leonid Gibiansky
> *Cc:* nmusers
> *Subject:* Re: [NMusers] Log transformation of concentration
> 
> Dear Leonid,
> Thank you very much for your explaination! I think I am now much clearer 

> about this.
> 
> Regards!
> 
> Chenguang
> 
> 
> 
> 2009/3/26 Leonid Gibiansky <[email protected] 
> <mailto:[email protected]>>
> 
>     Hi Chenguang,
>     The main reason to do the log transformation is the numerical
>     algorithm used in nonmem for error model. If you try to fit the
>     error model
>     Y=F*EXP(eps)
>     nonmem will take only the first term of the EXP function expansion
>     and will use the error model
>     Y=F*(1+EPS)
> 
>     Therefore, the only way to get true exponential (not proportional)
>     model is to log-transform both parts:
>     LOG(Y)=LOG(F)+EPS
> 
>     Note that this is done on the very last step.  All parameters have
>     the same meaning. All differential equations are written and solved
>     for F. Then, after you obtain F, you take the log. In the DV column,
>     you put the log of observed concentrations, so that your actual code 
is
>     Y=LOG(F)+EPS
> 
>     Last year I compared the performance of FOCE with interaction for
>     models with and without log-transformation, and found the
>     performance to be similar (in terms of bias and precision of
>     parameter estimates): you can find the poster on PAGE web site.
>     Still, for several real data sets, I've seen that the
>     log-transformed model provided slightly better fit, especially for
>     data with large residual error.
> 
>     Leonid
> 
>     --------------------------------------
>     Leonid Gibiansky, Ph.D.
>     President, QuantPharm LLC
>     web:    www.quantpharm.com <http://www.quantpharm.com/>
>     e-mail: LGibiansky at quantpharm.com <http://quantpharm.com/>
>     tel:    (301) 767 5566
> 
> 
> 
> 
> 
>     Chenguang Wang wrote:
> 
>         Dear NONMEM users,
> 
>         I am working on a PK model and using the log-transformed
>         concentration data. I'v read some discussions in the NONMEM user
>         group about the log-transformed concentration. But I am still
>         not very clear about this. Could anybody give me a reason to do
>         the transform on concentration? Also, I am curious that after
>         the transform, will the fixed effect have the same meaning as
>         that in the untransformed model? For example, theta1 is the
>         clearance, after log-transform of concentration, would the
>         estimation of theta1 still stands for the population clearance?
>         To my simple thinking about the differential equation,
> 
>         d(lnc)/dt= (dc/dt)*(1/c). Therefore, a "c" will be multiplied to
>         the right term of the orginal differential equation. I think the
>         solution of that equation might be different from the original
>         one. If it is different, how can I explain the theta1 in the log
>         transformed model?
> 
>         Would anyone please give me some explainations or references?
> 
>         Thanks a lot!
> 
>         Chenguang
> 
> 
> ------------------------------------------------------------------------
> This message and any attachments are solely for the intended recipient. 
> If you are not the intended recipient, disclosure, copying, use or 
> distribution of the information included in this message is prohibited 
> --- Please immediately and permanently delete.
> ------------------------------------------------------------------------

This message and any attachment are confidential and may be privileged or 
otherwise protected from disclosure. If you are not the intended recipient, you 
must not copy this message or attachment or disclose the contents to any other 
person. If you have received this transmission in error, please notify the 
sender immediately and delete the message and any attachment from your system. 
Merck KGaA, Darmstadt, Germany and any of its subsidiaries do not accept 
liability for any omissions or errors in this message which may arise as a 
result of E-Mail-transmission or for damages resulting from any unauthorized 
changes of the content of this message and any attachment thereto. Merck KGaA, 
Darmstadt, Germany and any of its subsidiaries do not guarantee that this 
message is free of viruses and does not accept liability for any damages caused 
by any virus transmitted therewith.

Click http://disclaimer.merck.de to access the German, French, Spanish and 
Portuguese versions of this disclaimer.

Reply via email to