Dear all,
I developing a mixed effects PK/PD model for VAS sleepiness reported by 20 healthy volunteers after 2 mg oral lorazpam administration. Since the VAS scale is bound, the distribution of VAS scores at various time points is right skewed. However, when I look at the distribution of my WRES in my model it is only very slighlty right skewed.
My questions are:
1) Do we base the need to do a Log transformation on diagnostics from the data (e.g. score distributions) or diagnostics of the model (e.g. WRES).
2) Also I have zero baseline data. I realize there is a need to bias the data with a constant if I am to Log transform. I added a small constant (0.01), but in my concordance plots I get all my baseline points below the line of concordance. Is this because the Log transformation treats data between 0 and 1 differently from numbers higher then 1, i.e. (taking the log 0f 0.01 results in a negative number, while doing so for numgers greater then 1 results in positive numbers. Would following the log-transformed model that introduces an additional theta to account for systematic bias be applicable in this scenario
(reported by by Beal, JPP 2001;28:481-504)? Has anybody tried this?
M = THETA(n)
Y = LOG(F+M) + (F/(F+M))*EPS(1) + (M/(F+M))*EPS(2)
3) My maximum VAS is 100 mm (or a log of 2). Yet when I log transform, I get predictions with Log values higher then 2. Is there any way to place a constraint so as not to get predictions higher than log 2.
Thanks in advnace, Mohamed
Mohamed A. Kamal, Pharm.D.
Ph.D. Candidate
Department of Pharmaceutical Sciences
University of Michigan
Log Transformation in NONMEM
3 messages
3 people
Latest: Jun 17, 2008
Dear Mohamed,
A logit transformation of data will transform your VAS scores from - infinity
to + infinity.
Varun Goel
--- On Mon, 6/16/08, [EMAIL PROTECTED] <[EMAIL PROTECTED]> wrote:
Quoted reply history
From: [EMAIL PROTECTED] <[EMAIL PROTECTED]>
Subject: [NMusers] Log Transformation in NONMEM
To: [email protected]
Date: Monday, June 16, 2008, 5:17 PM
Dear all,
I developing a mixed effects PK/PD model for VAS sleepiness reported
by 20 healthy volunteers after 2 mg oral lorazpam administration.
Since the VAS scale is bound, the distribution of VAS scores at
various time points is right skewed. However, when I look at the
distribution of my WRES in my model it is only very slighlty right
skewed.
My questions are:
1) Do we base the need to do a Log transformation on diagnostics from
the data (e.g. score distributions) or diagnostics of the model (e.g.
WRES).
2) Also I have zero baseline data. I realize there is a need to bias
the data with a constant if I am to Log transform. I added a small
constant (0.01), but in my concordance plots I get all my baseline
points below the line of concordance. Is this because the Log
transformation treats data between 0 and 1 differently from numbers
higher then 1, i.e. (taking the log 0f 0.01 results in a negative
number, while doing so for numgers greater then 1 results in positive
numbers.
Would following the log-transformed model that introduces an
additional theta to account for systematic bias be applicable in this
scenario
(reported by by Beal, JPP 2001;28:481-504)? Has anybody tried this?
M = THETA(n)
Y = LOG(F+M) + (F/(F+M))*EPS(1) + (M/(F+M))*EPS(2)
3) My maximum VAS is 100 mm (or a log of 2). Yet when I log
transform, I get predictions with Log values higher then 2. Is there
any way to place a constraint so as not to get predictions higher than
log 2.
Thanks in advnace, Mohamed
Mohamed A. Kamal, Pharm.D.
Ph.D. Candidate
Department of Pharmaceutical Sciences
University of Michigan
Hello Mohamed,
You may find the following reference useful for your problem :
Reference:
PAGE 14 (2005) Abstr 773 [www.page-meeting.org/?abstract=773]
Indirect-response model for the analysis of concentration-effect relationships
in clinical trials where response variables are scores. V. Piotrovsky
Regards,
Samer
Quoted reply history
-----Original Message-----
From: [EMAIL PROTECTED] on behalf of varun goel
Sent: Mon 6/16/2008 18:30
To: [email protected]; [EMAIL PROTECTED]
Subject: Re: [NMusers] Log Transformation in NONMEM
Dear Mohamed,
A logit transformation of data will transform your VAS scores from - infinity
to + infinity.
Varun Goel
--- On Mon, 6/16/08, [EMAIL PROTECTED] <[EMAIL PROTECTED]> wrote:
From: [EMAIL PROTECTED] <[EMAIL PROTECTED]>
Subject: [NMusers] Log Transformation in NONMEM
To: [email protected]
Date: Monday, June 16, 2008, 5:17 PM
Dear all,
I developing a mixed effects PK/PD model for VAS sleepiness reported
by 20 healthy volunteers after 2 mg oral lorazpam administration.
Since the VAS scale is bound, the distribution of VAS scores at
various time points is right skewed. However, when I look at the
distribution of my WRES in my model it is only very slighlty right
skewed.
My questions are:
1) Do we base the need to do a Log transformation on diagnostics from
the data (e.g. score distributions) or diagnostics of the model (e.g.
WRES).
2) Also I have zero baseline data. I realize there is a need to bias
the data with a constant if I am to Log transform. I added a small
constant (0.01), but in my concordance plots I get all my baseline
points below the line of concordance. Is this because the Log
transformation treats data between 0 and 1 differently from numbers
higher then 1, i.e. (taking the log 0f 0.01 results in a negative
number, while doing so for numgers greater then 1 results in positive
numbers.
Would following the log-transformed model that introduces an
additional theta to account for systematic bias be applicable in this
scenario
(reported by by Beal, JPP 2001;28:481-504)? Has anybody tried this?
M = THETA(n)
Y = LOG(F+M) + (F/(F+M))*EPS(1) + (M/(F+M))*EPS(2)
3) My maximum VAS is 100 mm (or a log of 2). Yet when I log
transform, I get predictions with Log values higher then 2. Is there
any way to place a constraint so as not to get predictions higher than
log 2.
Thanks in advnace, Mohamed
Mohamed A. Kamal, Pharm.D.
Ph.D. Candidate
Department of Pharmaceutical Sciences
University of Michigan