From: Ribbing, Jakob <*Jakob.Ribbing*>

Date: Mon, 17 Nov 2008 07:27:14 -0000

Xia,

I must admit, I am still confused. In my mind, you can not estimate

THETA(2) in your code, since it is completely confounded with THETA(1).

Moreover, if you fix THETA(2) to a non-zero value, THETA(1) will no

longer be the typical value of CL (or the population typical value of

CL), meaning that the interpretability of THETA(1) is lost.

Regarding your definition of omega^ I think this is an attempt to allow

a semi-parametric model. Can you please explain how equation 2 affects

equation 1, using code acceptable in the nonmem NONMEM program?

Currently, I am not clear on how many random effects you are estimating

for CL.

Thanks

Jakob

-----Original Message-----

From: owner-nmusers

On Behalf Of XIA LI

Sent: 17 November 2008 05:28

To: Leonid Gibiansky

Cc: 'Nick Holford'; 'nmusers'

Subject: Re: [NMusers] Very small P-Value for ETABAR

Leonid,

Sorry, I did make myself clear.

CL=THETA(1)*EXP(ETA(1)) (1)

where ETA(1) is Normal( 0, omega^2) or

log Normal(Eta_bar,omega^2)

Adding one more stage means giving some functions for the MEAN and

VARIANCE of ETA(1), say:

Eta_bar=THETA(2)

omega^= THETA(3)*EXP(ETA(2)) (2)

Sorry for any confusion!

Best,

Xia

---- Original message ----

*>Date: Fri, 14 Nov 2008 18:37:22 -0500
*

*>From: Leonid Gibiansky <LGibiansky *

*>Subject: Re: [NMusers] Very small P-Value for ETABAR
*

*>To: Xia Li <lix4 *

*>Cc: "'Nick Holford'" <n.holford *

<nmusers

*>
*

*>Xia,
*

*>I could be missing something but this
*

*> ETA(1)= THETA(2)*exp(ETA(2)) (Eq. 1)
*

*>does not make sense to me. In the original definition, ETA(1) is the
*

*>random variable with normal distribution. Even if posthoc ETAs are not
*

*>normal, they are still random. For example, it can be either positive
*

or

*>negative (unlike ETA1 given by (1)). If I the understood intentions
*

*>correctly, this is an attempt to describe a transformation of the
*

random

*>effects to make it normal:
*

*>
*

*>CL = THETA(1) exp(ETA(1)) is replaced by
*

*>CL = THETA(1) exp(THETA(2)*exp(ETA(1))) (2)
*

*>
*

*>But not every transformation is reasonable. I hardly can imagine the
*

*>case when you may want to use (2). Could you give some more realistic
*

*>examples, please, and situation when they were useful?
*

*>
*

*>On the separate note, mean of THETA(2)*exp(ETA(2)) is not equal to
*

*>THETA(2): geometric mean of THETA(2)*exp(ETA(2)) is equal to THETA(2)
*

*>
*

*>Thanks
*

*>Leonid
*

*>
*

*>--------------------------------------
*

*>Leonid Gibiansky, Ph.D.
*

*>President, QuantPharm LLC
*

*>web: www.quantpharm.com
*

*>e-mail: LGibiansky at quantpharm.com
*

*>tel: (301) 767 5566
*

*>
*

*>
*

*>
*

*>
*

*>Xia Li wrote:
*

*>> Hi Nick,
*

*>> My pleasure!
*

*>>
*

*>> This is a topic from Bayesian Hierarchical Model(BHM). If we look at
*

the

*>> simplest PK statement: CL=THETA(1)*EXP(ETA(1)), where ETA(1) is the
*

between

*>> subject random effect. We assume the "similarity" among the subjects
*

may be

*>> modeled by THETA(1) and ETA(1).
*

*>>
*

*>> Now here, if we observe that there is an underlying pattern between
*

*>> ETA(1)'s, i.e. deviation from zero or no longer normal and we assume
*

that

*>> there is a similarity among those patterns.
*

*>>
*

*>> Since ETA(1)'s are assumed similar, it is reasonable to model the
*

*>> "similarity" among the ETA(1)'s by THETA(2) and ETA(2): ETA(1)=
*

*>> THETA(2)*exp(ETA(2)). Hence we have one more stage, ETA(1) now is
*

*>> lognormal(nonsymmetrical) with mean THETA(2) (doesnt have to be
*

zero).

*>>
*

*>> We will not say the variance of ETA(1) is confounded with the
*

variance of

*>> ETA(2), we say it is a function of variance of ETA(2).In statistics,
*

*>> confounding means hard to distinguish from each other. Here, it is a
*

direct

*>> causation.
*

*>>
*

*>> Sorry I don't have a NM-TRAN code for this now. I usually use SAS and
*

Win

*>> bugs to do modeling and haven't tried this BHM in NONMEM. I will
*

figure out

*>> can I do it in NONMEM later.
*

*>>
*

*>> Best,
*

*>> Xia
*

*>>
*

*>> -----Original Message-----
*

*>> From: owner-nmusers *

[mailto:owner-nmusers

*>> Behalf Of Nick Holford
*

*>> Sent: Friday, November 14, 2008 3:34 PM
*

*>> To: nmusers
*

*>> Subject: Re: [NMusers] Very small P-Value for ETABAR
*

*>>
*

*>> Jakob, Mats,
*

*>>
*

*>> Thanks very much for your careful explanations of how asymmetric EBE
*

*>> distributions can arise. That is very helpful for my understanding.
*

*>>
*

*>> Xia,
*

*>>
*

*>> I am intrigued by your suggestion for how to estimate and account for
*

*>> the bias in the mean of the EBE distribution.
*

*>>
*

*>> In the usual ETA on EPS model I might write:
*

*>>
*

*>> ; SD of residual error for mixed proportional and additive random
*

effects

*>> PROP=THETA(1)*F
*

*>> ADD=THETA(2)
*

*>> SD=SQRT(PROP*PROP + ADD*ADD)
*

*>> Y=F + EPS(1)*SD*EXP(ETA(1))
*

*>>
*

*>> where EPS(1) is distributed mean zero, variance 1 FIXED
*

*>> and ETA(1) is the between subject random effect for residual error
*

*>>
*

*>> You seem to be suggesting:
*

*>> ETABAR=THETA(3)
*

*>> Y=F + EPS(1)*SD*EXP(ETA(1)) * ETABAR*EXP(ETA(2))
*

*>>
*

*>> It seems to me that the variance of ETA(1) will be confounded with
*

the

*>> variance of ETA(2). Would you please explain more clearly (with an
*

*>> explicit NM-TRAN code fragment if possible) what you are suggesting?
*

*>>
*

*>> Best wishes,
*

*>>
*

*>> Nick
*

*>>
*

*>> Xia Li wrote:
*

*>>> Hi Jakob,
*

*>>> Thank you very much for the information adding an "eta on epsilon".
*

This

*>> is
*

*>>> what I did in my research and I am glad to see people in
*

Pharmacometrics

*>> is
*

*>>> using it.
*

*>>>
*

*>>> And in Bayesian analysis, adding one more stage for ETA, i.e
*

*>>> ETA=ETABAR*exp(eta2), eta2~N(0,omega2) will allow the deviation =
*

from

zero

*>>> and shrinkage of ETA.
*

*>>>
*

*>>> Again, thanks all for your input.:)
*

*>>>
*

*>>> Best Regards,
*

*>>> Xia
*

*>>>
*

*>>> Xia Li
*

*>>> Mathematical Science Department
*

*>>> University of Cincinnati
*

*>>>
*

*>>
*

==========================

=============

Xia Li

Mathematical Science Department

University of Cincinnati

Received on Mon Nov 17 2008 - 02:27:14 EST

Date: Mon, 17 Nov 2008 07:27:14 -0000

Xia,

I must admit, I am still confused. In my mind, you can not estimate

THETA(2) in your code, since it is completely confounded with THETA(1).

Moreover, if you fix THETA(2) to a non-zero value, THETA(1) will no

longer be the typical value of CL (or the population typical value of

CL), meaning that the interpretability of THETA(1) is lost.

Regarding your definition of omega^ I think this is an attempt to allow

a semi-parametric model. Can you please explain how equation 2 affects

equation 1, using code acceptable in the nonmem NONMEM program?

Currently, I am not clear on how many random effects you are estimating

for CL.

Thanks

Jakob

-----Original Message-----

From: owner-nmusers

On Behalf Of XIA LI

Sent: 17 November 2008 05:28

To: Leonid Gibiansky

Cc: 'Nick Holford'; 'nmusers'

Subject: Re: [NMusers] Very small P-Value for ETABAR

Leonid,

Sorry, I did make myself clear.

CL=THETA(1)*EXP(ETA(1)) (1)

where ETA(1) is Normal( 0, omega^2) or

log Normal(Eta_bar,omega^2)

Adding one more stage means giving some functions for the MEAN and

VARIANCE of ETA(1), say:

Eta_bar=THETA(2)

omega^= THETA(3)*EXP(ETA(2)) (2)

Sorry for any confusion!

Best,

Xia

---- Original message ----

<nmusers

or

random

the

between

may be

that

zero).

variance of

direct

Win

figure out

[mailto:owner-nmusers

effects

the

This

Pharmacometrics

from

zero

==========================

=============

Xia Li

Mathematical Science Department

University of Cincinnati

Received on Mon Nov 17 2008 - 02:27:14 EST