RS_opt {PopED}R Documentation

Optimize the objective function using an adaptive random search algorithm for D-family and E-family designs.

Description

Optimize the objective function using an adaptive random search algorithm. Optimization can be performed for both D-family and E-family designs. The function works for both discrete and continuous optimization variables. This function takes information from the PopED database supplied as an argument. The PopED database supplies information about the the model, parameters, design and methods to use. Some of the arguments coming from the PopED database can be overwritten; by default these arguments are NULL in the function, if they are supplied then they are used instead of the arguments from the PopED database.

Usage

RS_opt(
  poped.db,
  ni = NULL,
  xt = NULL,
  model_switch = NULL,
  x = NULL,
  a = NULL,
  bpopdescr = NULL,
  ddescr = NULL,
  maxxt = NULL,
  minxt = NULL,
  maxa = NULL,
  mina = NULL,
  fmf = 0,
  dmf = 0,
  trflag = TRUE,
  opt_xt = poped.db$settings$optsw[2],
  opt_a = poped.db$settings$optsw[4],
  opt_x = poped.db$settings$optsw[3],
  cfaxt = poped.db$settings$cfaxt,
  cfaa = poped.db$settings$cfaa,
  rsit = poped.db$settings$rsit,
  rsit_output = poped.db$settings$rsit_output,
  fim.calc.type = poped.db$settings$iFIMCalculationType,
  approx_type = poped.db$settings$iApproximationMethod,
  iter = NULL,
  d_switch = poped.db$settings$d_switch,
  use_laplace = poped.db$settings$iEDCalculationType,
  laplace.fim = FALSE,
  header_flag = TRUE,
  footer_flag = TRUE,
  out_file = NULL,
  compute_inv = TRUE,
  ...
)

Arguments

poped.db

A PopED database.

ni

A vector of the number of samples in each group.

xt

A matrix of sample times. Each row is a vector of sample times for a group.

model_switch

A matrix that is the same size as xt, specifying which model each sample belongs to.

x

A matrix for the discrete design variables. Each row is a group.

a

A matrix of covariates. Each row is a group.

bpopdescr

Matrix defining the fixed effects, per row (row number = parameter_number) we should have:

  • column 1 the type of the distribution for E-family designs (0 = Fixed, 1 = Normal, 2 = Uniform, 3 = User Defined Distribution, 4 = lognormal and 5 = truncated normal)

  • column 2 defines the mean.

  • column 3 defines the variance of the distribution (or length of uniform distribution).

ddescr

Matrix defining the diagonals of the IIV (same logic as for the bpopdescr).

maxxt

Matrix or single value defining the maximum value for each xt sample. If a single value is supplied then all xt values are given the same maximum value.

minxt

Matrix or single value defining the minimum value for each xt sample. If a single value is supplied then all xt values are given the same minimum value

maxa

Vector defining the max value for each covariate. If a single value is supplied then all a values are given the same max value

mina

Vector defining the min value for each covariate. If a single value is supplied then all a values are given the same max value

fmf

The initial value of the FIM. If set to zero then it is computed.

dmf

The initial OFV. If set to zero then it is computed.

trflag

Should the optimization be output to the screen and to a file?

opt_xt

Should the sample times be optimized?

opt_a

Should the continuous design variables be optimized?

opt_x

Should the discrete design variables be optimized?

cfaxt

First step factor for sample times

cfaa

Stochastic Gradient search first step factor for covariates

rsit

Number of Random search iterations

rsit_output

Number of iterations in random search between screen output

fim.calc.type

The method used for calculating the FIM. Potential values:

  • 0 = Full FIM. No assumption that fixed and random effects are uncorrelated.

  • 1 = Reduced FIM. Assume that there is no correlation in the FIM between the fixed and random effects, and set these elements in the FIM to zero.

  • 2 = weighted models (placeholder).

  • 3 = Not currently used.

  • 4 = Reduced FIM and computing all derivatives with respect to the standard deviation of the residual unexplained variation (sqrt(SIGMA) in NONMEM). This matches what is done in PFIM, and assumes that the standard deviation of the residual unexplained variation is the estimated parameter (NOTE: NONMEM estimates the variance of the residual unexplained variation by default).

  • 5 = Full FIM parameterized with A,B,C matrices & derivative of variance.

  • 6 = Calculate one model switch at a time, good for large matrices.

  • 7 = Reduced FIM parameterized with A,B,C matrices & derivative of variance.

approx_type

Approximation method for model, 0=FO, 1=FOCE, 2=FOCEI, 3=FOI.

iter

The number of iterations entered into the blockheader_2 function.

d_switch

  • ******START OF CRITERION SPECIFICATION OPTIONS**********

D-family design (1) or ED-family design (0) (with or without parameter uncertainty)

use_laplace

Should the Laplace method be used in calculating the expectation of the OFV?

laplace.fim

Should an E(FIM) be calculated when computing the Laplace approximated E(OFV). Typically the FIM does not need to be computed and, if desired, this calculation is done using the standard MC integration technique, so can be slow.

header_flag

Should the header text be printed out?

footer_flag

Should the footer text be printed out?

out_file

Which file should the output be directed to? A string, a file handle using file or "" will output to the screen.

compute_inv

should the inverse of the FIM be used to compute expected RSE values? Often not needed except for diagnostic purposes.

...

arguments passed to evaluate.fim and ofv_fim.

References

  1. M. Foracchia, A.C. Hooker, P. Vicini and A. Ruggeri, "PopED, a software fir optimal experimental design in population kinetics", Computer Methods and Programs in Biomedicine, 74, 2004.

  2. J. Nyberg, S. Ueckert, E.A. Stroemberg, S. Hennig, M.O. Karlsson and A.C. Hooker, "PopED: An extended, parallelized, nonlinear mixed effects models optimal design tool", Computer Methods and Programs in Biomedicine, 108, 2012.

See Also

Other Optimize: Doptim(), LEDoptim(), a_line_search(), bfgsb_min(), calc_autofocus(), calc_ofv_and_grad(), mfea(), optim_ARS(), optim_LS(), poped_optim_1(), poped_optim_2(), poped_optim_3(), poped_optimize(), poped_optim()

Examples

library(PopED)

############# START #################
## Create PopED database
## (warfarin model for optimization
##  with parameter uncertainty)
#####################################

## Warfarin example from software comparison in:
## Nyberg et al., "Methods and software tools for design evaluation 
##   for population pharmacokinetics-pharmacodynamics studies", 
##   Br. J. Clin. Pharm., 2014. 

## Optimization using an additive + proportional reidual error
## to avoid sample times at very low concentrations (time 0 or very late samoples).

## find the parameters that are needed to define from the structural model
ff.PK.1.comp.oral.sd.CL

## -- parameter definition function 
## -- names match parameters in function ff
sfg <- function(x,a,bpop,b,bocc){
  parameters=c(CL=bpop[1]*exp(b[1]),
               V=bpop[2]*exp(b[2]),
               KA=bpop[3]*exp(b[3]),
               Favail=bpop[4],
               DOSE=a[1])
  return(parameters) 
}

# Adding 10% log-normal Uncertainty to fixed effects (not Favail)
bpop_vals <- c(CL=0.15, V=8, KA=1.0, Favail=1)
bpop_vals_ed_ln <- cbind(ones(length(bpop_vals),1)*4, # log-normal distribution
                         bpop_vals,
                         ones(length(bpop_vals),1)*(bpop_vals*0.1)^2) # 10% of bpop value
bpop_vals_ed_ln["Favail",]  <- c(0,1,0)
bpop_vals_ed_ln

## -- Define initial design  and design space
poped.db <- create.poped.database(ff_fun=ff.PK.1.comp.oral.sd.CL,
                                  fg_fun=sfg,
                                  fError_fun=feps.add.prop,
                                  bpop=bpop_vals_ed_ln, 
                                  notfixed_bpop=c(1,1,1,0),
                                  d=c(CL=0.07, V=0.02, KA=0.6), 
                                  sigma=c(0.01,0.25),
                                  groupsize=32,
                                  xt=c( 0.5,1,2,6,24,36,72,120),
                                  minxt=0,
                                  maxxt=120,
                                  a=70,
                                  mina=0,
                                  maxa=100)

############# END ###################
## Create PopED database
## (warfarin model for optimization
##  with parameter uncertainty)
#####################################


# Just a few iterations, optimize on DOSE and sample times using the full FIM
out_1 <- RS_opt(poped.db,opt_xt=1,opt_a=1,rsit=3,fim.calc.type=0, out_file = "")

## Not run: 
  
  RS_opt(poped.db)
  
  RS_opt(poped.db,opt_xt=TRUE,rsit=100,compute_inv=F)
  RS_opt(poped.db,opt_xt=TRUE,rsit=20,d_switch=0)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,d_switch=0,use_laplace=T)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,d_switch=0,use_laplace=T,laplace.fim=T)
  
  ## Different headers and footers of output
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,out_file="foo.txt")
  output <- RS_opt(poped.db,opt_xt=TRUE,rsit=100,trflag=FALSE)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,out_file="")
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,header_flag=FALSE)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,footer_flag=FALSE)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,header_flag=FALSE,footer_flag=FALSE)
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,header_flag=FALSE,footer_flag=FALSE,out_file="foo.txt")
  RS_opt(poped.db,opt_xt=TRUE,rsit=10,header_flag=FALSE,footer_flag=FALSE,out_file="") 


## End(Not run)
[Package PopED version 0.6.0 Index]