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---
title: Example evaluation of FOCUS dataset Z
author: Johannes Ranke
date: "`r Sys.Date()`"
output:
html_document:
toc: true
toc_float: true
code_folding: show
fig_retina: null
bibliography: references.bib
vignette: >
%\VignetteEngine{knitr::rmarkdown}
%\VignetteIndexEntry{Example evaluation of FOCUS dataset Z}
%\VignetteEncoding{UTF-8}
---
[Wissenschaftlicher Berater, Kronacher Str. 12, 79639 Grenzach-Wyhlen, Germany](http://www.jrwb.de)<br />
[Privatdozent at the University of Bremen](http://chem.uft.uni-bremen.de/ranke)
```{r, include = FALSE}
require(knitr)
opts_chunk$set(engine='R', tidy = FALSE)
```
# The data
The following code defines the example dataset from Appendix 7 to the FOCUS kinetics
report [@FOCUSkinetics2014, p. 354].
```{r, echo = TRUE, fig = TRUE, fig.width = 8, fig.height = 7}
library(mkin, quietly = TRUE)
LOD = 0.5
FOCUS_2006_Z = data.frame(
t = c(0, 0.04, 0.125, 0.29, 0.54, 1, 2, 3, 4, 7, 10, 14, 21,
42, 61, 96, 124),
Z0 = c(100, 81.7, 70.4, 51.1, 41.2, 6.6, 4.6, 3.9, 4.6, 4.3, 6.8,
2.9, 3.5, 5.3, 4.4, 1.2, 0.7),
Z1 = c(0, 18.3, 29.6, 46.3, 55.1, 65.7, 39.1, 36, 15.3, 5.6, 1.1,
1.6, 0.6, 0.5 * LOD, NA, NA, NA),
Z2 = c(0, NA, 0.5 * LOD, 2.6, 3.8, 15.3, 37.2, 31.7, 35.6, 14.5,
0.8, 2.1, 1.9, 0.5 * LOD, NA, NA, NA),
Z3 = c(0, NA, NA, NA, NA, 0.5 * LOD, 9.2, 13.1, 22.3, 28.4, 32.5,
25.2, 17.2, 4.8, 4.5, 2.8, 4.4))
FOCUS_2006_Z_mkin <- mkin_wide_to_long(FOCUS_2006_Z)
```
# Parent and one metabolite
The next step is to set up the models used for the kinetic analysis. As the
simultaneous fit of parent and the first metabolite is usually straightforward,
Step 1 (SFO for parent only) is skipped here. We start with the model 2a,
with formation and decline of metabolite Z1 and the pathway from parent
directly to sink included (default in mkin).
```{r FOCUS_2006_Z_fits_1, echo=TRUE, fig.height=6}
Z.2a <- mkinmod(Z0 = mkinsub("SFO", "Z1"),
Z1 = mkinsub("SFO"))
m.Z.2a <- mkinfit(Z.2a, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.2a)
summary(m.Z.2a, data = FALSE)$bpar
```
As obvious from the parameter summary (the \texttt{bpar} component of the
summary), the kinetic rate constant from parent compound Z to sink
is negligible. Accordingly, the exact magnitude of the fitted parameter
\texttt{log k\_Z0\_sink} is ill-defined and the covariance matrix is not
returned (not shown, would be visible in the complete summary).
This suggests, in agreement with the analysis in the FOCUS kinetics report, to
simplify the model by removing the pathway to sink.
A similar result can be obtained when formation fractions are used in the model
formulation:
```{r FOCUS_2006_Z_fits_2, echo=TRUE, fig.height=6}
Z.2a.ff <- mkinmod(Z0 = mkinsub("SFO", "Z1"),
Z1 = mkinsub("SFO"),
use_of_ff = "max")
m.Z.2a.ff <- mkinfit(Z.2a.ff, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.2a.ff)
summary(m.Z.2a.ff, data = FALSE)$bpar
```
Here, the ilr transformed formation fraction fitted in the model takes a very
large value, and the backtransformed formation fraction from parent Z to Z1 is
practically unity. Again, the covariance matrix is not returned as the model is
overparameterised.
The simplified model is obtained by setting the list component \texttt{sink} to
\texttt{FALSE}.\footnote{If the model formulation without formation fractions
is used, the same effect can be obtained by fixing the parameter \texttt{k\_Z\_sink}
to a value of zero.}
In the following, we use the parameterisation with formation fractions in order
to be able to compare with the results in the FOCUS guidance, and as it
makes it easier to use parameters obtained in a previous fit when adding a further
metabolite.
```{r FOCUS_2006_Z_fits_3, echo=TRUE, fig.height=6}
Z.3 <- mkinmod(Z0 = mkinsub("SFO", "Z1", sink = FALSE),
Z1 = mkinsub("SFO"), use_of_ff = "max")
m.Z.3 <- mkinfit(Z.3, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.3)
summary(m.Z.3, data = FALSE)$bpar
```
As there is only one transformation product for Z0 and no pathway
to sink, the formation fraction is internally fixed to unity.
# Metabolites Z2 and Z3
As suggested in the FOCUS report, the pathway to sink was removed for metabolite Z1 as
well in the next step. While this step appears questionable on the basis of the above results, it
is followed here for the purpose of comparison. Also, in the FOCUS report, it is
assumed that there is additional empirical evidence that Z1 quickly and exclusively
hydrolyses to Z2.
```{r FOCUS_2006_Z_fits_5, echo=TRUE, fig.height=7}
Z.5 <- mkinmod(Z0 = mkinsub("SFO", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO"), use_of_ff = "max")
m.Z.5 <- mkinfit(Z.5, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.5)
```
Finally, metabolite Z3 is added to the model. We use the optimised
differential equation parameter values from the previous fit in order to
accelerate the optimization.
```{r FOCUS_2006_Z_fits_6, echo=TRUE, fig.height=8}
Z.FOCUS <- mkinmod(Z0 = mkinsub("SFO", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO", "Z3"),
Z3 = mkinsub("SFO"),
use_of_ff = "max")
m.Z.FOCUS <- mkinfit(Z.FOCUS, FOCUS_2006_Z_mkin,
parms.ini = m.Z.5$bparms.ode,
quiet = TRUE)
plot_sep(m.Z.FOCUS)
summary(m.Z.FOCUS, data = FALSE)$bpar
endpoints(m.Z.FOCUS)
```
This fit corresponds to the final result chosen in Appendix 7 of the FOCUS
report. Confidence intervals returned by mkin are based on internally
transformed parameters, however.
# Using the SFORB model
As the FOCUS report states, there is a certain tailing of the time course of metabolite
Z3. Also, the time course of the parent compound is not fitted very well using the
SFO model, as residues at a certain low level remain.
Therefore, an additional model is offered here, using the single first-order
reversible binding (SFORB) model for metabolite Z3. As expected, the $\chi^2$
error level is lower for metabolite Z3 using this model and the graphical
fit for Z3 is improved. However, the covariance matrix is not returned.
```{r FOCUS_2006_Z_fits_7, echo=TRUE, fig.height=8}
Z.mkin.1 <- mkinmod(Z0 = mkinsub("SFO", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO", "Z3"),
Z3 = mkinsub("SFORB"))
m.Z.mkin.1 <- mkinfit(Z.mkin.1, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.mkin.1)
summary(m.Z.mkin.1, data = FALSE)$cov.unscaled
```
Therefore, a further stepwise model building is performed starting from the
stage of parent and two metabolites, starting from the assumption that the model
fit for the parent compound can be improved by using the SFORB model.
```{r FOCUS_2006_Z_fits_9, echo=TRUE, fig.height=8}
Z.mkin.3 <- mkinmod(Z0 = mkinsub("SFORB", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO"))
m.Z.mkin.3 <- mkinfit(Z.mkin.3, FOCUS_2006_Z_mkin, quiet = TRUE)
plot_sep(m.Z.mkin.3)
```
This results in a much better representation of the behaviour of the parent
compound Z0.
Finally, Z3 is added as well. These models appear overparameterised (no
covariance matrix returned) if the sink for Z1 is left in the models.
```{r FOCUS_2006_Z_fits_10, echo=TRUE, fig.height=8}
Z.mkin.4 <- mkinmod(Z0 = mkinsub("SFORB", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO", "Z3"),
Z3 = mkinsub("SFO"))
m.Z.mkin.4 <- mkinfit(Z.mkin.4, FOCUS_2006_Z_mkin,
parms.ini = m.Z.mkin.3$bparms.ode,
quiet = TRUE)
plot_sep(m.Z.mkin.4)
```
The error level of the fit, but especially of metabolite Z3, can be improved if
the SFORB model is chosen for this metabolite, as this model is capable of
representing the tailing of the metabolite decline phase.
```{r FOCUS_2006_Z_fits_11, echo=TRUE, fig.height=8}
Z.mkin.5 <- mkinmod(Z0 = mkinsub("SFORB", "Z1", sink = FALSE),
Z1 = mkinsub("SFO", "Z2", sink = FALSE),
Z2 = mkinsub("SFO", "Z3"),
Z3 = mkinsub("SFORB"))
m.Z.mkin.5 <- mkinfit(Z.mkin.5, FOCUS_2006_Z_mkin,
parms.ini = m.Z.mkin.4$bparms.ode[1:4],
quiet = TRUE)
plot_sep(m.Z.mkin.5)
```
The summary view of the backtransformed parameters shows that we get no
confidence intervals due to overparameterisation. As the optimized
\texttt{k\_Z3\_bound\_free} is excessively small, it seems reasonable to fix it to
zero.
```{r FOCUS_2006_Z_fits_11a, echo=TRUE}
m.Z.mkin.5a <- mkinfit(Z.mkin.5, FOCUS_2006_Z_mkin,
parms.ini = c(m.Z.mkin.5$bparms.ode[1:7],
k_Z3_bound_free = 0),
fixed_parms = "k_Z3_bound_free",
quiet = TRUE)
plot_sep(m.Z.mkin.5a)
```
As expected, the residual plots for Z0 and Z3 are more random than in the case of the
all SFO model for which they were shown above. In conclusion, the model
\texttt{Z.mkin.5a} is proposed as the best-fit model for the dataset from
Appendix 7 of the FOCUS report.
A graphical representation of the confidence intervals can finally be obtained.
```{r FOCUS_2006_Z_fits_11b, echo=TRUE}
mkinparplot(m.Z.mkin.5a)
```
The endpoints obtained with this model are
```{r FOCUS_2006_Z_fits_11b_endpoints, echo=TRUE}
endpoints(m.Z.mkin.5a)
```
It is clear the degradation rate of Z3 towards the end of the experiment
is very low as DT50\_Z3\_b2 (the second Eigenvalue of the system of two differential
equations representing the SFORB system for Z3, corresponding to the slower rate
constant of the DFOP model) is reported to be infinity. However, this appears
to be a feature of the data.
# References
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|
