I have a lme object, constructed from some repeated measures nutrient intake data (two 24-hour intake periods per RespondentID):
Male.lme2 <- lmer(BoxCoxXY ~ -1 + AgeFactor + IntakeDay + (1|RespondentID),
data = Male.Data,
weights = SampleWeight)
and I can successfully retrieve the random effects by RespondentID
using ranef(Male.lme1)
. I would also like to collect the result of the fixed effects by RespondentID
. coef(Male.lme1)
does not provide exactly what I need, as I show below.
> summary(Male.lme1)
Linear mixed model fit by REML
Formula: BoxCoxXY ~ AgeFactor + IntakeDay + (1 | RespondentID)
Data: Male.Data
AIC BIC logLik deviance REMLdev
9994 10039 -4990 9952 9980
Random effects:
Groups Name Variance Std.Dev.
RespondentID (Intercept) 0.19408 0.44055
Residual 0.37491 0.61230
Number of obs: 4498, groups: RespondentID, 2249
Fixed effects:
Estimate Std. Error t value
(Intercept) 13.98016 0.03405 410.6
AgeFactor4to8 0.50572 0.04084 12.4
AgeFactor9to13 0.94329 0.04159 22.7
AgeFactor14to18 1.30654 0.04312 30.3
IntakeDayDay2Intake -0.13871 0.01809 -7.7
Correlation of Fixed Effects:
(Intr) AgFc48 AgF913 AF1418
AgeFactr4t8 -0.775
AgeFctr9t13 -0.761 0.634
AgFctr14t18 -0.734 0.612 0.601
IntkDyDy2In -0.266 0.000 0.000 0.000
I have appended the fitted results to my data, head(Male.Data)
shows
NutrientID RespondentID Gender Age SampleWeight IntakeDay IntakeAmt AgeFactor BoxCoxXY lmefits
2 267 100020 1 12 0.4952835 Day1Intake 12145.852 9to13 15.61196 15.22633
7 267 100419 1 14 0.3632839 Day1Intake 9591.953 14to18 15.01444 15.31373
8 267 100459 1 11 0.4952835 Day1Intake 7838.713 9to13 14.51458 15.00062
12 267 101138 1 15 1.3258785 Day1Intake 11113.266 14to18 15.38541 15.75337
14 267 101214 1 6 2.1198688 Day1Intake 7150.133 4to8 14.29022 14.32658
18 267 101389 1 5 2.1198688 Day1Intake 5091.528 4to8 13.47928 14.58117
The first couple of lines from coef(Male.lme1)
are:
$RespondentID
(Intercept) AgeFactor4to8 AgeFactor9to13 AgeFactor14to18 IntakeDayDay2Intake
100020 14.28304 0.5057221 0.9432941 1.306542 -0.1387098
100419 14.00719 0.5057221 0.9432941 1.306542 -0.1387098
100459 14.05732 0.5057221 0.9432941 1.306542 -0.1387098
101138 14.44682 0.5057221 0.9432941 1.306542 -0.1387098
101214 13.82086 0.5057221 0.9432941 1.306542 -0.1387098
101389 14.07545 0.5057221 0.9432941 1.306542 -0.1387098
To demonstrate how the coef
results relate to the fitted estimates in Male.Data (which were grabbed using Male.Data$lmefits <- fitted(Male.lme1)
, for the first RespondentID, who has the AgeFactor level 9-13:
- the fitted value is 15.22633
, which equals - from the coeffs - (Intercept) + (AgeFactor9-13) = 14.28304 + 0.9432941
Is there a clever command for me to use that will do want I want automatically, which is to extract the fixed effect estimate for each subject, or am I faced with a series of if
statements trying to apply the correct AgeFactor level to each subject to get the correct fixed effect estimate, after deducting the random effect contribution off the Intercept?
Update, apologies, was trying to cut down on the output I was providing and forgot about str(). Output is:
>str(Male.Data)
'data.frame': 4498 obs. of 11 variables:
$ NutrientID : int 267 267 267 267 267 267 267 267 267 267 ...
$ RespondentID: Factor w/ 2249 levels "100020","100419",..: 1 2 3 4 5 6 7 8 9 10 ...
$ Gender : int 1 1 1 1 1 1 1 1 1 1 ...
$ Age : int 12 14 11 15 6 5 10 2 2 9 ...
$ BodyWeight : num 51.6 46.3 46.1 63.2 28.4 18 38.2 14.4 14.6 32.1 ...
$ SampleWeight: num 0.495 0.363 0.495 1.326 2.12 ...
$ IntakeDay : Factor w/ 2 levels "Day1Intake","Day2Intake": 1 1 1 1 1 1 1 1 1 1 ...
$ IntakeAmt : num 12146 9592 7839 11113 7150 ...
$ AgeFactor : Factor w/ 4 levels "1to3","4to8",..: 3 4 3 4 2 2 3 1 1 3 ...
$ BoxCoxXY : num 15.6 15 14.5 15.4 14.3 ...
$ lmefits : num 15.2 15.3 15 15.8 14.3 ...
The BodyWeight and Gender aren't being used (this is the males data, so all the Gender values are the same) and the NutrientID is similarly fixed for the data.
I have been doing horrible ifelse statements sinced I posted, so will try out your suggestion immediately. :)
Update2: this works perfectly with my current data and should be future-proof for new data, thanks to DWin for the extra help in the comment for this. :)
AgeLevels <- length(unique(Male.Data$AgeFactor))
Temp <- as.data.frame(fixef(Male.lme1)['(Intercept)'] +
c(0,fixef(Male.lme1)[2:AgeLevels])[
match(Male.Data$AgeFactor, c("1to3", "4to8", "9to13","14to18", "19to30","31to50","51to70","71Plus") )] +
c(0,fixef(Male.lme1)[(AgeLevels+1)])[
match(Male.Data$IntakeDay, c("Day1Intake","Day2Intake") )])
names(Temp) <- c("FxdEffct")
If we divide the covariance by the product of the standard errors, we get the correlation of fixed effects reported in the lmer() summary output. In fact this is the formula for the familiar correlation coefficient. Base R includes the convenient cov2cor() function to automatically make these calculations for us.
A noticeable difference between the lme and lmer outputs is that p-values are provided by lme but not lmer.
The most important practical difference between the two is this: Random effects are estimated with partial pooling, while fixed effects are not. Partial pooling means that, if you have few data points in a group, the group's effect estimate will be based partially on the more abundant data from other groups.
Below is how I've always found it easiest to extract the individuals' fixed effects and random effects components in the lme4-package. It actually extracts the corresponding fit to each observation. Assuming we have a mixed-effects model of form:
y = Xb + Zu + e
where Xb are the fixed effects and Zu are the random effects, we can extract the components (using lme4's sleepstudy as an example):
library(lme4)
fm1 <- lmer(Reaction ~ Days + (Days|Subject), sleepstudy)
# Xb
fix <- getME(fm1,'X') %*% fixef(fm1)
# Zu
ran <- t(as.matrix(getME(fm1,'Zt'))) %*% unlist(ranef(fm1))
# Xb + Zu
fixran <- fix + ran
I know that this works as a generalized approach to extracting components from linear mixed-effects models. For non-linear models, the model matrix X contains repeats and you may have to tailor the above code a bit. Here's some validation output as well as a visualization using lattice:
> head(cbind(fix, ran, fixran, fitted(fm1)))
[,1] [,2] [,3] [,4]
[1,] 251.4051 2.257187 253.6623 253.6623
[2,] 261.8724 11.456439 273.3288 273.3288
[3,] 272.3397 20.655691 292.9954 292.9954
[4,] 282.8070 29.854944 312.6619 312.6619
[5,] 293.2742 39.054196 332.3284 332.3284
[6,] 303.7415 48.253449 351.9950 351.9950
# Xb + Zu
> all(round((fixran),6) == round(fitted(fm1),6))
[1] TRUE
# e = y - (Xb + Zu)
> all(round(resid(fm1),6) == round(sleepstudy[,"Reaction"]-(fixran),6))
[1] TRUE
nobs <- 10 # 10 observations per subject
legend = list(text=list(c("y", "Xb + Zu", "Xb")), lines = list(col=c("blue", "red", "black"), pch=c(1,1,1), lwd=c(1,1,1), type=c("b","b","b")))
require(lattice)
xyplot(
Reaction ~ Days | Subject, data = sleepstudy,
panel = function(x, y, ...){
panel.points(x, y, type='b', col='blue')
panel.points(x, fix[(1+nobs*(panel.number()-1)):(nobs*(panel.number()))], type='b', col='black')
panel.points(x, fixran[(1+nobs*(panel.number()-1)):(nobs*(panel.number()))], type='b', col='red')
},
key = legend
)
It is going to be something like this (although you really should have given us the results of str(Male.Data) because model output does not tell us the factor levels for the baseline values:)
#First look at the coefficients
fixef(Male.lme2)
#Then do the calculations
fixef(Male.lme2)[`(Intercept)`] +
c(0,fixef(Male.lme2)[2:4])[
match(Male.Data$AgeFactor, c("1to3", "4to8", "9to13","14to18") )] +
c(0,fixef(Male.lme2)[5])[
match(Male.Data$IntakeDay, c("Day1Intake","Day2Intake") )]
You are basically running the original data through a match
function to pick the correct coefficient(s) to add to the intercept ... which will be 0 if the data is the factor's base level (whose spelling I am guessing at.)
EDIT: I just noticed that you put a "-1" in the formula so perhaps all of your AgeFactor terms are listed in the output and you can tale out the 0 in the coefficient vector and the invented AgeFactor level in the match table vector.
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