Mixed models for repeated measures (MMRM) are a popular choice for
analyzing longitudinal continuous outcomes in randomized clinical trials
and beyond; see Cnaan, Laird and Slasor
(1997)
for a tutorial and Mallinckrodt, Lane and Schnell
(2008) for a review. This
package implements MMRM based on the marginal linear model without
random effects using Template Model Builder (TMB
) which enables fast
and robust model fitting. Users can specify a variety of covariance
matrices, weight observations, fit models with restricted or standard
maximum likelihood inference, perform hypothesis testing with
Satterthwaite or Kenward-Roger adjustment, and extract least square
means estimates by using emmeans
.
Scope:
Main Features:
emmeans
packageC++
backend:C++
and automatic differentiation to
obtain precise gradient information for model fitting.mmrm
.mmrm
fit and generate tabulation
and plots of least square means per visit and treatment arm,
tabulation of model diagnostics, diagnostic graphs, and other
standard model outputs.You can install the current release version from CRAN with:
install.packages("mmrm")
You can install the current development version from R-Universe with:
install.packages(
"mmrm",
repos = c("https://openpharma.r-universe.dev", "https://cloud.r-project.org")
)
This is preferred, because for Windows and MacOS systems you can install pre-compiled binary versions of the packages, avoiding the need for compilation.
Alternatively, you can install the current development version from GitHub with:
if (!require("remotes")) {
install.packages("remotes")
}
remotes::install_github("openpharma/mmrm")
Note that this installation from source can take a substantial amount of
time, because compilation of the C++
sources is required.
See also the introductory vignette or get started by trying out the example:
library(mmrm)
fit <- mmrm(
formula = FEV1 ~ RACE + SEX + ARMCD * AVISIT + us(AVISIT | USUBJID),
data = fev_data
)
The code specifies an MMRM with the given covariates and an unstructured
covariance matrix for the timepoints (also called visits in the clinical
trial context, here given by AVISIT
) within the subjects (here
USUBJID
). While by default this uses restricted maximum likelihood
(REML), it is also possible to use ML, see ?mmrm
.
Printing the object will show you output which should be familiar to
anyone who has used any popular modeling functions such as
stats::lm()
, stats::glm()
, glmmTMB::glmmTMB()
, and
lme4::nlmer()
. From this print out we see the function call, the data
used, the covariance structure with number of variance parameters, as
well as the likelihood method, and model deviance achieved. Additionally
the user is provided a printout of the estimated coefficients and the
model convergence information:
fit
#> mmrm fit
#>
#> Formula: FEV1 ~ RACE + SEX + ARMCD * AVISIT + us(AVISIT | USUBJID)
#> Data: fev_data (used 537 observations from 197 subjects with maximum 4
#> timepoints)
#> Covariance: unstructured (10 variance parameters)
#> Inference: REML
#> Deviance: 3386.45
#>
#> Coefficients:
#> (Intercept) RACEBlack or African American
#> 30.77747548 1.53049977
#> RACEWhite SEXFemale
#> 5.64356535 0.32606192
#> ARMCDTRT AVISITVIS2
#> 3.77423004 4.83958845
#> AVISITVIS3 AVISITVIS4
#> 10.34211288 15.05389826
#> ARMCDTRT:AVISITVIS2 ARMCDTRT:AVISITVIS3
#> -0.04192625 -0.69368537
#> ARMCDTRT:AVISITVIS4
#> 0.62422703
#>
#> Model Inference Optimization:
#> Converged with code 0 and message: convergence: rel_reduction_of_f <= factr*epsmch
The summary()
method then provides the coefficients table with
Satterthwaite degrees of freedom as well as the covariance matrix
estimate:
summary(fit)
#> mmrm fit
#>
#> Formula: FEV1 ~ RACE + SEX + ARMCD * AVISIT + us(AVISIT | USUBJID)
#> Data: fev_data (used 537 observations from 197 subjects with maximum 4
#> timepoints)
#> Covariance: unstructured (10 variance parameters)
#> Method: Satterthwaite
#> Vcov Method: Asymptotic
#> Inference: REML
#>
#> Model selection criteria:
#> AIC BIC logLik deviance
#> 3406.4 3439.3 -1693.2 3386.4
#>
#> Coefficients:
#> Estimate Std. Error df t value Pr(>|t|)
#> (Intercept) 30.77748 0.88656 218.80000 34.715 < 2e-16
#> RACEBlack or African American 1.53050 0.62448 168.67000 2.451 0.015272
#> RACEWhite 5.64357 0.66561 157.14000 8.479 1.56e-14
#> SEXFemale 0.32606 0.53195 166.13000 0.613 0.540744
#> ARMCDTRT 3.77423 1.07415 145.55000 3.514 0.000589
#> AVISITVIS2 4.83959 0.80172 143.88000 6.037 1.27e-08
#> AVISITVIS3 10.34211 0.82269 155.56000 12.571 < 2e-16
#> AVISITVIS4 15.05390 1.31281 138.47000 11.467 < 2e-16
#> ARMCDTRT:AVISITVIS2 -0.04193 1.12932 138.56000 -0.037 0.970439
#> ARMCDTRT:AVISITVIS3 -0.69369 1.18765 158.17000 -0.584 0.559996
#> ARMCDTRT:AVISITVIS4 0.62423 1.85085 129.72000 0.337 0.736463
#>
#> (Intercept) ***
#> RACEBlack or African American *
#> RACEWhite ***
#> SEXFemale
#> ARMCDTRT ***
#> AVISITVIS2 ***
#> AVISITVIS3 ***
#> AVISITVIS4 ***
#> ARMCDTRT:AVISITVIS2
#> ARMCDTRT:AVISITVIS3
#> ARMCDTRT:AVISITVIS4
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Covariance estimate:
#> VIS1 VIS2 VIS3 VIS4
#> VIS1 40.5537 14.3960 4.9747 13.3867
#> VIS2 14.3960 26.5715 2.7855 7.4745
#> VIS3 4.9747 2.7855 14.8979 0.9082
#> VIS4 13.3867 7.4745 0.9082 95.5568
mmrm
To cite mmrm
please see
here.
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