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This vignette shows how to generate a simulated data set and analyze it using the model and estimation algorithm described in “Regression with Interval-Censored Covariates: Application to Cross-Sectional Incidence Estimation” by Morrison, Laeyendecker, and Brookmeyer (2021) in Biometrics: https://onlinelibrary.wiley.com/doi/10.1111/biom.13472.
First, we simulate some data:
set.seed(1)
library(rwicc)
= c(0.986, -3.88)
theta_true = 1
hazard_alpha = 0.5
hazard_beta = simulate_interval_censoring(
sim_data "theta" = theta_true,
"study_cohort_size" = 4500,
"preconversion_interval_length" = 365,
"hazard_alpha" = hazard_alpha,
"hazard_beta" = hazard_beta)
# extract the participant-level and observation-level simulated data:
= sim_data$pt_data
sim_participant_data = sim_data$obs_data
sim_obs_data rm(sim_data)
Here’s a look at the first few rows of participant-level data:
library(pander)
pander(head(sim_participant_data))
ID | E | L | R |
---|---|---|---|
1 | 2001-06-16 | 2001-06-16 | 2002-06-17 |
2 | 2001-05-09 | 2001-05-09 | 2002-05-06 |
3 | 2001-10-26 | 2001-10-26 | 2002-10-30 |
4 | 2001-09-27 | 2001-09-27 | 2002-09-25 |
5 | 2001-07-06 | 2001-07-06 | 2002-06-29 |
6 | 2001-11-03 | 2001-11-03 | 2002-11-02 |
E
is the individual’s enrollment dateL
is the date of the last HIV-negative testR
is the date of the first HIV-positive testNext, let’s look at the first few rows of observation-level (longitudinal) data:
pander(head(sim_obs_data))
ID | O | Y |
---|---|---|
1 | 2002-06-17 | 1 |
1 | 2002-07-15 | 0 |
1 | 2002-08-12 | 1 |
1 | 2002-09-09 | 0 |
1 | 2002-12-02 | 0 |
1 | 2003-02-24 | 0 |
O
is the observation dateY
is the MAA classification (1 = “recent infection”, 0 = “long-term infection”)The two tables are linked by the variable ID
.
Now, we will apply our proposed analysis (this takes a couple of minutes; use argument verbose = TRUE
to print progress messages):
= fit_joint_model(
EM_algorithm_outputs obs_level_data = sim_obs_data,
participant_level_data = sim_participant_data,
bin_width = 7,
verbose = FALSE)
The output of fit_joint_model()
is a list with several components:
names(EM_algorithm_outputs)
#> [1] "Theta" "Mu" "Omega"
#> [4] "converged" "iterations" "convergence_metrics"
Theta
is the vector of estimated logistic regression coefficients for \(P(Y|T)\) (intercept and slope):
pander(EM_algorithm_outputs$Theta)
(Intercept) | T |
---|---|
1.019 | -3.953 |
Mu
is the corresponding \(\hat{\mu}\) estimate:
= EM_algorithm_outputs$Mu
mu_est_EM print(mu_est_EM)
#> [1] 122.5193
converged
indicates whether the algorithm reached its convergence criterion (= 1 if converged, = 0 if not).
$converged
EM_algorithm_outputs#> [1] 1
iterations
is the number of EM iterations that the algorithm performed:
$iterations
EM_algorithm_outputs#> [1] 112
convergence_metrics
gives the values of all four metrics that we might use to evaluate convergence:
diff logL
: change in log-likelihood between iterationsdiff mu
: change in \(\hat{\mu}\)max abs diff coefs
: \(\max_{j\in 0:1} \{|\hat{\theta}_j^{(k)} - \hat{\theta}_j^{(k-1)}|\}\)max abs rel diff coefs
: \(\max_{j\in 0:1} \{|(\hat{\theta}_j^{(k)} - \hat{\theta}_j^{(k-1)})/\hat{\theta}_j^{(k-1)}|\}\)By default, the convergence criterion is: diff logL
< 0.1 and max abs rel diff coefs
< 0.0001.
pander(EM_algorithm_outputs$convergence_metrics)
diff logL | diff mu | max abs diff coefs | max abs rel diff coefs |
---|---|---|---|
0.008769 | 0.008171 | 0.0001012 | 9.931e-05 |
Next, we perform an alternative analysis using midpoint imputation:
= fit_midpoint_model(
theta_est_midpoint obs_level_data = sim_obs_data,
participant_level_data = sim_participant_data
)
pander(theta_est_midpoint)
(Intercept) | T_midpoint |
---|---|
0.7572 | -3.662 |
Here, we perform an alternative analysis using uniform imputation:
# uniform imputation:
= fit_uniform_model(
theta_est_uniform obs_level_data = sim_obs_data,
participant_level_data = sim_participant_data
)
pander(theta_est_uniform)
theta0 | theta1 |
---|---|
-0.549 | -2.037 |
Now, let’s graph the results. First, let’s plot the true and estimated CDFs for the distribution of seroconversion date, for individuals who enroll on the first calendar day of the cohort study:
= plot_CDF(
plot1 true_hazard_alpha = hazard_alpha,
true_hazard_beta = hazard_beta,
omega.hat = EM_algorithm_outputs$Omega)
print(plot1)
We can see that our joint modeling approach hasn’t estimated this distribution very accurately for this particular simulated dataset. Nevertheless, the next graph will show us that the joint model very accurately estimates the true distribution \(P(Y|T)\) and the true value of \(\mu\):
= plot_phi_curves(
plot2 theta_true = theta_true,
theta.hat_uniform = theta_est_uniform,
theta.hat_midpoint = theta_est_midpoint,
theta.hat_joint = EM_algorithm_outputs$Theta)
print(plot2)
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They may not be fully stable and should be used with caution. We make no claims about them.