Factor Analysis in Epidemiology

This is a short (15′!) presentation given for the Canadian Veterinary Epidemiology Club (CVEC) on February 26, 2016, about new epi tools.

What is Factor Analysis?

Factor analysis is a group of statistical methods used to identify the structure of data with the help of latent (not observed) variables. These latent variables, called factors, are identified by looking at clusters of correlated variables (the correlation between 2 variables proceed from the similarity of their relation with the latent variables).

In brief, we try to explain the correlation (covariance) between a large set of observed variables according to a smaller set of unobserved latent variables, a.k.a the factors. Therefore a factor is a cluster of related observed variables, representing the underlying dimension of a construct that is as distinct as possible from the other factors.

There are two main types of factor analysis: exploratory (EFA) and confirmatory (CFA).

Exploratory Factor Analysis (EFA)

It describes a group of variables by a linear combination of the underlying common factors.

Each observed variable is potentially a measure of every factor, and the goal is to determine the relationships between observed variables and factors that are the strongest. We don’t know a priori how many factors are needed to explain the relation among variables.

Confirmatory Factor Analysis (CFA)

We try to verify the ability of our theoretical model to explain the common variance between several variables with latent variables that we determined a priori. We have prior knowledge about the underlying structure of the construct under investigation. See structural Equation Modelling (SEM).

Why would you want to use it?

  • When you are more interested in identifying the structure underlying a particular phenomenon than testing a specific hypothesis.
  • You want to reduce the number of variables to a few factors explaining a large proportion of the original variables variance (Data reduction).
  • You want to identify groups of highly correlated variables, choose one among them to be used in subsequent analyses.

What are the 2 main methods?

Principal Component Analysis (PCA)

“The central idea of principal component analysis (PCA) is to reduce the dimensionality of a data set consisting of a large number of interrelated variables, while retaining as much as possible of the variation present in the data set” (Jolliffe 2002).

Objective: data reduction.

Factor Analysis

In factor analysis the goal is to explain the covariance among variables (the common variance between one variable and at least one another, a factor).

Objective: identifying data structure or causal modelling.

Assumptions

  • Within a set of observed variables there is a set of underlying factors (latent variables) that can explain the relationships among variables. The observed variables are dependent upon these latent variables but are also subject to random variation,
  • No outliers,
  • From Pearson correlation coefficient:
    • Large sample size (15-20 observations per variables),
    • Continuous distribution and sufficient variation within the variables,
    • Linear relationship among the correlated variables.

Examples

PCA for data reduction

See Prediction of bulk tank somatic cell count violations based on monthly individual cow somatic cell count data.

In this study, we started with ~30 variables that were potentially highly correlated. We had first to identify clusters of correlated variables to reduce the likelihood of overfitting the model. PCA was used to discard redundant variables.

BTSCC-pca12

 

We further used Lasso (least absolute shrinkage and selection operator) regression on the clusters identified by PCA.

Multiple Factor Analysis (MFA)

See Herd-Level Management Factors and Culling Rates in Québec Dairy Herds.

MFA is dedicated to datasets where variables are structured into groups, studying several set of variables simultaneously. If you have a set of variables, some may be related together and you might want to study the relationships between the groups of variables, not only the variables.

In the above study, we wanted to see if we could identify groups of herds according to certain factors. Cow-level data were aggregated to provide herd-level information. These aggregated data formed groups of variables related to management, reproduction, milk production, and health.

master-mfavar

Unfortunately there were no relationships between herds. However you can keep going your analysis and run a PCA on specific groups of variables.

master-aabp-pcarepro-1

Factor analysis

Here’s an example, on Q-methodology.

Softwares

Conclusion

Factor analyses are additional tools that allow epidemiologists to carry out a data-driven exploration of their dataset, addressing the impact of exposures and their context.

Ressources

Pourquoi s’inscrire à l’atelier Data Carpentry lors du prochain ISVEE14?

L’échéance approche à grands pas pour s’inscrire à un atelier lors du prochain ISVEE14 qui aura lieu à Merida, Mexique (31 juillet). Il y a un choix de plusieurs ateliers, tous aussi intéressants les uns que les autres, mais visant souvent un public qui a déjà une certaine expérience en épidémiologie et analyse de données. Cependant beaucoup de chercheurs ne sont pas familiers aux meilleures pratiques et outils requis dans le cycle de vie des données, de la gestion de ces données, la saisie et la création de métadonnées, l’analyse des données, à leur partage et leur ré-utilisation.

Data Carpentry vise à apprendre ces compétences qui permettent aux chercheurs d’être plus efficaces et productifs. Un atelier de 3 jours est proposé après la conférence ISVEE (8, 9 et 10 novembre).

Cet atelier est conçu pour les personnes avec peu ou pas d’expérience informatique (càd public novice), procurant les concepts de base, les compétences et outils pour travailler de manière plus efficace avec des données. Notre méthode d’enseignement est pratique, les participants doivent donc apporter leur propre ordinateur portable. Nous fournirons à l’avance les instructions nécessaires pour installer les logiciels requis et de l’aide sera disponible sur place. Aucun pré-requis n’est demandé et les outils utilisés ne requièrent pas de connaissances préalables. Aucune connaissance particulière en statistiques n’est demandée. Les chercheurs à différents niveaux dans leur carrière sont ciblés (étudiants au doctorat, chercheurs post-doctoraux, chercheurs associés, dans l’industrie ou au gouvernement, …). Le programme comprend:

  • comment utiliser des tableurs (tels que Excel) plus efficacement, et leurs limites,
  • passer de ces tableurs à des outils plus puissants pour manipuler et analyser les données, avec le logiciel statistique R,
  • se servir de bases de données, incluant les gérer et interroger avec SQL,
  • utiliser Git, un système de contrôle de version de pointe qui permet de suivre qui fait des changements à quoi et quand,
  • établir un flux de travail et automatiser les tâches répétitives, en particulier en ayant recours à la ligne de commande shell et aux scripts shell.

Les instructeurs ont appris beaucoup de ces compétences à leurs dépens et savent la différence qu’elles peuvent apporter à leur productivité et la possibilité de nouvelles ou meilleures recherches qu’elles permettent.

La recherche reproductible est importante et de bonnes pratiques sont essentielles.

On se revoit à Merida!

Plus d’informations à propos de l’atelier Data Carpentry à ISVEE ici.

Plus d’informations à propos de Data Carpentry et Software Carpentry.

Data Carpentry: Workshops to Increase Data Literacy for Researchers

Bias in Observational Studies – Sensitivity Analysis with R package episensr

When it’s time to interpret the study results from your observational study, you have to estimate if the effect measure you obtained is the truth, if it’s due to bias (systematic error, the effect measure’s precision), or if it’s due to chance (random error, the effect measure’s validity) (Rothman and Greenland, 2008, pp115-134). Every study has some random error due to its limited sample size, and is susceptible to systematic errors as well, from selection bias to the presence of (un)known confounders or information bias (measurement error, including misclassification).

Bias analysis, or sensitivity analysis, tries to quantify the direction, magnitude, and uncertainty of the bias affecting an estimate of association (Greenland and Lash, 2008, pp345-380; Lash et al., 2009).

Very often bias is evaluated qualitatively without any quantitative assessment of its magnitude. This might be due to the very few tools available to epidemiologists. Hence this R package, episensr, which is built following the book by Lash et al. I will illustrate its use with 3 studies from this book.

First you have to install and load the package.

install.packages("episensr")
# or get it from Github repo with
# library(devtools)
# install_github("dhaine/episensr")

library(episensr)

Selection Bias

We will use a case-control study by Stang et al. on the relation between mobile phone use and uveal melanoma. The observed odds ratio for the association between regular mobile phone use vs. no mobile phone use with uveal melanoma incidence is 0.71 [95% CI 0.51-0.97]. But there was a substantial difference in participation rates between cases and controls (94% vs 55%, respectively) and so selection bias could have an impact on the association estimate. The 2X2 table for this study is the following:

Regular Use No Use
Cases 136 107
Controls 297 165

We use the function selection as shown below.

selection(matrix(c(136, 107, 297, 165),
                 dimnames = list(c("UM+", "UM-"), c("Mobile+", "Mobile-")),
                 nrow = 2, byrow = TRUE),
          selprob = c(.94, .85, .64, .25))

Observed Data:
---------------------------------------------------
Outcome   : UM+
Comparing : Mobile+ vs. Mobile- 

    Mobile+ Mobile-
UM+     136     107
UM-     297     165

Data Corrected for Selected Proportions:
---------------------------------------------------

     Mobile+  Mobile-
UM+ 144.6809 125.8824
UM- 464.0625 660.0000

                               95% conf. interval
Observed Relative Risk: 0.7984    0.6518   0.9780
   Observed Odds Ratio: 0.7061    0.5144   0.9693

                                          [,1]
Selection Bias Corrected Relative Risk: 1.4838
   Selection Bias Corrected Odds Ratio: 1.6346

                                                [,1]
     Selection probability among cases exposed: 0.94
   Selection probability among cases unexposed: 0.85
  Selection probability among noncases exposed: 0.64
Selection probability among noncases unexposed: 0.25

The 2X2 table is provided as a matrix and selection probabilities given with the argument selprob, a vector with the 4 probabilities (guided by the participation rates in cases and controls) in the following order: among cases exposed, among cases unexposed, among noncases exposed, and among noncases unexposed. The output shows the observed 2X2 table, the same table corrected for the selection proportions, the observed odds ratio (and relative risk) followed by the corrected ones, and the input parameters.

Uncontrolled Confounders

We will use date from a cross-sectional study by Tyndall et al. on the association between male circumcision and the risk of acquiring HIV, which might be confounded by religion. The code to account for unmeasured or unknown confounders is the following, where the 2X2 table is given as a matrix. We choose a risk ratio implementation, provide a vector defining the prevalence of the confounder, religion, among the exposed and the unexposed, and give the risk ratio associating the confounder with the disease.

confounders(matrix(c(105, 85, 527, 93),
                   dimnames = list(c("HIV+", "HIV-"), c("Circ+", "Circ-")),
                   nrow = 2, byrow = TRUE),
            implement = "RR",
            p = c(.8, .05),
            RR.cd = .63)

Observed Data:
--------------
Outcome   : HIV+
Comparing : Circ+ vs. Circ- 

     Circ+ Circ-
HIV+   105    85
HIV-   527    93

Data, Counfounder +:
--------------------

        Circ+ Circ-
HIV+  75.1705 2.728
HIV- 430.4295 6.172

Data, Counfounder -:
--------------------

       Circ+  Circ-
HIV+ 29.8295 82.272
HIV- 96.5705 86.828

Crude and Unmeasured Confounder Specific Measures of Exposure-Outcome Relationship:
-----------------------------------------------------------------------------------

                                    95% conf. interval
        Crude Relative Risk: 0.3479    0.2757    0.439
Relative Risk, Confounder +: 0.4851
Relative Risk, Confounder -: 0.4851 

Exposure-Outcome Relationship Adjusted for Confounder:
------------------------------------------------------

Standardized Morbidity Ratio     SMRrr: 0.4851    RR adjusted using SMR estimate: 0.7173
Mantel-Haenszel                   MHrr: 0.4851     RR adjusted using MH estimate: 0.7173 

Bias Parameters:
----------------

p(Confounder+|Exposure+): 0.8
p(Confounder+|Exposure-): 0.05
  RR(Confounder-Outcome): 0.63

The output gives the crude 2X2 table, the 2X2 tables by levels of the confounder, the crude relative risk and confounder specific measures of association between exposure and outcome, and the relationship adjusted for the unknown confounder, using a standardized morbidity ratio (SMR) or a Mantel-Haenszel (MH) estimate of the risk ratio. Finally, the bias parameters are shown.

Probabilistic Sensitivity Analysis for Exposure Misclassification

We use a study on the effect of smoking during pregnancy on breast cancer risk (Fink and Lash), where we assume nondifferential misclassification of the exposure, smoking, with probability density functions for sensitivities (Se) and specificities (Sp) among cases and noncases equal to uniform distributions with a minimum of 0.7 and a maximum of 0.95 for sensitivities (0.9 and 0.99 respectively for specificities). As usual, the 2X2 table is provided as a matrix. We choose to correct for exposure misclassification with the argument type = exposure. We ask for 10000 replications (default is 1000). The Se and Sp for cases (seca, spca) are given as a list with its first element referring to the type of distribution (choice between uniform, triangular and trapezoidal) and the second element giving the distribution parameters (min and max for uniform distribution). By avoiding to provide information on the noncases (seexp, spexp), we are referring to a nondifferential misclassification.

smoke.nd <- probsens(matrix(c(215, 1449, 668, 4296),
                            dimnames = list(c("BC+", "BC-"), c("Smoke+", "Smoke-")),
                            nrow = 2, byrow = TRUE),
                     type = "exposure",
                     reps = 10000,
                     seca.parms = list("uniform", c(.7, .95)),
                     spca.parms = list("uniform", c(.9, .99)))

Observed Data:
--------------
Outcome   : BC+
Comparing : Smoke+ vs. Smoke- 

    Smoke+ Smoke-
BC+    215   1449
BC-    668   4296

Observed Measures of Exposure-Outcome Relationship:
-----------------------------------------------------------------------------------

                                95% conf. interval
 Observed Relative Risk: 0.9654    0.8524   1.0934
    Observed Odds Ratio: 0.9542    0.8092   1.1252

                                              Median 2.5th percentile
           Relative Risk -- systematic error: 0.9432           0.8816
              Odds Ratio -- systematic error: 0.9254           0.8477
Relative Risk -- systematic and random error: 0.9372           0.8181
   Odds Ratio -- systematic and random error: 0.9178           0.7671
                                              97.5th percentile
           Relative Risk -- systematic error:            0.9612
              Odds Ratio -- systematic error:            0.9488
Relative Risk -- systematic and random error:            1.0662
   Odds Ratio -- systematic and random error:            1.0884

Bias Parameters:
----------------

   Se|Cases: uniform ( 0.7 0.95 )
   Sp|Cases: uniform ( 0.9 0.99 )
Se|No-cases: ( )
Sp|No-cases: ( )

The output gives the 2X2 table, the observed measures of association, the corrected measures of association, and the input bias parameters.

We saved the probsens analysis in a new variable smoke.nd. We can see the element of the object probsens with the function str():

str(smoke.nd)

List of 4
 $ obs.data    : num [1:2, 1:2] 215 668 1449 4296
  ..- attr(*, "dimnames")=List of 2
  .. ..$ : chr [1:2] "BC+" "BC-"
  .. ..$ : chr [1:2] "Smoke+" "Smoke-"
 $ obs.measures: num [1:2, 1:3] 0.965 0.954 0.852 0.809 1.093 ...
  ..- attr(*, "dimnames")=List of 2
  .. ..$ : chr [1:2] " Observed Relative Risk:" "    Observed Odds Ratio:"
  .. ..$ : chr [1:3] "     " "95% conf." "interval"
 $ adj.measures: num [1:4, 1:3] 0.943 0.925 0.937 0.918 0.882 ...
  ..- attr(*, "dimnames")=List of 2
  .. ..$ : chr [1:4] "           Relative Risk -- systematic error:" "              Odds Ratio -- systematic error:" "Relative Risk -- systematic and random error:" "   Odds Ratio -- systematic and random error:"
  .. ..$ : chr [1:3] "Median" "2.5th percentile" "97.5th percentile"
 $ sim.df      :'data.frame':	10000 obs. of  12 variables:
  ..$ seca   : num [1:10000] 0.878 0.75 0.928 0.796 0.841 ...
  ..$ seexp  : num [1:10000] 0.878 0.75 0.928 0.796 0.841 ...
  ..$ spca   : num [1:10000] 0.958 0.948 0.971 0.906 0.969 ...
  ..$ spexp  : num [1:10000] 0.958 0.948 0.971 0.906 0.969 ...
  ..$ A1     : num [1:10000] 173.5 183.1 185.5 82.6 201.6 ...
  ..$ B1     : num [1:10000] 1490 1481 1479 1581 1462 ...
  ..$ C1     : num [1:10000] 550 584 583 284 634 ...
  ..$ D1     : num [1:10000] 4414 4380 4381 4680 4330 ...
  ..$ corr.RR: num [1:10000] 0.951 0.944 0.957 0.891 0.955 ...
  ..$ corr.OR: num [1:10000] 0.935 0.927 0.943 0.86 0.941 ...
  ..$ tot.RR : num [1:10000] 0.917 0.855 0.895 0.882 0.883 ...
  ..$ tot.OR : num [1:10000] 0.892 0.813 0.863 0.848 0.848 ...

smoke.nd is a list of 4 elements where different information on the analysis done are saved. We have smoke.nd$obs.data where we have the observed 2X2 table, smoke.nd$obs.measures (the observed measures of association), smoke.nd$adj.measures (the adjusted measures of association), and smoke.nd$sim.df, a data frame with the simulated variables from each replication, like the Se and Sp, the 4 cells of the adjusted 2X2 table, and the adjusted measures. We can plot the Se prior distribution (not forgetting to discard the draws that led to negative adjustments).

hist(smoke.nd$sim.df[!is.na(smoke.nd$sim.df$corr.RR), ]$seca,
     breaks = seq(0.65, 1, 0.01),
     col = "lightgreen",
     main = NULL,
     xlab = "Sensitivity for Cases")
Histogram of 10000 draws from uniform distribution for Se among cases
Histogram of 10000 draws from uniform distribution for Se among cases

 

Additional functions can be found on the reference manual and more will be added in the coming months.

Veterinary Epidemiologic Research: Modelling Survival Data – Parametric and Frailty Models

Last post on modelling survival data from Veterinary Epidemiologic Research: parametric analyses. The Cox proportional hazards model described in the last post make no assumption about the shape of the baseline hazard, which is an advantage if you have no idea about what that shape might be. With a parametric survival model, the survival time is assumed to follow a known distribution: Weibull, exponential (which is a special case of the Weibull), log-logistic, log-normal, and generalized gamma.

Exponential Model
The exponential model is the simplest, the hazard h_0(t) is constant over time: the rate at which failures are occurring is constant, h(t) = \lambda . We use again the pgtrial dataset:

temp <- tempfile()
download.file(
"http://ic.upei.ca/ver/sites/ic.upei.ca.ver/files/ver2_data_R.zip", temp)
load(unz(temp, "ver2_data_R/pgtrial.rdata"))
unlink(temp)

library(Hmisc)
pgtrial <- upData(pgtrial, labels = c(herd = 'Herd id', cow = 'Cow id',
tx = 'Treatment', lact = 'Lactation number',
thin = 'Body condition', dar = 'Days at risk',
preg = 'Pregnant or censored'),
levels = list(thin = list('normal' = 0, 'thin' = 1),
preg = list('censored' = 0, 'pregnant' = 1)))
pgtrial$herd <- as.factor(pgtrial$herd)

library(survival)
exp.mod <- survreg(Surv(dar, preg == 'pregnant') ~ herd + tx + (lact - 1) +
                   thin, data = pgtrial, dist = "exponential")
summary(exp.mod)

Call:
survreg(formula = Surv(dar, preg == "pregnant") ~ herd + tx + 
    (lact - 1) + thin, data = pgtrial, dist = "exponential")
           Value Std. Error     z         p
herd1     4.3629     0.1827 23.88 4.66e-126
herd2     4.6776     0.1711 27.34 1.41e-164
herd3     4.3253     0.1617 26.75 1.12e-157
tx       -0.2178     0.1255 -1.74  8.26e-02
lact      0.0416     0.0413  1.01  3.14e-01
thinthin  0.1574     0.1383  1.14  2.55e-01

Scale fixed at 1 

Exponential distribution
Loglik(model)= -1459.9   Loglik(intercept only)= -1465.6
	Chisq= 11.42 on 5 degrees of freedom, p= 0.044 
Number of Newton-Raphson Iterations: 5 
n= 319

Interpretation is the same as for a Cox model. Exponentiated coefficients are hazard ratios. R outputs the parameter estimates of the AFT (accelerated failure time) form of the exponential model. If you multiply the estimated coefficients by minus one you get estimates that are consistent with the proportional hazards parameterization of the model. So for tx, the estimated hazard ratio is exp(0.2178) = 1.24 (at any given point in time, a treated cow is 1.24 times more likely to conceive than a non-treated cow). The corresponding accelerating factor for an exponential model is the reciprocal of the hazard ratio, exp(-0.2178) = 0.80: treating a cow accelerates the time to conception by a factor of 0.80.

Weibull Model

In a Weibull model, the hazard function is h(t) = \lambda p t^{p-1} where p and \lambda are > 0. p is the shape parameter and determines the shape of the hazard function. If it’s > 1 , the hazard increases with time. If p = 1 , the hazard is constant and the model reduces to an exponential model. If p < 1 , the hazard decreases over time.

library(car)
pgtrial$parity <- recode(pgtrial$lact, "1 = 1; 2:hi = '2+'")
weib.mod <- survreg(Surv(dar, preg == 'pregnant') ~ herd + tx + parity +
                   thin, data = pgtrial, dist = "weibull")
summary(weib.mod)

Call:
survreg(formula = Surv(dar, preg == "pregnant") ~ herd + tx + 
    parity + thin, data = pgtrial, dist = "weibull")
               Value Std. Error       z         p
(Intercept)  4.23053     0.1937 21.8412 9.42e-106
herd2        0.36117     0.1947  1.8548  6.36e-02
herd3       -0.00822     0.1980 -0.0415  9.67e-01
tx          -0.23386     0.1438 -1.6262  1.04e-01
parity2+     0.33819     0.1490  2.2698  2.32e-02
thinthin     0.11222     0.1576  0.7119  4.77e-01
Log(scale)   0.13959     0.0509  2.7407  6.13e-03

Scale= 1.15 

Weibull distribution
Loglik(model)= -1453.7   Loglik(intercept only)= -1460.7
	Chisq= 14 on 5 degrees of freedom, p= 0.016 
Number of Newton-Raphson Iterations: 5 
n= 319 

The shape parameter is the reciprocal of what is called by R the scale parameter. The shape parameter is then 1/1.15 = 0.869.

We can also use a piecewise constant exponential regression model, which is a model allowing the baseline hazard to vary between time periods but forces it to remain constant within time periods. In order to run such a model, we need data in a counting process format with a start and stop time for each interval. However, survreg does not allow for a data in that format. The trick would be to use a glm and fitting a Poisson model, including time intervals. See this post by Stephanie Kovalchik which explains how to construct the data and model. The example below is using the same approach, for a time interval of 40 days:

interval.width <- 40
# function to compute time breaks given the exit time = dar
cow.breaks <- function(dar) unique(c(seq(0, dar, by = interval.width),
                                      dar))
# list of each subject's time periods
the.breaks <- lapply(unique(pgtrial$cow), function(id){
  cow.breaks(max(pgtrial$dar[pgtrial$cow == id]))
})
# the expanded period of observation:
start <- lapply(the.breaks, function(x) x[-length(x)]) # for left time points
stop <-  lapply(the.breaks, function(x) x[-1]) # for right time points

count.per.cow <- sapply(start, length)
index <- tapply(pgtrial$cow, pgtrial$cow, length)
index <- cumsum(index) # index of last observation for each cow

event <- rep(0, sum(count.per.cow))
event[cumsum(count.per.cow)] <- pgtrial$preg[index]

# creating the expanded dataset
pw.pgtrial <- data.frame(
    cow = rep(pgtrial$cow[index], count.per.cow),
    dar = rep(pgtrial$dar[index], count.per.cow),
    herd = rep(pgtrial$herd[index], count.per.cow),
    tx = rep(pgtrial$tx[index], count.per.cow),
    lact = rep(pgtrial$lact[index], count.per.cow),
    thin = rep(pgtrial$thin[index], count.per.cow),
    start = unlist(start),
    stop = unlist(stop),
    event = event
  )

# create time variable which indicates the period of observation (offset in Poisson model)
pw.pgtrial$time <- pw.pgtrial$stop - pw.pgtrial$start # length of observation

# create a factor for each interval, allowing to have a different rate for each period
pw.pgtrial$interval <- factor(pw.pgtrial$start)

pw.pgtrial[100:110, ]
    cow dar herd tx lact   thin start stop event time interval
100  61 113    1  1    4   thin     0   40     0   40        0
101  61 113    1  1    4   thin    40   80     0   40       40
102  61 113    1  1    4   thin    80  113     1   33       80
103  62 117    1  0    7 normal     0   40     0   40        0
104  62 117    1  0    7 normal    40   80     0   40       40
105  62 117    1  0    7 normal    80  117     2   37       80
106  63 121    1  1    1   thin     0   40     0   40        0
107  63 121    1  1    1   thin    40   80     0   40       40
108  63 121    1  1    1   thin    80  120     0   40       80
109  63 121    1  1    1   thin   120  121     2    1      120
110  64 122    1  1    3 normal     0   40     0   40        0

# Poisson model
pw.model <- glm(event ~ offset(log(time)) + interval + herd + tx + lact +
+                 thin, data = pw.pgtrial, family = "poisson")
summary(pw.model)

Call:
glm(formula = event ~ offset(log(time)) + interval + herd + tx + 
    lact + thin, family = "poisson", data = pw.pgtrial)

Deviance Residuals: 
   Min      1Q  Median      3Q     Max  
-1.858  -1.373  -1.227   1.357   3.904  

Coefficients:
             Estimate Std. Error z value Pr(>|z|)    
(Intercept) -3.602545   0.132436 -27.202  < 2e-16 ***
interval40  -0.112838   0.106807  -1.056  0.29076    
interval80  -0.064105   0.125396  -0.511  0.60920    
interval120 -0.007682   0.147919  -0.052  0.95858    
interval160 -0.005743   0.191778  -0.030  0.97611    
interval200 -0.427775   0.309143  -1.384  0.16644    
interval240  0.199904   0.297331   0.672  0.50137    
interval280  0.737508   0.385648   1.912  0.05583 .  
interval320  0.622366   1.006559   0.618  0.53637    
herd2       -0.254389   0.114467  -2.222  0.02626 *  
herd3        0.026851   0.119416   0.225  0.82209    
tx           0.219584   0.084824   2.589  0.00963 ** 
lact        -0.023528   0.027511  -0.855  0.39241    
thinthin    -0.139915   0.093632  -1.494  0.13509    
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

(Dispersion parameter for poisson family taken to be 1)

    Null deviance: 2155.6  on 798  degrees of freedom
Residual deviance: 2131.1  on 785  degrees of freedom
AIC: 2959.1

Number of Fisher Scoring iterations: 7

Log-logistic Model

loglog.mod <- survreg(Surv(dar, preg == 'pregnant') ~ herd + tx + lact +
                   thin, data = pgtrial, dist = "loglogistic")
summary(loglog.mod)

Call:
survreg(formula = Surv(dar, preg == "pregnant") ~ herd + tx + 
    lact + thin, data = pgtrial, dist = "loglogistic")
              Value Std. Error      z        p
(Intercept)  3.9544     0.2531 15.625 4.91e-55
herd2        0.2537     0.2355  1.077 2.81e-01
herd3       -0.1019     0.2437 -0.418 6.76e-01
tx          -0.3869     0.1768 -2.189 2.86e-02
lact         0.0612     0.0550  1.112 2.66e-01
thinthin     0.0400     0.1894  0.211 8.33e-01
Log(scale)  -0.1260     0.0515 -2.447 1.44e-02

Scale= 0.882 

Log logistic distribution
Loglik(model)= -1467.2   Loglik(intercept only)= -1472.2
	Chisq= 9.85 on 5 degrees of freedom, p= 0.08 
Number of Newton-Raphson Iterations: 4 
n= 319 

Individual Frailty Model
In an individual frailty model, we add variance unique to individuals in order to account for additional variability in the hazard (like negative binomial model vs. Poisson model). For example, let’s fit a Weibull model with gamma individual frailty to the prostaglandin dataset:

library(parfm)
pgtrial$preg.bin <- as.numeric(pgtrial$preg) - 1
indfr.mod <- parfm(Surv(dar, preg.bin) ~ herd + tx + lact + thin,
             cluster = "cow", data = pgtrial, dist = "weibull",
             frailty = "gamma")
Execution time: 17.872 second(s) 
indfr.mod
Frailty distribution: gamma 
Baseline hazard distribution: Weibull 
Loglikelihood: -1455.679 

         ESTIMATE SE    p-val    
theta     0.000   0.003          
rho       0.867   0.044          
lambda    0.024   0.006          
herd2    -0.289   0.169 0.088 .  
herd3     0.039   0.175 0.824    
tx        0.204   0.125 0.103    
lact     -0.041   0.041 0.314    
thinthin -0.136   0.138 0.323    
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1

Shared Frailty
Shared frailty is a way to deal with clustered data. We will use the “culling” dataset and fit a shared frailty model with a Weibull distribution and a gamma distributed frailty common to all cows in a herd:

temp <- tempfile()
download.file(
  "http://ic.upei.ca/ver/sites/ic.upei.ca.ver/files/ver2_data_R.zip", temp)
load(unz(temp, "ver2_data_R/culling.rdata"))
unlink(temp)

library(frailtypack)
shfrw.mod <- frailtyPenal(Surv(dar, culled) ~ as.factor(lact_c3) + johnes +
                          cluster(herd),
                          hazard = 'Weibull', data = culling, Frailty = TRUE)
shfrw.sum <- cbind(shfrw.mod$coef, sqrt(diag(shfrw.mod$varH)), 
                 shfrw.mod$coef / sqrt(diag(shfrw.mod$varH)), 
        signif(1 - pchisq((shfrw.mod$coef/sqrt(diag(shfrw.mod$varH)))^2, 1)),
                   exp(shfrw.mod$coef),
 exp(shfrw.mod$coef - abs(qnorm((1 - 0.95) / 2)) * sqrt(diag(shfrw.mod$varH))), 
 exp(shfrw.mod$coef + abs(qnorm((1 - 0.95) / 2)) * sqrt(diag(shfrw.mod$varH))))
row.names(shfrw.sum) <- c("Lactation 2", "Lactation 3+", "Johnes")
colnames(shfrw.sum) <- c("Coef.", "Std. Err.", "z", "p-value", "Hazard Ratio", 
                       "Lower CI", "Upper CI")
shfrw.sum
                 Coef. Std. Err.        z     p-value Hazard Ratio  Lower CI
Lactation 2  0.2518627 0.1450806 1.736019 8.25605e-02     1.286419 0.9680321
Lactation 3+ 0.7636558 0.1227840 6.219508 4.98717e-10     2.146108 1.6870874
Johnes       0.5914741 0.3045475 1.942141 5.21200e-02     1.806650 0.9945867
             Upper CI
Lactation 2  1.709525
Lactation 3+ 2.730017
Johnes       3.281748

That’s it for reproducing the examples from Dohoo’s book, chapter on modelling survival data. Next time I’ll look at mixed models.

Veterinary Epidemiologic Research: Modelling Survival Data – Semi-Parametric Analyses

Next on modelling survival data from Veterinary Epidemiologic Research: semi-parametric analyses. With non-parametric analyses, we could only evaluate the effect one or a small number of variables. To evaluate multiple explanatory variables, we analyze data with a proportional hazards model, the Cox regression. The functional form of the baseline hazard is not specified, which make the Cox model a semi-parametric model.
A Cox proportional hazards model is fit hereafter, on data from a clinical trial of the effect of prostaglandin adminsitration on the start of breeding period of dairy cows:

temp <- tempfile()
download.file(
"http://ic.upei.ca/ver/sites/ic.upei.ca.ver/files/ver2_data_R.zip", temp)
load(unz(temp, "ver2_data_R/pgtrial.rdata"))
unlink(temp)

library(Hmisc)
pgtrial <- upData(pgtrial, labels = c(herd = 'Herd id', cow = 'Cow id',
                             tx = 'Treatment', lact = 'Lactation number',
                             thin = 'Body condition', dar = 'Days at risk',
                             preg = 'Pregnant or censored'),
                  levels = list(thin = list('normal' = 0, 'thin' = 1),
                    preg = list('censored' = 0, 'pregnant' = 1)))
pgtrial$herd <- as.factor(pgtrial$herd)

library(survival)
coxph.mod <- coxph(Surv(dar, preg == 'pregnant') ~ herd + tx + lact + thin,
                   data = pgtrial, ties = 'breslow')
(coxph.sum <- summary(coxph.mod))
Call:
coxph(formula = Surv(dar, preg == "pregnant") ~ herd + tx + lact + 
    thin, data = pgtrial, ties = "breslow")

  n= 319, number of events= 264 

             coef exp(coef) se(coef)      z Pr(>|z|)  
herd2    -0.28445   0.75243  0.16981 -1.675   0.0939 .
herd3     0.03676   1.03744  0.17426  0.211   0.8329  
tx        0.18359   1.20152  0.12543  1.464   0.1433  
lact     -0.04283   0.95807  0.04109 -1.042   0.2972  
thinthin -0.14557   0.86453  0.13794 -1.055   0.2913  
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

         exp(coef) exp(-coef) lower .95 upper .95
herd2       0.7524     1.3290    0.5394     1.050
herd3       1.0374     0.9639    0.7373     1.460
tx          1.2015     0.8323    0.9396     1.536
lact        0.9581     1.0438    0.8839     1.038
thinthin    0.8645     1.1567    0.6597     1.133

Concordance= 0.564  (se = 0.021 )
Rsquare= 0.029   (max possible= 1 )
Likelihood ratio test= 9.5  on 5 df,   p=0.09084
Wald test            = 9.32  on 5 df,   p=0.09685
Score (logrank) test = 9.34  on 5 df,   p=0.09611

R gives several options to control ties in case several events occurred at the same time: the Efron method (default in R), Breslow method (default in software like SAS or Stata), and the exact method. Breslow is the simplest and adequate if not too many ties in the dataset. Efron is closer to the exact approximation.

Stratified Cox Propotional Hazards Model

In a stratified Cox model, different baseline hazards are assumed across groups of subjects. The Cox model is modified to allow the control of a predictor which do not satisfy the proportional hazards (PH) assumption. We refit the above model by stratifying by herd and including a treatment by herd interaction:

scoxph.mod <- coxph(Surv(dar, preg == 'pregnant') ~ tx + tx*herd + lact + thin +
                    strata(herd), data = pgtrial, method = 'breslow')
summary(scoxph.mod)
Call:
coxph(formula = Surv(dar, preg == "pregnant") ~ tx + tx * herd + 
    lact + thin + strata(herd), data = pgtrial, method = "breslow")

  n= 319, number of events= 264 

             coef exp(coef) se(coef)      z Pr(>|z|)  
tx       -0.02160   0.97863  0.25528 -0.085   0.9326  
herd2          NA        NA  0.00000     NA       NA  
herd3          NA        NA  0.00000     NA       NA  
lact     -0.04600   0.95504  0.04065 -1.132   0.2578  
thinthin -0.13593   0.87291  0.13833 -0.983   0.3258  
tx:herd2 -0.05659   0.94498  0.33570 -0.169   0.8661  
tx:herd3  0.54494   1.72451  0.31823  1.712   0.0868 .
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

         exp(coef) exp(-coef) lower .95 upper .95
tx          0.9786     1.0218    0.5934     1.614
herd2           NA         NA        NA        NA
herd3           NA         NA        NA        NA
lact        0.9550     1.0471    0.8819     1.034
thinthin    0.8729     1.1456    0.6656     1.145
tx:herd2    0.9450     1.0582    0.4894     1.825
tx:herd3    1.7245     0.5799    0.9242     3.218

Concordance= 0.56  (se = 0.035 )
Rsquare= 0.032   (max possible= 0.998 )
Likelihood ratio test= 10.32  on 5 df,   p=0.06658
Wald test            = 10.5  on 5 df,   p=0.0623
Score (logrank) test = 10.66  on 5 df,   p=0.05851

Evaluating the Assumption of Proportional Hazards

We can evaluate it graphically, by examining the log-cumulative hazard plot vs. ln(time) and check if the curves are parallel:

coxph.mod2 <- coxph(Surv(dar, preg == 'pregnant') ~ tx, data = pgtrial,
                   ties = 'breslow')
pgtrial2 <- with(pgtrial, data.frame(tx = c(0, 1)))
tfit.add <- survfit(coxph.mod2, newdata = pgtrial2)
df1 <- data.frame(
    time    = tfit.add[1, ]$time,
    n.risk  = tfit.add[1, ]$n.risk,
    n.event = tfit.add[1, ]$n.event,
    surv    = tfit.add[1, ]$surv,
    strata  = "0",
    upper   = tfit.add[1, ]$upper,
    lower   = tfit.add[1, ]$lower,
    log.surv = log(-log(tfit.add[1, ]$surv))
 ) 
df2 <- data.frame(
    time    = tfit.add[2, ]$time,
    n.risk  = tfit.add[2, ]$n.risk,
    n.event = tfit.add[2, ]$n.event,
    surv    = tfit.add[2, ]$surv,
    strata  = "1",
    upper   = tfit.add[2, ]$upper,
    lower   = tfit.add[2, ]$lower,
    log.surv = log(-log(tfit.add[2, ]$surv))
 )
dfpar.add <- rbind(df1, df2)
zeros <- data.frame(time = 0, surv = 1, strata = c(1, 2), 
                     upper = 1, lower = 1)
dfpar.add <- rbind.fill(zeros, dfpar.add)
dfpar.add$strata <- factor(dfpar.add$strata, labels = c("No tx", "Tx"))
ggplot(dfpar.add, aes(log(time), log.surv, colour = strata)) + 
  geom_step(size = 0.6) + 
  scale_color_manual("Tx", values = c('blue4', 'darkorange')) + 
  xlab("ln(time)") + ylab("Log-log survival")
Log cumulative hazard plot
Log cumulative hazard plot

Another graphical approach is to compare plots of predicted survival times from a Cox model (assuming PH) to Kaplan-Meier survivor function (which do not assume PH):

tfit.km <- survfit(Surv(dar, preg == 'pregnant') ~ tx, data = pgtrial)
df3.km <- data.frame(
    time    = tfit.km$time,
    n.risk  = tfit.km$n.risk,
    n.event = tfit.km$n.event,
    surv    = tfit.km$surv,
    strata  = gsub("tx=", "", summary(tfit.km, censored = T)$strata),
    upper   = tfit.km$upper,
    lower   = tfit.km$lower
 ) 
zeros <- data.frame(time = 0, surv = 1, strata = gsub("tx=", "", 
                                          levels(summary(tfit.km)$strata)), 
                     upper = 1, lower = 1)
df3.km <- rbind.fill(df3.km, zeros)
df3.km$cat <- with(df3.km, ifelse(strata == "0", "No tx, observed",
                                  "Tx, observed"))
dfpar.add$cat <- with(dfpar.add, ifelse(strata == "No tx", "No tx, expected",
                                        "Tx, expected"))
dfpar.obs <- rbind.fill(dfpar.add, df3.km)
ggplot(dfpar.obs, aes(time, surv, colour = cat)) + 
   geom_step(size = 0.6) + 
   scale_color_manual("", values = c('blue1', 'blue4', 'darkorange1',
                            'darkorange4')) + 
   xlab("time") + ylab("survival probability")
Kaplan-Meier Cox plot
Kaplan-Meier Cox plot

You can also assess PH statistically with the Schoenfeld residuals using cox.zph function:

(schoen <- cox.zph(coxph.mod))
             rho chisq      p
herd2    -0.0630 1.100 0.2942
herd3    -0.0443 0.569 0.4506
tx       -0.1078 3.141 0.0763
lact      0.0377 0.447 0.5035
thinthin -0.0844 2.012 0.1560
GLOBAL        NA 7.631 0.1778

plot(schoen, var = 4)
Schoenfeld residuals for lactation
Schoenfeld residuals for lactation

Evaluating the Overall Fit of the Model

First we can look at the Cox-Snell residuals, which are the estimated cumulative hazards for individuals at their failure (or censoring) times. The default residuals of coxph in R are the martingale residuals, not the Cox-Snell. But it can be computed:

cox.snell <- (as.numeric(pgtrial$preg) - 1) - resid(coxph.mod,
                                                    type = "martingale")
coxph.res <- survfit(coxph(Surv(cox.snell, pgtrial$preg == 'pregnant') ~ 1,
                           method = 'breslow'), type = 'aalen')

plot(coxph.res$time, -log(coxph.res$surv), type = 's',
     xlab = 'Modified Cox-Snell residuals', ylab = 'Cumulative hazard')
abline(0, 1, col = 'red', lty = 2)

## Alternatively:
coxph.res2 <- survfit(Surv(cox.snell, pgtrial$preg == 'pregnant') ~ 1)
Htilde <- cumsum(coxph.res2$n.event / coxph.res$n.risk)
plot(coxph.res2$time, Htilde, type = 's', col = 'blue')
abline(0, 1, col = 'red', lty = 2)
Plot of Cox-Snell residuals
Plot of Cox-Snell residuals

We can also use a goodness-of-fit test:

## GOF (Gronnesby and Borgan omnibus gof)
library(gof)
cumres(coxph.mod)

Kolmogorov-Smirnov-test: p-value=0.35
Cramer von Mises-test: p-value=0.506
Based on 1000 realizations. Cumulated residuals ordered by herd2-variable.
---
Kolmogorov-Smirnov-test: p-value=0.041
Cramer von Mises-test: p-value=0.589
Based on 1000 realizations. Cumulated residuals ordered by herd3-variable.
---
Kolmogorov-Smirnov-test: p-value=0
Cramer von Mises-test: p-value=0.071
Based on 1000 realizations. Cumulated residuals ordered by tx-variable.
---
Kolmogorov-Smirnov-test: p-value=0.728
Cramer von Mises-test: p-value=0.733
Based on 1000 realizations. Cumulated residuals ordered by lact-variable.
---
Kolmogorov-Smirnov-test: p-value=0.106
Cramer von Mises-test: p-value=0.091
Based on 1000 realizations. Cumulated residuals ordered by thinthin-variable.

We can evaluate the concordance between the predicted and observed sequence of pairs of events. Harrell’s c index computes the proportion of all pairs of subjects in which the model correctly predicts the sequence of events. It ranges from 0 to 1 with 0.5 for random predictions and 1 for a perfectly discriminating model. It is obtained from the Somer’s Dxy rank correlation:

library(rms)
fit.cph <- cph(Surv(dar, preg == 'pregnant') ~ herd + tx + lact + thin,
               data = pgtrial, x = TRUE, y = TRUE, surv = TRUE)
v <- validate(fit.cph, dxy = TRUE, B = 100)
Dxy <- v[rownames(v) == "Dxy", colnames(v) == "index.corrected"]
(Dxy / 2) + 0.5 # c index
[1] 0.4538712

Evaluating the Functional Form of Predictors

We can use martingale residuals to evaluate the functional form of the relationship between a continuous predictor and the survival expectation for individuals:

lact.mod <- coxph(Surv(dar, preg == 'pregnant') ~ lact, data = pgtrial,
                  ties = 'breslow')
lact.res <- resid(lact.mod, type = "martingale")
plot(pgtrial$lact, lact.res, xlab = 'lactation', ylab = 'Martingale residuals')
lines(lowess(pgtrial$lact, lact.res, iter = 0))
 
# adding quadratic term
lact.mod <- update(lact.mod, . ~ . + I(lact^2))
lact.res <- resid(lact.mod, type = "martingale")
plot(pgtrial$lact, lact.res, xlab = 'lactation', ylab = 'Martingale residuals')
lines(lowess(pgtrial$lact, lact.res, iter = 0))
Plot of marrtingale residuals vs. lactation number
Plot of marrtingale residuals vs. lactation number
Plot of martingale residuals vs. lactation number (as quadratic term)
Plot of martingale residuals vs. lactation number (as quadratic term)

Checking for Outliers

Deviance residuals can be used to identify outliers:

## deviance residuals
dev.res <- resid(coxph.mod, type = "deviance")
plot(pgtrial$dar, dev.res, xlab = 'time (days)', ylab = 'deviance residuals')

cbind(dev.res, pgtrial)[abs(dev.res) > 2, ]
      dev.res herd cow tx lact   thin dar     preg
1    2.557832    1   1  0    1 normal   1 pregnant
2    2.592492    1   2  1    4   thin   1 pregnant
3    2.319351    1   3  1    1 normal   2 pregnant
73  -2.693731    1  76  1    1 normal 277 censored
74   2.734508    2  78  0    2   thin   1 pregnant
75   2.644885    2  79  1    4 normal   1 pregnant
76   2.436308    2  80  1    1 normal   2 pregnant
176 -2.015925    2 180  1    2 normal 201 censored
180 -2.196008    2 184  1    2 normal 250 censored
183 -2.081493    2 187  1    3   thin 288 censored
185 -2.238729    2 189  0    1 normal 346 censored
314 -2.274912    3 318  0    1   thin 262 censored
315 -2.226711    3 319  0    2   thin 262 censored
316 -2.182517    3 320  0    4   thin 287 censored
317 -2.278029    3 321  0    2   thin 288 censored
318 -2.341736    3 322  0    3   thin 308 censored
319 -2.392427    3 323  0    2   thin 320 censored
Deviance residuals
Deviance residuals

Score residuals and scaled score residuals can be used to identify influential observations:

### Detecting influential points
# score residuals
score.res <- resid(coxph.mod, type = "score")
# score residuals for tx
plot(pgtrial$dar, score.res[ , 3], xlab = 'time (days)',
     ylab = 'score residuals')
text(pgtrial$dar, score.res[ , 3], rownames(pgtrial), cex = 0.6, pos = 4)

cbind(score.res[ , 3], pgtrial)[abs(score.res[ , 3]) > 2, ]
   score.res[, 3] herd cow tx lact   thin dar     preg
73      -2.025537    1  76  1    1 normal 277 censored

## influential observations
dfbeta <- resid(coxph.mod, type = "dfbeta")
# dfbeta residuals for tx
plot(pgtrial$dar, dfbeta[ , 3], xlab = 'time (days)',
     ylab = 'scaled score residual')
text(pgtrial$dar, dfbeta[ , 3], rownames(pgtrial), cex = 0.6, pos = 4)

# with standardized dfbeta
dfbetas <- resid(coxph.mod, type = "dfbetas")
plot(pgtrial$dar, dfbetas[ , 3], xlab = 'time (days)',
     ylab = 'standardized score residuals')
text(pgtrial$dar, dfbetas[ , 3], rownames(pgtrial), cex = 0.6, pos = 4)
Score residuals
Score residuals
Scaled score residuals (delta-beta)
Scaled score residuals (delta-beta)
Standardized score residuals
Standardized score residuals

Veterinary Epidemiologic Research: Modelling Survival Data – Non-Parametric Analyses

Next topic from Veterinary Epidemiologic Research: chapter 19, modelling survival data. We start with non-parametric analyses where we make no assumptions about either the distribution of survival times or the functional form of the relationship between a predictor and survival. There are 3 non-parametric methods to describe time-to-event data: actuarial life tables, Kaplan-Meier method, and Nelson-Aalen method.
We use data on occurrence of calf pneumonia in calves raised in 2 different housing systems. Calves surviving to 150 days without pneumonia are considered censored at that time.

temp <- tempfile()
download.file(
"http://ic.upei.ca/ver/sites/ic.upei.ca.ver/files/ver2_data_R.zip", temp)
load(unz(temp, "ver2_data_R/calf_pneu.rdata"))
unlink(temp)

library(Hmisc)
calf_pneu <- upData(calf_pneu, labels = c(calf = 'Calf id',
                                  stock = 'Stocking method',
                             days = 'Time to onset of pneumonia or censoring',
                                  pn = 'Pneumonia'),
                  levels = list(stock = list('batch' = 0, 'continuous' = 1)))

Actuarial Life Table

To create a life table, we use the function lifetab from package KMsurv, after calculating the number of censored and events at each time point and grouping them by time interval (with gsummary from package nlme).

library(KMsurv)
interval <- seq(from = 30, to = 165, by = 15)
interval <- floor(calf_pneu$days/15)
interval.censor <- data.frame(interval, calf_pneu$pn)
library(nlme)
pneumonia <- gsummary(interval.censor, sum, groups = interval)
total <- gsummary(interval.censor, length, groups = interval)
lt.data <- cbind(pneumonia[ , 1:2], total[ , 2])
length <- length(lt.data$interval)
lt.data[length + 1, ]$interval <- NA
nevent <- lt.data[ , 2]
nlost <- lt.data[ , 3] - lt.data[ , 2]
(life.table <- lifetab(lt.data$interval, 24, nlost, nevent))
      nsubs nlost nrisk nevent      surv        pdf     hazard    se.surv
1-3      24     0  24.0      1 1.0000000 0.02083333 0.02127660 0.00000000
3-4      23     0  23.0      1 0.9583333 0.04166667 0.04444444 0.04078938
4-5      22     0  22.0      1 0.9166667 0.04166667 0.04651163 0.05641693
5-6      21     0  21.0      3 0.8750000 0.12500000 0.15384615 0.06750772
6-7      18     1  17.5      2 0.7500000 0.08571429 0.12121212 0.08838835
7-8      15     6  12.0      3 0.6642857 0.16607143 0.28571429 0.09686316
8-10      6     0   6.0      1 0.4982143 0.04151786 0.09090909 0.11032937
10-NA     5     5   2.5      0 0.4151786         NA         NA 0.11915934
NA-3      0    NA    NA     NA 0.4151786         NA         NA 0.11915934
          se.pdf  se.hazard
1-3   0.02039469 0.02127178
3-4   0.04078938 0.04443347
4-5   0.04078938 0.04649905
5-6   0.06750772 0.08855994
6-7   0.05792828 0.08555236
7-8   0.08649471 0.16326531
8-10  0.03899969 0.09053265
10-NA         NA         NA
NA-3          NA         NA

Kaplan-Meier Method

To compute the Kaplan-Meier estimator we use the function survfit from package survival. It takes as argument a Surv object, which gives the time variable and the event of interest. You get the Kaplan-Meier estimate with the summary of the survfit object. We can then plot the estimates to show the Kaplan-Meier survivor function.

library(survival)
km.sf <- survfit(Surv(days, pn == 1) ~ 1, data = calf_pneu)
summary(km.sf)
Call: survfit(formula = Surv(days, pn == 1) ~ 1, data = calf_pneu)

 time n.risk n.event survival std.err lower 95% CI upper 95% CI
   27     24       1    0.958  0.0408        0.882        1.000
   49     23       1    0.917  0.0564        0.813        1.000
   72     22       1    0.875  0.0675        0.752        1.000
   79     21       2    0.792  0.0829        0.645        0.972
   89     19       1    0.750  0.0884        0.595        0.945
   90     18       1    0.708  0.0928        0.548        0.916
  101     17       1    0.667  0.0962        0.502        0.885
  113     15       2    0.578  0.1019        0.409        0.816
  117      9       1    0.514  0.1089        0.339        0.778
  123      6       1    0.428  0.1198        0.247        0.741

plot(km.sf, xlab = "time (days)", ylab = "cumulative survival probability", conf.int = TRUE)
Kaplan-Meier survivor function (95% CI)
Kaplan-Meier survivor function (95% CI)

Nelson-Aalen Method

A “hazard” is the probability of failure at a point in time, given that the calf had survived up to that point in time. A cumulative hazard, the Nelson-Aaalen estimate, can be computed. The Nelson-Aalen estimate can be calculated by transforming the Fleming-Harrington estimate of survival.

fh.sf <- survfit(Surv(days, pn == 1) ~ 1, data = calf_pneu, type = "fleming")

plot(stepfun(fh.sf$time, c(0, -log(fh.sf$surv))), do.points = FALSE, 
      xlab = "time (days)", ylab = "cumulative hazard",
      main = "", ylim = c(0, 1.5))
lines(stepfun(fh.sf$time, c(0, -log(fh.sf$upper))), lty = 5, do.points = FALSE)
lines(stepfun(fh.sf$time, c(0, -log(fh.sf$lower))), lty = 5, do.points = FALSE)
Nelson-Aalen cumulative hazard function
Nelson-Aalen cumulative hazard function (95% CI)

Tests of the Overall Survival Curve

Several tests are available to test whether the overall survivor functions in 2 or more groups are equal. We can use the log-rank test, the simplest test, assigning equal weight to each time point estimate and equivalent to a standard Mantel-Haenszel test. Also, there’s the Peto-Peto-Prentice test which weights the stratum-specific estimates by the overall survival experience and so reduces the influence of different censoring patterns between groups.
To do these tests, we apply the survdiff function to the Surv object. The argument rho gives the weights according to S^{(t)}\rho and may be any numeric value. Default is rho = 0 which gives the log-rank test. Rho = 1 gives the “Peto & Peto modification of the Gehan-Wilcoxon test”. Rho larger than zero gives greater weight to the first part of the survival curves. Rho smaller than zero gives weight to the later part of the survival curves.

survdiff(Surv(days, pn == 1) ~ stock, data = calf_pneu, rho = 0) # rho is optional
Call:
survdiff(formula = Surv(days, pn == 1) ~ stock, data = calf_pneu, 
    rho = 0)

                  N Observed Expected (O-E)^2/E (O-E)^2/V
stock=batch      12        4     6.89      1.21      2.99
stock=continuous 12        8     5.11      1.63      2.99

 Chisq= 3  on 1 degrees of freedom, p= 0.084

survdiff(Surv(days, pn == 1) ~ stock, data = calf_pneu, rho = 1) # rho=1 asks for Peto-Peto test
Call:
survdiff(formula = Surv(days, pn == 1) ~ stock, data = calf_pneu, 
    rho = 1)

                  N Observed Expected (O-E)^2/E (O-E)^2/V
stock=batch      12     2.89     5.25      1.06      3.13
stock=continuous 12     6.41     4.05      1.38      3.13

 Chisq= 3.1  on 1 degrees of freedom, p= 0.0766

Finally we can compare survivor function with stock R plot or using ggplot2. With ggplot2, you get the necessary data from the survfit object and create a new data frame from it. The baseline data (time = 0) are not there so you create it yourself:

(km.stock <- survfit(Surv(days, pn == 1) ~ stock, data = calf_pneu))
Call: survfit(formula = Surv(days, pn == 1) ~ stock, data = calf_pneu)

                 records n.max n.start events median 0.95LCL 0.95UCL
stock=batch           12    12      12      4     NA     123      NA
stock=continuous      12    12      12      8    113      79      NA

plot(km.stock, conf.int = FALSE, col = c("blue4", "darkorange"),
      xlab = "time (days)", ylab = "cumulative survival probability")
legend("bottomleft", inset = .05, c("batch", "continuous"),
        text.col = c("blue4", "darkorange"))

km.df <- data.frame(
    time    = km.stock$time,
    n.risk  = km.stock$n.risk,
    n.event = km.stock$n.event,
    surv    = km.stock$surv,
    strata  = gsub("stock=", "", summary(km.stock, censored = T)$strata),
    upper   = km.stock$upper,
    lower   = km.stock$lower
 ) 
zeros <- data.frame(time = 0, surv = 1, strata = gsub("stock=", "",
                                           levels(summary(km.stock)$strata)), 
                     upper = 1, lower = 1)
library(plyr)
km.df <- rbind.fill(zeros, km.df)
km.df$strata <- ordered(km.df$strata, levels = c("batch", "continuous"))
library(ggplot2)
ggplot(km.df, aes(time, surv, colour = strata)) + 
   geom_step(size = 0.6) + xlim(0, 150) + ylim(0, 1) + 
   xlab("time (days)") + ylab("cumulative survival probability") +
   labs(colour = "stock")
K-M survival curves, by stocking type
K-M survival curves, by stocking type

kmc-gg

Veterinary Epidemiologic Research: Count and Rate Data – Poisson Regression and Risk Ratios

As noted on paragraph 18.4.1 of the book Veterinary Epidemiologic Research, logistic regression is widely used for binary data, with the estimates reported as odds ratios (OR). If it’s appropriate for case-control studies, risk ratios (RR) are preferred for cohort studies as RR provides estimates of probabilities directly. Moreover, it is often forgotten the assumption of rare event rate, and the OR will overestimate the true effect.

One approach to get RR is to fit a generalised linear model (GLM) with a binomial distribution and a log link. But these models may sometimes fail to converge (Zou, 2004). Another option is to use a Poisson regression with no exposure or offset specified (McNutt, 2003). It gives estimates with very little bias but confidence intervals that are too wide. However, using robust standard errors gives correct confidence intervals (Greenland, 2004, Zou, 2004).

We use data on culling of dairy cows to demonstrate this.

temp <- tempfile()
download.file(
"http://ic.upei.ca/ver/sites/ic.upei.ca.ver/files/ver2_data_R.zip",
temp)
load(unz(temp, "ver2_data_R/culling.rdata"))
unlink(temp)

table(culling$culled)

  0   1 
255 466 
### recoding number of lactation
culling$lact <- with(culling, ifelse(lact_c3 > 1, 2, lact_c3))

The logistic regression:

log.reg <- glm(culled ~ lact, family = binomial("logit"), data = culling)
summary(log.reg)

Call:
glm(formula = culled ~ lact, family = binomial("logit"), data = culling)

Deviance Residuals: 
   Min      1Q  Median      3Q     Max  
-1.546  -1.199   0.849   0.849   1.156  

Coefficients:
            Estimate Std. Error z value Pr(>|z|)    
(Intercept)   -0.734      0.299   -2.45    0.014 *  
lact           0.784      0.171    4.59  4.4e-06 ***
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1 

(Dispersion parameter for binomial family taken to be 1)

    Null deviance: 936.86  on 720  degrees of freedom
Residual deviance: 915.84  on 719  degrees of freedom
AIC: 919.8

Number of Fisher Scoring iterations: 4

cbind(exp(coef(log.reg)), exp(confint(log.reg)))
Waiting for profiling to be done...
                 2.5 % 97.5 %
(Intercept) 0.48 0.267  0.864
lact        2.19 1.568  3.065

We could compute by hand the OR and RR:

with(culling, table(culled, lact))
      lact
culled   1   2
     0  97 158
     1 102 364
## OR is 2.19:
(364 / 158) / (102 / 97)
[1] 2.19
## or the ratio between the cross-products
(364 * 97) / (158 * 102)
[1] 2.19
## or with epicalc
library(epicalc)
with(culling, cc(culled, lact, graph = FALSE))

       lact
culled    1   2 Total
  0      97 158   255
  1     102 364   466
  Total 199 522   721

OR =  2.19 
Exact 95% CI =  1.54, 3.1  
Chi-squared = 21.51, 1 d.f., P value = 0
Fisher's exact test (2-sided) P value = 0 

# RR is 1.36:
(364 / 522) / (102 / 199)
[1] 1.36

The GLM with binomial distribution and log link:

log.reg2 <- glm(culled ~ lact, family = binomial(link = "log"), data = culling)
summary(log.reg2)

Call:
glm(formula = culled ~ lact, family = binomial(link = "log"), 
    data = culling)

Deviance Residuals: 
   Min      1Q  Median      3Q     Max  
-1.546  -1.199   0.849   0.849   1.156  

Coefficients:
            Estimate Std. Error z value Pr(>|z|)    
(Intercept)  -0.9762     0.1412   -6.91  4.8e-12 ***
lact          0.3078     0.0749    4.11  4.0e-05 ***
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1 

(Dispersion parameter for binomial family taken to be 1)

    Null deviance: 936.86  on 720  degrees of freedom
Residual deviance: 915.84  on 719  degrees of freedom
AIC: 919.8

Number of Fisher Scoring iterations: 5

cbind(exp(coef(log.reg2)), exp(confint(log.reg2)))
Waiting for profiling to be done...
                  2.5 % 97.5 %
(Intercept) 0.377  0.28  0.488
lact        1.360  1.18  1.588

The modified Poisson with robust estimator as described by Zou, 2004 (GEE with individual observations treated as a repeated measure):

## create id for each observation
culling$id <- 1:length(culling$herd)
library(geepack)
zou.mod <- geeglm(culled ~ lact, family = poisson(link = "log"), id = id, corstr = "exchangeable", data = culling)
summary(zou.mod)

Call:
geeglm(formula = culled ~ lact, family = poisson(link = "log"), 
    data = culling, id = id, corstr = "exchangeable")

 Coefficients:
            Estimate Std.err Wald Pr(>|W|)    
(Intercept)  -0.9762  0.1412 47.8  4.8e-12 ***
lact          0.3078  0.0749 16.9  4.0e-05 ***
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1 

Estimated Scale Parameters:
            Estimate Std.err
(Intercept)    0.354   0.021

Correlation: Structure = exchangeable  Link = identity 

Estimated Correlation Parameters:
      Estimate Std.err
alpha        0       0
Number of clusters:   721   Maximum cluster size: 1 
## exponentiated coefficients
exp(coef(zou.mod))
(Intercept)        lact 
      0.377       1.360 
## getting confidence intervals
library(doBy)
zou.mod.coefci <- esticon(zou.mod, diag(2))
zou.mod.expci <- exp(cbind(zou.mod.coefci$Estimate, zou.mod.coefci$Lower, zou.mod.coefci$Upper))
rownames(zou.mod.expci) <- names(coef(zou.mod))
colnames(zou.mod.expci) <- c("RR", "Lower RR", "Upper RR")
zou.mod.expci
               RR Lower RR Upper RR
(Intercept) 0.377    0.286    0.497
lact        1.360    1.175    1.576

Or the same using glm() and then getting robust standard errors:

pois.reg <- glm(culled ~ lact, family = poisson(link = "log"), data = culling)
library(sandwich) # to get robust estimators
library(lmtest) # to test coefficients
coeftest(pois.reg, vcov = sandwich)

z test of coefficients:

            Estimate Std. Error z value Pr(>|z|)    
(Intercept)  -0.9762     0.1412   -6.91  4.8e-12 ***
lact          0.3078     0.0749    4.11  4.0e-05 ***
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1 

## RR
exp(coef(pois.reg))
(Intercept)        lact 
      0.377       1.360 
## CI
0.3078 + qnorm(0.05 / 2) * 0.0749 # upper 95% CI
[1] 0.161
exp(0.3078 + qnorm(0.05 / 2) * 0.0749)
[1] 1.17
0.3078 + qnorm(1 - 0.05 / 2) * 0.0749 # lower 95% CI
[1] 0.455
exp(0.3078 + qnorm(1 - 0.05 / 2) * 0.0749)
[1] 1.58

So no excuse to use odds ratios when risk ratios are more appropriate!

Addition: Plotting the Risk Ratios

zou.mod2 <- geeglm(culled ~ lact + johnes, family = poisson(link = "log"),
                   id = id, corstr = "exchangeable", data = culling)
zou.mod2.coefci <- esticon(zou.mod2, diag(3))
zou.mod2.expci <- exp(cbind(zou.mod2.coefci$Estimate, zou.mod2.coefci$Lower,
                           zou.mod2.coefci$Upper))
rownames(zou.mod2.expci) <- names(coef(zou.mod2))
colnames(zou.mod2.expci) <- c("RR", "LowerCI", "UpperCI")
zou.df <- as.data.frame(zou.mod2.expci)
zou.df$var <- row.names(zou.df)
library(ggplot2)
ggplot(zou.df[2:3, ], aes(y = RR, x = reorder(var, RR))) +
  geom_point() +
  geom_pointrange(aes(ymin = LowerCI, ymax = UpperCI)) + 
  scale_x_discrete(labels = c("Lactation", "Johnes")) + 
  scale_y_log10(breaks = seq(1, 2, by = 0.1)) +
  xlab("") + 
  geom_hline(yintercept = 1, linetype = "dotdash", colour = "blue") +
  coord_flip()

Thanks to Tal Galili for suggesting this addition.