SimCiRat {SimComp}R Documentation

Simultaneous Confidence Intervals for General Contrasts (Ratios) of Means of Multiple Endpoints

Description

Simultaneous confidence intervals for general contrasts (linear functions) of normal means (e.g., "Dunnett", "Tukey", "Williams" ect.), and for single or multiple endpoints (primary response variables) simultaneously. The procedure of Hasler and Hothorn (2012) <doi:10.1080/19466315.2011.633868> is applied for ratios of means of normally distributed data. The variances/ covariance matrices of the treatment groups (containing the covariances between the endpoints) may be assumed to be equal or possibly unequal for the different groups (Hasler, 2014 <doi:10.1515/ijb-2012-0015>). For the case of only a single endpoint and unequal covariance matrices (variances), the procedure coincides with the PI procedure of Hasler and Hothorn (2008) <doi:10.1002/bimj.200710466>.

Usage

## Default S3 method:
SimCiRat(data, grp, resp = NULL, na.action = "na.error", type = "Dunnett", 
  base = 1, Num.Contrast = NULL, Den.Contrast = NULL, alternative = "two.sided", 
  covar.equal = FALSE, conf.level = 0.95, CorrMatDat = NULL, ...)
## S3 method for class 'formula'
SimCiRat(formula, ...)

Arguments

data

a data frame containing a grouping variable and the endpoints as columns

grp

a character string with the name of the grouping variable

resp

a vector of character strings with the names of the endpoints; if resp=NULL (default), all column names of the data frame without the grouping variable are chosen automatically

formula

a formula specifying a numerical response and a grouping factor (e.g. response ~ treatment)

na.action

a character string indicating what should happen when the data contain NAs; if na.action="na.error" (default) the procedure stops with an error message; if na.action="multi.df" a new experimental version is used (details will follow soon)

type

a character string, defining the type of contrast, with the following options:

  • "Dunnett": many-to-one comparisons

  • "Tukey": all-pair comparisons

  • "Sequen": comparisons of consecutive groups

  • "AVE": comparison of each group with average of all others

  • "GrandMean": comparison of each group with grand mean of all groups

  • "Changepoint": differences of averages of groups of higher order to averages of groups of lower order

  • "Marcus": Marcus contrasts

  • "McDermott": McDermott contrasts

  • "Williams": Williams trend tests

  • "UmbrellaWilliams": Umbrella-protected Williams trend tests

note that type is ignored if Num.Contrast or Den.Contrast is specified by the user (see below)

base

a single integer specifying the control group for Dunnett contrasts, ignored otherwise

Num.Contrast

a numerator contrast matrix, where columns correspond to groups and rows correspond to contrasts

Den.Contrast

a denominator contrast matrix, where columns correspond to groups and rows correspond to contrasts

alternative

a character string specifying the alternative hypothesis, must be one of "two.sided" (default), "greater" or "less"

covar.equal

a logical variable indicating whether to treat the variances/ covariance matrices of the treatment groups (containing the covariances between the endpoints) as being equal; if TRUE then the pooled variance/ covariance matrix is used, otherwise the Satterthwaite approximation to the degrees of freedom is used

conf.level

a numeric value defining the simultaneous confidence level

CorrMatDat

a correlation matrix of the endpoints, if NULL (default) it is estimated from the data

...

arguments to be passed to SimCiRat.default

Details

The interest is in simultaneous confidence intervals for several linear combinations (contrasts) of treatment means in a one-way ANOVA model, and for single or multiple endpoints simultaneously. For example, corresponding intervals for the all- pair comparison of Tukey (1953) and the many-to-one comparison of Dunnett (1955) are implemented, but allowing for heteroscedasticity and multiple endpoints, and in terms of ratios of means. The user is also free to create other interesting problem-specific contrasts. Approximate multivariate t-distributions are used to calculate lower and upper limits (Hasler and Hothorn, 2012 <doi:10.1080/19466315.2011.633868>). Simultaneous tests based on these intervals control the familywise error rate in admissible ranges and in the strong sense. The variances/ covariance matrices of the treatment groups (containing the covariances between the endpoints) can be assumed to be equal (covar.equal=TRUE) or unequal (covar.equal=FALSE). If being equal, the pooled variance/ covariance matrix is used, otherwise approximations to the degrees of freedom (Satterthwaite, 1946) are used (Hasler, 2014 <doi:10.1515/ijb-2012-0015>; Hasler and Hothorn, 2008 <doi:10.1002/bimj.200710466>). Unequal covariance matrices occure if variances or correlations of some endpoints differ depending on the treatment groups.

Value

An object of class SimCi containing:

estimate

a matrix of estimated ratios

lower.raw

a matrix of raw (unadjusted) lower limits

upper.raw

a matrix of raw (unadjusted) upper limits

lower

a matrix of lower limits adjusted for multiplicity

upper

a matrix of upper limits adjusted for multiplicity

CorrMatDat

if not prespecified by CorrMatDat, either the estimated common correlation matrix of the endpoints (covar.equal=TRUE) or a list of different (one for each treatment) estimated correlation matrices of the endpoints (covar.equal=FALSE)

CorrMatComp

the estimated correlation matrix of the comparisons

degr.fr

a matrix of degrees of freedom

Note

By default (na.action="na.error"), the procedure stops if there are missing values. A new experimental version for missing values is used if na.action="multi.df". If covar.equal=TRUE, the number of endpoints must not be greater than the total sample size minus the number of treatment groups. If covar.equal=FALSE, the number of endpoints must not be greater than the minimal sample size minus 1. Otherwise the procedure stops.

All intervals have the same direction for all comparisons and endpoints (alternative="..."). In case of doubt, use "two.sided".

The correlation matrix for the multivariate t-distribution also depends on the unknown ratios. The same problem also arises for the degrees of freedom if the covariance matrices for the different groups are assumed to be unequal (covar.equal=FALSE). Both problems are handled by a plug-in approach, see the references therefore.

Author(s)

Mario Hasler

References

Hasler, M. (2014): Multiple contrast tests for multiple endpoints in the presence of heteroscedasticity. The International Journal of Biostatistics 10, 17–28, <doi:10.1515/ijb-2012-0015>.

Hasler, M. and Hothorn, L.A. (2012): A multivariate Williams-type trend procedure. Statistics in Biopharmaceutical Research 4, 57–65, <doi:10.1080/19466315.2011.633868>.

Hasler, M. and Hothorn, L.A. (2008): Multiple contrast tests in the presence of heteroscedasticity. Biometrical Journal 50, 793–800, <doi:10.1002/bimj.200710466>.

Dilba, G. et al. (2006): Simultaneous confidence sets and confidence intervals for multiple ratios. Journal of Statistical Planning and Inference 136, 2640–2658, <DOI:10.1016/j.jspi.2004.11.009>.

See Also

SimTestRat, SimTestDiff, SimCiDiff

Examples

# Example 1:
# Simultaneous confidence intervals related to a comparison of the groups
# B and H against the standard S, for endpoint Thromb.count, assuming unequal
# variances for the groups. This is an extension of the well-known Dunnett-
# intervals to the case of heteroscedasticity and in terms of ratios of means
# instead of differences.

data(coagulation)

interv1 <- SimCiRat(data=coagulation, grp="Group", resp="Thromb.count",
  type="Dunnett", base=3, alternative="greater", covar.equal=FALSE)
interv1
plot(interv1)

# Example 2:
# Simultaneous confidence intervals related to a comparisons of the groups
# B and H against the standard S, simultaneously for all endpoints, assuming
# unequal covariance matrices for the groups. This is an extension of the well-
# known Dunnett-intervals to the case of heteroscedasticity and multiple
# endpoints and in terms of ratios of means instead of differences.

data(coagulation)

interv2 <- SimCiRat(data=coagulation, grp="Group", resp=c("Thromb.count","ADP","TRAP"),
  type="Dunnett", base=3, alternative="greater", covar.equal=FALSE)
summary(interv2)
plot(interv2)
[Package SimComp version 3.3 Index]