When looking at bivariate binomial data with the aim of learning about the dependence that is present, possibly after correcting for some covariates many models are available.
in the mets package you can fit the
Pairwise odds ratio model
Bivariate Probit model
Additive gamma random effects model
Typically it can be hard or impossible to specify random effects models with special structure among the parameters of the random effects. This is possible in our models.
To be concrete about the model structure assume that we have paired binomial data (Y1, Y2, X1, X)2 where the responses are Y1, Y2 and we have covariates X1, X2.
We start by giving a brief description of these different models. First we for bivariate data one can specify the marginal probability using logistic regression models logit(P(Yi = 1|Xi)) = αi + XiTβi = 1, 2. These model can be estimated under working independence .
A typical twin analysis will typically consist of looking at both
Pairwise odds ratio model
Bivariate Probit model
The additive gamma can be used for the same as the bivariate probit model but is more restrictive in terms of dependence structure, but is nevertheless still valuable to have also as a check of results of the bivariate probit model.
For these model we assume that given random effects Z and a covariate vector V12 we have independent logistic regression models probit(P(Yi = 1|Xi, Z)) = αi + XiTβ + V12TZi = 1, 2. where Z$ is a bivariate normal distribution with some covariance Σ. The general covariance structure Σ makes the model very flexible.
We note that
The more standard link function logit rather than the probit link is often used and implemented in for example . The advantage is that one now gets an odds-ratio interpretation of the subject specific effects, but one then needs numerical integration to fit the model.
Now the pairwise odds ratio model the specifies that given $ X_1, X_2 $ the marginal models are logit(P(Yi = 1|Xi)) = αi + XiTβi = 1, 2
The primary object of interest are the odds ratio between Y1 and Y2 $$ \gamma_{12} = \frac{ P( Y_{ki} =1 , Y_{kj} =1) P( Y_{ki} =0 , Y_{kj} =0) }{ P( Y_{ki} =1 , Y_{kj} =0) P( Y_{ki} =0 , Y_{kj} =1) } $$ given Xki, Xkj, and Zkji.
We model the odds ratio with the regression γ12 = exp (Z12Tλ) Where Z12 are some covarites that may influence the odds-ratio between between Y1 and Y2 and contains the marginal covariates, . This odds-ratio is given covariates as well as marginal covariates. The odds-ratio and marginals specify the joint bivariate distribution via the so-called Placckett-distribution.
One way of fitting this model is the ALR algoritm, the alternating logistic regression ahd this has been described in several papers . We here simply estimate the parameters in a two stage-procedure
This gives efficient estimates of the dependence parameters because of orthogonality, but some efficiency may be gained for the marginal parameters by using the full likelihood or iterative fitting such as for the ALR.
The pairwise odds-ratio model is very useful, but one do not have a random effects model.
Again we operate under marginal logistic regression models are logit(P(Yi = 1|Xi)) = αi + XiTβi = 1, 2
First with just one random effect Z we assume that conditional on Z the responses are independent and follow the model logit(P(Yi = 1|Xi, Z)) = exp(−Z ⋅ Ψ−1(λ•, λ•, P(Yi = 1|Xi))) where Ψ is the laplace transform of Z where we assume that Z is gamma distributed with variance λ•−1 and mean 1. In general Ψ(λ1, λ2) is the laplace transform of a Gamma distributed random effect with Z with mean λ1/λ2 and variance λ1/λ22.
We fit this model by
To deal with multiple random effects we consider random effects Zii = 1, ..., d such that Zi is gamma distributed with * mean: λj/λ• * variance: λj/λ•2, where we define the scalar λ• below.
Now given a cluster-specific design vector V12 we assume that V12TZ is gamma distributed with mean 1 and variance λ•−1 such that critically the random effect variance is the same for all clusters. That is λ• = V12T(λ1, ..., λd)T We return to some specific models below, and show how to fit the ACE and AE model using this set-up.
One last option in the model-specification is to specify how the parameters λ1, ..., λd are related. We thus can specify a matrix M of dimension p × d such that (λ1, ..., λd)T = Mθ where θ is d-dimensional. If M is diagonal we have no restrictions on parameters.
This parametrization is obtained with the var.par=0 option that thus estimates θ.
The DEFAULT parametrization instead estimates the variances of the random effecs (var.par=1) via the parameters ν Mν = (λ1/λ•2, ..., λd/λ•2)T
The basic modelling assumption is now that given random effects Z = (Z1, ..., Zd) we have independent probabilites logit(P(Yi = 1|Xi, Z)) = exp(−V12, iTZ ⋅ Ψ−1(λ•, λ•, P(Yi = 1|Xi)))i = 1, 2
We fit this model by
Even though the model not formaly in this formulation allows negative correlation in practice the paramters can be negative and this reflects negative correlation. An advanatage is that no numerical integration is needed.
We consider the twin-stutter where for pairs of twins that are either dizygotic or monozygotic we have recorded whether the twins are stuttering
We here consider MZ and same sex DZ twins.
Looking at the data
library(mets)
data(twinstut)
twinstut$binstut <- 1*(twinstut$stutter=="yes")
twinsall <- twinstut
twinstut <- subset(twinstut,zyg%in%c("mz","dz"))
head(twinstut)
#> tvparnr zyg stutter sex age nr binstut
#> 1 1 mz no female 71 1 0
#> 2 1 mz no female 71 2 0
#> 3 2 dz no female 71 1 0
#> 8 5 mz no female 71 1 0
#> 9 5 mz no female 71 2 0
#> 11 7 dz no male 71 1 0
twinstut <- subset(twinstut,tvparnr < 3000)We start by fitting an overall dependence OR for both MZ and DZ even though the dependence is expected to be different across zygosity.
The first step is to fit the marginal model adjusting for marginal covariates. We here note that there is a rather strong gender effect in the risk of stuttering.
margbin <- glm(binstut~factor(sex)+age,data=twinstut,family=binomial())
summary(margbin)
#>
#> Call:
#> glm(formula = binstut ~ factor(sex) + age, family = binomial(),
#> data = twinstut)
#>
#> Coefficients:
#> Estimate Std. Error z value Pr(>|z|)
#> (Intercept) 0.03033 2.16166 0.014 0.9888
#> factor(sex)male 0.80288 0.20272 3.961 7.48e-05 ***
#> age -0.05471 0.03295 -1.660 0.0968 .
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> (Dispersion parameter for binomial family taken to be 1)
#>
#> Null deviance: 940.43 on 2650 degrees of freedom
#> Residual deviance: 921.01 on 2648 degrees of freedom
#> AIC: 927.01
#>
#> Number of Fisher Scoring iterations: 6Now estimating the OR parameter. We see a strong dependence with an OR at around 8 that is clearly significant.
bina <- binomial.twostage(margbin,data=twinstut,var.link=1,
clusters=twinstut$tvparnr,detail=0)
summary(bina)
#> Dependence parameter for Odds-Ratio (Plackett) model
#> With log-link
#> $estimates
#> theta se
#> dependence1 1.859712 0.481585
#>
#> $or
#> Estimate Std.Err 2.5% 97.5% P-value
#> dependence1 6.422 3.093 0.3603 12.48 0.03785
#>
#> $type
#> [1] "plackett"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"Now, and more interestingly, we consider an OR that depends on zygosity and note that MZ have a much larger OR than DZ twins. This type of trait is somewhat complicated to interpret, but clearly, one option is that that there is a genetic effect, alternatively there might be a stronger environmental effect for MZ twins.
# design for OR dependence
theta.des <- model.matrix( ~-1+factor(zyg),data=twinstut)
bin <- binomial.twostage(margbin,data=twinstut,var.link=1,
clusters=twinstut$tvparnr,theta.des=theta.des)
summary(bin)
#> Dependence parameter for Odds-Ratio (Plackett) model
#> With log-link
#> $estimates
#> theta se
#> factor(zyg)dz 0.1624942 1.0050473
#> factor(zyg)mz 3.7460315 0.7259771
#>
#> $or
#> Estimate Std.Err 2.5% 97.5% P-value
#> factor(zyg)dz 1.176 1.182 -1.141 3.494 0.3197
#> factor(zyg)mz 42.353 30.747 -17.910 102.616 0.1684
#>
#> $type
#> [1] "plackett"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"We now consider further regression modelling of the OR structure by considering possible interactions between sex and zygozsity. We see that MZ has a much higher dependence and that males have a much lower dependence. We tested for interaction in this model and these were not significant.
twinstut$cage <- scale(twinstut$age)
theta.des <- model.matrix( ~-1+factor(zyg)+factor(sex),data=twinstut)
bina <- binomial.twostage(margbin,data=twinstut,var.link=1,
clusters=twinstut$tvparnr,theta.des=theta.des)
summary(bina)
#> Dependence parameter for Odds-Ratio (Plackett) model
#> With log-link
#> $estimates
#> theta se
#> factor(zyg)dz 1.238547 1.118919
#> factor(zyg)mz 6.078248 1.536564
#> factor(sex)male -3.233772 1.776972
#>
#> $or
#> Estimate Std.Err 2.5% 97.5% P-value
#> factor(zyg)dz 3.45059 3.86094 -4.11670 11.0179 0.3715
#> factor(zyg)mz 436.26434 670.34797 -877.59353 1750.1222 0.5152
#> factor(sex)male 0.03941 0.07003 -0.09784 0.1767 0.5736
#>
#> $type
#> [1] "plackett"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"We now demonstrate how the models can fitted jointly and with anohter syntax, that ofcourse just fits the marginal model and subsequently fits the pairwise OR model.
First noticing as before that MZ twins have a much higher dependence.
# refers to zygosity of first subject in eash pair : zyg1
# could also use zyg2 (since zyg2=zyg1 within twinpair's)
out <- easy.binomial.twostage(stutter~factor(sex)+age,data=twinstut,
response="binstut",id="tvparnr",var.link=1,
theta.formula=~-1+factor(zyg1))
summary(out)
#> Dependence parameter for Odds-Ratio (Plackett) model
#> With log-link
#> $estimates
#> theta se
#> factor(zyg1)dz 0.1624942 1.0050473
#> factor(zyg1)mz 3.7460315 0.7259771
#>
#> $or
#> Estimate Std.Err 2.5% 97.5% P-value
#> factor(zyg1)dz 1.176 1.182 -1.141 3.494 0.3197
#> factor(zyg1)mz 42.353 30.747 -17.910 102.616 0.1684
#>
#> $type
#> [1] "plackett"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"Now considering all data and estimating separate effects for the OR for opposite sex DZ twins and same sex twins. We here find that os twins are not markedly different from the same sex DZ twins.
# refers to zygosity of first subject in eash pair : zyg1
# could also use zyg2 (since zyg2=zyg1 within twinpair's))
desfs<-function(x,num1="zyg1",num2="zyg2")
c(x[num1]=="dz",x[num1]=="mz",x[num1]=="os")*1
margbinall <- glm(binstut~factor(sex)+age,data=twinsall,family=binomial())
out3 <- easy.binomial.twostage(binstut~factor(sex)+age,
data=twinsall,response="binstut",id="tvparnr",var.link=1,
theta.formula=desfs,desnames=c("dz","mz","os"))
summary(out3)
#> Dependence parameter for Odds-Ratio (Plackett) model
#> With log-link
#> $estimates
#> theta se
#> dz 0.5278527 0.2396796
#> mz 3.4850037 0.1864190
#> os 0.7802940 0.2894394
#>
#> $or
#> Estimate Std.Err 2.5% 97.5% P-value
#> dz 1.695 0.4063 0.8989 2.492 3.016e-05
#> mz 32.623 6.0815 20.7031 44.542 8.128e-08
#> os 2.182 0.6316 0.9442 3.420 5.504e-04
#>
#> $type
#> [1] "plackett"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"library(mets)
data(twinstut)
twinstut <- subset(twinstut,zyg%in%c("mz","dz"))
twinstut$binstut <- 1*(twinstut$stutter=="yes")
head(twinstut)
#> tvparnr zyg stutter sex age nr binstut
#> 1 1 mz no female 71 1 0
#> 2 1 mz no female 71 2 0
#> 3 2 dz no female 71 1 0
#> 8 5 mz no female 71 1 0
#> 9 5 mz no female 71 2 0
#> 11 7 dz no male 71 1 0
twinstut <- subset(twinstut,tvparnr < 2000)First testing for same dependence in MZ and DZ that we recommend doing by comparing the correlations of MZ and DZ twins. Apart from regression correction in the mean this is an un-structured model, and the useful concordance and casewise concordance estimates can be reported from this analysis.
b1 <- bptwin(binstut~sex,data=twinstut,id="tvparnr",zyg="zyg",DZ="dz",type="un")
summary(b1)
#>
#> Estimate Std.Err Z p-value
#> (Intercept) -2.04432 0.10246 -19.9532 < 2.2e-16 ***
#> sexmale 0.41203 0.12392 3.3249 0.0008844 ***
#> atanh(rho) MZ 1.11748 0.43188 2.5875 0.0096683 **
#> atanh(rho) DZ 0.23000 0.25889 0.8884 0.3743295
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Total MZ/DZ Complete pairs MZ/DZ
#> 583/1192 212/354
#>
#> Estimate 2.5% 97.5%
#> Tetrachoric correlation MZ 0.80669 0.26456 0.96139
#> Tetrachoric correlation DZ 0.22603 -0.27052 0.62759
#>
#> MZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00886 0.00272 0.02840
#> Casewise Concordance 0.43282 0.13214 0.79272
#> Marginal 0.02046 0.01258 0.03312
#> Rel.Recur.Risk 21.15321 2.70681 39.59960
#> log(OR) 4.15336 1.96005 6.34666
#> DZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00128 0.00013 0.01240
#> Casewise Concordance 0.06251 0.00705 0.38497
#> Marginal 0.02046 0.01258 0.03312
#> Rel.Recur.Risk 3.05481 -3.12067 9.23029
#> log(OR) 1.20535 -1.09090 3.50161
#>
#> Estimate 2.5% 97.5%
#> Broad-sense heritability 1 NaN NaNWe now turn attention to specific polygenic modelling where special random effects are used to specify ACE, AE, ADE models and so forth. This is very easy with the bptwin function. The key parts of the output are the sizes of the genetic component A and the environmental component, and we can compare with the results of the unstructed model above. Also formally we can test if this submodel is acceptable by a likelihood ratio test.
b1 <- bptwin(binstut~sex,data=twinstut,id="tvparnr",zyg="zyg",DZ="dz",type="ace")
summary(b1)
#>
#> Estimate Std.Err Z p-value
#> (Intercept) -4.20958 1.55369 -2.7094 0.00674 **
#> sexmale 0.85990 0.36387 2.3632 0.01812 *
#> log(var(A)) 1.17018 0.99695 1.1738 0.24049
#> log(var(C)) -23.53038 NaN NaN NaN
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Total MZ/DZ Complete pairs MZ/DZ
#> 583/1192 212/354
#>
#> Estimate 2.5% 97.5%
#> A 0.76318 0.41002 1.11633
#> C 0.00000 0.00000 0.00000
#> E 0.23682 -0.11633 0.58998
#> MZ Tetrachoric Cor 0.76318 0.15672 0.95170
#> DZ Tetrachoric Cor 0.38159 0.19280 0.54313
#>
#> MZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00768 0.00201 0.02893
#> Casewise Concordance 0.37943 0.09711 0.77658
#> Marginal 0.02025 0.01241 0.03289
#> Rel.Recur.Risk 18.73516 -0.13385 37.60417
#> log(OR) 3.85127 1.58182 6.12072
#> DZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00230 0.00077 0.00688
#> Casewise Concordance 0.11369 0.05266 0.22841
#> Marginal 0.02025 0.01241 0.03289
#> Rel.Recur.Risk 5.61371 2.19257 9.03484
#> log(OR) 1.92764 1.16374 2.69154
#>
#> Estimate 2.5% 97.5%
#> Broad-sense heritability 0.76318 0.41002 1.11633b0 <- bptwin(binstut~sex,data=twinstut,id="tvparnr",zyg="zyg",DZ="dz",type="ae")
summary(b0)
#>
#> Estimate Std.Err Z p-value
#> (Intercept) -4.20958 1.55369 -2.7094 0.00674 **
#> sexmale 0.85990 0.36387 2.3632 0.01812 *
#> log(var(A)) 1.17018 0.99695 1.1738 0.24049
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Total MZ/DZ Complete pairs MZ/DZ
#> 583/1192 212/354
#>
#> Estimate 2.5% 97.5%
#> A 0.76318 0.41002 1.11633
#> E 0.23682 -0.11633 0.58998
#> MZ Tetrachoric Cor 0.76318 0.15672 0.95170
#> DZ Tetrachoric Cor 0.38159 0.19280 0.54313
#>
#> MZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00768 0.00201 0.02893
#> Casewise Concordance 0.37943 0.09711 0.77658
#> Marginal 0.02025 0.01241 0.03289
#> Rel.Recur.Risk 18.73517 -0.13386 37.60419
#> log(OR) 3.85127 1.58182 6.12072
#> DZ:
#> Estimate 2.5% 97.5%
#> Concordance 0.00230 0.00077 0.00688
#> Casewise Concordance 0.11369 0.05266 0.22841
#> Marginal 0.02025 0.01241 0.03289
#> Rel.Recur.Risk 5.61371 2.19257 9.03484
#> log(OR) 1.92764 1.16374 2.69154
#>
#> Estimate 2.5% 97.5%
#> Broad-sense heritability 0.76318 0.41002 1.11633Fitting first a model with different size random effects for MZ and DZ. We note that as before in the OR and biprobit model the dependence is much stronger for MZ twins. We also test if these are the same by parametrizing the OR model with an intercept. This clearly shows a significant difference.
theta.des <- model.matrix( ~-1+factor(zyg),data=twinstut)
margbin <- glm(binstut~sex,data=twinstut,family=binomial())
bintwin <- binomial.twostage(margbin,data=twinstut,model="gamma",
clusters=twinstut$tvparnr,detail=0,theta=c(0.1)/1,var.link=1,
theta.des=theta.des)
summary(bintwin)
#> Dependence parameter for Clayton-Oakes model
#> Variance of Gamma distributed random effects
#> With log-link
#> $estimates
#> theta se
#> factor(zyg)dz -2.13348460 1.0821489
#> factor(zyg)mz -0.07740026 0.5790839
#>
#> $vargam
#> Estimate Std.Err 2.5% 97.5% P-value
#> factor(zyg)dz 0.1184 0.1282 -0.1327 0.3696 0.35544
#> factor(zyg)mz 0.9255 0.5360 -0.1249 1.9760 0.08419
#>
#> $type
#> [1] "gamma"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"
# test for same dependence in MZ and DZ
theta.des <- model.matrix( ~factor(zyg),data=twinstut)
margbin <- glm(binstut~sex,data=twinstut,family=binomial())
bintwin <- binomial.twostage(margbin,data=twinstut,model="gamma",
clusters=twinstut$tvparnr,detail=0,theta=c(0.1)/1,var.link=1,
theta.des=theta.des)
summary(bintwin)
#> Dependence parameter for Clayton-Oakes model
#> Variance of Gamma distributed random effects
#> With log-link
#> $estimates
#> theta se
#> (Intercept) -2.133485 1.082149
#> factor(zyg)mz 2.056084 1.227348
#>
#> $vargam
#> Estimate Std.Err 2.5% 97.5% P-value
#> (Intercept) 0.1184 0.1282 -0.1327 0.3696 0.3554
#> factor(zyg)mz 7.8153 9.5921 -10.9849 26.6155 0.4152
#>
#> $type
#> [1] "gamma"
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"First setting up the random effects design for the random effects and the the relationship between variance parameters. We see that the genetic random effect has size one for MZ and 0.5 for DZ subjects, that have shared and non-shared genetic components with variance 0.5 such that the total genetic variance is the same for all subjects. The shared environmental effect is the samme for all. Thus two parameters with these bands.
out <- twin.polygen.design(twinstut,id="tvparnr",zygname="zyg",zyg="dz",type="ace")
head(cbind(out$des.rv,twinstut$tvparnr),10)
#> MZ DZ DZns1 DZns2 env
#> 1 1 0 0 0 1 1
#> 2 1 0 0 0 1 1
#> 3 0 1 1 0 1 2
#> 8 1 0 0 0 1 5
#> 9 1 0 0 0 1 5
#> 11 0 1 1 0 1 7
#> 12 0 1 1 0 1 8
#> 13 0 1 0 1 1 8
#> 15 0 1 1 0 1 10
#> 18 0 1 1 0 1 12
out$pardes
#> [,1] [,2]
#> [1,] 1.0 0
#> [2,] 0.5 0
#> [3,] 0.5 0
#> [4,] 0.5 0
#> [5,] 0.0 1Now, fitting the ACE model, we see that the variance of the genetic, component, is 1.5 and the environmental variance is -0.5. Thus suggesting that the ACE model does not fit the data. When the random design is given we automatically use the gamma fralty model.
margbin <- glm(binstut~sex,data=twinstut,family=binomial())
bintwin1 <- binomial.twostage(margbin,data=twinstut,
clusters=twinstut$tvparnr,detail=0,theta=c(0.1)/1,var.link=0,
random.design=out$des.rv,theta.des=out$pardes)
summary(bintwin1)
#> Dependence parameter for Clayton-Oakes model
#> Variance of Gamma distributed random effects
#> $estimates
#> theta se
#> dependence1 1.1700713 0.9350041
#> dependence2 -0.2552978 0.5910697
#>
#> $type
#> [1] "clayton.oakes"
#>
#> $h
#> Estimate Std.Err 2.5% 97.5% P-value
#> dependence1 1.2791 0.6039 0.09552 2.4626 0.03416
#> dependence2 -0.2791 0.6039 -1.46265 0.9045 0.64397
#>
#> $vare
#> NULL
#>
#> $vartot
#> Estimate Std.Err 2.5% 97.5% P-value
#> p1 0.9148 0.5352 -0.1343 1.964 0.08744
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"For this model we estimate the concordance and casewise concordance as well as the marginal rates of stuttering for females.
concordanceTwinACE(bintwin1,type="ace")
#> $MZ
#> Estimate Std.Err 2.5% 97.5% P-value
#> concordance 0.009738 0.004010 0.001878 0.01760 1.517e-02
#> casewise concordance 0.476141 0.190613 0.102547 0.84974 1.249e-02
#> marginal 0.020452 0.005083 0.010489 0.03041 5.733e-05
#>
#> $DZ
#> Estimate Std.Err 2.5% 97.5% P-value
#> concordance 0.001301 0.001158 -0.0009681 0.00357 2.611e-01
#> casewise concordance 0.063604 0.057255 -0.0486137 0.17582 2.666e-01
#> marginal 0.020452 0.005083 0.0104894 0.03041 5.733e-05The E component was not consistent with the fit of the data and we now consider instead the AE model.
out <- twin.polygen.design(twinstut,id="tvparnr",zygname="zyg",zyg="dz",type="ae")
bintwin <- binomial.twostage(margbin,data=twinstut,
clusters=twinstut$tvparnr,detail=0,theta=c(0.1)/1,var.link=0,
random.design=out$des.rv,theta.des=out$pardes)
summary(bintwin)
#> Dependence parameter for Clayton-Oakes model
#> Variance of Gamma distributed random effects
#> $estimates
#> theta se
#> dependence1 0.8485392 0.4941264
#>
#> $type
#> [1] "clayton.oakes"
#>
#> $h
#> Estimate Std.Err 2.5% 97.5% P-value
#> dependence1 1 0 1 1 0
#>
#> $vare
#> NULL
#>
#> $vartot
#> Estimate Std.Err 2.5% 97.5% P-value
#> p1 0.8485 0.4941 -0.1199 1.817 0.08593
#>
#> attr(,"class")
#> [1] "summary.mets.twostage"Again, the concordance can be computed:
concordanceTwinACE(bintwin,type="ae")
#> $MZ
#> Estimate Std.Err 2.5% 97.5% P-value
#> concordance 0.009236 0.003778 0.001831 0.01664 1.450e-02
#> casewise concordance 0.451605 0.189131 0.080916 0.82229 1.695e-02
#> marginal 0.020452 0.005083 0.010489 0.03041 5.733e-05
#>
#> $DZ
#> Estimate Std.Err 2.5% 97.5% P-value
#> concordance 0.001966 0.0007099 0.0005741 0.003357 5.628e-03
#> casewise concordance 0.096106 0.0196561 0.0575803 0.134631 1.012e-06
#> marginal 0.020452 0.0050831 0.0104894 0.030415 5.733e-05sessionInfo()
#> R version 4.4.2 (2024-10-31)
#> Platform: x86_64-pc-linux-gnu
#> Running under: Ubuntu 24.04.1 LTS
#>
#> Matrix products: default
#> BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
#> LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.26.so; LAPACK version 3.12.0
#>
#> locale:
#> [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
#> [3] LC_TIME=en_US.UTF-8 LC_COLLATE=C
#> [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
#> [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
#> [9] LC_ADDRESS=C LC_TELEPHONE=C
#> [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
#>
#> time zone: Etc/UTC
#> tzcode source: system (glibc)
#>
#> attached base packages:
#> [1] stats graphics grDevices utils datasets methods base
#>
#> other attached packages:
#> [1] mets_1.3.4 timereg_2.0.6 survival_3.7-0 rmarkdown_2.29
#>
#> loaded via a namespace (and not attached):
#> [1] cli_3.6.3 knitr_1.49 rlang_1.1.4
#> [4] xfun_0.49 jsonlite_1.8.9 listenv_0.9.1
#> [7] future.apply_1.11.3 buildtools_1.0.0 lava_1.8.0
#> [10] htmltools_0.5.8.1 maketools_1.3.1 sys_3.4.3
#> [13] sass_0.4.9 grid_4.4.2 evaluate_1.0.1
#> [16] jquerylib_0.1.4 fastmap_1.2.0 mvtnorm_1.3-2
#> [19] yaml_2.3.10 lifecycle_1.0.4 numDeriv_2016.8-1.1
#> [22] compiler_4.4.2 codetools_0.2-20 ucminf_1.2.2
#> [25] Rcpp_1.0.13-1 future_1.34.0 lattice_0.22-6
#> [28] digest_0.6.37 R6_2.5.1 parallelly_1.39.0
#> [31] parallel_4.4.2 splines_4.4.2 bslib_0.8.0
#> [34] Matrix_1.7-1 tools_4.4.2 globals_0.16.3
#> [37] cachem_1.1.0