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Introduction

In the present vignette, we want to discuss how to specify multivariate multilevel models using brms. We call a model multivariate if it contains multiple response variables, each being predicted by its own set of predictors. Consider an example from biology. Hadfield, Nutall, Osorio, and Owens (2007) analyzed data of the Eurasian blue tit (https://en.wikipedia.org/wiki/Eurasian_blue_tit). They predicted the tarsus length as well as the back color of chicks. Half of the brood were put into another fosternest, while the other half stayed in the fosternest of their own dam. This allows to separate genetic from environmental factors. Additionally, we have information about the hatchdate and sex of the chicks (the latter being known for 94% of the animals).

data("BTdata", package = "MCMCglmm")
head(BTdata)
       tarsus       back  animal     dam fosternest  hatchdate  sex
1 -1.89229718  1.1464212 R187142 R187557      F2102 -0.6874021  Fem
2  1.13610981 -0.7596521 R187154 R187559      F1902 -0.6874021 Male
3  0.98468946  0.1449373 R187341 R187568       A602 -0.4279814 Male
4  0.37900806  0.2555847 R046169 R187518      A1302 -1.4656641 Male
5 -0.07525299 -0.3006992 R046161 R187528      A2602 -1.4656641  Fem
6 -1.13519543  1.5577219 R187409 R187945      C2302  0.3502805  Fem

Basic Multivariate Models

We begin with a relatively simple multivariate normal model.

bform1 <- 
  bf(mvbind(tarsus, back) ~ sex + hatchdate + (1|p|fosternest) + (1|q|dam)) +
  set_rescor(TRUE)

fit1 <- brm(bform1, data = BTdata, chains = 2, cores = 2)

As can be seen in the model code, we have used mvbind notation to tell brms that both tarsus and back are separate response variables. The term (1|p|fosternest) indicates a varying intercept over fosternest. By writing |p| in between we indicate that all varying effects of fosternest should be modeled as correlated. This makes sense since we actually have two model parts, one for tarsus and one for back. The indicator p is arbitrary and can be replaced by other symbols that comes into your mind (for details about the multilevel syntax of brms, see help("brmsformula") and vignette("brms_multilevel")). Similarly, the term (1|q|dam) indicates correlated varying effects of the genetic mother of the chicks. Alternatively, we could have also modeled the genetic similarities through pedigrees and corresponding relatedness matrices, but this is not the focus of this vignette (please see vignette("brms_phylogenetics")). The model results are readily summarized via

fit1 <- add_criterion(fit1, "loo")
summary(fit1)
 Family: MV(gaussian, gaussian) 
  Links: mu = identity
         mu = identity 
Formula: tarsus ~ sex + hatchdate + (1 | p | fosternest) + (1 | q | dam) 
         back ~ sex + hatchdate + (1 | p | fosternest) + (1 | q | dam) 
   Data: BTdata (Number of observations: 828) 
  Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
         total post-warmup draws = 2000

Multilevel Hyperparameters:
~dam (Number of levels: 106) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.49      0.05     0.39     0.59 1.00      667
sd(back_Intercept)                       0.25      0.07     0.10     0.40 1.00      261
cor(tarsus_Intercept,back_Intercept)    -0.52      0.22    -0.93    -0.07 1.00      426
                                     Tail_ESS
sd(tarsus_Intercept)                      860
sd(back_Intercept)                        499
cor(tarsus_Intercept,back_Intercept)      623

~fosternest (Number of levels: 104) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.27      0.06     0.16     0.38 1.00      589
sd(back_Intercept)                       0.35      0.06     0.23     0.47 1.00      416
cor(tarsus_Intercept,back_Intercept)     0.71      0.21     0.23     0.99 1.00      224
                                     Tail_ESS
sd(tarsus_Intercept)                     1019
sd(back_Intercept)                        847
cor(tarsus_Intercept,back_Intercept)      332

Regression Coefficients:
                 Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept    -0.41      0.07    -0.54    -0.28 1.00      659      855
back_Intercept      -0.01      0.06    -0.14     0.12 1.00     1285     1336
tarsus_sexMale       0.77      0.06     0.66     0.88 1.00     2512     1387
tarsus_sexUNK        0.23      0.13    -0.02     0.48 1.00     2273     1533
tarsus_hatchdate    -0.04      0.06    -0.16     0.07 1.00      669     1086
back_sexMale         0.01      0.07    -0.12     0.14 1.00     2355     1415
back_sexUNK          0.15      0.15    -0.16     0.44 1.00     2504     1785
back_hatchdate      -0.09      0.05    -0.19     0.02 1.00     1197     1235

Further Distributional Parameters:
             Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus     0.76      0.02     0.72     0.80 1.00     2013     1525
sigma_back       0.90      0.02     0.85     0.95 1.00     1872     1417

Residual Correlations: 
                    Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
rescor(tarsus,back)    -0.05      0.04    -0.12     0.02 1.00     1981     1515

Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).

The summary output of multivariate models closely resembles those of univariate models, except that the parameters now have the corresponding response variable as prefix. Across dams, tarsus length and back color seem to be negatively correlated, while across fosternests the opposite is true. This indicates differential effects of genetic and environmental factors on these two characteristics. Further, the small residual correlation rescor(tarsus, back) on the bottom of the output indicates that there is little unmodeled dependency between tarsus length and back color. Although not necessary at this point, we have already computed and stored the LOO information criterion of fit1, which we will use for model comparisons. Next, let’s take a look at some posterior-predictive checks, which give us a first impression of the model fit.

pp_check(fit1, resp = "tarsus")

pp_check(fit1, resp = "back")

This looks pretty solid, but we notice a slight unmodeled left skewness in the distribution of tarsus. We will come back to this later on. Next, we want to investigate how much variation in the response variables can be explained by our model and we use a Bayesian generalization of the \(R^2\) coefficient.

bayes_R2(fit1)
          Estimate Est.Error      Q2.5     Q97.5
R2tarsus 0.4340254 0.0264582 0.3797048 0.4826320
R2back   0.1985098 0.0286021 0.1440022 0.2539625

Clearly, there is much variation in both animal characteristics that we can not explain, but apparently we can explain more of the variation in tarsus length than in back color.

More Complex Multivariate Models

Now, suppose we only want to control for sex in tarsus but not in back and vice versa for hatchdate. Not that this is particular reasonable for the present example, but it allows us to illustrate how to specify different formulas for different response variables. We can no longer use mvbind syntax and so we have to use a more verbose approach:

bf_tarsus <- bf(tarsus ~ sex + (1|p|fosternest) + (1|q|dam))
bf_back <- bf(back ~ hatchdate + (1|p|fosternest) + (1|q|dam))
fit2 <- brm(bf_tarsus + bf_back + set_rescor(TRUE), 
            data = BTdata, chains = 2, cores = 2)

Note that we have literally added the two model parts via the + operator, which is in this case equivalent to writing mvbf(bf_tarsus, bf_back). See help("brmsformula") and help("mvbrmsformula") for more details about this syntax. Again, we summarize the model first.

fit2 <- add_criterion(fit2, "loo")
summary(fit2)
 Family: MV(gaussian, gaussian) 
  Links: mu = identity
         mu = identity 
Formula: tarsus ~ sex + (1 | p | fosternest) + (1 | q | dam) 
         back ~ hatchdate + (1 | p | fosternest) + (1 | q | dam) 
   Data: BTdata (Number of observations: 828) 
  Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
         total post-warmup draws = 2000

Multilevel Hyperparameters:
~dam (Number of levels: 106) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.48      0.05     0.39     0.58 1.00      619
sd(back_Intercept)                       0.25      0.07     0.11     0.40 1.00      296
cor(tarsus_Intercept,back_Intercept)    -0.50      0.22    -0.93    -0.06 1.01      310
                                     Tail_ESS
sd(tarsus_Intercept)                     1275
sd(back_Intercept)                        578
cor(tarsus_Intercept,back_Intercept)      548

~fosternest (Number of levels: 104) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.27      0.06     0.16     0.38 1.00      466
sd(back_Intercept)                       0.35      0.06     0.23     0.47 1.00      533
cor(tarsus_Intercept,back_Intercept)     0.70      0.19     0.26     0.98 1.00      254
                                     Tail_ESS
sd(tarsus_Intercept)                      800
sd(back_Intercept)                        805
cor(tarsus_Intercept,back_Intercept)      349

Regression Coefficients:
                 Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept    -0.41      0.07    -0.55    -0.28 1.01      824      855
back_Intercept       0.00      0.05    -0.11     0.10 1.00     1320     1339
tarsus_sexMale       0.77      0.06     0.66     0.88 1.00     2459     1397
tarsus_sexUNK        0.22      0.13    -0.04     0.48 1.00     2948     1425
back_hatchdate      -0.08      0.05    -0.19     0.02 1.00     1255     1687

Further Distributional Parameters:
             Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus     0.76      0.02     0.72     0.80 1.00     1571     1120
sigma_back       0.90      0.02     0.85     0.95 1.00     1718     1480

Residual Correlations: 
                    Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
rescor(tarsus,back)    -0.05      0.04    -0.12     0.02 1.00     2187     1296

Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).

Let’s find out, how model fit changed due to excluding certain effects from the initial model:

loo(fit1, fit2)
Output of model 'fit1':

Computed from 2000 by 828 log-likelihood matrix.

         Estimate   SE
elpd_loo  -2124.4 33.6
p_loo       174.5  7.3
looic      4248.9 67.1
------
MCSE of elpd_loo is 0.4.
MCSE and ESS estimates assume MCMC draws (r_eff in [0.3, 1.8]).

All Pareto k estimates are good (k < 0.7).
See help('pareto-k-diagnostic') for details.

Output of model 'fit2':

Computed from 2000 by 828 log-likelihood matrix.

         Estimate   SE
elpd_loo  -2123.7 33.6
p_loo       173.5  7.3
looic      4247.3 67.2
------
MCSE of elpd_loo is NA.
MCSE and ESS estimates assume MCMC draws (r_eff in [0.4, 1.6]).

Pareto k diagnostic values:
                         Count Pct.    Min. ESS
(-Inf, 0.7]   (good)     827   99.9%   96      
   (0.7, 1]   (bad)        1    0.1%   <NA>    
   (1, Inf)   (very bad)   0    0.0%   <NA>    
See help('pareto-k-diagnostic') for details.

Model comparisons:
 model elpd_diff se_diff p_worse       diag_diff      diag_elpd
  fit2       0.0     0.0      NA                 1 k_psis > 0.7
  fit1      -0.8     1.3    0.72 |elpd_diff| < 4               

Apparently, there is no noteworthy difference in the model fit. Accordingly, we do not really need to model sex and hatchdate for both response variables, but there is also no harm in including them (so I would probably just include them).

To give you a glimpse of the capabilities of brms’ multivariate syntax, we change our model in various directions at the same time. Remember the slight left skewness of tarsus, which we will now model by using the skew_normal family instead of the gaussian family. Since we do not have a multivariate normal (or student-t) model, anymore, estimating residual correlations is no longer possible. We make this explicit using the set_rescor function. Further, we investigate if the relationship of back and hatchdate is really linear as previously assumed by fitting a non-linear spline of hatchdate. On top of it, we model separate residual variances of tarsus for male and female chicks.

bf_tarsus <- bf(tarsus ~ sex + (1|p|fosternest) + (1|q|dam)) +
  lf(sigma ~ 0 + sex) + skew_normal()
bf_back <- bf(back ~ s(hatchdate) + (1|p|fosternest) + (1|q|dam)) +
  gaussian()

fit3 <- brm(
  bf_tarsus + bf_back + set_rescor(FALSE),
  data = BTdata, chains = 2, cores = 2,
  control = list(adapt_delta = 0.95)
)

Again, we summarize the model and look at some posterior-predictive checks.

fit3 <- add_criterion(fit3, "loo")
summary(fit3)
 Family: MV(skew_normal, gaussian) 
  Links: mu = identity; sigma = log
         mu = identity 
Formula: tarsus ~ sex + (1 | p | fosternest) + (1 | q | dam) 
         sigma ~ 0 + sex
         back ~ s(hatchdate) + (1 | p | fosternest) + (1 | q | dam) 
   Data: BTdata (Number of observations: 828) 
  Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
         total post-warmup draws = 2000

Smoothing Spline Hyperparameters:
                       Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sds(back_shatchdate_1)     2.05      1.08     0.35     4.61 1.00      439      390

Multilevel Hyperparameters:
~dam (Number of levels: 106) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.47      0.05     0.38     0.57 1.01      496
sd(back_Intercept)                       0.23      0.07     0.10     0.36 1.01      250
cor(tarsus_Intercept,back_Intercept)    -0.53      0.23    -0.95    -0.06 1.01      362
                                     Tail_ESS
sd(tarsus_Intercept)                      716
sd(back_Intercept)                        419
cor(tarsus_Intercept,back_Intercept)      464

~fosternest (Number of levels: 104) 
                                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept)                     0.27      0.06     0.15     0.38 1.00      401
sd(back_Intercept)                       0.31      0.06     0.20     0.42 1.00      357
cor(tarsus_Intercept,back_Intercept)     0.65      0.21     0.18     0.97 1.02      210
                                     Tail_ESS
sd(tarsus_Intercept)                      700
sd(back_Intercept)                        662
cor(tarsus_Intercept,back_Intercept)      486

Regression Coefficients:
                     Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept        -0.41      0.07    -0.55    -0.28 1.00      794     1109
back_Intercept           0.00      0.05    -0.10     0.10 1.00     1120     1482
tarsus_sexMale           0.77      0.06     0.66     0.88 1.00     2457     1507
tarsus_sexUNK            0.22      0.12    -0.00     0.45 1.00     2078     1422
sigma_tarsus_sexFem     -0.30      0.04    -0.38    -0.22 1.00     2417     1555
sigma_tarsus_sexMale    -0.25      0.04    -0.32    -0.16 1.00     2146     1753
sigma_tarsus_sexUNK     -0.40      0.13    -0.66    -0.15 1.00     2056     1415
back_shatchdate_1       -0.07      3.19    -5.79     7.17 1.00      823     1172

Further Distributional Parameters:
             Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_back       0.90      0.02     0.86     0.95 1.00     1379     1297
alpha_tarsus    -1.25      0.42    -1.91    -0.14 1.00     1304      553

Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).

We see that the (log) residual standard deviation of tarsus is somewhat larger for chicks whose sex could not be identified as compared to male or female chicks. Further, we see from the negative alpha (skewness) parameter of tarsus that the residuals are indeed slightly left-skewed. Lastly, running

conditional_effects(fit3, "hatchdate", resp = "back")

reveals a non-linear relationship of hatchdate on the back color, which seems to change in waves over the course of the hatch dates.

There are many more modeling options for multivariate models, which are not discussed in this vignette. Examples include autocorrelation structures, Gaussian processes, or explicit non-linear predictors (e.g., see help("brmsformula") or vignette("brms_multilevel")). In fact, nearly all the flexibility of univariate models is retained in multivariate models.

References

Hadfield JD, Nutall A, Osorio D, Owens IPF (2007). Testing the phenotypic gambit: phenotypic, genetic and environmental correlations of colour. Journal of Evolutionary Biology, 20(2), 549-557.