Two Different Questions About Information
In a mixed-effects study, data can tell us about the population and about particular individuals. These are related questions, but they are not the same. Population information describes how precisely the full study can estimate shared parameters, such as a population mean or a random-effect variance. Individual empirical Bayes (EB) precision describes how concentrated the model-based estimate of one subject’s latent random effect is, conditional on the population model.
The distinction matters in design. Adding subjects can improve estimation of population parameters even if each subject contributes little information about their own random effect. Repeating measurements on a subject can sharpen that subject’s EB estimate, but it does not necessarily improve every population parameter at the same rate. The calculations below separate these targets in a Gaussian random-intercept model.
A Random-Intercept Model
Suppose subject \(i\) has \(m\) measurements, all made under the same condition. Let \(Y_{ij}\) be measurement \(j\) on subject \(i\), in the measurement’s units. Consider
Here \(\beta\) is the population mean, \(b_i\) is subject \(i\)’s deviation from that mean, and \(\varepsilon_{ij}\) is residual error. Assume random effects are independent across subjects, residual errors are independent across observations and subjects, and the random effects and residual errors are mutually independent. For the calculations, \(\sigma^2\) and \(\omega^2\) are positive and treated as known when calculating EB precision. For population Fisher information, they are the true local values at which information is evaluated.
After integrating out \(b_i\), the vector of a subject’s \(m\) observations has a multivariate normal distribution:
The off-diagonal covariances are \(\omega^2\): two measurements on the same subject share the random intercept. This marginal distribution is the basis for population information. By contrast, EB estimation conditions on the measurements of one subject and combines those data with the random-effect distribution.
Individual EB Estimate and Conditional Precision
For known \(\beta,\omega^2,\sigma^2\), the subject’s data provide the sample mean \(\bar{Y}_i\). The likelihood for \(b_i\) is proportional to a normal density centered at \(\bar{Y}_i-\beta\), with variance \(\sigma^2/m\). Combining it with the normal distribution \(N(0,\omega^2)\) gives a normal conditional distribution for \(b_i\):
The conditional mean is the EB estimate in this known-parameter model. It is a shrunken version of the subject’s raw deviation \(\bar{Y}_i-\beta\). The shrinkage factor is \(\omega^2/(\omega^2+\sigma^2/m)\), between zero and one. The conditional precision, the reciprocal of the conditional variance, is \(1/\omega^2+m/\sigma^2\). It includes information from both the population distribution of random effects and the subject’s own measurements.
In practical empirical Bayes estimation, population parameters are generally estimated from the study and then substituted into these calculations. The resulting conditional variance is therefore a plug-in precision: it treats estimated population parameters as if they were known. It does not, by itself, include uncertainty in those estimates.
Worked Example: Shrinkage for One Subject
Consider a hypothetical study with \(\beta=10\) mg/L, \(\omega^2=4\) (mg/L)\(^2\), and \(\sigma^2=9\) (mg/L)\(^2\). One subject has three measurements: 12, 15, and 18 mg/L. Calculate the EB estimate and its conditional variance, treating the population parameters as known.
The subject mean is \(\bar{Y}_i=(12+15+18)/3=15\) mg/L, so the raw deviation is \(15-10=5\) mg/L. The shrinkage factor is
Thus the EB estimate is \(0.5714(5)=2.857\) mg/L. The posterior conditional variance is
The corresponding conditional standard deviation is \(\sqrt{1.714}=1.309\) mg/L. The estimate is closer to zero than the raw deviation because the model allows substantial residual variation relative to the information from these three measurements. The calculation describes uncertainty about this subject’s \(b_i\), conditional on the specified population parameters; it is not a standard error for \(\beta\) or \(\omega^2\).
Population Fisher Information in the Same Model
For \(N\) independent subjects with the same \(m\), population information is obtained from the marginal likelihood of their observation vectors. For the fixed mean \(\beta\), the Fisher information from one subject is \(\mathbf{1}^{\mathsf T}V^{-1}\mathbf{1}\). Since \(V\mathbf{1}=(\sigma^2+m\omega^2)\mathbf{1}\), it follows that \(V^{-1}\mathbf{1}=\mathbf{1}/(\sigma^2+m\omega^2)\). Therefore,
This is information about the shared population mean, not about any one \(b_i\). The denominator reflects the covariance among repeated observations: extra measurements on one subject share the subject-level random intercept.
The marginal information about \(\omega^2\) is also distinct from EB precision. For a multivariate normal observation with mean not depending on \(\omega^2\), and covariance derivative \(J=\partial V/\partial\omega^2=\mathbf{1}\mathbf{1}^{\mathsf T}\), the covariance-parameter Fisher information is
To see the simplification, \(V^{-1}\mathbf{1}=\mathbf{1}/(\sigma^2+m\omega^2)\) implies \(V^{-1}J=\mathbf{1}\mathbf{1}^{\mathsf T}/(\sigma^2+m\omega^2)\). Squaring this rank-one matrix and taking its trace gives \(m^2/(\sigma^2+m\omega^2)^2\); the Fisher-information formula contributes the factor \(1/2\). Independent subjects contribute additive information, so the total is \(N\) times the per-subject expression. The units are inverse squared units of \(\omega^2\), as required for information about a variance parameter.
These formulas rely on the stated Gaussian model and a balanced design with common \(m\). They describe expected local curvature of the marginal log likelihood. They are not the realized curvature for every possible data set, nor do they guarantee that a variance-component estimate will behave like a normal estimator, especially near the boundary \(\omega^2=0\).
Worked Example: Population Information for a Cohort
Suppose a hypothetical design enrolls \(N=20\) subjects, each measured \(m=3\) times, with \(\sigma^2=9\) (mg/L)\(^2\) and \(\omega^2=4\) (mg/L)\(^2\). Calculate the Fisher information for \(\beta\) and \(\omega^2\).
For the mean,
The inverse square root, \(1/\sqrt{2.857}=0.5916\) mg/L, is the model-based Cramér–Rao standard-error benchmark for an unbiased estimator under regularity conditions. It is a local information summary, not a confidence interval or a claim about the realized uncertainty in a particular fitted study.
For the random-effect variance,
The inverse square root is \(2.214\) (mg/L)\(^2\). The two information quantities concern different population parameters and have different units. Neither is the conditional precision of the individual EB estimate calculated in the preceding example.
Why Design Can Affect the Two Quantities Differently
A useful comparison holds the total number of measurements fixed while changing how they are allocated. More subjects provide more independent realizations of the random effect; more repeated observations per subject reduce residual noise in that subject’s mean. Those changes enter population information and EB precision through different expressions.
Worked Example: Twelve Measurements, Two Allocations
Compare two hypothetical designs with the same total of 12 observations and the same known variances, \(\sigma^2=9\) (mg/L)\(^2\) and \(\omega^2=4\) (mg/L)\(^2\): Design A has four subjects with three measurements each; Design B has 12 subjects with one measurement each.
For a subject with \(m=3\), the EB conditional variance is \((1/4+3/9)^{-1}=1.714\) (mg/L)\(^2\). With \(m=1\), it is \((1/4+1/9)^{-1}=2.769\) (mg/L)\(^2\). Thus Design A gives each subject a more precise conditional estimate of their random intercept than Design B does for each subject.
The population information for \(\beta\) is different. In Design A it is
In Design B it is
Under this model, the allocation across more independent subjects gives greater information about the population mean. For \(\omega^2\), the totals are \(4[3^2/(2(21)^2)]=0.04082\) (L/mg)\(^4\) for Design A and \(12[1^2/(2(13)^2)]=0.03550\) (L/mg)\(^4\) for Design B. In this particular comparison, Design A gives slightly more information about the random-effect variance. The result is parameter-specific: the allocation that improves individual EB precision need not maximize information for every population parameter.
Interpretation, Diagnostics, and Limitations
Population information and EB precision should not be compared as if they were interchangeable versions of one quantity. Population information is a matrix (or a component of a matrix) for shared parameters, based on the marginal distribution across subjects. EB precision is conditional on one subject’s data and the assumed population distribution. Its value is strongly affected by the amount and timing of that subject’s data, while population information also depends on the number and distribution of subjects.
A useful diagnostic is to inspect the ingredients of the calculation against the design and fitted model. For the random-intercept example, check that repeated measurements are genuinely comparable, that residual errors are reasonably represented by the assumed covariance, and that the random-intercept distribution is plausible. If residual errors are correlated but treated as independent, the term \(m/\sigma^2\) can overstate the information contributed by repeated observations and make EB estimates appear too precise. If substantial between-subject structure is omitted, the assumed \(\omega^2\) may also fail to represent the actual heterogeneity.
A common warning sign is a large change in EB estimates or their conditional variances after modest changes to the assumed \(\omega^2\), \(\sigma^2\), or fixed effects. This may indicate that an individual has limited data and is being strongly guided by the population distribution. Conversely, a precise-looking conditional EB variance does not establish that the population variance was estimated precisely: that requires information across subjects. Check both levels, and remember that a plug-in EB variance omits uncertainty in the estimated population parameters.
Alternative summaries answer different questions. A subject-specific likelihood estimate uses that subject’s data without the population shrinkage distribution; it can be unstable when the subject has few observations. A population marginal-likelihood analysis estimates shared parameters from all subjects and is the relevant basis for population information. A full Bayesian analysis can represent uncertainty in both population parameters and individual effects jointly, rather than treating estimated population parameters as fixed. These approaches are not interchangeable: the appropriate one depends on whether the target is a population parameter, an individual effect, or their joint uncertainty.
The formulas here are a transparent reference case, not a universal design rule. Unbalanced sampling, covariates, nonlinear models, non-Gaussian outcomes, estimated nuisance parameters, and more complex random effects change the information calculations. In particular, the displayed EB variance is exact only for the stated Gaussian random-intercept model with known parameters. In applications it is often a conditional approximation based on fitted population parameters.
Check Your Understanding
Answer each question using the model and assumptions in this tutorial. Brief solutions are included below the questions.
- With known population parameters, what happens to the conditional variance of an individual random intercept as the number of independent repeated measurements increases?
- For \(m=2\), \(\sigma^2=8\) (mg/L)\(^2\), and \(\omega^2=2\) (mg/L)\(^2\), calculate the shrinkage factor.
- Why is the information for \(\beta\) not the same quantity as the conditional precision for \(b_i\)?
- What key uncertainty is omitted when a plug-in EB conditional variance treats fitted population parameters as known?
Solutions. (1) The conditional variance is \((1/\omega^2+m/\sigma^2)^{-1}\). Increasing \(m\) increases the precision term \(m/\sigma^2\), so the variance decreases. (2) The shrinkage factor is \(\omega^2/(\omega^2+\sigma^2/m)=2/(2+8/2)=2/6=0.3333\). (3) \(\beta\) is a shared population parameter informed by marginal data across subjects; \(b_i\) is a latent effect for one subject, whose conditional distribution combines that subject’s observations with the random-effect distribution. They have different targets and units. (4) It omits uncertainty in the estimated population parameters, including uncertainty in the estimated random-effect and residual variances.