Realistic priors for related parameters

 

In certain statistical applications the inference regarding a parameter of principle interest is

strongly dependent on the value of a nuisance parameter. For example, in cross-over trials the

inference regarding the direct effect of treatment will be strongly dependent on assumptions

regarding the carry-over effect. In a random effects meta-analysis the inferences about the overall

effect of treatment may be strongly dependent on assumptions about the random-effects variance,

in particular if the number of trials is small. In many such cases, however, putting uninformative

priors on the nuisance parameter can be dangerous. For instance, if an uninformative prior is put

on the carry-over effect for an AB/BA cross-over, then inference about the treatment is reduced to

a comparison of the first period values only. Furthermore, such independent specification of priors

for main and nuisance parameters can exhibit incoherence. As a concrete example consider the

trial by Martin and Browning (1985). The ratio of the interval of measurement between the last dose

of the previous treatment and the last dose of the current treatment was at least 125. Thus to use

the same prior for carry-over and direct effect is to say that it is just as likely that the former will be

greater than the latter as vice-versa despite the fact that the duration of action would have to be

125 times as great. Similarly for random effects meta-analysis it is much more plausible that the

random effect variance can be large if the treatment effect is large than if it is small.

 

This project will look at possible Bayesian approaches to analysis using linked  (joint) priors to

see whether any practical contribution can be made to modelling in  such cases. It is likely to include an

empirical investigation of published meta-analyses to compare estimated random effect variances to treatment

estimates.

 

References

 

Martin A, Browning RC. Metoprolol in the aged hypertensive: a comparison  of two dosage

schedules. Postgrad Med J 1985;61(713):225-7.

Senn SJ. Consensus and controversy in pharmaceutical statistics (with  discussion). The

Statistician 2000;49:135-176.

Senn SJ. Cross-over Trials in Clinical Research. Second ed. Chichester:  Wiley, 2002.

Senn, SJ. Trying to be precise about vagueness Statistics in Medicine, 2007: 26, 1417-1430.

 

 

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