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In spatio-temporal disease mapping models, identifiability constraints affect PQL and INLA results
被引:53
|作者:
Goicoa, T.
[1
,2
,4
]
Adin, A.
[1
,2
]
Ugarte, M. D.
[1
,2
]
Hodges, J. S.
[3
]
机构:
[1] Univ Publ Navarra, Dept Stat & OR, Pamplona, Spain
[2] Univ Publ Navarra, Inst Adv Mat InaMat, Pamplona, Spain
[3] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN 55455 USA
[4] Res Network Hlth Serv Chron Dis REDISSEC, Madrid, Spain
关键词:
Breast cancer;
INLA;
Leroux CAR prior;
PQL;
Space-time interactions;
SPACE-TIME VARIATION;
APPROXIMATE INFERENCE;
EMPIRICAL BAYES;
RISK;
LIKELIHOOD;
D O I:
10.1007/s00477-017-1405-0
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Disease mapping studies the distribution of relative risks or rates in space and time, and typically relies on generalized linear mixed models (GLMMs) including fixed effects and spatial, temporal, and spatio-temporal random effects. These GLMMs are typically not identifiable and constraints are required to achieve sensible results. However, automatic specification of constraints can sometimes lead to misleading results. In particular, the penalized quasi-likelihood fitting technique automatically centers the random effects even when this is not necessary. In the Bayesian approach, the recently-introduced integrated nested Laplace approximations computing technique can also produce wrong results if constraints are not well-specified. In this paper the spatial, temporal, and spatio-temporal interaction random effects are reparameterized using the spectral decompositions of their precision matrices to establish the appropriate identifiability constraints. Breast cancer mortality data from Spain is used to illustrate the ideas.
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页码:749 / 770
页数:22
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