Estimation of infection prevalence from correlated binomial samples

被引:21
作者
Condon, J [1 ]
Kelly, G
Bradshaw, B
Leonard, N
机构
[1] Queens Univ Belfast, Dept Appl Math & Theoret Phys, Belfast BT7 1NN, Antrim, North Ireland
[2] Univ Coll Dublin, Dept Stat, Dublin 4, Ireland
[3] Cent Vet Res Lab, Dept Agr & Food, Dublin 15, Ireland
[4] Univ Coll Dublin, Fac Vet Med, Dublin 4, Ireland
关键词
nonparametric random effects; generalised linear mixed model; GLIMMIX; Proc NLMIXED; generalised estimating equations;
D O I
10.1016/j.prevetmed.2004.03.003
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Infection prevalence in a population often is estimated from grouped binary data expressed as proportions. The groups can be families, herds, flocks, farms, etc. The observed number of cases generally is assumed to have a Binomial distribution and the estimate of prevalence is then the sample proportion of cases. However, the individual binary observations might not be independent-leading to overdispersion. The goal of this paper was to demonstrate random-effects models for the estimation of infection prevalence from data which are correlated and in particular, to illustrate a nonparametric, random-effects model for this purpose. The nonparametric approach is a relatively recent addition to the random-effects class of models and does not appear to have been discussed previously in the veterinary epidemiology literature. The assumptions for a logistic-regression model with a nonparametric random effect were outlined. In a demonstration of the method on data relating to Salmonella infection in Irish pig herds, the nonparametric method resulted in the classification of herds into a small number of distinct prevalence groups (i.e. low, medium and high prevalence) and also estimated the relative frequency of each prevalence category in the population. We compared the estimates from a logistic model with a nonparametric distribution for the random effects with four alternative models: a logistic-regression model with no random effects, a marginal model using a generalised estimating equation (GEE) and two methods of fitting a Normally distributed random effect (the GLIMMIX macro and the NLMIXED procedure both in SAS). Parameter estimates from random-effects models are not readily interpretable in terms of prevalences. Therefore, we outlined two methods for calculating population-averaged estimates of prevalence from random-effects models: one using numerical integration and the other using Monte Carlo simulation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 30 条
[1]   A general maximum likelihood analysis of variance components in generalized linear models [J].
Aitkin, M .
BIOMETRICS, 1999, 55 (01) :117-128
[2]   Impact on human health of Salmonella spp. on pork in The Netherlands and the anticipated effects of some currently proposed control strategies [J].
Berends, BR ;
Van Knapen, F ;
Mossel, DAA ;
Burt, SA ;
Snijders, JMA .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1998, 44 (03) :219-229
[3]   Identification and quantification of risk factors regarding Salmonella spp. On pork carcasses [J].
Berends, BR ;
VanKnapen, F ;
Snijders, JMA ;
Mossel, DAA .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1997, 36 (2-3) :199-206
[4]   APPROXIMATE INFERENCE IN GENERALIZED LINEAR MIXED MODELS [J].
BRESLOW, NE ;
CLAYTON, DG .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1993, 88 (421) :9-25
[5]   Herd size and sero-prevalence of Salmonella enterica in Danish swine herds: a random-effects model for register data [J].
Carstensen, B ;
Christensen, J .
PREVENTIVE VETERINARY MEDICINE, 1998, 34 (2-3) :191-203
[6]   Generalised linear mixed models analysis of risk factors for contamination of Danish broiler flocks with Salmonella typhimurium [J].
Chriél, M ;
Stryhn, H ;
Dauphin, G .
PREVENTIVE VETERINARY MEDICINE, 1999, 40 (01) :1-17
[7]   Estimating the annual fraction of eggs contaminated with Salmonella enteritidis in the United States [J].
Ebel, E ;
Schlosser, W .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2000, 61 (01) :51-62
[8]   Describing heterogeneous effects in stratified ordinal contingency tables, with application to multi-center clinical trials [J].
Hartzel, J ;
Liu, IM ;
Agresti, A .
COMPUTATIONAL STATISTICS & DATA ANALYSIS, 2001, 35 (04) :429-449
[9]  
HINDE JP, 1982, GLIM82
[10]  
Ihaka R., 1996, J COMPUTATIONAL GRAP, V5, P299, DOI [10.1080/10618600.1996.10474713, 10.2307/1390807, DOI 10.1080/10618600.1996.10474713]