 Research article
 Open Access
 Published:
A poisson regression approach for modelling spatial autocorrelation between geographically referenced observations
BMC Medical Research Methodology volume 11, Article number: 133 (2011)
Abstract
Background
Analytic methods commonly used in epidemiology do not account for spatial correlation between observations. In regression analyses, omission of that autocorrelation can bias parameter estimates and yield incorrect standard error estimates.
Methods
We used age standardised incidence ratios (SIRs) of esophageal cancer (EC) from the Babol cancer registry from 2001 to 2005, and extracted socioeconomic indices from the Statistical Centre of Iran. The following models for SIR were used: (1) Poisson regression with agglomerationspecific nonspatial random effects; (2) Poisson regression with agglomerationspecific spatial random effects. Distancebased and neighbourhoodbased autocorrelation structures were used for defining the spatial random effects and a pseudolikelihood approach was applied to estimate model parameters. The Bayesian information criterion (BIC), Akaike's information criterion (AIC) and adjusted pseudo R^{2}, were used for model comparison.
Results
A Gaussian semivariogram with an effective range of 225 km best fit spatial autocorrelation in agglomerationlevel EC incidence. The Moran's I index was greater than its expected value indicating systematic geographical clustering of EC. The distancebased and neighbourhoodbased Poisson regression estimates were generally similar. When residual spatial dependence was modelled, point and interval estimates of covariate effects were different to those obtained from the nonspatial Poisson model.
Conclusions
The spatial pattern evident in the EC SIR and the observation that point estimates and standard errors differed depending on the modelling approach indicate the importance of accounting for residual spatial correlation in analyses of EC incidence in the Caspian region of Iran. Our results also illustrate that spatial smoothing must be applied with care.
Background
In general, disease counts in areas that are geographically proximate will display residual spatial dependence; 'residual' here acknowledging that dependence of these counts on known risk factors has been taken account of in the analysis model. Spatially correlated observations do not satisfy the independence assumption central to generalized linear model (GLM) theory [1]. However, generalized linear mixed models (GLMMs) can accommodate spatial random effects and provide a flexible means of analysing spatially correlated disease counts [2]. Left unaddressed, residual spatial correlation can bias regression parameter estimates and cause standard errors to be underestimated, leading to confidence intervals that are too narrow and, potentially leading to incorrect inferences regarding exposuredisease associations [3].
The purpose of this paper is to demonstrate for medical statisticians and health researchers how to fit common types of GLMMs with spatially autocorrelated random effects. While Bayesian or frequentist approaches can be used, we limit attention to frequentist approaches here. Most applications of GLMMs use approximate likelihood methods to estimate model parameters. Rather than try to cover a broad array of models (without providing sufficient depth for the reader to understand the logic behind the model), we focus on Poisson regression with three of the most common autocorrelation structures: Poisson regression with agglomerationspecific nonspatial random effects; Poisson regression with distancebased agglomerationspecific spatial random effects; and Poisson regression with neighbourhoodbased agglomerationspecific spatial random effects. We aim to compare these three autocorrelation structure approaches for Poisson regression models. In this study these methods are illustrated by investigating the association between the geographic pattern of esophageal cancer, EC, incidence and socioeconomic pattern in the Caspian region of Iran.
The structure of this paper is as follows: In the methods section, the EC study's setting and data collection are described and exploratory analysis methods are detailed; then regression models for count data incorporating different assumptions about spatial correlation are presented. In the results section, the application of the different models to the EC data is described, and finally conclusions from these analyses are presented.
Methods
Study Population
Residents of Mazandaran and Golestan provinces constitute the study population (see Figure 1). The estimated midyear population of Mazandaran and Golestan provinces between 2001 and 2005, stratified for age in fiveyear intervals and place of residence, was obtained from the statistical centre of Iran [4]. These estimates were projections for 2001 to 2005 based on 1995 census data using the 2000 geographic boundaries [5, 6]. Geographic coordinates for each agglomeration were also obtained that approximately reflected the geographical centroid of each agglomeration [4].
Geographic region
Iran has high rates of EC (esophageal cancer) [7, 8]. Strong spatial aggregations in esophageal cancer have been identified in the two study provinces with a tendency for high rates in eastern and central wards and low rates in the west [9]. A recent study showed EC was associated with aggregated risk factors related to socioeconomic status (SES) including income and urbanisation [10]. The total population of these two provinces is approximately 4.5 million (1.6 million in Golestan province) [4]. The provinces of Iran are subdivided into wards. There are usually a few cities and rural agglomerations in each ward. Rural agglomerations are a collection of a number of villages. Currently, Mazandaran province has 15 wards, 46 cities and 110 agglomerations and Golestan province has 11 wards, 24 cities and 50 agglomerations. Figure 1 shows geographic boundaries of cities and rural agglomerations within wards in Mazandaran and Golestan provinces.
Data sources
The cases of interest were all EC patients registered between 2001 and 2005 among the study population. The results for both sexes combined are presented in this paper. Data on incident cases of cancer were obtained from the Babol Cancer Registry; issues related to methods, quality and completeness of data collection for this cancer registry are described elsewhere [9, 11]. In summary, the major sources of data collection related to cancer in the Babol cancer registry were reports from pathology laboratories, hospitals, and radiology clinics.
For each agglomeration the following socioeconomic variables were obtained from the 1995 statistical yearbooks of Mazandaran and Golestan [5, 6] and the income and expenses survey in urban and rural areas in 1995 [12, 13]: population density (inhabitants per square kilometre), relative level of activity (a synthetic indicator devised by the statistical centre of Iran that is calculated from the number of households, number of telephone lines, number of bank offices, number of commercial licences, electricity consumption, annual construction budget), annual income per family, annual expenditure on food per family, annual expenditure on fruit and vegetables per family, percentage of occupation in the industrial sector, percentage of occupation in the services sector, percentage of occupation in the agricultural sector, percentage of occupation in the construction sector, percentage of male unemployment, and percentage of illiteracy for males and females. In addition to the villages, some agglomerations contain one or more cities; a proportional aslikely basis method was used to calculate socioeconomic characteristics of these agglomerations.
Factor analysis of socioeconomic variables
A factor analysis was performed to synthesize the socioeconomic variables into a few independent and uncorrelated factors. A Varimax rotation with Kaiser normalisation was used to facilitate interpretation of the factors. The AndersonRubin method was used to create factor scores from the factor solution [14]. The factor scores extracted with this method are uncorrelated with a zero average and variance of one. We attached labels to the factors by interpreting coefficients of the items. This process identified three factors: income, urbanisation and literacy. Scores for these factors for each agglomeration were subsequently used in regression models.
Standardised incidence rates calculation
Adjustment of incidence rates for differences in the age structure of agglomerations was accomplished by agestandardisation. The SIR for an agglomeration was obtained from the ratio of the observed and expected number of cases in that agglomeration. The indirect method of standardisation was used for internal comparisons[15]. Since the population of the region was stable between 2001 and 2005, the 2003 population size was used for computing the incidence rates in age categories of the overall region and the subsequent expected number of cases in each agglomeration. Fiveyear intervals were used for age categorisation.
Exploratory spatial data analysis
Two methods were used to measure spatial aggregation of the agglomeration SIRs; Moran's I [16] and semivariograms [17]. Moran's I was adjusted for agglomeration counts by comparing the observed count in a region with its expected count under the constant risk hypothesis [18].
To calculate the empirical semivariogram, we used studentised residuals (residuals that are each divided by their estimated standard error) obtained from a weighted least squares (WLS) regression. This involved a linear regression model of the form
where α_{0} was an intercept parameter to be estimated,∈_{i} was the residual error of the i^{th} agglomeration, and Z_{i} was a BoxCox transformation of the SIRs. The weights used in parameter estimation by WLS were proportional to the population size at risk within each agglomeration. To obtain a succinct statistical description of the spatial correlation three different parametric models (exponential, Gaussian, and spherical) were fitted to the empirical semivariogram, each of which can be described in terms of nugget, sill and range parameters[17]. The model considered most appropriate was that which minimized the residual sum of squares between the theoretical model and the empirical semivariogram [17].
Analytic methods
Three approaches for modelling with agglomerationspecific random effects were considered: (1) a standard Poisson GLMM with independent agglomerationspecific random effects (nonspatial Poisson GLMM); (2) a discrete autocorrelation structure for agglomerationspecific random effects (neighbourhoodbased spatial Poisson GLMM); and (3) a continuous autocorrelation structure for agglomerationspecific random effects (distancebased spatial Poisson GLMM).
For all approaches it was assumed that, conditional on random effects, the number of cancer cases in each of the N agglomerations, Y_{1}, . . . , Y_{N}, were independent Poisson random variables each with mean μ_{i}.
The models contained income, urbanisation and literacy. The aim of the analyses was to identify macro scale SES factors that determine the distribution of EC at the agglomeration level.
where X_{SES} is a design matrix for the three socioeconomic factors; β_{0} is an intercept parameter to be estimated, β_{SES} is a vector of parameters that describe the socioeconomic factor effects on EC and the offset term log(E_{i}) is the logarithm of the expected number of cases for that agglomeration (assumed fixed). Since theoretical $\mathsf{\text{SIR}}=\frac{{\mu}_{\mathsf{\text{i}}}}{{\mathsf{\text{E}}}_{\mathsf{\text{i}}}}$, this is a model for observed agglomeration level SIRs and the parameters β_{SES} describe association between factor scores and (log) SIR with exp(β_{SES}) interpretable as relative risk parameters within each agglomeration.
Nonspatial Poisson generalized linear mixed model (nonspatial GLMM)
A nonspatial GLMM for the number of cases can be specified as
where u_{i} is the random effect (one for each agglomeration). These are independent random effects, and as per convention, were assumed to be distributed as N(0, ${\zeta}_{{}_{\mathsf{\text{i}}}}^{2}$)[2]. The parameter ${\zeta}_{{}_{\mathsf{\text{i}}}}^{2}$ indicates the variance in the population distribution, and therefore the degree of heterogeneity of agglomerations. These random effects represent the influence of agglomeration i that is not captured by the observed covariates.
Neighbourhoodbased spatial Poisson generalized linear mixed model (neighbourhoodbased GLMM)
The neighbourhoodbased GLMMs took the following form:
The vector of random effects Θ_{i} was assumed to have conditional autoregressive structure (CAR) [19, 20]. A generalization of the CAR called the intrinsic conditional autoregressive structure (ICAR) was used here, where the conditional distribution of the random effects Θ_{i} is
where$\overline{{\Theta}_{\mathsf{\text{i}}}}={\sum}_{\mathsf{\text{j}}\in {\delta}_{\mathsf{\text{i}}}}\frac{{\Theta}_{\mathsf{\text{j}}}}{{\mathsf{\text{n}}}_{\mathsf{\text{i}}}}$, n_{i} is the number of neighbours for agglomeration i, and δ_{i} indicates the neighbourhood of agglomeration i [21]. Using the properties of the multivariate normal distribution, Eq. (4) can be specified in a joint formulation, where $\mathsf{\text{Q}}={\sum}_{\Theta}^{1}\phantom{\rule{0.3em}{0ex}}\left(1\mathsf{\text{W}}\right)$ is the precision matrix as Θ ~ MVN(0, (σ^{2}Q)^{1}). The diagonal matrix Σ_{Θ} has entries $\frac{1}{{\mathsf{\text{n}}}_{\mathsf{\text{i}}}}$ and W has entries ${\mathsf{\text{W}}}_{\mathsf{\text{ij}}}=\left\{\begin{array}{c}\hfill \frac{1}{{\mathsf{\text{n}}}_{\mathsf{\text{i}}}}\phantom{\rule{1em}{0ex}}\mathsf{\text{if}}\phantom{\rule{0.3em}{0ex}}\mathsf{\text{j}}\in {\delta}_{\mathsf{\text{i}}}\hfill \\ \hfill 0\phantom{\rule{1em}{0ex}}\mathsf{\text{otherwise}}\hfill \end{array}\right.$.
In this way, the precision matrix has a rather simple form in ICAR, with the number of neighbours n_{i} on the diagonal and offdiagonal entries 1, where i and j are neighbours and zero otherwise.
Distancebased spatial Poisson generalized linear mixed models (distancebased GLMMs)
Distancebased GLMMs took the following form
The vector of random effects was assumed to be MVN(0, Σ_{Θ}(θ)) with parameters that are jointly referred to as$\Theta \phantom{\rule{0.3em}{0ex}}=\phantom{\rule{0.3em}{0ex}}\left[\begin{array}{c}\hfill {\tau}^{2}\hfill \\ \hfill {\nu}^{2}\hfill \\ \hfill \phi \hfill \end{array}\right]$. If d_{ij} denotes the distance between agglomeration centroid i and j, where counts y_{i} and y_{j} were observed, then
where the matrix F has elements F_{ij} given by $exp\phantom{\rule{0.3em}{0ex}}\left(\frac{{\mathsf{\text{d}}}_{\mathsf{\text{ij}}}}{\phi}\right)$ for exponential, $exp\phantom{\rule{0.3em}{0ex}}\left(\frac{{\mathsf{\text{d}}}_{{}_{\mathsf{\text{ij}}}}^{\mathsf{\text{2}}}}{{\phi}^{2}}\right)$ for Gaussian, and $exp\phantom{\rule{0.3em}{0ex}}\left[\frac{2}{3}\left(\frac{{\mathsf{\text{d}}}_{\mathsf{\text{ij}}}}{\phi}\right)\phantom{\rule{0.3em}{0ex}}\frac{1}{2}{\left(\frac{{\mathsf{\text{d}}}_{\mathsf{\text{ij}}}}{\phi}\right)}^{3}\right]$ for spherical semivariogram models. The unknown parameters in these models, namely, τ^{2} (the nugget), ν^{2} (the sill), and φ (the range), can be obtained from a variogram of the data.
Parameter Estimation
We used a pseudolikelihood approach to estimate unknown parameters in the GLMMs [22]. This approach first assumed that Δ, the vector of variancecovariance parameters, was fixed and used maximum likelihood to estimate β; and then, from the residuals, r, revised the estimate of Δ and iterated until convergence. The following steps were carried out:
1. An initial estimate ${\widehat{\beta}}_{0}$ of β was made by assuming no spatial correlation, that is, with Σ as a diagonal matrix.
The deviance residuals r_{0} were calculated using ${\widehat{\beta}}_{0}$, and Δ was estimated by using maximum likelihood.
2. A new set of estimates ${\widehat{\beta}}_{1}$was found with Δ assumed fixed at the values ${\widehat{\Delta}}_{0}$; hence, a new set of deviance residuals r_{1} was calculated.
3. These estimates were used in a new cycle to redraw Δ and thus derive fresh estimates${\widehat{\Delta}}_{1}$.
Steps 2 and 3 formed an iterative cycle that continued until there was no further change in the estimates.
Model comparison
The 2 LogLikelihood statistic and two commonly used penalized model selection criteria, the Bayesian information criterion (BIC) and Akaike's information criterion (AIC), were used for model comparison. Adjusted pseudo R^{2} was also used to compare the different models with
where y_{i} was the observed count and ${\widehat{\lambda}}_{\mathsf{\text{i}}}$was the model expected count, and adjusted pseudo R^{2} was given by ${\mathsf{\text{R}}}_{{}^{\mathsf{\text{adj}}}}^{\mathsf{\text{2}}}\phantom{\rule{0.3em}{0ex}}=\phantom{\rule{0.3em}{0ex}}1\frac{\mathsf{\text{N}}1}{\mathsf{\text{d}}\mathsf{\text{.f}}.}\phantom{\rule{0.3em}{0ex}}{\left(1\phantom{\rule{0.3em}{0ex}}\phantom{\rule{0.3em}{0ex}}\mathsf{\text{R}}\right)}^{2}$. The adjustment was for the number of degrees of freedom (d.f. = Nno. of model parameters)[23].
Cartographic display
In this study the RR (risk ratio) break points were determined by considering values in the range 0.1 to 10. This corresponds to the range 1 to +1 upon logarithmic transformation. Then this logarithmic scale was divided into 11 equal intervals centred on zero, the break point values were transformed back to the original RR scale, and the five middle intervals were used in the maps. As shown in Figure 2, the middle category was further divided above and below 1. A redgreen colour scheme was used for the maps, with shading of red for areas with the highest SIR (> 1.33), followed by orange and yellow for areas with moderately elevated SIR, light and medium green for areas with moderately low SIR, and dark green representing areas with the lowest SIR (< 0.75).
Software
SIR calculation was done by Microsoft Excel, exploratory spatial analyses were performed using the SAS VARIOGRAM Procedure[24], factor analyses performed using SPSS 17 and the SAS Glimmix procedure was used to carry out the random effect regression models [25, 26].
Results
Factor analysis
Factor analysis identified three factors with eigenvalues greater than 1. Table 1 shows the correlations between socioeconomic items and the extracted factors. The three factors account for 53% of total variance in socioeconomic variables and individually the factors account for: income: 25%, urbanisation: 15% and literacy: 13%.
Exploratory analysis
A total of 1693 new EC cases were diagnosed in 20012005 in Mazandaran and Golestan. The observed Moran index was 0.22 which was greater than its expected value 0.0066, indicating systematic clustering in the region. Consistent with Moran's I, Figure 2(a) showed strong spatial aggregations, with a tendency for high rates in the eastern and central agglomerations and low rates in the west.
A Gaussian semivariogram best fitted the empirical semivariogram as illustrated in Figure 3(a). The effective range of spatial autocorrelation was 225 km. The nugget/sill ratio was 0.28, indicating a moderate degree of spatial autocorrelation (Figure 3(b)).
Spatial regression
As illustrated in Figure 3(b), exponential, Gaussian and spherical semivariogram models smoothed out the fluctuations of, and provided a reasonable overall fit to, the empirical semivariogram. Hence we used all three models for Σ_{Φ}(θ) and compared the results in Table 2. While the Gaussian model had slightly better fit, the choice of autocorrelation structure had little effect on the results from the distancebased GLMMs. We decided to select the Gaussian distancebased GLMM for further comparisons.
Comparison of the overall fit of nonspatial and spatial regression approaches is provided in Table 3. Based on the likelihood ratio, AIC and BIC the neighbourhoodbased autocorrelation structure had the best fit to observed EC counts compared to the competing methods. The PseudoR^{2} diagnostic suggested that nearly 25% of the total variation in EC counts could be explained by the three SES factors. This measure also indicated best fit for neighbourhoodbased Poisson regression. Figure 4 shows the scatter plots of the observed SIR against the model predicted SIRs for each of the three models. Large observed SIR are smoothed towards 1 in all three approaches, i.e. for those agglomerations model predicted SIRs are closer to 1 and the agglomeration is represented in Figure 4 with a point below the line of equality. This smoothing was most marked in the nonspatial model and least marked in the neighbourhoodbased model.
Table 4 presents the point and interval estimates for parameters of interest in the nonspatial GLMM, neighbourhoodbased GLMM and distancebased GLMM. The two spatial models had RR estimates that were qualitatively similar to the nonspatial GLMM model in finding all three risk factors to be, if anything, protective. However the two spatial GLMMs' RR estimates were considerably further from the null than their nonspatial counterparts, a point returned to below.
In general, 95% CIs for relative risks in the two spatial GLMMs were wider than the corresponding intervals in the nonspatial GLMM, reflecting the reasonably strong interagglomeration correlation being taken into account by the spatial model approaches and corresponding effective reduction in sample size in comparison with the nonspatial model that assumes independence of these agglomerations.
As mentioned above, the neighbourhoodbased GLMM and distancebased GLMM point estimates were systematically smaller compared with the nonspatial GLMM. This attenuation of effect away from the null was especially marked for the income and urbanisation factors.
The neighbourhoodbased GLMM and distancebased GLMM RR estimates had comparable conclusions based on inspection of pvalues but all three associations were more strongly protective in the neighbourhoodbased model. The results for the neighbourhoodbased autocorrelation structure indicated that an increase in the score of the income or urbanisation factor was significantly associated with decreasing EC SIR. Model smoothed SIR maps after adjustment for the three factors in Table 3 in a neighbourhoodbased GLMM are illustrated in Figure 2(b).
Discussion
In this ecologic study we observed significant associations between agglomerationspecific EC SIR and SES. The geographic pattern of cancer SIR was consistently stronger among eastern regions and among rural agglomerations. However this conclusion depended on the choice of model.
Multiple forms of residual correlation were potentially present in the cancer SIR data; we considered models addressing 2 types of geographical correlation. A semivariogram plot confirmed the presence of substantial distancebased residual spatial correlation in the EC SIR; agglomerations greater than 225 km apart behaved essentially as independent observations in EC, but at lesser distances, SIR were increasingly correlated as the distance between agglomerations centroids diminished. The global Moran's I showed the importance of neighbourhoodbased residual correlation in the data. CAR spatial smoothing works by making neighbours more alike than nonneighbours, and careful consideration must be given to the way in which neighbours are defined. By defining neighbours based on sharing a border, artificial similarities between some agglomerations may have been induced and would have had the effect of producing some attenuation of fixedeffect estimates. However there was little evidence of this in Figure 4.
The studentised residuals should approximately have a zero mean and a constant variance (1), and their distribution should be roughly Gaussian. We found little deviation from these assumptions in the residual analysis of the transformed SIR data (Z_{i}'s). Thus, the studentised residuals should approximately satisfy the assumption of intrinsic stationary. As discussed by Cressie [17], semivariogram estimators based on the residuals are biased and in this case the covariance of the error could depend on the agglomerations' population sizes. We weighted the semivariogram parameter estimation by agglomeration population size to minimise this bias. When the aim of semivariogram estimation is perfection such as in the Poisson kriging method, Poisson semivariogram estimation taking into account the size of the administrative units can be used [27].
Useful information for model selection can be obtained from using AIC and BIC together, particularly from trying as far as possible to find models favoured by both criteria. Quantitatively, the BIC puts more penalty on the loglikelihood function and the BIC favours more parsimonious models [28]. In the present study the neighbourhoodbased Poisson regression was favoured by AIC, BIC and adjusted pseudo R^{2} indices, although the distancebased Poisson model was closer to the neighbourhoodbased GLMM results than was the nonspatial Poisson regression.
Ignoring spatial autocorrelation can result in explanatory variables apparently being associated with incidence as a result of overstatement of the degrees of freedom in the data and consequent underestimation of standard errors. In our analysis, the standard errors of the regression coefficients were smaller by as much as 35 percent in the model that ignored spatial effects compared with the models that adjusted for spatial effects. As a result, accounting for spatial autocorrelation increased the width of confidence intervals for point estimates. We also observed modest attenuation of SES factor associations with EC in the direction of the null, i.e. a risk ratio of 1, in the nonspatial model. In general it is difficult to predict the direction and nature of this attenuation when a spatial random effect is added to model [29]. Results of simulation studies suggest that the importance of accounting for spatial autocorrelation will depend on the similarity in the spatial variation of the agglomerationlevel exposure with the extraPoisson variation in the outcome, as well as the strength of that correlation. If the agglomerationlevel exposure varies on a larger scale over space relative to the spatial structure of the residuals, then ignoring the spatial autocorrelation may lead to underestimation of the exposure effect. If the spatial structures of exposure and disease incidence are similar, then the exposure effect may be confounded by the inclusion of spatial random effects [30–32].
It is noteworthy that the neighbourhoodbased GLMM is optimal if all agglomerations are of similar size and arranged in a regular pattern and the distancebased GLMM is optimal if all inhabitants of each agglomeration live at their agglomeration's centroid and the measured rate thus refers to this specific location. There have been attempts to model Poisson kriging accounting for size and shape of administrative units as well as population density [33, 34].
Bayesian methods have been widely used for the analysis of spatially correlated count data using software such as WinBUGS and MLwiN. WinBUGS was developed purely for Bayesian analysis, while MLwiN also allows likelihood approaches to GLMMs. Bayesian models have to specify prior distributions for all parameters and require computationally intensive MCMC sampling. Likelihood and Bayesian approaches for spatial Poisson regression have been compared for several case studies with similar results found [35].
Valid inference in spatial regression requires acknowledgment of residual spatial dependence, since regression coefficients of interest will often be sensitive to the form of the dependence assumed, as was observed in this study. The exploratory data analysis showed significant geographic autocorrelation suggesting that the nonspatial GLMM, which ignored this type of correlation, was inappropriate. In the nonspatial GLMM presented here, the agglomerationspecific random effects, assumed to be independent, introduced extraPoisson variation in EC counts but ignored betweenagglomeration spatial correlation. In contrast, the spatial GLMMs explicitly defined spatiallystructured random effects, accounting for betweenagglomeration spatial correlation but not addressing extraPoisson variation, which would have required a second set of agglomerationspecific random effects. While we have illustrated the use of SAS, one widely available statistical software package, implementations of these methods also exist in R and WinBugs [25, 26].
Conclusions
Our results illustrate the importance of accounting for residual spatial correlation in analyses of ecologic studies of disease incidence.
GLMMs are accessible, flexible methods that enable epidemiologists to account for residual spatial correlation. With careful definition of correlation structure and careful application of spatial smoothing, spatial GLMMs are a valuable tool to account explicitly for the effects of residual spatial correlation during the regression modelling process.
Abbreviations
 AIC:

Akaike's information criterion
 BIC:

Bayesian information criterion
 CAR:

Conditional autoregressive
 Distancebased GLMM:

Distance based spatial Poisson generalized linear mixed model
 EC:

Esophageal cancer
 GLM:

Generalized linear model
 GLMM:

Generalized linear mixed model
 ICAR:

Intrinsic conditional autoregressive
 Neighbourhoodbased GLMM:

Neighbourhood based spatial Poisson generalized linear mixed model
 Nonspatial GLMM:

Nonspatial Poisson generalized linear mixed model
 RR:

Risk ratio
 SES:

Socioeconomic status
 SIR:

Standardised incidence ratio
 WLS:

Weighted least squares
References
 1.
McCullagh P, Nelder JA: Generalized Linear Models. 1989, London: Chapman and Hall
 2.
Breslow NE, Clayton DG: Approximate inference in generalized linear mixed models. J Am Stat Assoc. 1993, 88: 925. 10.2307/2290687.
 3.
Waller L, Gotway C: Applied Spatial Statistics for Public Health Data. 2004, New York: Wiley
 4.
Iran statistical yearbook. 2000, Tehran: Statistical Center of Iran
 5.
Reconstruction and estimation of Golestan province population according to 2000 geographic boundaries. 2003, Tehran: Statistical Center of Iran
 6.
Reconstruction and estimation of Mazandaran province population according to 2000 geographic boundaries. 2003, Tehran: Statistical Center of Iran
 7.
Mahboubi E, Kmet J, Cook P, Day N, Ghadirian P, Salmasizadeh S: Oesophageal cancer studies in the Caspian Littoral of Iran:the caspian cancer registry. Br J Cancer. 1973, 28: 197214. 10.1038/bjc.1973.138.
 8.
Saidi F, Sepehr A, Fahimi S, Farahvash MJ, Salehian P, Esmailzadeh A, Keshoofy M, Pirmoazen N, Yazdanbod M, Roshan MK: Oesophageal cancer among the Turkomans of northeast Iran. Br J Cancer. 2000, 83: 12491254. 10.1054/bjoc.2000.1414.
 9.
Mohebbi M, Mahmoodi M, Wolfe R, Nourijelyani K, Mohammad K, Zeraati H, Fotouhi A: Geographical spread of gastrointestinal tract cancer incidence in the Caspian Sea region of Iran: spatial analysis of cancer registry data. BMC Cancer. 2008, 8: 13710.1186/147124078137.
 10.
Mohebbi M, Wolfe R, Jolley D, Forbes A, Mahmoodi M, Burton R: The spatial distribution of esophageal and gastric cancer in Caspian region of Iran: an ecological analysis of diet and socioeconomic influences. International Journal of Health Geographics. 2011, 10: 1310.1186/1476072X1013.
 11.
Mohebbi M, Nourijelyani K, Mahmoudi M, Mohammad K, Zeraati H, Fotouhi A, Moghadaszadeh B: Time of occurrence and age distribution of digestive tract cancers in northern Iran. Iranian J Publ Health. 2008, 37: 819.
 12.
Income and expenses survey in rural families in 1995. 1996, Tehran: Statistical Center of Iran
 13.
Income and expenses survey in urban families in 1995. 1996, Tehran: Statistical Center of Iran
 14.
Anderson T, (Ed.): An introduction to multivariate statistical analysis. 1984, New York: John Wiley & Sons
 15.
Esteve J, Benhamou E, Raymond L: Descriptive Epidemiology. 1994, Lyon: IARC Scientific Publication, Iv:
 16.
Moran P: Notes on continuous stochastic phenomena. Biometrika. 1950, 37: 1723.
 17.
Cressie N: Statistics for Spatial Data, rev. edn. 1993, New York: Wiley
 18.
Walter SD: The analysis of regional patterns in health data: I. Distributional considerations. Am J Epidemiol. 1992, 730741. 136
 19.
Langford IH, Leyland AH, Rasbash J, Goldstein H: Multilevel modelling of the geographical distributions of diseases. J R Stat Soc Ser C Appl Stat. 1999, 48: 253268. 10.1111/14679876.00153.
 20.
Clayton D, Kaldor J: Empirical Bayes estimates of agestandardized relative risks for use in disease mapping. Biometrics. 1987, 43: 671681. 10.2307/2532003.
 21.
Besag J, York J, Mollié A: Bayesian image restoration with two applications in spatial statistics. Ann Inst Stat Math. 1991, 120. 43
 22.
Wolfinger R, O'Connell M: Generalized linear mixed models a pseudolikelihood approach. Journal of Statistical Computation and Simulation. 1993, 48: 233243. 10.1080/00949659308811554.
 23.
Cameron A, Windmeijer F: R^{2} measures for count data regression models with applications to healthcare utilization. Journal of Business and Economic Statistics. 1996, 14: 209220. 10.2307/1392433.
 24.
SAS/STAT 9.2 User's Guide, Chapter 95: The VARIOGRAM Procedure. 2008, SAS Publishing
 25.
Littell R, Milliken G, Stroup W, Wolfinger R: SAS system for mixed models; Chapter 11: Spatial Variability. 2006, Cary, NC: SAS Institute, Inc, 2
 26.
Rasmussen S: Modelling of discrete spatial variation in epidemiology with SAS using GLIMMIX. Computer Methods and Programs in Biomedicine. 2004, 76: 8389. 10.1016/j.cmpb.2004.03.003.
 27.
Monestiez P, Dubroca L, Bonnin E, Durbec JP, Guinet C: Geostatistical modelling of spatial distribution of balaenoptera physalus in the Northwestern Mediterranean sea from sparse count data and heterogeneous observation efforts. Ecological Modelling. 2006, 193: 615628. 10.1016/j.ecolmodel.2005.08.042.
 28.
Kuha J: AIC and BIC comparisons of assumptions and performance. Sociological Methods & Research. 2004, 33: 188229.
 29.
Best NG, Arnold RA, Thomas A, Waller LA, Conlon EM: Bayesian models for spatially correlated disease and exposure data. Bayesian statistics 6, eds. Edited by: Bernardo JM, Berger JO, Dawid AP, Smith AFM. 1999, Oxford: Clarendon Press, 131156.
 30.
Clayton D, Bernardinelli L: Bayesian methods for mapping disease risks. Methods for Small area studies in geographical and environmental epidemiology. Edited by: Cuzick J, Elliott P. 1992, Oxford: Oxford University Press, 205220.
 31.
Guthrie KA, Sheppard L, Wakefield J: A hierarchical aggregate data model with spatially correlated disease rates. Biometrics. 2002, 58: 898905. 10.1111/j.0006341X.2002.00898.x.
 32.
Wakefield J, Salway R: A statistical framework for ecological and aggregate studies. Journal of the Royal Statistical Society Series A. 2001, 164: 119137. 10.1111/1467985X.00191.
 33.
Goovaerts P: Geostatistical analysis of disease data: accounting for spatial support and population density in the isopleth mapping of cancer mortality risk using areatopoint Poisson kriging. International Journal of Health Geographics. 2006, 5: 5210.1186/1476072X552.
 34.
Goovaerts p: Kriging and semivariogram deconvolution in the presence of irregular geographical units. Mathematical Geology. 2008, 40: 101128.
 35.
Jang M, Lee Y, Lawson A, Browne W: A comparison of the hierarchical likelihood and Bayesian approaches to spatial epidemiological modelling. Environmetrics. 2007, 18: 809821. 10.1002/env.877.
Prepublication history
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Acknowledgements
We would like to thank the survey team and colleagues of the Babol Cancer Registry.
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The authors declare that they have no competing interests.
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MM was responsible for the data collection process and issues related to data quality. MM performed the statistical analysis. MM and RW wrote the first draft of the manuscript to which all authors subsequently contributed. All authors read and revised the manuscript for important intellectual content and approved the final manuscript.
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Mohebbi, M., Wolfe, R. & Jolley, D. A poisson regression approach for modelling spatial autocorrelation between geographically referenced observations. BMC Med Res Methodol 11, 133 (2011). https://doi.org/10.1186/1471228811133
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Keywords
 Cancer incidence
 Dietary pattern
 Disease mapping
 Multilevel generalised linear model
 Socioeconomic status
 Spatial analysis