| Literature DB >> 35897258 |
Ropo E Ogunsakin1, Themba G Ginindza1,2.
Abstract
Determining spatial links between disease risk and socio-demographic characteristics is vital in disease management and policymaking. However, data are subject to complexities caused by heterogeneity across host classes and space epidemic processes. This study aims to implement a spatially varying coefficient (SVC) model to account for non-stationarity in the effect of covariates. Using the South Africa general household survey, we study the provincial variation of people living with diabetes and hypertension risk through the SVC model. The people living with diabetes and hypertension risk are modeled using a logistic model that includes spatially unstructured and spatially structured random effects. Spatial smoothness priors for the spatially structured component are employed in modeling, namely, a Gaussian Markov random field (GMRF), a second-order random walk (RW2), and a conditional autoregressive (CAR) model. The SVC model is used to relax the stationarity assumption in which non-linear effects of age are captured through the RW2 and allow the mean effect to vary spatially using a CAR model. Results highlight a non-linear relationship between age and people living with diabetes and hypertension. The SVC models outperform the stationary models. The results suggest significant provincial differences, and the maps provided can guide policymakers in carefully exploiting the available resources for more cost-effective interventions.Entities:
Keywords: Bayesian inference; conditional autoregressive; diabetes; hypertension; spatially varying coefficients
Mesh:
Year: 2022 PMID: 35897258 PMCID: PMC9331550 DOI: 10.3390/ijerph19158886
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 4.614
Figure 1Map of South Africa showing the nine provinces and major cities [34].
Descriptive summary of variables utilized in the study.
| Description | ||
|---|---|---|
| Metrical Variable | Mean (SD) | |
| Age | Age of the respondent | 46.45 ± 8.22 |
| Socio-demographic variables | ||
| Sex | ||
| Male | 2807 (50.4) | |
| Female | 2764 (49.6) | |
| Marital status | ||
| Single | 1701(30.5) | |
| Married | 3203 (57.5) | |
| Divorced/Separated/Widowed | 667 (12.0) | |
| Educational status | ||
| No primary education | 225 (4.0) | |
| Primary | 990 (17.8) | |
| Secondary | 3508 (63.0) | |
| Tertiary | 848 (15.2) | |
| Race | ||
| African | 4718 (84.7) | |
| Colored | 496 (8.9) | |
| Indian/Asian | 57 (1.0) | |
| White | 300 (5.4) | |
| Working for a wage | ||
| Yes | 4547 (81.6) | |
| No | 1024 (18.4) | |
| Working without remuneration | ||
| Yes | 83 (1.5) | |
| No | 5498 (98.5) | |
| Salary period | ||
| Per week | 762 (13.7) | |
| Per month | 4775 (85.7) | |
| Annually | 34 (0.6) | |
| Residence type | ||
| Urban | 3861(69.3) | |
| Rural | 1710 (0.6) | |
| Province | ||
| Western Cape | 489 (8.8) | |
| Eastern Cape | 700 (12.6) | |
| Northern Cape | 380 (6.8) | |
| Free State | 398 (7.1) | |
| KwaZulu-Natal | 548 (9.8) | |
| North West | 387 (6.9) | |
| Gauteng | 1557 (27.9) | |
| Mpumalanga | 600 (10.8) | |
| Limpopo | 512 (9.2) |
Bayesian values of stationary model diagnostic measures.
| Outcome | Model Fit Statistics | Model 1 | Model 2 | Model 3 | Model 4 |
|---|---|---|---|---|---|
| Diabetes |
| 14.78 | 17.77 | 17.71 | 17.65 |
|
| 2166.80 | 2067.81 | 2068.02 | 2068.16 | |
|
| 2181.58 | 2085.58 | 2085.73 | 2087.37 | |
| Hypertension |
| 14.91 | 24.85 | 21.67 | 24.19 |
|
| 4723.10 | 4382.83 | 4391.61 | 4389.19 | |
|
| 4738.01 | 4407.68 | 4413.28 | 4413.38 |
Bayesian values of SVC model diagnostic measures.
| Outcome | Model Fit Statistics | Model 5 | Model 6 | Model 7 | Model 8 |
|---|---|---|---|---|---|
| Diabetes |
| 12.11 | 12.41 | 12.92 | 12.35 |
|
| 2074.84 | 2074.41 | 2073.74 | 2074.49 | |
|
| 2086.95 | 2086.82 | 2086.66 | 2086.84 | |
| Hypertension |
| 16.97 | 17.26 | 16.91 | 17.91 |
|
| 4385.94 | 4386.39 | 4383.82 | 4388.54 | |
|
| 4402.91 | 4403.65 | 4400.73 | 4406.45 |
Figure 2Spatially varying effects of covariates on diabetes.
Figure 3Spatial varying effects of covariates on hypertension.
Figure 4Map of South Africa showing posterior means of spatial effects of diabetes and hypertension.
Figure 5(a) Non-linear effects of age on the log-odds of diabetes (posterior means with the 97.5% credible interval). (b) Non-linear effects of age on the log-odds of hypertension (posterior means with the 97.5% credible interval).