Next Article in Journal
Correction: Perakanya et al. Prevalence and Risk Factors of Opisthorchis viverrini Infection in Sakon Nakhon Province, Thailand. Trop. Med. Infect. Dis. 2022, 7, 313
Previous Article in Journal
Seroepidemiological Survey of Anti-Toxoplasma gondii and Anti-Neospora caninum Antibodies in Domestic Cats (Felis catus) in Rolim de Moura, State of Rondônia, North Brazil
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
TropicalMed
Volume 8
Issue 4
10.3390/tropicalmed8040221
tropicalmed-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Spatial Autocorrelation Method for Taenia solium Risk Mapping: The Case of Lao PDR

by
Andrew Larkins
1,2,*,
Mieghan Bruce
2,3 and
Amanda Ash
1,2
1
School of Medical, Molecular and Forensic Sciences, Murdoch University, Perth, WA 6150, Australia
2
Centre for Biosecurity and One Health, Harry Butler Institute, Murdoch University, Perth, WA 6150, Australia
3
School of Veterinary Medicine, Murdoch University, Perth, WA 6150, Australia
*
Author to whom correspondence should be addressed.
Trop. Med. Infect. Dis. 2023, 8(4), 221; https://doi.org/10.3390/tropicalmed8040221
Submission received: 13 March 2023 / Revised: 6 April 2023 / Accepted: 9 April 2023 / Published: 10 April 2023
(This article belongs to the Section Neglected and Emerging Tropical Diseases)
Browse Figures
Versions Notes

Abstract

:
Background: The World Health Organization has identified Taenia solium mapping tools as an important development for intensifying control in hyperendemic areas. Taenia solium has also been identified as a priority by the Lao PDR government. There is a limited understanding of the distribution of T. solium due to inherent diagnostic challenges. Method: Global and local autocorrelation statistics were applied to available risk factor data sourced from national censuses to map the risk of Taenia solium in Lao PDR. Results: Approximately 50% of villages could be considered hot spots for one or more risk factors. Different risk factor hot spots co-occurred in 30% of villages. Twenty per cent of villages were classified as hot spots for the proportion of households owning pigs and another risk factor. Northern Lao PDR was the dominant high-risk area. This is consistent with passive reports, limited surveys, and anecdotal reports. One smaller area in southern Lao PDR was also identified as high-risk. This is of particular interest because T. solium has not previously been investigated in this area. Conclusions: The methods applied provide a simple, rapid, and versatile approach that allows endemic countries to begin mapping the risk of T. solium at a sub-national level.

1. Introduction

Taenia solium has been recognised by the World Health Organization (WHO) as the world’s most significant foodborne parasite and the leading cause of preventable epilepsy in low- and middle-income countries [1,2]. It is a zoonotic parasite with a lifecycle predominantly involving humans and pigs. As the definitive host, humans are susceptible to taeniasis, a condition in which adult T. solium worms develop and are carried in the gastrointestinal tract after ingesting raw or undercooked pork containing viable cysticerci. People with taeniasis generally do not suffer from substantial illness; however, they distribute infectious eggs or proglottids into the environment via their faeces. These eggs or proglottids are a source of infection for the carriers themselves, other people, and pigs. If ingested, both pigs and humans may become intermediate hosts and develop cysticercosis. Cysticercosis in humans can have major consequences on a person’s health, particularly when cysts develop in the central nervous system, a condition known as neurocysticercosis (NCC). The most common consequence of NCC is epilepsy [3]. Beyond the immediate illness, patients potentially lose the ability to earn an income and participate in daily life, and they may become ostracised by their community [4].
Definitively diagnosing a person with NCC can be a difficult task and requires advanced neuroimaging, brain or spinal cord biopsy, or, in rare cases, visualization of subretinal cysticerci [5]. These diagnostic tools are rarely available in the low and middle-income countries where T. solium is endemic. Not only is NCC difficult to definitively diagnose, but methods for diagnosing porcine cysticercosis and human taeniasis due to T. solium also present challenges. Often, tests are inaccessible for use in endemic communities, do not differentiate between different Taenia species, or suffer from poor field performance [6,7]. An accurate, precise, and field-ready diagnostic test for any stage of T. solium does not currently exist, and this is a major limitation to understanding the true extent of the disease in endemic countries. Despite the inherent complexities, foundational observational research has identified multiple key risk factors related to poor water, sanitation, and hygiene; pig rearing; pork consumption; and cultural behaviours [8,9].

1.1. Risk Mapping

Given the diagnostic challenges of T. solium, the WHO has called for the development of mapping tools that have the potential to identify hyperendemic areas [10]. Such tools may be able to highlight areas where intensified control efforts would provide benefits without the significant resource requirements of expansive prevalence surveys with sophisticated diagnostics [11,12]. Recent efforts have been made to map the occurrence and endemicity of T. solium at the global and regional levels using the available literature on populations, disease occurrence, and risk factors [12,13,14,15]. Whilst this is critical work that highlights the scale of the disease on a broad scale, these efforts do not provide countries with detailed information that can aid current control efforts. At this point in time, studies on the spatial epidemiology of T. solium from academic institutes have primarily focussed on the observational occurrence and association of human and porcine cases [16,17,18,19,20,21]. To date, there have been no published efforts that have investigated the spatial autocorrelation of risk factors to identify high-risk areas. In situations in which disease occurrence data are lacking, the distribution of risk factors may act as an effective proxy to inform decision-making.

1.2. The Lao People’s Democratic Republic

The Lao People’s Democratic Republic (PDR) is the smallest and only landlocked country in Southeast Asia. It is a country with a diverse population that has seen conditions within the country change significantly since its establishment in 1975. Vast improvements to health care and standards of living have been made in recent decades; however, there is still significant variability across the country. Subsistence agriculture continues to employ over 60% of people in the country, and agricultural households are twice as likely to fall back into poverty [22]. Livestock is the second largest agricultural industry in the country, yet 95% of livestock owners are considered subsistence or smallholder farmers, with livestock sales contributing up to 50% of cash income in some northern districts [23]. Pig production is a central practice for these livestock households, particularly in the northern regions [24]. Pigs are a valuable source of income and have cultural and ceremonial significance in many communities [25]. The levels of sanitation and health provision in rural areas, combined with the nature of pig rearing and raw pork consumption, mean that T. solium is a substantial risk. Ensuring that subsistence and smallholder pigs can be raised safely and sustainably is critical for the livelihoods of much of the population in Lao PDR.
Multiple biological surveys investigating human taeniasis have been conducted in Lao PDR over the past 30 years. However, the diagnostic tests used in these surveys generally do not differentiate between different species of Taenia [26]. The government of Lao PDR has highlighted T. solium as a priority disease; however, further investigation into the epidemiology of T. solium in Lao PDR has been delayed due to the complexity and resources required for diagnosis. The use of spatial statistics has the potential to inform T. solium activities in Lao PDR, where larger structured surveys are not currently feasible.
Given the significance of T. solium as a neglected tropical disease and the ongoing calls for methods to identify hyperendemic areas, the objective of this study was to apply spatial autocorrelation statistics to readily available data to identify high-risk areas in Lao PDR. This objective aims to support decision-making for the control of T. solium in Lao PDR and provide an example of how such an approach may be applied in other endemic countries.

2. Materials and Methods

This study had four main methodological parts:
  • Obtain and handle risk factor data;
  • Apply global spatial autocorrelation statistics to determine whether spatial dependency was present for each risk factor on a national scale;
  • Identify which villages were considered hot spots for each risk factor using local indicators of spatial autocorrelation;
  • Assess the co-occurrence of risk factor hot spots and calculate a risk score for each village.

2.1. Data

Risk factor data from the Lao PDR 2011 Agricultural Census and 2015 Housing and Population Census were accessed via the Lao Decide Info platform [24]. Five key risk factors were selected for analysis on the basis of an unstructured literature review and expert opinion (Table 1). Risk factor data were standardised by the number of households in a village to control for the effect of village size. The two censuses were conflated so that risk factors could be considered in all villages. Polygon geometries from the 2015 census were considered the most representative of the current population. Consequently, point geometries of the 2011 villages were aggregated into the 2015 villages. After conflation, 185 of 8499 (2.2%) villages were missing agricultural data. Missing data were imputed using the mean of the district for the respective risk factor. All statistical analysis was completed using RStudio [27].

2.2. Global Spatial Autocorrelation

Global autocorrelation was assessed using global Moran’s I and global join count statistics [28]. Moran’s I statistic describes the similarity in values of a numerical variable between locations [29]. The relationship between locations is realised through a spatial matrix, where locations closer in space are weighted more heavily than those that are distant. Moran’s I generally ranges between +1 and −1, where a result of +1 represents perfect positive autocorrelation, and locations near each other have similar values. A result of −1 represents negative autocorrelation, and locations near each other have dissimilar values. A result of zero reflects no spatial autocorrelation, with values being randomly distributed. The significance of the statistic is inferred against the null hypothesis that no spatial autocorrelation is present and that values are randomly distributed.
Moran’s I is not an appropriate choice of test for categorical data, and global autocorrelation of binary risk factors was assessed using the global join count statistic [30]. The join count statistic involves counting the number of different joins between neighbouring locations. The joins considered were 1–1, 1–0, and 0–0. For the two binary risk factors of the main water or sanitation type, these values represented the following categorical joins between two neighbours: unimproved–unimproved (U–U), unimproved–improved (U–I), and improved–improved (I–I). If autocorrelation was present, then similar values were located closer to each other, and we would expect more U–U and I–I joins than I–U joins. The resulting I–I and U–U counts were significance-tested against their expected numbers if there was no autocorrelation, the null hypothesis.

2.3. Local Spatial Autocorrelation

Global measures of autocorrelation are extremely useful in providing analysts with an overview of spatial dependency; however, these do not consider the potential for instability in dependency across an area. More detailed information on local spatial dependency is often required for decision-makers, particularly in resource-limited settings. Local Getis–Ord and local join count statistics were assessed as measures of local autocorrelation, with their significance tested using conditional random permutations [31]. Local Getis–Ord, or G, statistics examined each village and its neighbours, comparing their mean value to an expected value based on the global mean [32]. Positive results indicated clusters of values higher than the mean (hot spots), and negative results indicated clusters of low values (cold spots).
In a similar fashion, the local join count statistic was applied to binary variables [33]. Neighbouring joins of 1–1 (U–U) were counted for each location and tested for significance against the expected value given spatial independence. Due to the nature of the local statistic equation, any joins including zero (1–0 or 0–0) multiplied to zero and were not considered. As a result, the statistic was only of use in locations with a value of one (i.e., hot spots). The categorisation of the one and zero binary values could simply be reversed to assess hot spots of the second category, for example, improved sanitation or water rather than the unimproved category, if necessary.

2.4. Village Risk Scores

The ability to examine a single risk metric is extremely useful for decision-makers. To accommodate this, each village was provided with a risk score based on the count of risk factors that was classified as a hot spot in that village. Due to the importance of pig households in the epidemiology of T. solium, this calculation was repeated and limited to villages that were pig hot spots.

3. Results

All risk factors related to T. solium in Lao PDR were spatially dependent in Lao PDR. Moran’s I statistic was positive and significant across five orders of spatial lag. The results ranged from 0.74–0.51, 0.71–0.43, and 0.59–0.25 for pig households, poverty, and subsistence households, respectively (Supplementary File S1). The binary risk factors of the main sanitation or the main water source being unimproved also demonstrated spatial dependency (Supplementary File S1). Local autocorrelation statistics illustrated that this dependency was not homogenous, with 15–26% of villages being identified as hot spots depending on the risk factor (Table 2). The locations of the risk factor hot spots illustrated that northern Lao PDR appears to have a larger number of hot spots of pig households and unimproved water. Meanwhile, hot spots of subsistence households were more evenly distributed. The majority of poverty and unimproved sanitation hotpots were found in southern Lao PDR; however, there were hot spots for all risk factors scattered throughout the country (Figure 1).
The co-occurrence of risk factor hot spots was present in approximately one in three villages (31%) (Table 3). This percentage decreased when considering only pig hot spots and the co-occurrence of other risk factors. One in five villages (20%) was classified as a hot spot for pigs and another risk factor (Table 3). Mapping these villages revealed northern Lao PDR as the largest area with overlapping hot spots for pigs and other risk factors. However, there was a smaller area in southern Lao PDR where villages were considered hot spots for almost all risk factors (Figure 2).

4. Discussion

Passive reporting, anecdotal knowledge, and limited surveys all support the major finding that northern Lao PDR is the largest area of high risk for T. solium in Lao PDR [9,34,35,36,37]. The identification of a second high-risk area in southern Lao PDR is of interest, as there has been little investigation in this location. It is hoped that these results can encourage further research and targeted investigation where appropriate. To date, only a single hyperendemic village has been documented in Lao PDR [26]. The village of Om Phalong in the northern province of Phongsaly was identified in 2013 [35]. The subsequent trial of porcine and human interventions in a One Health manner led to the cost-effective control of T. solium and soil-transmitted helminths in the village [38]. This trial provided some of the first empirical evidence for how health can be enhanced through a One Health approach in Southeast Asia; however, the village has now reverted to a hyperendemic state five years later (unpublished data). A wider body of evidence for cost-effective interventions for the control of T. solium is currently lacking and has been identified by experts as a critical research area [39]. The results presented above classified this hyperendemic village as a hot spot for pig, subsistence, and water risk factors and revealed other areas that are high-risk and may include similar villages.
This study presents a tool that may allow endemic countries to take the first steps in planning for the eventual control of T. solium by identifying high-risk areas that should be prioritised for further investigation. The recently released WHO risk-mapping tool [40] uses a semi-quantitative method to combine binary data on porcine cysticercosis, T. solium taeniasis, unknown taeniasis, neurocysticercosis, open defaecation, and backyard pigs to produce a risk level for a given area. This method is heavily reliant on disease occurrence data, with four of six factors focussed on this, and it only considers binary risk factors. Relying on disease occurrence data means accepting the limitations of suboptimal T. solium diagnostics and the health systems needed to capture, analyse, and store such data. These limitations have been noted in regional attempts to map the risk of T. solium [13,14,15]. The use of pre-existing census data highlights the utility of what already exists, and it is hoped that this tool can be applied in other endemic countries. The use of readily available non-biological data is particularly relevant in Lao PDR, where health and veterinary services are limited. Public spending remains low in both sectors, with a reliance on out-of-pocket spending and external funding. This context means that the efficient identification or screening of hyperendemic villages is increasingly important.
The use of open-source software and versatile methods was an important feature of this study. The analysis can be completed by national staff on software that only requires basic training or extension. This kind of analysis and training on existing data is critical to capacity development and the next users who may wish to repeat or alter the analytic method in the future or apply similar approaches to other issues or locations. Although the national results presented provide an indication of the high-risk areas, as more is learnt about the occurrence and associations of T. solium in Lao PDR, repeated spatial analysis on future census data and at a finer scale has the potential to reveal further local spatial patterns that may be hidden in this study and prove critical to local control.
This study considered a small number of risk factors on the basis of their availability in census data, an informal search of the literature, and expert opinion. Other risk factors, such as those relating to culture and ethnicity, were considered relevant and potentially important; however, their data were not available, and evidence of the association between these factors and T. solium in Lao PDR is limited. This sparsity of data is also the reason why this risk mapping tool has not yet been validated against biological data. Due to the diagnostic challenges previously mentioned, there are insufficient data at the village level to appropriately validate this tool [26]. This lack of data also prevented the application of more sophisticated risk mapping methods that use prevalence as the outcome or dependent variable. As more prevalence data become available in Lao PDR, such an approach is encouraged. This issue of data sparsity is common across many endemic countries; it is why a non-biological risk mapping approach was taken in this case, and it is believed to be relevant to the many endemic countries that are trying to better understand their own risk patterns of T. solium.
Further validation of this tool is necessary because whilst the hyperendemic village mentioned above was correctly identified by the tool, the only village where there was a published case of neurocysticercosis [37] was not identified as a hotspot for any risk factors. It is hoped that this tool can be validated in a stepwise manner as T. solium research and control progress in Lao PDR. There is also the potential to apply species-specific molecular diagnostics to taeniasis-positive patients in national helminth surveys, which may provide a suitable validation dataset and rapidly progress the understanding of all Taenia species in Lao PDR. This includes T. asiatica, which shares similar biological features to T. solium and may be present in similar high-risk locations; however, the current epidemiology and significance of T. asiatica remain unknown in Lao PDR, as it has only been identified in three cases [26]. The tool is not presented here and should not yet be interpreted as a complete predictor for disease occurrence. Rather, it is a risk mapping and decision support tool that helps to identify high-risk locations for further investigation, analysis, and ground truthing. The tool should be used in combination with passive surveillance systems, existing knowledge, and other methods prior to significant resource allocation.
This study has four other limitations that are worthy of discussion. Firstly, the method for hot spot classification is data-driven and based on first-degree neighbours. Consequently, it does not consider biological or epidemiological thresholds that may be linked to disease occurrence. This is simply because these thresholds are currently unknown in Lao PDR. Secondly, the nature of local autocorrelation statistics means that a village’s hot spot status is impacted by its neighbours’ values. There is the possibility that a single outlier village may have its value averaged out by its neighbours, resulting in it potentially not being classified as a cluster. Whilst described elsewhere as a significant limitation [41], the purpose of this analysis was to identify broad areas for further investigation. The inclusion of neighbouring values may begin to account for porous village borders and the fluid nature of many communities. As such, the use of first-degree neighbours may be a limitation or a strength of this approach. This will not become clear until there are further studies related to the village-level occurrence of T. solium in Lao PDR and elsewhere. Thirdly, the strong global autocorrelation that is present in the national data may make the detection of local clusters more difficult and hide distinct local patterns [32]. This limitation could potentially be overcome by repeating the analysis on smaller scales, focusing on the now-identified high-risk areas. This limitation highlights the importance of simple and versatile methods that can be reapplied readily as new information comes to hand. Finally, when examining the co-occurrence of hot spots, it should be remembered that these results only reflect co-occurrence and, importantly, do not consider the correlation, interaction, or relative weight of each risk factor. Further investigation of combined risk could be achieved through multi-criteria decision analysis or other methods. This study is a starting point in the investigation of T. solium risk in Lao PDR; however, these limitations are a reminder that multiple lenses should be applied in health planning prior to decision-making. Assumptions and analyses should be regularly re-examined as new data and information become available. For this reason, future risk mapping tools for T. solium should ideally continue to be simple, rapid, and versatile.

5. Conclusions

This study applied simple spatial autocorrelation statistics to pre-existing data and produced results that are relevant to local stakeholders and illustrate the spatial heterogeneity of T. solium risk factors at a sub-national level. The information provided by this study allows for the targeted application of further research and control activities in Lao PDR in a clear and transparent manner. Investigating the spatial clustering of risk factors offers a simple, versatile, and rapid approach that can assist decision makers in identifying high-risk areas. This approach is pertinent to T. solium due to the current lack of accurate, reliable, and practical diagnostic tests. Further research and significant investment into the fundamental epidemiology of T. solium and options for its control are required in Southeast Asia if the disease situation is to be better understood. Given the intrinsic link between living conditions and other neglected tropical diseases, the approach presented here has the potential to inform control efforts for other neglected tropical diseases in Lao PDR and other countries.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/tropicalmed8040221/s1, Supplementary File S1: Global autocorrelation results.

Author Contributions

Conceptualization, A.L., A.A., M.B.; methodology, A.L., A.A., M.B.; formal analysis, A.L.; writing—original draft preparation, A.L.; writing—review and editing, A.L., A.A., M.B.; supervision, A.A., M.B. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Australian Centre for International Agricultural Research (LS/2014/055) and a Murdoch University Strategic Scholarship.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data generated or analysed during this study are included in this published article (and its Supplementary Information Files).

Acknowledgments

The authors would like to thank Kongxay Luangphengsouk and Eleanor Bruce for their discussion during the conception of this study. The authors would also like to thank Rattanaxay Phetsouvanh, Bounnaloth Insisiengmay, and Boualy Keokhamphavanh for their feedback on interim results and their efforts in controlling Taenia solium in Lao PDR.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. WHO. Preventable Epilepsy: Taenia solium Infection Burdens Economies, Societies and Individuals: A Rationale for Investment and Action; WHO: Geneva, Switzerland, 2016. [Google Scholar]
  2. FAO; WHO (Eds.). Multicriteria-Based Ranking for Risk Management of Food-Borne Parasites; FAO/WHO: Rome, Italy, 2014. [Google Scholar]
  3. Garcia, H.H.; Nash, T.E.; Del Brutto, O.H. Clinical symptoms, diagnosis, and treatment of neurocysticercosis. Lancet Neurol. 2014, 13, 1202–1215. [Google Scholar] [CrossRef] [PubMed]
  4. Tran, D.S.; Odermatt, P.; Singphuoangphet, S.; Druet-Cabanac, M.; Preux, P.M.; Strobel, M.; Barennes, H. Epilepsy in Laos: Knowledge, attitudes, and practices in the community. Epilepsy Behav. 2007, 10, 565–570. [Google Scholar] [CrossRef] [PubMed]
  5. Del Brutto, O.H.; Nash, T.E.; White, A.C., Jr.; Rajshekhar, V.; Wilkins, P.P.; Singh, G.; Vasquez, C.M.; Salgado, P.; Gilman, R.H.; Garcia, H.H. Revised diagnostic criteria for neurocysticercosis. J. Neurol. Sci. 2017, 372, 202–210. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Mubanga, C.; Mwape, K.E.; Phiri, I.K.; Trevisan, C.; Zulu, G.; Chabala, C.; van Damme, I.; Schmidt, V.; Dorny, P.; Gabriël, S. Progress on the development of rapid diagnostic tests for foodborne neglected zoonotic helminthiases: A systematic review. Acta Trop. 2019, 194, 135–147. [Google Scholar] [CrossRef]
  7. Mubanga, C.; Van Damme, I.; Trevisan, C.; Schmidt, V.; Phiri, I.K.; Zulu, G.; Noh, J.; Handali, S.; Mambo, R.; Chembensofu, M.; et al. Evaluation of an Antibody Detecting Point of Care Test for Diagnosis of Taenia solium Cysticercosis in a Zambian Rural Community: A Prospective Diagnostic Accuracy Study. Diagnostics 2021, 11, 2121. [Google Scholar] [CrossRef]
  8. Coral-Almeida, M.; Gabriël, S.; Abatih, E.N.; Praet, N.; Benitez, W.; Dorny, P. Taenia solium Human Cysticercosis: A Systematic Review of Sero-epidemiological Data from Endemic Zones around the World. PLoS Negl. Trop. Dis. 2015, 9, e0003919. [Google Scholar] [CrossRef] [Green Version]
  9. Holt, H.R.; Inthavong, P.; Khamlome, B.; Blaszak, K.; Keokamphe, C.; Somoulay, V.; Phongmany, A.; Durr, P.; Graham, K.; Allen, J.; et al. Endemicity of Zoonotic Diseases in Pigs and Humans in Lowland and Upland Lao PDR: Identification of Socio-cultural Risk Factors. PLoS Negl. Trop. Dis. 2016, 10, e0003913. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. WHO. Ending the Neglect to Attain the Sustainable Development Goals: A Road Map for Neglected Tropical Diseases; WHO: Geneva, Switzerland, 2020; p. 9789240010352. [Google Scholar]
  11. Braae, U.C.; Gabriel, S.; Trevisan, C.; Thomas, L.F.; Magnussen, P.; Abela-Ridder, B.; Ngowi, H.; Johansen, M.V. Stepwise approach for the control and eventual elimination of Taenia solium as a public health problem. BMC Infect. Dis. 2019, 19, 182. [Google Scholar] [CrossRef]
  12. WHO. WHO Taenia solium endemicity map—2022 update. Wkly. Epidemiol. Rec. 2022, 97, 169–172. [Google Scholar]
  13. Braae, U.C.; Devleesschauwer, B.; Sithole, F.; Wang, Z.; Willingham, A.L. Mapping occurrence of Taenia solium taeniosis/cysticercosis and areas at risk of porcine cysticercosis in Central America and the Caribbean basin. Parasit. Vectors 2017, 10, 424. [Google Scholar] [CrossRef] [PubMed]
  14. Braae, U.C.; Hung, N.M.; Satrija, F.; Khieu, V.; Zhou, X.-N.; Willingham, A.L. Porcine cysticercosis (Taenia solium and Taenia asiatica): Mapping occurrence and areas potentially at risk in East and Southeast Asia. Parasit. Vectors 2018, 11, 613. [Google Scholar] [CrossRef]
  15. Braae, U.C.; Saarnak, C.F.L.; Mukaratirwa, S.; Devleesschauwer, B.; Magnussen, P.; Johansen, M.V. Taenia solium taeniosis/cysticercosis and the co-distribution with schistosomiasis in Africa. Parasit. Vectors 2015, 8, 323. [Google Scholar] [CrossRef] [Green Version]
  16. Lescano, A.G.; Garcia, H.H.; Gilman, R.H.; Guezala, M.C.; Tsang, V.C.W.; Moulton, L.; Garcia, H.H.; Gavidia, C.M.; Green, J.A.; Gilman, R.H. Swine cysticercosis hotspots surrounding Taenia solium tapeworm carriers. Am. J. Trop. Med. Hyg. 2007, 76, 376–383. [Google Scholar] [CrossRef]
  17. O’Neal, S.E.; Moyano, L.M.; Ayvar, V.; Gonzalvez, G.; Diaz, A.; Rodriguez, S.; Wilkins, P.P.; Tsang, V.C.W.; Gilman, R.H.; García, H.H.; et al. Geographic Correlation between Tapeworm Carriers and Heavily Infected Cysticercotic Pigs. PLoS Negl. Trop. Dis. 2012, 6, e1953. [Google Scholar] [CrossRef] [PubMed]
  18. Pray, I.W.; Ayvar, V.; Gamboa, R.; Muro, C.; Moyano, L.M.; Benavides, V.; Flecker, R.H.; Garcia, H.H.; O’Neal, S.E. Spatial relationship between Taenia solium tapeworm carriers and necropsy cyst burden in pigs. PLoS Negl. Trop. Dis. 2017, 11, e0005536. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Ngowi, H.A.; Kassuku, A.A.; Carabin, H.; Mlangwa, J.E.D.; Mlozi, M.R.S.; Mbilinyi, B.P.; Willingham, A.L. Spatial Clustering of Porcine Cysticercosis in Mbulu District, Northern Tanzania. PLoS Negl. Trop. Dis. 2010, 4, e652. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Coral-Almeida, M.; Henriquez-Trujillo, A.R.; Asanza, S.; Erazo, C.; Paucar, M.; Calvopiña, M. Assessing the burden and spatial distribution of human neurocysticercosis in Ecuador (2013–2017). PLoS Negl. Trop. Dis. 2020, 14, e0008384. [Google Scholar] [CrossRef]
  21. Raghava, M.V.; Prabhakaran, V.; Jayaraman, T.; Muliyil, J.; Oommen, A.; Dorny, P.; Vercruysse, J.; Rajshekhar, V. Detecting spatial clusters of Taenia solium infections in a rural block in South India. Trans. R. Soc. Trop. Med. Hyg. 2010, 104, 601–612. [Google Scholar] [CrossRef]
  22. World Bank Group. Lao People’s Democratic Republic—Systematic Country Diagnostic: Priorities for Ending Poverty and Boosting Shared Prosperity; World Bank Group: Washington, DC, USA, 2017; Report No.: 112241-LA. [Google Scholar]
  23. Bastiaensen, P.; Kamakawa, A.; Varas, M. OIE—PVS Evaluation Report of the Veterinary Services of the Lao People’s Democratic Republic; OIE: Paris, France, 2011. [Google Scholar]
  24. Government of the Lao PDR. Lao DECIDE Info: Informing Decisions for Sustainable Development 2021. Available online: http://www.decide.la/ (accessed on 1 November 2021).
  25. Bardosh, K.; Inthavong, P.; Xayaheuang, S.; Okello, A.L. Controlling parasites, understanding practices: The biosocial complexity of a One Health intervention for neglected zoonotic helminths in northern Lao PDR. Soc. Sci. Med. 2014, 120, 215–223. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Larkins, A.; Keatley, S.; Insisiengmay, B.; Phetsouvanh, R.; Bruce, M.; Ash, A. The challenges of detecting Taenia solium and neurocysticercosis in low and middle-income countries: A scoping review of Lao People’s Democratic Republic. Trop. Med. Int. Health 2023. [Google Scholar] [CrossRef]
  27. RStudio Team. RStudio: Integrated Development for R, 1.4.1 ed.; RStudio, PBC: Boston, MA, USA, 2021. [Google Scholar]
  28. Bivand, R.S.; Wong, D.W.S. Comparing implementations of global and local indicators of spatial association. Test 2018, 27, 716–748. [Google Scholar] [CrossRef]
  29. Moran, P.A.P. The Interpretation of Statistical Maps. J. R. Stat. Soc. Ser. B Methodol. 1948, 10, 243–251. [Google Scholar] [CrossRef]
  30. Cliff, A.D.; Ord, K. Spatial Autocorrelation: A Review of Existing and New Measures with Applications. Econ. Geogr. 1970, 46, 269–292. [Google Scholar] [CrossRef]
  31. Anselin, L.; Ibnu, S.; Youngihn, K. GeoDa: An Introduction to Spatial Data Analysis. Geogr. Anal. 2006, 38, 5–22. [Google Scholar] [CrossRef]
  32. Ord, J.K.; Getis, A. Local Spatial Autocorrelation Statistics: Distributional Issues and an Application. Geogr. Anal. 1995, 27, 286–306. [Google Scholar] [CrossRef]
  33. Anselin, L.; Li, X. Operational local join count statistics for cluster detection. J. Geogr. Syst. 2019, 21, 189–210. [Google Scholar] [CrossRef]
  34. Jeon, H.-K.; Yong, T.-S.; Sohn, W.-M.; Chai, J.-Y.; Min, D.-Y.; Yun, C.-H.; Rim, H.-J.; Pongvongsa, T.; Banouvong, V.; Insisiengmay, B.; et al. Current Status of Human Taeniasis in Lao People’s Democratic Republic. Korean J. Parasitol. 2013, 51, 259–263. [Google Scholar] [CrossRef] [PubMed]
  35. Okello, A.; Ash, A.; Keokhamphet, C.; Hobbs, E.; Khamlome, B.; Dorny, P.; Thomas, L.; Allen, J. Investigating a hyper-endemic focus of Taenia solium in northern Lao PDR. Parasit. Vectors 2014, 7, 134. [Google Scholar] [CrossRef] [Green Version]
  36. Okello, A.L.; Burniston, S.; Conlan, J.V.; Inthavong, P.; Khamlome, B.; Welburn, S.C.; Gilbert, J.; Allen, J.; Blacksell, S.D. Prevalence of Endemic Pig-Associated Zoonoses in Southeast Asia: A Review of Findings from the Lao People’s Democratic Republic. Am. J. Trop. Med. Hyg. 2015, 92, 1059–1066. [Google Scholar] [CrossRef] [Green Version]
  37. Jeon, H.-K.; Yong, T.-S.; Sohn, W.-M.; Chai, J.-Y.; Min, D.-Y.; Rim, H.-J.; Insisiengmay, B.; Eom, K.S. Human Neurocysticercosis Case and an Endemic Focus of Taenia solium in Lao PDR. Korean J. Parasitol. 2013, 51, 599–602. [Google Scholar] [CrossRef]
  38. Okello, W.O.; Okello, A.L.; Inthavong, P.; Tiemann, T.; Phengsivalouk, A.; Devleesschauwer, B.; Shaw, A.; Allen, J. Improved methods to capture the total societal benefits of zoonotic disease control: Demonstrating the cost-effectiveness of an integrated control programme for Taenia solium, soil transmitted helminths and classical swine fever in northern Lao PDR. PLoS Negl. Trop. Dis. 2018, 12, e0006782. [Google Scholar] [CrossRef] [PubMed]
  39. WHO. Expert Consultation to Accelerate Control of Foodborne Trematode Infections, Taeniasis and Cysticercosis; WHO Regional Office for the Western Pacific: Seoul, Republic of Korea, 2017; RS-2017-GE-35-KOR. [Google Scholar]
  40. WHO. Launch of New Tools for the Control of Taenia solium; WHO: Geneva, Switzerland, 2021; Available online: https://www.who.int/news/item/12-09-2021-launch-of-new-tools-for-the-control-of-taenia-solium (accessed on 30 January 2023).
  41. Wong, D.W.S. Issues in the Current Practices of Spatial Cluster Detection and Exploring Alternative Methods. Int. J. Environ. Res. Public Health 2021, 18, 9848. [Google Scholar] [CrossRef] [PubMed]
Tropicalmed 08 00221 g001 550
Figure 1. Mapping of local autocorrelation statistics.
Figure 1. Mapping of local autocorrelation statistics.
Tropicalmed 08 00221 g001
Tropicalmed 08 00221 g002 550
Figure 2. Mapping of local autocorrelation statistics. a Not a pig hot spot. b Pig hot spot only.
Figure 2. Mapping of local autocorrelation statistics. a Not a pig hot spot. b Pig hot spot only.
Tropicalmed 08 00221 g002
Table
Table 1. Risk factor data.
Table 1. Risk factor data.
Risk FactorData TypeSource
Pig-owning householdsProportion in village2011 Agricultural
Census
Subsistence householdsProportion in village
People living in povertyProportion in village2015 Housing
and Population
Census
Main sanitation unimprovedBinary
Main water source unimprovedBinary
Table
Table 2. Summary of local autocorrelation statistics with 95% significance.
Table 2. Summary of local autocorrelation statistics with 95% significance.
Risk FactorNumber of Villages (% of Total)
Cold SpotNot SignificantHot Spot
Pig households2413 (28%)3866 (46%)2220 (26%)
Subsistence households1494 (18%)5113 (60%)1892 (22%)
Poverty1897 (22%)5120 (60%)1482 (17%)
Main sanitation typen.a. 17219 (85%)1280 (15%)
Main water sourcen.a. 16796 (80%)1703 (20%)
1 See interpretation of binary local join count statistics described in methods.
Table
Table 3. Summary of village risk scores.
Table 3. Summary of village risk scores.
Risk ScoreNumber of Villages (% of Total)
Any Risk FactorPig Hot Spot
04192(49.3%)6279(73.9%) a
11663(19.6%)480(5.7%) b
21439(16.9%)802(9.4%)
3831(9.8%)595(7.0%)
4327(3.9%)296(3.5%)
547(0.5%)47(0.6%)
Total8499(100%)8499(100%)
a Not a pig hot spot. b Pig hot spot only.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Larkins, A.; Bruce, M.; Ash, A. A Spatial Autocorrelation Method for Taenia solium Risk Mapping: The Case of Lao PDR. Trop. Med. Infect. Dis. 2023, 8, 221. https://doi.org/10.3390/tropicalmed8040221

AMA Style

Larkins A, Bruce M, Ash A. A Spatial Autocorrelation Method for Taenia solium Risk Mapping: The Case of Lao PDR. Tropical Medicine and Infectious Disease. 2023; 8(4):221. https://doi.org/10.3390/tropicalmed8040221

Chicago/Turabian Style

Larkins, Andrew, Mieghan Bruce, and Amanda Ash. 2023. "A Spatial Autocorrelation Method for Taenia solium Risk Mapping: The Case of Lao PDR" Tropical Medicine and Infectious Disease 8, no. 4: 221. https://doi.org/10.3390/tropicalmed8040221

APA Style

Larkins, A., Bruce, M., & Ash, A. (2023). A Spatial Autocorrelation Method for Taenia solium Risk Mapping: The Case of Lao PDR. Tropical Medicine and Infectious Disease, 8(4), 221. https://doi.org/10.3390/tropicalmed8040221

Article Metrics

Back to TopTop