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Seroprevalence and spatial epidemiology of lymphatic filariasis in American Samoa after successful mass drug administration

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dc.contributor.author Lau, Colleen L
dc.contributor.author Won, Kimberly Y
dc.contributor.author Becker, Luke
dc.contributor.author Magalhaels, Ricardo J. Soares
dc.contributor.author Fuimaono, Saipale
dc.contributor.author Melrose, Wayne
dc.contributor.author Lammie, Patrick J
dc.contributor.author Graves, Patricia M
dc.date.accessioned 2021-12-01T21:07:36Z
dc.date.available 2021-12-01T21:07:36Z
dc.date.issued 2014
dc.identifier.citation Lau CL, Won KY, Becker L, Soares Magalhaes RJ, Fuimaono S, et al. (2014) Seroprevalence and Spatial Epidemiology of Lymphatic Filariasis in American Samoa after Successful Mass Drug Administration. PLoS Negl Trop Dis 8(11): e3297. doi:10.1371/journal.pntd.0003297 en_US
dc.identifier.uri ${sadil.baseUrl}/handle/123456789/956
dc.description 12 p. ; 29 cm en_US
dc.description.abstract Background: As part of the Global Programme to Eliminate Lymphatic Filariasis (LF), American Samoa conducted mass drug administration (MDA) from 2000–2006, and passed transmission assessment surveys in 2011–2012. We examined the seroprevalence and spatial epidemiology of LF post-MDA to inform strategies for ongoing surveillance and to reduce resurgence risk. Methods: ELISA for LF antigen (Og4C3) and antibodies (Wb123, Bm14) were performed on a geo-referenced serum bank of 807 adults collected in 2010. Risk factors assessed for association with sero-positivity included age, sex, years lived in American Samoa, and occupation. Geographic clustering of serological indicators was investigated to identify spatial dependence and household-level clustering. Results: Og4C3 antigen of .128 units (positive) were found in 0.75% (95% CI 0.3–1.6%) of participants, and .32 units (equivocal plus positive) in 3.2% (95% CI 0.6–4.7%). Seroprevalence of Wb123 and Bm14 antibodies were 8.1% (95% CI 6.3–10.2%) and 17.9% (95% CI 15.3–20.7%) respectively. Antigen-positive individuals were identified in all ages, and antibody prevalence higher in older ages. Prevalence was higher in males, and inversely associated with years lived in American Samoa. Spatial distribution of individuals varied significantly with positive and equivocal levels of Og4C3 antigen, but not with antibodies. Using Og4C3 cutoff points of .128 units and .32 units, average cluster sizes were 1,242 m and 1,498 m, and geographical proximity of households explained 85% and 62% of the spatial variation respectively. Conclusions: High-risk populations for LF in American Samoa include adult males and recent migrants. We identified locations and estimated the size of possible residual foci of antigen-positive adults, demonstrating the value of spatial analysis in post-MDA surveillance. Strategies to monitor cluster residents and high-risk groups are needed to reduce resurgence risk. Further research is required to quantify factors contributing to LF transmission at the last stages of elimination to ensure that programme achievements are sustained. en_US
dc.language.iso en en_US
dc.publisher PLOS Neglected Tropical Diseases en_US
dc.relation.ispartofseries Article in PLOS Neglected Tropical Diseases;Volume 8 Issue 11
dc.subject Filariasis - prevention - American Samoa en_US
dc.subject Mosquitoes as carriers of diseases en_US
dc.subject Parasitic diseases en_US
dc.title Seroprevalence and spatial epidemiology of lymphatic filariasis in American Samoa after successful mass drug administration en_US
dc.type Article en_US


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