Epidemiology of periportal fibrosis and relevance of current Schistosoma mansoni infection within the context of repeated mass drug administration in rural Uganda: a population-based, cross-sectional study

dc.contributor.authorAnjorin, Seun
dc.contributor.authorNabatte, Betty
dc.contributor.authorMpooya, Simon
dc.contributor.authorTinkitina, Benjamin
dc.contributor.authorOpio, Christopher K
dc.contributor.authorKabatereine, Narcis B
dc.contributor.authorChami, Goylette F
dc.date.accessioned2024-10-24T10:30:01Z
dc.date.available2024-10-24T10:30:01Z
dc.date.issued2024-10
dc.description.abstractWHO guidelines for schistosomiasis-related morbidity control and elimination rely on current infection as a proxy indicator for morbidity. We evaluated these guidelines within the context of repeated mass drug administration and periportal fibrosis attributable to chronic intestinal schistosomiasis. We examined 1442 households randomly sampled from 38 villages in Buliisa, Pakwach, and Mayuge districts of Uganda within the SchistoTrack cohort. Periportal fibrosis was diagnosed in 2834 individuals aged 5–90 years using ultrasound and image patterns C–F from the Niamey protocol. Schistosoma mansoni status and intensity were diagnosed by Kato-Katz microscopy and point-of-care circulating cathodic antigen tests. Schistosome infection, co-infections, and comorbidities were examined as exposures for periportal fibrosis. Multivariable logistic regressions were run with SEs clustered by household. Between Jan 6 and Feb 3, 2022, 342 (12·1%) of participants were diagnosed with periportal fibrosis. By Kato-Katz microscopy, 1229 (43·4%) of 2834 participants were infected. 1863 (65·7%) of 2834 participants had trace positive point-of-care circulating cathodic antigen tests, which was higher than prevalence by Kato-Katz microscopy, and 1158 (40·9%) of 2834 participants had trace negative point-of-care circulating cathodic antigen tests. Individual schistosome status, intensity, and prevalence of heavy intensity infections of less than 1% and less than 5% were not correlated with periportal fibrosis likelihood or village prevalence. Periportal fibrosis likelihood linearly increased with age from 5–25 years, non-linearly increased from 26–45 years, attenuated or remain unchanged from 46–60 years, and steadily decreased past 60 years of age. History of liver diseases, HIV, and ultrasound-detected chronic hepatitis or early cirrhosis-like disease were associated with more than two-times increased periportal fibrosis likelihood. WHO guidelines reliant on current schistosome status and intensity are uninformative for identifying probable cases or communities with periportal fibrosis. History of HIV and underlying chronic hepatitis or early cirrhosis-like disease are risk factors that could be investigated for periportal fibrosis surveillance and management. NDPH Pump Priming Fund, Wellcome Trust, John Fell Fund, Robertson Foundation, and UK Research and Innovation Engineering and Physical Sciences Research Council.
dc.description.sponsorshipNDPH Pump Priming Fund, Wellcome Trust, John Fell Fund, Robertson Foundation, and UK Research and Innovation Engineering and Physical Sciences Research Council
dc.identifier.citationAnjorin, Seun, Betty Nabatte, Simon Mpooya, et al. 'Epidemiology of Periportal Fibrosis and Relevance of Current Schistosoma Mansoni Infection within the Context of Repeated Mass Drug Administration in Rural Uganda: A Population-Based, Cross-Sectional Study', The Lancet. Microbe, (2024), pp. 100944.
dc.identifier.issnISSN 2666-5247
dc.identifier.issnEISSN 2666-5247
dc.identifier.urihttps://nru.uncst.go.ug/handle/123456789/9690
dc.language.isoen
dc.publisherElsevier Ltd
dc.titleEpidemiology of periportal fibrosis and relevance of current Schistosoma mansoni infection within the context of repeated mass drug administration in rural Uganda: a population-based, cross-sectional study
dc.typeArticle
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