Development of prediction models to identify hotspots of schistosomiasis in endemic regions to guide mass drug administration

Author:

Singer Benjamin J.1,Coulibaly Jean T.2345,Park Hailey J.1,Andrews Jason R.1,Bogoch Isaac I.6,Lo Nathan C.1ORCID

Affiliation:

1. Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University, Stanford, CA 94304

2. Unité de Formation et de Recherche Biosciences, Université Félix Houphouët-Boigny, Abidjan, Côte d’Ivoire

3. Centre Suisse de Recherches Scientifiques en Côte d’Ivoire, Abidjan, Côte d’Ivoire

4. Swiss Tropical and Public Health Institute, Basel, Allschwil 4123 Switzerland

5. University of Basel, Basel 4001, Switzerland

6. Department of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada

Abstract

Schistosomiasis is a neglected tropical disease affecting over 150 million people. Hotspots of Schistosoma transmission—communities where infection prevalence does not decline adequately with mass drug administration—present a key challenge in eliminating schistosomiasis. Current approaches to identify hotspots require evaluation 2–5 y after a baseline survey and subsequent mass drug administration. Here, we develop statistical models to predict hotspots at baseline prior to treatment comparing three common hotspot definitions, using epidemiologic, survey-based, and remote sensing data. In a reanalysis of randomized trials in 589 communities in five endemic countries, a regression model predicts whether Schistosoma mansoni infection prevalence will exceed the WHO threshold of 10% in year 5 (“prevalence hotspot”) with 86% sensitivity, 74% specificity, and 93% negative predictive value (NPV; assuming 30% hotspot prevalence), and a regression model for Schistosoma haematobium achieves 90% sensitivity, 90% specificity, and 96% NPV. A random forest model predicts whether S. mansoni moderate and heavy infection prevalence will exceed a public health goal of 1% in year 5 (“intensity hotspot”) with 92% sensitivity, 79% specificity, and 96% NPV, and a boosted trees model for S. haematobium achieves 77% sensitivity, 95% specificity, and 91% NPV. Baseline prevalence is a top predictor in all models. Prediction is less accurate in countries not represented in training data and for a third hotspot definition based on relative prevalence reduction over time (“persistent hotspot”). These models may be a tool to prioritize high-risk communities for more frequent surveillance or intervention against schistosomiasis, but prediction of hotspots remains a challenge.

Funder

UC | UCSF | School of Medicine, University of California, San Francisco

University Health Network

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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