TY - JOUR KW - Hotspots KW - machine learning KW - Neglected Tropical Diseases KW - Public health KW - schistosomiasis AU - Singer B AU - Coulibaly J AU - Park H AU - Andrews J AU - Bogoch I AU - Lo N AB -
Schistosomiasis is a neglected tropical disease affecting over 150 million people. Hotspots of 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 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 achieves 90% sensitivity, 90% specificity, and 96% NPV. A random forest model predicts whether 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 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.
BT - Proceedings of the National Academy of Sciences of the United States of America C1 -https://www.ncbi.nlm.nih.gov/pubmed/38181058
DA - 01/2024 DO - 10.1073/pnas.2315463120 IS - 2 J2 - Proc Natl Acad Sci U S A LA - eng N2 -Schistosomiasis is a neglected tropical disease affecting over 150 million people. Hotspots of 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 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 achieves 90% sensitivity, 90% specificity, and 96% NPV. A random forest model predicts whether 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 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.
PY - 2024 T2 - Proceedings of the National Academy of Sciences of the United States of America TI - Development of prediction models to identify hotspots of schistosomiasis in endemic regions to guide mass drug administration. UR - https://www.pnas.org/doi/10.1073/pnas.2315463120 VL - 121 SN - 1091-6490 ER -