Evidence map›Paper›PMID 42842616›Full record

ArticlePLoS neglected tropical diseases2026

Assessing diagnostic accuracy of onchocerciasis rapid diagnostic tests using Bayesian latent class models.

Jayla Norman, N'Deye-Marie Bassabi-Alladjie, Pelagie M Boko-Collins, Dziedzom K de Souza, Katherine Gass, Louise Hamill, Jerónimo Langa, Carson Moore, Nelvina Mucato, Rassul Nala and 2 more

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Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

12 authors.

Jayla NormanNeglected Tropical Diseases Support Center, Task Force for Global Health, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0009-0005-7437-3154
N'Deye-Marie Bassabi-AlladjieNational Control Programme of Communicable Diseases, Ministry of Health Benin, Cotonou, Benin.
Pelagie M Boko-CollinsSightsavers, Benin Country Office, Cotonou, Benin.
Dziedzom K de SouzaNoguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Accra, Ghana.
Katherine GassNeglected Tropical Diseases Support Center, Task Force for Global Health, Atlanta, Georgia, United States of America.
Louise HamillSightsavers, Haywards Heath, United Kingdom.
Jerónimo LangaInstituto Nacional de Saúde, Maputo, Mozambique.
Carson MooreNeglected Tropical Diseases Support Center, Task Force for Global Health, Atlanta, Georgia, United States of America.
Nelvina MucatoSightsavers, Mozambique Country Office, Nampula, Mozambique.
Rassul NalaInstituto Nacional de Saúde, Maputo, Mozambique.
Sarah SullivanNeglected Tropical Diseases Support Center, Task Force for Global Health, Atlanta, Georgia, United States of America.
Emanuele GiorgiDepartment of Applied Health Sciences, University of Birmingham, Birmingham, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOnchocerciasis elimination programs increasingly rely on rapid diagnostic tests (RDTs) that detect antibodies to the Ov16 antigen, yet the performance of currently available rapid tests remains uncertain. The commercially available SD BIOLINE Ov16 RDT has shown inconsistent sensitivity when used on whole blood and does not consistently meet international performance thresholds for mapping or decisions to stop mass drug administration (MDA). Two novel onchocerciasis RDTs have been developed, DDTD RDT and GADx RDT, but their diagnostic accuracy has not been fully evaluated using methods that account for the absence of a true reference standard. METHODOLOGY/PRINCIPAL

findingsWe pooled participant-level data from three field studies conducted in Mozambique, Ghana, and Benin in 2023 to evaluate two novel onchocerciasis RDTs and the commercially available SD BIOLINE Ov16 RDT. A Bayesian latent class model was used to estimate diagnostic sensitivity and specificity without assuming any test was a perfect reference standard. Across all model specifications, the GADx rapid test showed the highest sensitivity, with posterior median estimates (92.0%-92.8%) consistently above the 89% threshold recommended for decisions to stop mass drug administration (MDA). Posterior median sensitivity for the SD BIOLINE test was above this threshold in most models but below it under the field-based prior (83.2%). The DDTD RDT demonstrated lower sensitivity overall (86.6%-88.4%). Specificity estimates were consistently high for all tests but remained below the recommended threshold of 99.8% (highest median: 98.8%). Alternative definitions of a positive result for the multi-antigen DDTD RDT did not meaningfully alter its estimated performance. CONCLUSIONS/SIGNIFICANCE: In the study communities sampled, the two novel onchocerciasis RDTs generally yielded higher sensitivity estimates than the commercially available SD BIOLINE Ov16 RDT, with the GADx assay having the highest estimated sensitivity. However, posterior estimates for none of the evaluated tests reached the specificity threshold recommended to support decisions to stop MDA on their own. These findings highlight the need for improved diagnostic tools or complementary testing strategies to support elimination decision-making.

Indexed as

OnchocerciasisRapid Diagnostic TestsAnimalsAntibodies, HelminthAntigens, HelminthBayes TheoremBeninFemaleGhanaHumansLatent Class AnalysisMaleMozambiqueOnchocerca volvulusSensitivity and SpecificityAntibodies, HelminthAntigens, Helminth

Identifiers

PMID42842616
PMCPMC13660989

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.