Accuracy of a new rapid diagnostic test for urinary antigen detection and assessment of drug treatment in opisthorchiasis.

Enzyme-linked immunosorbent assay Liver fluke Opisthorchis viverrini Quantitative formalin-ethyl acetate concentration technique Urinary Opisthorchis viverrini rapid diagnosis test Urinary antigen detection

Journal

Infectious diseases of poverty
ISSN: 2049-9957
Titre abrégé: Infect Dis Poverty
Pays: England
ID NLM: 101606645

Informations de publication

Date de publication:
21 Nov 2023
Historique:
received: 14 08 2023
accepted: 15 11 2023
medline: 23 11 2023
pubmed: 22 11 2023
entrez: 22 11 2023
Statut: epublish

Résumé

Screening for opisthorchiasis, a parasitic worm infection affecting many millions of people in Southeast Asia, has traditionally relied on faecal egg examination such as the formalin-ethyl acetate concentration technique (FECT) and Kato-Katz method. Although the urinary enzyme-linked immunosorbent assay (ELISA) has been used more recently, we developed a urinary antigen-based rapid diagnostic test (RDT) to simplify diagnosis and as a point-of-care testing (POCT) and field applications for surveillance and control of opisthorchiasis. A urinary Opisthorchis viverrini (OV)-RDT was developed using immunochromatographic methodology with a specific monoclonal antibody against OV. The diagnostic performance of the urinary OV-RDT was compared to that of quantitative faecal FECT and urinary antigen ELISA (n = 493). Cross-reactivities of urinary OV-RDT with other helminthiases coexisted with O. viverrini were determined (n = 96). A field trial in the application of urinary OV-RDT was compared with urinary antigen ELISA at baseline screening and assessment of drug treatment outcomes in opisthorchiasis (n = 1629). The McNemar chi-square, Kruskal-Wallis and Cohen's kappa coefficient (κ-value) tests were used for statistical analyses. Urinary OV-RDT had sensitivity of 94.2% and specificity of 93.2%, compared to faecal FECT. Urinary OV-RDT had high diagnostic agreement (Kappa = 0.842-0.874, P < 0.001) and quantitative correlation with urinary antigen ELISA (Kruskal-Wallis tests = 316.2, P < 0.0001) and faecal FECT (Kruskal-Wallis tests = 362.3, P < 0.0001). The positive rates by OV-RDT, ELISA and FECT were 48.9%, 52.5% and 49.3%, respectively. Cross-reactions of urinary OV-RDT with other helminthiases were few (2%). Field trials of urinary OV-RDT yielded comparable prevalence of O. viverrini between urinary OV-RDT (53.2%) and urinary antigen ELISA (54.0%). OV screening showed high diagnostic agreement (kappa > 0.8, P < 0.0001) between urinary OV-RDT and urinary antigen ELISA. The cure rates of opisthorchiasis at 1 month post-praziquantel treatment determined by urinary OV-RDT (86.6%) and urinary antigen ELISA (80.5%) were similar (P > 0.05). The urinary OV-RDT test has high potential as a new tool for screening and evaluating treatment outcomes in opisthorchiasis. The ease of sample collection and simplicity of urinary OV-RDT may facilitate mass screening, control and elimination of opisthorchiasis, thereby contributing to a reduction in the disease burden in Southeast Asia.

Sections du résumé

BACKGROUND BACKGROUND
Screening for opisthorchiasis, a parasitic worm infection affecting many millions of people in Southeast Asia, has traditionally relied on faecal egg examination such as the formalin-ethyl acetate concentration technique (FECT) and Kato-Katz method. Although the urinary enzyme-linked immunosorbent assay (ELISA) has been used more recently, we developed a urinary antigen-based rapid diagnostic test (RDT) to simplify diagnosis and as a point-of-care testing (POCT) and field applications for surveillance and control of opisthorchiasis.
METHODS METHODS
A urinary Opisthorchis viverrini (OV)-RDT was developed using immunochromatographic methodology with a specific monoclonal antibody against OV. The diagnostic performance of the urinary OV-RDT was compared to that of quantitative faecal FECT and urinary antigen ELISA (n = 493). Cross-reactivities of urinary OV-RDT with other helminthiases coexisted with O. viverrini were determined (n = 96). A field trial in the application of urinary OV-RDT was compared with urinary antigen ELISA at baseline screening and assessment of drug treatment outcomes in opisthorchiasis (n = 1629). The McNemar chi-square, Kruskal-Wallis and Cohen's kappa coefficient (κ-value) tests were used for statistical analyses.
RESULTS RESULTS
Urinary OV-RDT had sensitivity of 94.2% and specificity of 93.2%, compared to faecal FECT. Urinary OV-RDT had high diagnostic agreement (Kappa = 0.842-0.874, P < 0.001) and quantitative correlation with urinary antigen ELISA (Kruskal-Wallis tests = 316.2, P < 0.0001) and faecal FECT (Kruskal-Wallis tests = 362.3, P < 0.0001). The positive rates by OV-RDT, ELISA and FECT were 48.9%, 52.5% and 49.3%, respectively. Cross-reactions of urinary OV-RDT with other helminthiases were few (2%). Field trials of urinary OV-RDT yielded comparable prevalence of O. viverrini between urinary OV-RDT (53.2%) and urinary antigen ELISA (54.0%). OV screening showed high diagnostic agreement (kappa > 0.8, P < 0.0001) between urinary OV-RDT and urinary antigen ELISA. The cure rates of opisthorchiasis at 1 month post-praziquantel treatment determined by urinary OV-RDT (86.6%) and urinary antigen ELISA (80.5%) were similar (P > 0.05).
CONCLUSIONS CONCLUSIONS
The urinary OV-RDT test has high potential as a new tool for screening and evaluating treatment outcomes in opisthorchiasis. The ease of sample collection and simplicity of urinary OV-RDT may facilitate mass screening, control and elimination of opisthorchiasis, thereby contributing to a reduction in the disease burden in Southeast Asia.

Identifiants

pubmed: 37990282
doi: 10.1186/s40249-023-01162-4
pii: 10.1186/s40249-023-01162-4
pmc: PMC10662682
doi:

Substances chimiques

Praziquantel 6490C9U457

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© 2023. The Author(s).

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Auteurs

Chanika Worasith (C)

Department of Adult Nursing, Faculty of Nursing, Khon Kaen University, Khon Kaen, Thailand.
Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.

Jiraporn Sithithaworn (J)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.

Phattharaphon Wongphutorn (P)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Biomedical Science Program, Graduate School, Khon Kaen University, Khon Kaen, Thailand.

Chutima Homwong (C)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.

Kanoknan Khongsukwiwat (K)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.

Anchalee Techasen (A)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.

Kulthida Y Kopolrat (KY)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Faculty of Public Health, Kasetsart University Chalermphrakiat Sakon Nakhon Province Campus, Sakon Nakhon, Thailand.

Watcharin Loilome (W)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Department of Systems Biosciences and Computational Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Khon Kaen University Phenome Centre, Khon Kaen University, Khon Kaen, Thailand.

Nisana Namwat (N)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Department of Systems Biosciences and Computational Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Khon Kaen University Phenome Centre, Khon Kaen University, Khon Kaen, Thailand.

Bandit Thinkamrop (B)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Department of Epidemiology and Biostatistics, Faculty of Public Health, Khon Kaen University, Khon Kaen, Thailand.

Chaiwat Tawarungruang (C)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Department of Epidemiology and Biostatistics, Faculty of Public Health, Khon Kaen University, Khon Kaen, Thailand.

Attapol Titapun (A)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Department of Surgery, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Thewarach Laha (T)

Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Ross H Andrews (RH)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand.
Faculty of Medicine, St Mary's Campus, Imperial College London, London, UK.

Simon D Taylor-Robinson (SD)

Division of Digestive Health, Department of Surgery and Cancer, Imperial College London, London, UK.

Paiboon Sithithaworn (P)

Cholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Thailand. paib_sit@kku.ac.th.
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand. paib_sit@kku.ac.th.

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