Performance characteristics of diagnostic assays for schistosomiasis in Ontario, Canada

Introduction: Due to lower intensity of infection and greater intervals from last exposure, parasitologic detection methods for schistosomiasis are poorly sensitive in non-endemic areas, challenging accurate diagnosis. Methods: We evaluated parasitologic versus indirect detection methods for schisto...

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Bibliographic Details
Published in:	Therapeutic advances in infectious disease Vol. 10
Main Authors:	Lau, Rachel, Makhani, Leila, Omoruna, Osaru, Lecce, Celine, Shao, Eric, Cunanan, Marlou, Ralevski, Filip, Cheema, Karamjit, Boggild, Andrea K.
Format:	Journal Article
Language:	English
Published:	London, England SAGE Publications 01-01-2023 Sage Publications Ltd SAGE Publishing
Subjects:	Cross-reactivity Eggs Medical diagnosis Microscopy Original Research Ova Polymerase chain reaction Schistosoma Schistosoma mansoni Schistosomiasis Serology Canada schistosomiasis diagnosis PCR
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Summary:	Introduction: Due to lower intensity of infection and greater intervals from last exposure, parasitologic detection methods for schistosomiasis are poorly sensitive in non-endemic areas, challenging accurate diagnosis. Methods: We evaluated parasitologic versus indirect detection methods for schistosomiasis. We included specimens submitted for Schistosoma serology, and stool for ova and parasite microscopy. Three real-time PCR assays targeting Schistosoma mansoni and S. haematobium were performed. Primary outcome measures were sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), where both microscopy and serology were the composite reference standard against serum PCR. Results: Of 8168 serum specimens submitted for Schistosoma serology, 638 (7.8%) were reactive and 6705 (82.1%) were non-reactive. Of 156,771 stool specimens submitted for ova and parasite testing, 46 (0.03%) were positive for eggs of S. mansoni. Four (0.5%) urine specimens were positive for eggs of S. haematobium. Combined serum PCRs targeting S. mansoni had a sensitivity and specificity of 27.8% (95% CI = 18.3–39.1%) and 100% (95% CI = 83.9–100%), respectively, with PPV of 100% (95% CI = 100%) and NPV of 26.9% (95% CI = 24.3–29.7%). The one serum sample positive for S. haematobium was also detectable by our S. haematobium PCR. No cross-reactivity was observed for all three PCR assays. Conclusions: Although serology is highly sensitive, parasitologic tests signify active infection, but are limited by low population-level sensitivity, particularly in non-endemic settings. Although serum PCR offered no performance advantage over stool microscopy, its role in diagnostic parasitology should be pursued due to its high-throughput and operator-independent nature.
ISSN:	2049-9361 2049-937X
DOI:	10.1177/20499361231173843