Assessment of urine metabolite biomarkers for the detection of S. haematobium infection in pre-school aged children in a rural community in Zimbabwe.

S. haematobium biomarkers diagnosis metabolites

Journal

Acta tropica
ISSN: 1873-6254
Titre abrégé: Acta Trop
Pays: Netherlands
ID NLM: 0370374

Informations de publication

Date de publication:
08 Aug 2024
Historique:
received: 09 11 2023
revised: 15 07 2024
accepted: 16 07 2024
medline: 11 8 2024
pubmed: 11 8 2024
entrez: 10 8 2024
Statut: aheadofprint

Résumé

Early diagnosis of urogenital schistosomiasis is key to its control and elimination. The current gold standard microscopic examination techniques lack sensitivity in detecting light Schistosomiasis infections in pre-school aged children thus it is urgent to develop diagnostic tools that may be integrated into control programs. In this study, we evaluated the diagnostic performance of urine metabolite biomarkers using a chemical reagent strip in the detection of S. haematobium infection in pre-school aged children. A case-control study was conducted involving 82 pre-school aged children that were age and sex matched. Urine samples were collected for 3 consecutive days and were evaluated using urine filtration gold techniques as the gold standard method. The samples were simultaneously measured for metabolite biomarkers specifically haematuria, proteins, ketones, nitrites, glucose, bilirubin and urobilinogen using chemical reagent strips. Pearson correlation test was used to measure the relationship between S. haematobium infection and the urine metabolite biomarkers. The diagnostic performance of urine biomarkers were correlated with the microscopic examination urine filtration technique. Haematuria (r = 0.592, p = 0.0001) and proteinuria (r = 0.448, p = 0.0001) were correlated to S. haematobium infection. Negative correlations with p > 0.05 were recorded for ketones and urobilinogen. Highest sensitivity was 65.9% (CI, 49.4 - 79.9) for haematuria whilst protein (albumin) biomarker had a lower specificity value of 43.9% (28.5 - 60.3). Inversely, highest sensitivity was 87.8% (73.8 - 95.9) for proteinuria whilst haematuria had a lower sensitivity value of 82.9% (67.9 - 92.8). The positive predictive values ranged from 57.7% (41.6 - 72.2) to 79.4% (65.5 - 88.7) whereas negative predictive values ranged from 70.8% (60.8 - 79.2) to 52.0% (48.7 - 55.3). With respect to diagnostic efficiency, haematuria had a fair diagnostic performance with an area under the curve of 0.76 followed by proteinuria with proteinuria whilst the remaining metabolites fail discriminating ability with an area under the curve of less than 0.5. Although haematuria and protein biomarkers in urine are moderately sensitive and specific, they are important morbidity indicators of urogenital schistosomiasis in pre-school aged that may be utilised during screening in schistosomiasis control programs. We recommend comprehensive analysis of biomarkers using metabolomics techniques to identify novel urine biomarkers.

Sections du résumé

BACKGROUND BACKGROUND
Early diagnosis of urogenital schistosomiasis is key to its control and elimination. The current gold standard microscopic examination techniques lack sensitivity in detecting light Schistosomiasis infections in pre-school aged children thus it is urgent to develop diagnostic tools that may be integrated into control programs. In this study, we evaluated the diagnostic performance of urine metabolite biomarkers using a chemical reagent strip in the detection of S. haematobium infection in pre-school aged children.
METHODS METHODS
A case-control study was conducted involving 82 pre-school aged children that were age and sex matched. Urine samples were collected for 3 consecutive days and were evaluated using urine filtration gold techniques as the gold standard method. The samples were simultaneously measured for metabolite biomarkers specifically haematuria, proteins, ketones, nitrites, glucose, bilirubin and urobilinogen using chemical reagent strips. Pearson correlation test was used to measure the relationship between S. haematobium infection and the urine metabolite biomarkers.
RESULTS RESULTS
The diagnostic performance of urine biomarkers were correlated with the microscopic examination urine filtration technique. Haematuria (r = 0.592, p = 0.0001) and proteinuria (r = 0.448, p = 0.0001) were correlated to S. haematobium infection. Negative correlations with p > 0.05 were recorded for ketones and urobilinogen. Highest sensitivity was 65.9% (CI, 49.4 - 79.9) for haematuria whilst protein (albumin) biomarker had a lower specificity value of 43.9% (28.5 - 60.3). Inversely, highest sensitivity was 87.8% (73.8 - 95.9) for proteinuria whilst haematuria had a lower sensitivity value of 82.9% (67.9 - 92.8). The positive predictive values ranged from 57.7% (41.6 - 72.2) to 79.4% (65.5 - 88.7) whereas negative predictive values ranged from 70.8% (60.8 - 79.2) to 52.0% (48.7 - 55.3). With respect to diagnostic efficiency, haematuria had a fair diagnostic performance with an area under the curve of 0.76 followed by proteinuria with proteinuria whilst the remaining metabolites fail discriminating ability with an area under the curve of less than 0.5.
CONCLUSION CONCLUSIONS
Although haematuria and protein biomarkers in urine are moderately sensitive and specific, they are important morbidity indicators of urogenital schistosomiasis in pre-school aged that may be utilised during screening in schistosomiasis control programs. We recommend comprehensive analysis of biomarkers using metabolomics techniques to identify novel urine biomarkers.

Identifiants

pubmed: 39127139
pii: S0001-706X(24)00209-2
doi: 10.1016/j.actatropica.2024.107327
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107327

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors declare that they have no conflict of interest.

Auteurs

Herald Midzi (H)

Department of Biochemistry and Biotechnology, University of Zimbabwe, Harare, Zimbabwe.; Optics & Imaging, Doris Duke Medical Research Institute, College of Health Sciences, University of KwaZulu-Natal, KwaZulu-Natal, South Africa.. Electronic address: midziherald@gmail.com.

Thajasvarie Naicker (T)

Optics & Imaging, Doris Duke Medical Research Institute, College of Health Sciences, University of KwaZulu-Natal, KwaZulu-Natal, South Africa.

Arthur Vengesai (A)

Faculty of Medicine and Health Sciences, Department of Biochemistry, Midlands State University, Gweru, Zimbabwe.

Lucy Mabaya (L)

Midlands State University, National Pathology Research and Diagnostic Centre, Gweru, Zimbabwe.

Petros Muchesa (P)

Water and Health Research Centre, University of Johannesburg, South Africa.

Tariro L Mduluza-Jokonya (TL)

Optics & Imaging, Doris Duke Medical Research Institute, College of Health Sciences, University of KwaZulu-Natal, KwaZulu-Natal, South Africa.; Faculty of Medicine and Health Science, University of Zimbabwe, Harare, Zimbabwe.

Aaron Garikai Katerere (AG)

Department of Biochemistry and Biotechnology, University of Zimbabwe, Harare, Zimbabwe.

Donald Kapanga (D)

Midlands State University, National Pathology Research and Diagnostic Centre, Gweru, Zimbabwe.

Maritha Kasambala (M)

Department of Biological Sciences and Ecology, University of Zimbabwe, Harare, Zimbabwe.

Francisca Mutapi (F)

Ashworth Laboratories, Institute for Immunology and Infection Research and Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh, Scotland.

Takafira Mduluza (T)

Department of Biochemistry and Biotechnology, University of Zimbabwe, Harare, Zimbabwe.

Classifications MeSH