Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/34573
Title: Urinary N-acetyltyramine-O,β-glucuronide in Persons with Onchocerciasis-Associated Epilepsy
Authors: Hotterbeekx, An
Dusabimana, Alfred
Mandro, Michel
Abhafule, Germain M
Deogratias, Wonya’Rossy
Siewe Fodjo, Joseph N.
ABRAMS, Steven 
Colebunders, Robert
Issue Date: 2020
Publisher: MDPI
Source: Pathogens, 9 (3) (Art N° 191)
Abstract: We investigated urinary N-acetyltyramine-O,beta-glucuronide (NATOG) levels as a biomarker for active Onchocerca volvulus infection in an onchocerciasis-endemic area in the Democratic Republic of Congo with a high epilepsy prevalence. Urinary NATOG was measured in non-epileptic men with and without O. volvulus infection, and in O. volvulus-infected persons with epilepsy (PWE). Urinary NATOG concentration was positively associated with microfilarial density (p < 0.001). The median urinary NATOG concentration was higher in PWE (3.67 mu M) compared to men without epilepsy (1.74 mu M), p = 0.017; and was higher in persons with severe (7.62 mu M) compared to mild epilepsy (2.16 mu M); p = 0.008. Non-epileptic participants with and without O. volvulus infection had similar NATOG levels (2.23 mu M and 0.71 mu M, p = 0.426). In a receiver operating characteristic curve analysis to investigate the diagnostic value of urinary NATOG, the area under the curve was 0.721 (95% CI: 0.633-0.797). Using the previously proposed cut-off value of 13 mu M to distinguish between an active O. volvulus infection and an uninfected state, the sensitivity was 15.9% and the specificity 95.9%. In conclusion, an O. volvulus infection is associated with an increased urinary NATOG concentration, which correlates with the individual parasitic load. However, the NATOG concentration has a low discriminating power to differentiate between infected and uninfected individuals.
Keywords: Onchocerca volvulus;N-acetyltyramine-O,β-glucuronide (NATOG), epilepsy;Africa;biomarker;urine
Document URI: http://hdl.handle.net/1942/34573
e-ISSN: 2076-0817
DOI: 10.3390/pathogens9030191
ISI #: WOS:000524306100018
Rights: 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Category: A1
Type: Journal Contribution
Validations: ecoom 2021
Appears in Collections:Research publications

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