High prevalence of cysticercosis in people with epilepsy in southern Rwanda.

BACKGROUND: Neurocysticercosis (NCC), the central nervous system infection by Taenia solium larvae, is a preventable and treatable cause of epilepsy. In Sub-Saharan Africa, the role of NCC in epilepsy differs geographically and, overall, is poorly defined. We aimed at contributing specific, first da...

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Main Authors: Ruth Rottbeck, Jules Fidèle Nshimiyimana, Pierrot Tugirimana, Uta E Düll, Janko Sattler, Jean-Claudien Hategekimana, Janvier Hitayezu, Irmengard Bruckmaier, Matthias Borchert, Jean Bosco Gahutu, Sebastian Dieckmann, Gundel Harms, Frank P Mockenhaupt, Ralf Ignatius
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-11-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC3828157?pdf=render
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author Ruth Rottbeck
Jules Fidèle Nshimiyimana
Pierrot Tugirimana
Uta E Düll
Janko Sattler
Jean-Claudien Hategekimana
Janvier Hitayezu
Irmengard Bruckmaier
Matthias Borchert
Jean Bosco Gahutu
Sebastian Dieckmann
Gundel Harms
Frank P Mockenhaupt
Ralf Ignatius
author_facet Ruth Rottbeck
Jules Fidèle Nshimiyimana
Pierrot Tugirimana
Uta E Düll
Janko Sattler
Jean-Claudien Hategekimana
Janvier Hitayezu
Irmengard Bruckmaier
Matthias Borchert
Jean Bosco Gahutu
Sebastian Dieckmann
Gundel Harms
Frank P Mockenhaupt
Ralf Ignatius
author_sort Ruth Rottbeck
collection DOAJ
description BACKGROUND: Neurocysticercosis (NCC), the central nervous system infection by Taenia solium larvae, is a preventable and treatable cause of epilepsy. In Sub-Saharan Africa, the role of NCC in epilepsy differs geographically and, overall, is poorly defined. We aimed at contributing specific, first data for Rwanda, assessing factors associated with NCC, and evaluating a real-time PCR assay to diagnose NCC in cerebrospinal fluid (CSF). METHODOLOGY/PRINCIPAL FINDINGS: At three healthcare facilities in southern Rwanda, 215 people with epilepsy (PWE) and 51 controls were clinically examined, interviewed, and tested by immunoblot for cysticerci-specific serum antibodies. Additionally, CSF samples from PWE were tested for anticysticercal antibodies by ELISA and for parasite DNA by PCR. Cranial computer tomography (CT) scans were available for 12.1% of PWE with additional symptoms suggestive of NCC. The Del Brutto criteria were applied for NCC diagnosis. Cysticerci-specific serum antibodies were found in 21.8% of PWE and 4% of controls (odds ratio (OR), 6.69; 95% confidence interval (95%CI), 1.6-58.7). Seropositivity was associated with age and lack of safe drinking water. Fifty (23.3%) PWE were considered NCC cases (definitive, based on CT scans, 7.4%; probable, mainly based on positive immunoblots, 15.8%). In CSF samples from NCC cases, anticysticercal antibodies were detected in 10% (definitive cases, 25%) and parasite DNA in 16% (definitive cases, 44%). Immunoblot-positive PWE were older (medians, 30 vs. 22 years), more frequently had late-onset epilepsy (at age >25 years; 43.5% vs. 8.5%; OR, 8.30; 95%CI, 3.5-20.0), and suffered from significantly fewer episodes of seizures in the preceding six months than immunoblot-negative PWE. CONCLUSIONS/SIGNIFICANCE: NCC is present and contributes to epilepsy in southern Rwanda. Systematic investigations into porcine and human cysticercosis as well as health education and hygiene measures for T. solium control are needed. PCR might provide an additional, highly specific tool in NCC diagnosis.
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spelling doaj.art-b8e356e85fcb4dc7b0101474691e4adb2022-12-21T22:50:47ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352013-11-01711e255810.1371/journal.pntd.0002558High prevalence of cysticercosis in people with epilepsy in southern Rwanda.Ruth RottbeckJules Fidèle NshimiyimanaPierrot TugirimanaUta E DüllJanko SattlerJean-Claudien HategekimanaJanvier HitayezuIrmengard BruckmaierMatthias BorchertJean Bosco GahutuSebastian DieckmannGundel HarmsFrank P MockenhauptRalf IgnatiusBACKGROUND: Neurocysticercosis (NCC), the central nervous system infection by Taenia solium larvae, is a preventable and treatable cause of epilepsy. In Sub-Saharan Africa, the role of NCC in epilepsy differs geographically and, overall, is poorly defined. We aimed at contributing specific, first data for Rwanda, assessing factors associated with NCC, and evaluating a real-time PCR assay to diagnose NCC in cerebrospinal fluid (CSF). METHODOLOGY/PRINCIPAL FINDINGS: At three healthcare facilities in southern Rwanda, 215 people with epilepsy (PWE) and 51 controls were clinically examined, interviewed, and tested by immunoblot for cysticerci-specific serum antibodies. Additionally, CSF samples from PWE were tested for anticysticercal antibodies by ELISA and for parasite DNA by PCR. Cranial computer tomography (CT) scans were available for 12.1% of PWE with additional symptoms suggestive of NCC. The Del Brutto criteria were applied for NCC diagnosis. Cysticerci-specific serum antibodies were found in 21.8% of PWE and 4% of controls (odds ratio (OR), 6.69; 95% confidence interval (95%CI), 1.6-58.7). Seropositivity was associated with age and lack of safe drinking water. Fifty (23.3%) PWE were considered NCC cases (definitive, based on CT scans, 7.4%; probable, mainly based on positive immunoblots, 15.8%). In CSF samples from NCC cases, anticysticercal antibodies were detected in 10% (definitive cases, 25%) and parasite DNA in 16% (definitive cases, 44%). Immunoblot-positive PWE were older (medians, 30 vs. 22 years), more frequently had late-onset epilepsy (at age >25 years; 43.5% vs. 8.5%; OR, 8.30; 95%CI, 3.5-20.0), and suffered from significantly fewer episodes of seizures in the preceding six months than immunoblot-negative PWE. CONCLUSIONS/SIGNIFICANCE: NCC is present and contributes to epilepsy in southern Rwanda. Systematic investigations into porcine and human cysticercosis as well as health education and hygiene measures for T. solium control are needed. PCR might provide an additional, highly specific tool in NCC diagnosis.http://europepmc.org/articles/PMC3828157?pdf=render
spellingShingle Ruth Rottbeck
Jules Fidèle Nshimiyimana
Pierrot Tugirimana
Uta E Düll
Janko Sattler
Jean-Claudien Hategekimana
Janvier Hitayezu
Irmengard Bruckmaier
Matthias Borchert
Jean Bosco Gahutu
Sebastian Dieckmann
Gundel Harms
Frank P Mockenhaupt
Ralf Ignatius
High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
PLoS Neglected Tropical Diseases
title High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
title_full High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
title_fullStr High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
title_full_unstemmed High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
title_short High prevalence of cysticercosis in people with epilepsy in southern Rwanda.
title_sort high prevalence of cysticercosis in people with epilepsy in southern rwanda
url http://europepmc.org/articles/PMC3828157?pdf=render
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