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      Nodding syndrome and epilepsy in onchocerciasis endemic regions: comparing preliminary observations from South Sudan and the Democratic Republic of the Congo with data from Uganda

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          Abstract

          Background

          Nodding syndrome (NS) is an epilepsy disorder occurring in children in South Sudan, northern Uganda and Tanzania. The etiology of NS is unknown, but epidemiological studies demonstrate an association between NS and onchocerciasis.

          Methods

          Between November 2013 and July 2015 we visited onchocerciasis endemic regions in South Sudan, Uganda, and the Democratic Republic of the Congo (DRC) to assess the epilepsy situation. In South Sudan we interviewed patients and affected families, health officials, colleagues and healthcare workers, and performed a small household survey to estimate the epilepsy prevalence in the village of Mvolo, Western Equatoria State. Most information from Uganda was collected through discussions with colleagues and a review of published literature and reports. In the Bas-Uélé district of the DRC, we visited the villages of Liguga, Titule and Dingila, interviewed patients with epilepsy and family members and conducted a preliminary entomological assessment.

          Results

          In South Sudan there is an ongoing NS and epilepsy epidemic in the Western Equatoria state that started around 1990. A survey of 22 households in Mvolo revealed that 28 out of 168 (16.7 %) children suffered from NS or another form of epilepsy. Thirteen (59 %) households had at least one child, and nine (41 %) households at least two children with NS or another form of epilepsy. In northern Uganda, an NS and epilepsy epidemic started around 2000. The occurrence of new NS cases has been in decline since 2008 and no new NS cases were officially reported in 2013. The decline in NS cases coincided with the bi-annual distribution of ivermectin and the treatment of blackfly-breeding rivers with larvicides. In Bas-Uélé district in the DRC, epilepsy appears to be endemic with cases clustered in villages close to blackfly-infested, rapid-flowing rivers. The majority of epilepsy cases in Liguga, Dingila and Titule presented with generalized (tonic–clonic) seizures without nodding, but with mental retardation. In Titule, an epilepsy prevalence of 2.3 % was documented. The only anthropophilic species of blackfly collected in the region belonged to the Simulium damnosum complex.

          Conclusion

          Blackflies may play a key role in the transmission of an etiological agent that either directly or indirectly cause, not only NS, but also other forms of epilepsy in onchocerciasis endemic regions.

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          Most cited references40

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          Clinical, neurological, and electrophysiological features of nodding syndrome in Kitgum, Uganda: an observational case series.

          Nodding syndrome is an unexplained illness characterised by head-bobbing spells. The clinical and epidemiological features are incompletely described, and the explanation for the nodding and the underlying cause of nodding syndrome are unknown. We aimed to describe the clinical and neurological diagnostic features of this illness. In December, 2009, we did a multifaceted investigation to assess epidemiological and clinical illness features in 13 parishes in Kitgum District, Uganda. We defined a case as a previously healthy child aged 5-15 years with reported nodding and at least one other neurological deficit. Children from a systematic sample of a case-control investigation were enrolled in a clinical case series which included history, physical assessment, and neurological examinations; a subset had electroencephalography (EEG), electromyography, brain MRI, CSF analysis, or a combination of these analyses. We reassessed the available children 8 months later. We enrolled 23 children (median age 12 years, range 7-15 years) in the case-series investigation, all of whom reported at least daily head nodding. 14 children had reported seizures. Seven (30%) children had gross cognitive impairment, and children with nodding did worse on cognitive tasks than did age-matched controls, with significantly lower scores on tests of short-term recall and attention, semantic fluency and fund of knowledge, and motor praxis. We obtained CSF samples from 16 children, all of which had normal glucose and protein concentrations. EEG of 12 children with nodding syndrome showed disorganised, slow background (n=10), and interictal generalised 2·5-3·0 Hz spike and slow waves (n=10). Two children had nodding episodes during EEG, which showed generalised electrodecrement and paraspinal electromyography dropout consistent with atonic seizures. MRI in four of five children showed generalised cerebral and cerebellar atrophy. Reassessment of 12 children found that six worsened in their clinical condition between the first evaluation and the follow-up evaluation interval, as indicated by more frequent head nodding or seizure episodes, and none had cessation or decrease in frequency of these episodes. Nodding syndrome is an epidemic epilepsy associated with encephalopathy, with head nodding caused by atonic seizures. The natural history, cause, and management of the disorder remain to be determined. Division of Global Disease Detection and Emergency Response, US Centers for Disease Control and Prevention. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Nodding Syndrome

            An epidemic illness characterized by head nodding associated with onchocerciasis has been described in eastern Africa since the early 1960s; we summarize published reports and recent studies. Onset of nodding occurs in previously healthy 5–15-year-old children and is often triggered by eating or cold temperatures and accompanied by cognitive impairment. Its incidence has increased in Uganda and South Sudan over the past 10 years. Four case–control studies identified modest and inconsistent associations. There were nonspecific lesions seen by magnetic resonance imaging, no cerebrospinal fluid inflammation, and markedly abnormal electroencephalography results. Nodding episodes are atonic seizures. Testing has failed to demonstrate associations with trypanosomiasis, cysticercosis, loiasis, lymphatic filariasis, cerebral malaria, measles, prion disease, or novel pathogens; or deficiencies of folate, cobalamin, pyridoxine, retinol, or zinc; or toxicity from mercury, copper, or homocysteine. There is a consistent enigmatic association with onchocerciasis detected by skin snip or serologic analysis. Nodding syndrome is an unexplained epidemic epilepsy.
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              Clinical and epidemiologic characteristics of nodding syndrome in Mundri County, southern Sudan.

              Nodding syndrome (repetitive nodding and progressive generalized seizures) is assuming epidemic proportions in South Sudan, Tanzania and Uganda. To describe clinical and epidemiological features of nodding syndrome in southern Sudan based on preliminary investigations conducted in 2001 and 2002. Household surveys, clinical, electrophysiological (EEG) assessments, informant interviews and case-control studies were conducted in the town of Lui and the village of Amadi in southern Sudan. Nodding syndrome is characterized by involuntary repetitive nodding of the head, progressing to generalized seizures; mental and physical deterioration. The EEGs were consistent with progressive epileptic encephalopathy. Prevalence of Nodding syndrome in Lui and Amadi was 2.3% and 6.7% respectively. All case control studies showed a positive association between cases and Onchocerca volvulus. A history of measles was negatively associated with being a case: 2/13 of cases and 11/19 of controls had had measles: odds ratio 0.13 (95% CI 0.02, 0.76). Environmental assessment did not reveal any naturally occurring or manmade neurotoxic factors to explain Nodding Syndrome, although fungal contamination of food could not be ruled out. Nodding Syndrome was strongly associated with Onchocerca volvulus. There was no evidence to suggest an environmental pollutant, chemical agent, or other toxic factor.
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                Author and article information

                Contributors
                32486920149 , robert.colebunders@uantwerpen.be
                ahendy@itg.be
                jmokili@gmail.com
                j_wamala@yahoo.com
                kaducuj@yahoo.com
                Luciaku55@yahoo.com
                floritepage@yahoo.fr
                mandhura@yahoo.fr
                mucinyagisele@gmail.com
                glmambandu@gmail.com
                kombayendema1@yahoo.fr
                lumaliza.jeanlouis@gmail.com
                m.vanoijen@erasmusmc.nl
                Anne.Laudisoit@liverpool.ac.uk
                Journal
                BMC Res Notes
                BMC Res Notes
                BMC Research Notes
                BioMed Central (London )
                1756-0500
                22 March 2016
                22 March 2016
                2016
                : 9
                : 182
                Affiliations
                [ ]Global Health Institute, Gouverneur Kinsbergen Centrum, University of Antwerp, Doornstraat 331, 2610 Antwerp, Belgium
                [ ]Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium
                [ ]Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium
                [ ]Biology Department, San Diego State University, San Diego, USA
                [ ]Ministry of Health, Kampala, Uganda
                [ ]Faculty of Medicine, Gulu University, Gulu, Uganda
                [ ]Department of Neglected Tropical Diseases, Ministry of Health, Juba, Republic of South Sudan
                [ ]National Onchocercosis Control Program, Ministry of Health, Kisangani, Democratic Republic of the Congo
                [ ]Provincial Health Division Ituri, Ministry of Health, Bunia, Democratic Republic of the Congo
                [ ]Medical Doctor Bunia, Bunia, Province Orientale Democratic Republic of the Congo
                [ ]Provincial Ministry of Public Health, Kisangani, Province Orientale Democratic Republic of the Congo
                [ ]Biodiversity Surveillance Center, Kisangani University, Kisangani, Democratic Republic of the Congo
                [ ]General Reference Hospital of Dingila, Dingila, Democratic Republic of the Congo
                [ ]Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
                [ ]Institute of Integrative Ecology, School of Biological Sciences, University of Liverpool, Liverpool, UK
                Article
                1993
                10.1186/s13104-016-1993-7
                4802870
                27005304
                0f2ba00e-b46b-4c43-8afd-ca90436bf69b
                © Colebunders et al. 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 15 September 2015
                : 15 March 2016
                Funding
                Funded by: Flemish Interuniversity council
                Funded by: Doctors Without Borders Switzerland
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Medicine
                epilepsy,nodding syndrome,africa,onchocerca,blackflies,simulium
                Medicine
                epilepsy, nodding syndrome, africa, onchocerca, blackflies, simulium

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