Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Jun 20;7(1):64.
doi: 10.1186/s40249-018-0450-3.

High prevalence of epilepsy in two rural onchocerciasis endemic villages in the Mahenge area, Tanzania, after 20 years of community directed treatment with ivermectin

Affiliations

High prevalence of epilepsy in two rural onchocerciasis endemic villages in the Mahenge area, Tanzania, after 20 years of community directed treatment with ivermectin

Bruno P Mmbando et al. Infect Dis Poverty. .

Abstract

Background: Epilepsy is a neurological disorder with a multitude of underlying causes, which may include infection with Onchocerca volvulus, the parasitic worm that causes human onchocerciasis. A survey carried out in 1989 revealed a high prevalence of epilepsy (1.02% overall, ranging from 0.51 to 3.71% in ten villages) in the Mahenge area of Ulanga district, an onchocerciasis endemic region in south eastern Tanzania. This study aimed to determine the prevalence and incidence of epilepsy following 20 years of onchocerciasis control through annual community directed treatment with ivermectin (CDTI).

Methods: The study was conducted in January 2017 in two suburban and two rural villages in the Mahenge area. Door-to-door household visits were carried out by trained community health workers and data assistants to screen for persons suspected of having epilepsy, using a standardised questionnaire. Persons with suspected epilepsy were then interviewed and examined by a neurologist for case verification. Onchocerciasis associated epilepsy was defined as epilepsy without an obvious cause, with an onset of seizures between the ages of 3-18 years in previously healthy children. In each village, fifty males aged ≥20 years were tested for onchocerciasis antibodies using an OV16 rapid test and were examined for presence of onchocerciasis nodules. Children aged 6-10 years were also tested using OV16 tests.

Results: 5117 individuals (median age 18.5 years, 53.2% female) from 1168 households were screened. 244 (4.8%) were suspected of having epilepsy and invited for neurological assessment. Prevalence of epilepsy was 2.5%, with the rural villages having the highest rate (3.5% vs 1.5%), P < 0.001. Overall incidence of epilepsy was 111 cases (95% CI: 73-161) per 100 000 person-years, while that of onchocerciasis associated epilepsy was 131 (95% CI: 70-223). Prevalence of OV16 antibodies in adult males and among children 6-10 years old was higher in rural villages than in suburban villages (76.5% vs 50.6, and 42.6% vs 4.7% respectively), (P < 0.001), while overall prevalence of onchocerciasis nodules was 1.8%.

Conclusions: This survey revealed a high prevalence and incidence of epilepsy in two rural onchocerciasis endemic villages in the Mahenge area. Despite 20 years of CDTI, a high prevalence of OV16 antibodies in children aged 6-10 years suggests on-going O. volvulus transmission. Reasons for the persistence of on-going parasite transmission in the Mahenge area need to be investigated.

Keywords: Epilepsy; Mahenge; Onchocerciasis; Tanzania.

PubMed Disclaimer

Conflict of interest statement

Ethics approval and consent to participate

This study was approved by the ethical committees of the National Institute for Medical Research in Tanzania and the University of Antwerp in Belgium. The study was carried out adhering to the principles of the Declaration of Helsinki. Meetings were held with the community leaders to explain the aims and procedures of the study. During the screening phase, consent was obtained from heads of households or adults who were available at the household during the interviews. For persons suspected to have epilepsy and individuals who participated in REMO and in OV16 testing, individual written consent was obtained. Individuals aged 18 years and above provided their own consent, while children and minors had their consent signed by their parents or guardians. Moreover, assent was obtained from those aged 12 years or above.

Competing interests

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Map of the Mahenge area
Fig. 2
Fig. 2
Risk of epilepsy adjusted by village (a) and prevalence of epilepsy by strata (b)
Fig. 3
Fig. 3
Distribution of age at onset of nodding syndrome and other types of epilepsy
Fig. 4
Fig. 4
OV16 positivity rate in children 6–10 years by village (a), and age in urban (b) and rural (c)
Fig. 5
Fig. 5
Distribution of OV16 positivity rate among individuals with confirmed and without epilepsy by age group
Fig. 6
Fig. 6
Proportion of children aged 7–10 years enrolled in primary school at different classes by village

Comment in

References

    1. World Health Organisation. Epilepsy 2017. http://www.who.int/mediacentre/factsheets/fs999/en/. Accessed 28 Sep 2017.
    1. Paul A, Adeloye D, George-Carey R, Kolčić I, Grant L, Chan KY. An estimate of the prevalence of epilepsy in sub–Saharan Africa: a systematic analysis. J Glob Health. 2012;2:20405. doi: 10.7189/jogh.02.020405. - DOI - PMC - PubMed
    1. Aall-Jilek LM. Epilepsy in the Wapogoro tribe in Tanganyika. Acta Psychiatr Scand. 1965;41:57–86. doi: 10.1111/j.1600-0447.1965.tb04970.x. - DOI
    1. Dowell SF, Sejvar JJ, Riek L, Vandemaele KAH, Lamunu M, Kuesel AC, et al. Nodding syndrome. Emerg Infect Dis. 2013;19:1374. doi: 10.3201/eid1909.130401. - DOI - PMC - PubMed
    1. Tumwine JK, Vandemaele K, Chungong S, Richer M, Anker M, Ayana Y, et al. Clinical and epidemiologic characteristics of nodding syndrome in Mundri County, southern Sudan. Afr Health Sci. 2012;12:242–248. - PMC - PubMed