Abstract

BackgroundSurveys conducted in 1991–1992 in the Mbam Valley (Cameroon) revealed that onchocerciasis was highly endemic, with community microfilarial loads (CMFL) > 100 microfilariae/snip in some villages. Also in 1991–1992, a survey of suspected cases of epilepsy (SCE) found 746 SCE using a questionnaire administered to individuals identified by key informants, with prevalences reaching 13.6% in some communities. From 1998, annual community-directed treatment with ivermectin (CDTI) was implemented to control onchocerciasis. In 2017, a door-to-door household survey was conducted in three of the villages visited in 1991–1992, using a standardized 5-item epilepsy screening questionnaire.ResultsIn 2017, a total of 2286 individuals living in 324 households were screened (582 in Bayomen, 553 in Ngongol and 1151 in Nyamongo) and 112 SCE were identified (4.9%). Neurologists examined 92 of these SCE and confirmed the diagnosis of epilepsy for 81 of them (3.5%). Between the surveys in 1991–1992 and 2017, the prevalence of SCE decreased from 13.6% to 2.5% in Bayomen (P = 0.001), from 8.7% to 6.6% in Ngongol (P = 0.205) and from 6.4% to 5.4% in Nyamongo (P = 0.282). The median age of SCE shifted from 20 (IQR: 12–23) to 29 years (IQR: 18–33; P = 0.018) in Bayomen, from 16 (IQR: 12–21) to 26 years (IQR: 21–39; P < 0.001) in Ngongol and from 16 (IQR: 13–19) to 24 years (IQR: 19–32; P < 0.001) in Nyamongo. The proportions of SCE aged < 10, 10–19, 20–29 and ≥ 30 years shifted from 9.5, 58.3, 25.0 and 7.1% in 1991–1992 to 2.7, 20.5, 39.3 and 37.5% in 2017, respectively.ConclusionsSCE prevalence decreased overall between 1991–1992 and 2017. The age shift observed is probably due to a decrease in the number of new cases of epilepsy resulting from the dramatic reduction of Onchocerca volvulus transmission after 19 years of CDTI.

Highlights

  • Surveys conducted in 1991–1992 in the Mbam Valley (Cameroon) revealed that onchocerciasis was highly endemic, with community microfilarial loads (CMFL) > 100 microfilariae/snip in some villages

  • Recent meta-analyses confirmed that neurocysticercosis, toxocariasis, toxoplasmosis and cerebral malaria are closely associated with epilepsy, with common odds ratios of 2.7 (95% confidence interval, CI: 2.1–3.6), 1.69, 2.25 and 4.68, respectively [5,6,7,8]

  • We considered that the death and migrations of new cases of epilepsy during the 5-year period would have a minimal effect on the incidence

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Summary

Introduction

Surveys conducted in 1991–1992 in the Mbam Valley (Cameroon) revealed that onchocerciasis was highly endemic, with community microfilarial loads (CMFL) > 100 microfilariae/snip in some villages. In 2017, a door-to-door household survey was conducted in three of the villages visited in 1991–1992, using a standardized 5-item epilepsy screening questionnaire. Estimated prevalences in Africa are amongst the highest observed worldwide, with 0.9% and 6.0% in sub-Saharan Africa and central Africa, respectively [3]. Incidence rates of epilepsy in sub-Saharan Africa range from 64 to 187 per 100,000 person-years [4]. Evident causes including perinatal brain damage or parasitic diseases that are highly endemic in sub-Saharan Africa partly account for the high epilepsy burden endured by the region. Recent meta-analyses confirmed that neurocysticercosis, toxocariasis, toxoplasmosis and cerebral malaria are closely associated with epilepsy, with common odds ratios of 2.7 (95% confidence interval, CI: 2.1–3.6), 1.69 (95% CI: 1.42–2.01), 2.25 (95% CI: 1.27–3.9) and 4.68 (95% CI: 2.52–5.70), respectively [5,6,7,8]

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