Risk Factors for Nodding Syndrome and Other Forms of Epilepsy in Northern Uganda: A Case-Control Study

Epidemiological studies suggest a link between onchocerciasis and various forms of epilepsy, including nodding syndrome (NS). The aetiopathology of onchocerciasis associated epilepsy remains unknown. This case-control study investigated potential risk factors that may lead to NS and other forms of n...

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Autores principales: Nolbert Gumisiriza, Marina Kugler, Nele Brusselaers, Frank Mubiru, Ronald Anguzu, Albert Ningwa, Rodney Ogwang, Pamela Akun, Amos Deogratius Mwaka, Catherine Abbo, Rogers Sekibira, An Hotterbeekx, Robert Colebunders, Kevin Marsh, Richard Idro
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/b8a8b4dab12144a687e5d024378acf72
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Sumario:Epidemiological studies suggest a link between onchocerciasis and various forms of epilepsy, including nodding syndrome (NS). The aetiopathology of onchocerciasis associated epilepsy remains unknown. This case-control study investigated potential risk factors that may lead to NS and other forms of non-nodding epilepsy (OFE) in northern Uganda. We consecutively recruited 154 persons with NS (aged between 8 and 20 years), and age-frequency matched them with 154 with OFE and 154 healthy community controls. Participants’ socio-demography, medical, family, and migration histories were recorded. We tested participants for <i>O. volvulus</i> serum antibodies. The 154 controls were used for both OFE and NS separately to determine associations. We recruited 462 people with a median age of 15 years (IQR 14, 17); 260 (56.4%) were males. Independent risk factors associated with the development of NS were the presence of <i>O. volvulus</i> antibodies [aOR 8.79, 95% CI (4.15–18.65), <i>p</i>-value < 0.001] and preterm birth [aOR 2.54, 95% CI (1.02–6.33), <i>p</i>-value = 0.046]. Risk factors for developing OFE were the presence of O. volvulus antibodies [aOR 8.83, 95% CI (4.48–17.86), <i>p</i>-value < 0.001] and being born in the period before migration to IDP camps [aOR 4.28, 95% CI (1.20–15.15), <i>p</i>-value = 0.024]. In conclusion, <i>O. volvulus seropositivity</i> was a risk factor to develop NS and OFE; premature birth was a potential co-factor. Living in IDP camps was not a risk factor for developing NS or OFE.