4.5 Article

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

Journal

PATHOGENS
Volume 10, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens10111451

Keywords

nodding syndrome; epilepsy; onchocerciasis; Uganda; risk factors

Categories

Funding

  1. Medical Research Council (MRC)
  2. United Kingdom Department for International Development
  3. African Research Leadership Award [MR/M025489/1]
  4. Dubois Brigue foundation
  5. VLIR-UOS (Flemish Interuniversity Council for University Development Cooperation)
  6. DELTAS Africa Initiative [DEL-15-003]
  7. MRC [MR/M025489/1] Funding Source: UKRI

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This study found that O. volvulus seropositivity and premature birth are risk factors for developing nodding syndrome and other forms of non-nodding epilepsy. Being born before the migration to internally displaced persons (IDP) camps was a risk factor for developing other forms of non-nodding epilepsy.
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 O. volvulus 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 O. volvulus antibodies [aOR 8.79, 95% CI (4.15-18.65), p-value < 0.001] and preterm birth [aOR 2.54, 95% CI (1.02-6.33), p-value = 0.046]. Risk factors for developing OFE were the presence of O. volvulus antibodies [aOR 8.83, 95% CI (4.48-17.86), p-value < 0.001] and being born in the period before migration to IDP camps [aOR 4.28, 95% CI (1.20-15.15), p-value = 0.024]. In conclusion, O. volvulus seropositivity 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.

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