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Prevalence of epilepsy, human and porcine cysticercosis in western Kenya
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Prevalence of epilepsy, human and porcine cysticercosis in western Kenya

  1. • Study population: • Village with high proportion of pig-keeping households (HH) and suspected high rate of porcine cysticercosis, Busibwabo sub-location, Busia County, Kenya (Figure 1) • Sampling: • Three-stage door-to-door community based survey (Figure 2) • Pigs: Assessment of individual characteristics, lingual exam (Figure 3) • Exam not performed on pigs that were pregnant, lactating, or under 3 months of age • Humans: • Stage 1: • Humans: Assessment of household characteristics, individual survey and epilepsy screening questionnaire • Stage 2: • Screen positive for epilepsy: Neurologist evaluation to confirm epilepsy diagnosis and blood test for cysticercal antigen (Ag) • Screen negative for epilepsy: A random sample of 2% of individuals who were negative on epilepsy screening questions had blood test for cysticercal Ag • Stage 3: • Confirmed Lifetime Epilepsy ≥5 yrs old: Computed Tomography (CT) brain • CT done in Children <5yrs if focal neurological deficit or positive cysticercal Ag • 2% sample of screen negative and positive cysticercal Ag: CT brain • Procedures: • Epilepsy Screening: 9-question epilepsy screening questionnaire was adapted from a widely used instrument and translated into the predominant local languages12 • Lifetime Epilepsy: ILAE 1993 criteria.13 • Porcine Cysticercosis: Presence of one or more palpable lingual cysts • Human Cysticercosis: Blood was tested for circulating cysticercal antigen using the apDia Cysticercosis Antigen ELISA, a commercially available enzyme immunoassay for qualitative determination of viable metacestodes (cysticerci) of Taenia spp. Cut-off values were calculated according to kit instructions. • Human Neurocysticercosis: Contrast-enhanced Computed Tomography (CT) of the brain was performed using standard protocols and read by a radiologist blinded to the serostatus and presence or absence of epilepsy • Analysis: Fishers exact tests were used to compare proportions. Methods Conclusions Prevalence of Epilepsy, Human and Porcine Cysticercosis in Western Kenya 1. Meyer, A., et al., Global disparities in the epilepsy treatment gap: a systematic review. Bull World Health Organ, 2010. 88: 260-266. 2. Leonardi, M. and T. Ustun, The global burden of epilepsy. Epilepsia, 2002. 43(sup6):21-25. 3. Del Brutto, O.H., Neurocysticercosis: A Review. The Scientific World Journal, 2012. 4. Ndimubanzi, P., et al., A Systematic Review of the Frequency of Neurocysticercosis with a Focus on People with Epilepsy. PLoS Negl Trop Dis, 2010. 4(11): e870. 5. Ngugi, A., et al., Estimation of the burden of active and life-time epilepsy: A meta-analytic approach. Epilepsia, 2010. 51(5): 883-890. 6. Carabin, H., et al., Clinical manifestations associated with neurocysticercosis: A systematic review. PLoS Negl Trop Dis, 2011. 5(5): e1152. 7. Mafojane, N., et al., The current status of neurocysticercosis in Eastern and Southern Africa. Acta Tropica, 2003. 87:25-33. 8. Balogou, A., et al., Cysticercose et épilepsie au nord du Togo dans le Tone. Rev Neurol (Paris), 2000. 156(3):270-273. 9. Blocher, J., et al., A Cross-Sectionnal Study of People with Epilepsy and Neurocysticercosis in Tanzania: Clinical Characteristics and Diagnostic Approaches. PLoS Negl Trop Dis, 2011. 5(6): e1185. 10. Dongmo, L., et al., Cysticercose et épilepsie: étude cas-témoins dans la Vallée du Mbam, Cameroun. Bull Soc Pathol Exot, 2004. 97(2): 105-8. 11. Nsengiyumva, G., et al., Cysticercosis as a major risk factor for epilepys in Burundi, East Africa. Epilepsia, 2003. 44(7): 950-5. 12. Placencia, M, Shorvon, SD, Paredes, V, Bimos, C, Sander JWAS, Suarez, J, Cascante, SM. Epileptic Seizures in an Andean Region of Ecuador. Brain (1992), 115, 771-782. 13. Commission on Epidemiology and Prognosis ILAE. Guidelines for Epidemiologic Studies on Epilepsy. Epilepsia 1993;34:592-6. Results Introduction References • Epilepsy affects 50 million people worldwide, of whom 80% live in resource-limited settings where there are high treatment gaps1,2 • Neurocysticercosis (NCC) is the leading cause of acquired epilepsy worldwide3,4 • In Latin American regions with endemic NCC, epilepsy prevalence is 2-3x higher than global rates4-6 • Human cysticercosis is strongly associated with keeping free-ranging pigs and lack of latrines7 • Most studies from African settings derive only from clinic-based settings7-11 Objectives • To estimate the prevalence of epilepsy and NCC- associated epilepsy in humans in a region with suspected high porcine cysticercosis in Western Kenya • To estimate the prevalence of human and porcine cysticercosis • Age- and gender- adjusted human epilepsy prevalence is 3-7 times higher than global estimates of 5-10 per 1000 population5 • Human cysticercosis prevalence was moderate • Surprisingly, there were no cases of NCC-associated epilepsy • Prevalence of porcine cysticercosis is comparable to other areas of East/Southern Africa but lower than Latin America • Limitations include: • apDia Ag ELISA only detects viable cysticerci and is more sensitive in extra-parenchymal disease • small absolute number of people with epilepsy • porcine lingual exam has limited sensitivity • Additional research to identify potential protective factors explaining the low prevalence of human cysticercosis despite high rates in pigs is essential Meyer, AC1, Sokhi, D,2 Ngugi, A,3 Solomon, T, 4 Févre, E 2,4 1Yale University, 2 International Livestock Research Institute, 3Aga Khan University East Africa, 4University of Liverpool Acknowledgements • Chiefs, Assistant Chiefs and the communities in Busibwabo sub-location • Ministry of Agriculture, Livestock and Fisheries, Ministries of Medical Services and Public Health, County Government of Busia, Kenya • Leadership and staff, Ministry of Health facilities near Busibwabo sub-location • Dr. Prabhakar Reddi, Dr. Sam Oula, Aga Khan Hospital Kisumu • EPICC Study staff • Fogarty International Center, NIH (K01TW008764- Meyer) • Global Health Equity Scholars Program, Yale University (Meyer) • CGIAR Research Program on Agriculture for Nutrition and Health (A4NH) led by IFPRI (Fevre) • International League Against Epilepsy, UK Chapter (Sokhi) • Association of British Neurologists (Sokhi) • Epilepsy Research UK (Sokhi) Kenya Lake Victoria Busibwabo Sub-location Busia Figure 1. Map of Study Area. Prevalence per 1000 population [95% CI] Lifetime Epilepsy Crude 26.2 [15.4-41.7] Crude Female 21.7 [9.4-42.3] Crude Male 32.1 [14.8-60.1] Age-Adjusted 30.4 [12.1-48.8] Age-Sex-Adjusted 36.0 [13.1-58.9] Cysticercosis Human Epilepsy 0 [0, 195.0]* Without Epilepsy 83.3 [2.1, 384.8] Porcine 84.5 [31.6, 174.9] * One sided 97.5% confidence interval Table 1. Prevalence of Epilepsy and Cysticercosis. Humans • Mean 4.5 people per HH [Range:1-20] • 57% were female (368/648) • 60% were children <18 yrs (392/648) • Among adults: • 72% had a primary school education or less (185/256) • 75% were farmers (193/256) • 73% always used latrine (474/648) • 27% had a worm in their faeces in the last one year (158/579) • 2% had taken de-worming medication in the last month (14/648) • Epilepsy • 37 people screened positive for epilepsy • of whom 16 were confirmed after neurology review • One additional individual with epilepsy was identified by her mother • Crude and adjusted epilepsy prevalence is presented in Table 1. • Cysticercosis prevalence is presented in Table 1 • No neurocysticercosis was identified. Pigs • 28% of HH kept pigs (41/145) • Mean of 1.8 pigs per HH [Range:1-7] • Median age was 4 months [IQR: 2-6] • 69% of pigs were always tethered in both wet and dry seasons (50/72) • No associations were observed between porcine cysticercosis and: • allowing pigs to range freely in wet (p=0.66) or dry (p=0.67) seasons • presence of a latrine (p=0.32) or all closed latrines (p=0.34) in the HH • Having an ill pig in the HH in last 12 mos (p=0.10) • We evaluated 145 households, containing 648 humans and 72 pigs between 2/25-6/3/15 Figure 3. Lingual examination for cysticercosis. 154 Households 810 Humans 5 HH did not consent 4 HH missed after 2 visits 660 humans present on study day 654 consented 648 participated 37 pos screen 12 neg screen random sample 2.6% (17/648) epilepsy 0% (0/10) +apDia 0% (0/15) CT+NCC 8.3%(1/12) +apDia 0% (0/1) CT+NCC 145 HH participated 72 pigs evaluated 8.4% (6/71) cysts on lingual exam Stage 1 Stage 2 Stage 3 Figure 2. Recruitment and Study Flow. +apDia: apDia Cysticercosis Antigen ELISA above cut-off value; CT+NCC: Contrast-enhanced Computed Tomography of the Brain consistent with diagnosis of neurocysticercosis; HH: Household. LB-5329
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