Magnetic resonance imaging findings in Kenyans and South Africans with active convulsive epilepsy: An observational study

Author:

Kariuki Symon M.12ORCID,Wagner Ryan G.3ORCID,Gunny Roxana4,D'Arco Felice4ORCID,Kombe Martha1,Ngugi Anthony K.5,White Steven6,Odhiambo Rachael5,Cross J. Helen7ORCID,Sander Josemir W.89101112ORCID,Newton Charles R. J. C.12

Affiliation:

1. Neurosciences Unit KEMRI‐Wellcome Trust Research Programme Kilifi Kenya

2. Department of Psychiatry University of Oxford Oxford UK

3. MRC/Wits Rural Public Health and Health Transitions Research Unit (Agincourt), School of Public Health, Faculty of Health Sciences University of the Witwatersrand Johannesburg South Africa

4. Department of Neuroradiology Great Ormond Street Hospital London UK

5. Department of Population Health, Medical College Aga Khan University of East Africa Nairobi Kenya

6. Cromwell Hospital London UK

7. Developmental Neurosciences UCL, NIHR BRC Great Ormond Street Institute of Child Health London UK

8. Department of Clinical & Experimental Epilepsy UCL Queen Square Institute of Neurology London UK

9. Chalfont Centre for Epilepsy Chalfont St Peter UK

10. Stichting Epilepsie Instellingen Nederland (SEIN) Heemstede The Netherlands

11. Department of Neurology West China Hospital Chengdu China

12. Institute of Brain Science & Brain‐Inspired Technology, Sichuan University Chengdu China

Abstract

AbstractObjectiveFocal epilepsy is common in low‐ and middle‐income countries. The frequency and nature of possible underlying structural brain abnormalities have, however, not been fully assessed.MethodsWe evaluated the possible structural causes of epilepsy in 331 people with epilepsy (240 from Kenya and 91 from South Africa) identified from community surveys of active convulsive epilepsy. Magnetic resonance imaging (MRI) scans were acquired on 1.5‐Tesla scanners to determine the frequency and nature of any underlying lesions. We estimated the prevalence of these abnormalities using Bayesian priors (from an earlier pilot study) and observed data (from this study). We used a mixed‐effect modified Poisson regression approach with the site as a random effect to determine the clinical features associated with neuropathology.ResultsMRI abnormalities were found in 140 of 240 (modeled prevalence = 59%, 95% confidence interval [CI]: 53%–64%) of people with epilepsy in Kenya, and in 62 of 91 (modeled prevalence = 65%, 95% CI: 57%–73%) in South Africa, with a pooled modeled prevalence of 61% (95% CI: 56%–66%). Abnormalities were common in those with a history of adverse perinatal events (15/23 [65%, 95% CI: 43%–84%]), exposure to parasitic infections (83/120 [69%, 95% CI: 60%–77%]) and focal electroencephalographic features (97/142 [68%, 95% CI: 60%–76%]), but less frequent in individuals with generalized electroencephalographic features (44/99 [44%, 95% CI: 34%–55%]). Most abnormalities were potentially epileptogenic (167/202, 82%), of which mesial temporal sclerosis (43%) and gliosis (34%) were the most frequent. Abnormalities were associated with co‐occurrence of generalized non‐convulsive seizures (relative risk [RR] = 1.12, 95% CI: 1.04–1.25), lack of family history of seizures (RR = 0.91, 0.86–0.96), convulsive status epilepticus (RR = 1.14, 1.08–1.21), frequent seizures (RR = 1.12, 1.04–1.20), and reported use of anti‐seizure medication (RR = 1.22, 1.18–1.26).SignificanceMRI identified pathologies are common in people with epilepsy in Kenya and South Africa. Mesial temporal sclerosis, the most common abnormality, may be amenable to surgical correction. MRI may have a diagnostic value in rural Africa, but future longitudinal studies should examine the prognostic role.

Funder

Wellcome Trust

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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