TY - JOUR
T1 - Etiology of active epilepsy in adults
T2 - A Latin American multicenter hospital-based study
AU - Carpio Rodas, Luis Arturo
AU - Cuero Vidal, Olga
AU - Giagante, Brenda
AU - Nuñez, Lilia
AU - Plascencia, Noel
AU - Briseño, Alvarez Pedro
AU - Hamamoto-Filho, Pedro
AU - Rezk, Eduardo
AU - Pinheiro, Mariana
AU - Fleury, Agnes
AU - Suastegui, Roberto
AU - Gaytán, Andrea
AU - Rios-Patiño, David
AU - Morcillo Muñoz, Andrés
AU - Di Capua, Daniela
AU - Mullo, Elena
AU - Braga, Patricia
AU - Demicheli, Elisa
AU - Preve, Federico
AU - Monllor, Enrique
AU - Villanueva, Manuela
AU - Jerez, Juan
AU - Zambrano, José A.
AU - Andrieu, Florencia
AU - Pino-Salgado, Stephanie
AU - Gomez-Gulfo, Vanessa
AU - Márquez, Arturo
AU - Uribe, Reinaldo
AU - Aguilera, Ledda
AU - Quijada, Alonso
AU - Abudinen, Gabriel
AU - Rivas, Julia
AU - Rivas, Luis
AU - Solis-Cabrera, Vanessa
AU - Resendiz-Aparicio, Juan
AU - Kelvin, Elizabeth A.
N1 - Publisher Copyright:
© 2026 British Epilepsy Association.
PY - 2026/5/10
Y1 - 2026/5/10
N2 - Purpose
Etiologic patterns of epilepsy in low- and middle-income countries (LMICs) remain insufficiently characterized. We aimed to describe the causes and clinical features of active epilepsy in adults from seven Latin American (LA) countries using the 2017 ILAE etiologic classification.
Methods
We performed a retrospective multicenter case series based on medical records from 12 tertiary hospitals in Argentina, Brazil, Chile, Colombia, Ecuador, Mexico, and Uruguay (2019–2023). Adults (≥16 years) with active epilepsy, defined as at least one seizure in the past five years or ongoing antiseizure medication (ASM) use, were included. Etiology was categorized using the 2017 ILAE classification.
Results
A total of 3033 patients were included (mean age 32 years; 53 % women). Most had focal-onset seizures (73.5 %), and 63 % showed epileptiform EEG abnormalities. Etiology was identified in 65 % of cases and remained unknown in 35 %. Structural etiologies predominated (47 %), followed by genetic (10.5 %), infectious (5.4 %), immune (1 %), metabolic/toxic (0.8 %), and neurodegenerative (0.3 %). The most frequent structural causes were hippocampal sclerosis (25.8 %), malformations of cortical development (24.8 %), and stroke (18.6 %). Neurocysticercosis accounted for 41.6 % of infectious cases but only 2.3 % of the entire cohort. Etiologic distribution varied across countries and age groups.
Conclusions
In this large Latin American case series, structural etiologies were the leading identified cause of active epilepsy, while one-third-of cases remained of unknown etiology. The relatively low prevalence of neurocysticercosis contrasts with classical assumptions and highlights the need for updated, region-specific data. Population-based and incident studies remain essential to better define etiologic determinants across Latin America.
AB - Purpose
Etiologic patterns of epilepsy in low- and middle-income countries (LMICs) remain insufficiently characterized. We aimed to describe the causes and clinical features of active epilepsy in adults from seven Latin American (LA) countries using the 2017 ILAE etiologic classification.
Methods
We performed a retrospective multicenter case series based on medical records from 12 tertiary hospitals in Argentina, Brazil, Chile, Colombia, Ecuador, Mexico, and Uruguay (2019–2023). Adults (≥16 years) with active epilepsy, defined as at least one seizure in the past five years or ongoing antiseizure medication (ASM) use, were included. Etiology was categorized using the 2017 ILAE classification.
Results
A total of 3033 patients were included (mean age 32 years; 53 % women). Most had focal-onset seizures (73.5 %), and 63 % showed epileptiform EEG abnormalities. Etiology was identified in 65 % of cases and remained unknown in 35 %. Structural etiologies predominated (47 %), followed by genetic (10.5 %), infectious (5.4 %), immune (1 %), metabolic/toxic (0.8 %), and neurodegenerative (0.3 %). The most frequent structural causes were hippocampal sclerosis (25.8 %), malformations of cortical development (24.8 %), and stroke (18.6 %). Neurocysticercosis accounted for 41.6 % of infectious cases but only 2.3 % of the entire cohort. Etiologic distribution varied across countries and age groups.
Conclusions
In this large Latin American case series, structural etiologies were the leading identified cause of active epilepsy, while one-third-of cases remained of unknown etiology. The relatively low prevalence of neurocysticercosis contrasts with classical assumptions and highlights the need for updated, region-specific data. Population-based and incident studies remain essential to better define etiologic determinants across Latin America.
KW - Active epilepsy
KW - Middle-low-income countries
KW - Neurocysticercosis
KW - Seizures
KW - Structural epilepsy
KW - Active epilepsy
KW - Middle-low-income countries
KW - Neurocysticercosis
KW - Seizures
KW - Structural epilepsy
UR - https://www.scopus.com/pages/publications/105039556939
UR - https://www.seizure-journal.com/article/S1059-1311(26)00142-1
U2 - 10.1016/j.seizure.2026.05.012
DO - 10.1016/j.seizure.2026.05.012
M3 - Artículo
AN - SCOPUS:105039556939
SN - 1059-1311
VL - 139
SP - 182
EP - 192
JO - Seizure
JF - Seizure
ER -