Age at onset of epilepsy, pharmacoresistance, and cognitive outcomes: a prospective cohort study

AT Berg, FA Zelko, SR Levy, FM Testa - Neurology, 2012 - AAN Enterprises
AT Berg, FA Zelko, SR Levy, FM Testa
Neurology, 2012AAN Enterprises
Objectives: Increasing evidence suggests that uncontrolled seizures have deleterious effects
on cognition and behavior, particularly in the developing brain. Methods: In a community-
based cohort, 198 children, aged< 8 years with new-onset epilepsy were followed
prospectively and reassessed with the Wechsler Intelligence Scales for Children, Third
Edition (WISC-III) 8–9 years later. Linear regression analyses with interactions between age
at onset (age) and pharmacoresistance (PR) were used to test whether earlier onset …
Objectives
Increasing evidence suggests that uncontrolled seizures have deleterious effects on cognition and behavior, particularly in the developing brain.
Methods
In a community-based cohort, 198 children, aged <8 years with new-onset epilepsy were followed prospectively and reassessed with the Wechsler Intelligence Scales for Children, Third Edition (WISC-III) 8–9 years later. Linear regression analyses with interactions between age at onset (age) and pharmacoresistance (PR) were used to test whether earlier onset conveyed greater vulnerability to the effects of uncontrolled seizures. Full-scale IQ (FSIQ) and the 4 subdomain scores were examined. Adjustment for adaptive behavior scores in a subset was performed. A dichotomous indicator for IQ <80 or ≥80 was used to permit inclusion of children who were not tested, particularly those who were untestable.
Results
FSIQ was not correlated with age. PR was associated with an 11.4 point lower FSIQ (p = 0.002) and similar decrements in each WISC-III domain. There were substantial age-PR interactions for FSIQ (p = 0.003) and 3 domain scores, indicating a lessening impact of PR with increasing age. The dichotomous IQ indicator was strongly correlated with age at onset in the pharmacoresistant group (p < 0.0001) and not in the non-pharmacoresistant group (p = 0.61). Adjustment for adaptive behavior measured near onset did not alter the conclusions.
Conclusions
Uncontrolled seizures impair cognitive function with effects being most severe in infancy and lessening with increasing age at onset. These findings further emphasize the need for early aggressive treatment and seizure control in infants and young children.
American Academy of Neurology