SCN2A‐Developmental and Epileptic Encephalopathies: Challenges to trial‐readiness for non‐seizure outcomes

• Published in: Epilepsia (Copenhagen) Vol. 62; no. 1; pp. 258 - 268
• Main Authors: Berg, Anne T., Palac, Hannah, Wilkening, Greta, Zelko, Frank, Schust Meyer, Leah
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01-01-2021
• Subjects: Adaptation, Psychological; Adolescent; Age; Behavior rating scales; Brain Diseases - genetics; Brain Diseases - physiopathology; Child; Child, Preschool; Children; Clinical trials; Clinical Trials as Topic; Communication; Convulsions & seizures; Epilepsy; Epileptic Syndromes - genetics; Epileptic Syndromes - physiopathology; Female; Humans; Infant; Language Development; Male; Motor Skills; NAV1.2 Voltage-Gated Sodium Channel - genetics; Neonates; Neurodevelopmental Disorders - genetics; Neurodevelopmental Disorders - physiopathology; phenotype; Seizures; Simons SearchLight; trial readiness; Vineland Adaptive Behavior Scales; Young Adult; phenotype; Vineland Adaptive Behavior Scales; Simons SearchLight; trial readiness
• ISSN: 0013-9580; 1528-1167
• DOI: 10.1111/epi.16750

Objective
SCN2A‐associated developmental and epileptic encephalopathies (DEEs) present with seizures, developmental impairments, and often both. We sought to characterize the level and pattern of development in children with SCN2A variants, and to address the sensitivity of the Vineland Adaptive Behavior Scales (VABS) in measuring changes over time in children with SCN2A‐DEEs.
Methods
Clinical histories for participants with pathogenic SCN2A variants in the Simons SearchLight project were analyzed for descriptive purposes. VABS scores obtained at study entry and yearly thereafter were analyzed for floor and ceiling effects, change with age, and association with epilepsy through use of regression and longitudinal regression methods.
Results
Sixty‐four participants (50 with epilepsy, 30 [47%] female, median age 49 months, interquartile range [IQR] 28 to 101) were included. Histories of birth complications (N = 34, 54%), neonatal neurological signs (N = 45, 74%), and other neurological symptoms (N = 31, 48%) were common and similar in epilepsy and nonepilepsy subgroups. Mean standardized VABS scores (Composite 53.5; Motor, 55.8, Communication, 54.1, Socialization, 59.4, and Daily living skills, 55.1) reflected performance ~3 standard deviations below the normative test average. In longitudinal regression analyses, standardized scores decreased between 1.3 and 2.8 points per year, suggesting regression of abilities. Raw score analyses, however, revealed several subdomains with substantial floor effects (eg, community use); other raw scores increased with increasing age. Participants with epilepsy scored 0.6 to 1 SD lower than those without epilepsy (all P’s < .05).
Significance
The VABS, as standardly administered, has shortcomings for addressing growth or regression in individuals with SCN2A‐DEEs. Some subdomain raw scores reflected substantial floor effects. Raw scores increased so slowly over time that standardized scores declined. Alternative measures sensitive to incremental meaningful change are required if outcomes such as adaptive behavior are to be primary outcomes in short‐term clinical trials.