TY - JOUR
T1 - SCN2A-Developmental and Epileptic Encephalopathies
T2 - Challenges to trial-readiness for non-seizure outcomes
AU - Berg, Anne T.
AU - Palac, Hannah
AU - Wilkening, Greta
AU - Zelko, Frank
AU - Schust Meyer, Leah
N1 - Funding Information:
The analyses for this project were funded by The FamilieSCN2A Foundation and by the Stanley Manne Children's Research Institute and Ann & Robert H. Lurie Children's Hospital of Chicago under the Precision Medicine Strategic Research Initiative and by a grant from the Pediatric Epilepsy Research Foundation, Dallas, TX.
Funding Information:
The analyses for this project were funded by The FamilieSCN2A Foundation and by the Stanley Manne Children's Research Institute and Ann & Robert H. Lurie Children's Hospital of Chicago under the Precision Medicine Strategic Research Initiative and by a grant from the Pediatric Epilepsy Research Foundation, Dallas, TX. We would like to extend a special thanks to Drs. John Spiro and LeeAnne Snyder for their kind assistance in understanding the SearchLight data and methods. We are grateful to all of the families at the participating Simons SearchLight project (formally known as Simons Variation?in Individuals Project). We appreciate obtaining access to the data from the phenotype and genotype data for the SCN2A in the SFARI Base. Approved researchers can obtain the SSC population data set described in this study by applying at https://base.sfari.org.
Publisher Copyright:
© 2020 International League Against Epilepsy
PY - 2021/1
Y1 - 2021/1
N2 - 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.
AB - 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.
KW - Simons SearchLight
KW - Vineland Adaptive Behavior Scales
KW - phenotype
KW - trial readiness
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UR - http://www.scopus.com/inward/citedby.url?scp=85096653539&partnerID=8YFLogxK
U2 - 10.1111/epi.16750
DO - 10.1111/epi.16750
M3 - Article
C2 - 33236786
AN - SCOPUS:85096653539
SN - 0013-9580
VL - 62
SP - 258
EP - 268
JO - Epilepsia
JF - Epilepsia
IS - 1
ER -