Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study

Author:

Perry M. Scott1ORCID,Scheffer Ingrid E.2ORCID,Sullivan Joseph3,Brunklaus Andreas4ORCID,Boronat Susana5,Wheless James W.6,Laux Linda7,Patel Anup D.8ORCID,Roberts Colin M.9,Dlugos Dennis10,Holder Deborah11,Knupp Kelly G.12ORCID,Lallas Matt13,Phillips Steven14,Segal Eric15,Smeyers Patricia16,Lal Dennis17ORCID,Wirrell Elaine18ORCID,Zuberi Sameer4,Brünger Tobias17,Wojnaroski Mary8,Maru Benit19,O'Donnell Penrose20,Morton Magda20,James Emma20,Vila Maria Candida20ORCID,Huang Norman20,Gofshteyn Jacqueline S.20ORCID,Rico Salvador20ORCID

Affiliation:

1. Cook Children's Medical Center Fort Worth Texas USA

2. University of Melbourne, Austin Health Melbourne Victoria Australia

3. University of California, San Francisco San Francisco California USA

4. School of Health & Wellbeing University of Glasgow Glasgow UK

5. Hospital de la Santa Creu i Sant Pau Barcelona Spain

6. Le Bonheur Children's Hospital Memphis Tennessee USA

7. Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois USA

8. Nationwide Children's Hospital Columbus Ohio USA

9. Doernbecher Children's Hospital Portland Oregon USA

10. Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

11. Cedars‐Sinai Medical Center Los Angeles California USA

12. Children's Hospital Colorado Aurora Colorado USA

13. Nicklaus Children's Hospital Miami Florida USA

14. Multicare Health System Tacoma Washington USA

15. Northeast Regional Epilepsy Group & Hackensack University Medical Center, Hackensack Meridian School of Medicine Hackensack New Jersey USA

16. Hospital Universitari i Politècnic la Fe Valencia Spain

17. UTHealth Houston Houston Texas USA

18. Mayo Clinic Rochester Minnesota USA

19. SSI Strategy London UK

20. Encoded Therapeutics South San Francisco California USA

Abstract

AbstractObjectiveDravet syndrome (DS) is a developmental and epileptic encephalopathy characterized by high seizure burden, treatment‐resistant epilepsy, and developmental stagnation. Family members rate communication deficits among the most impactful disease manifestations. We evaluated seizure burden and language/communication development in children with DS.MethodsENVISION was a prospective, observational study evaluating children with DS associated with SCN1A pathogenic variants (SCN1A+ DS) enrolled at age ≤5 years. Seizure burden and antiseizure medications were assessed every 3 months and communication and language every 6 months with the Bayley Scales of Infant and Toddler Development 3rd edition and the parent‐reported Vineland Adaptive Behavior Scales 3rd edition. We report data from the first year of observation, including analyses stratified by age at Baseline: 0:6–2:0 years:months (Y:M; youngest), 2:1–3:6 Y:M (middle), and 3:7–5:0 Y:M (oldest).ResultsBetween December 2020 and March 2023, 58 children with DS enrolled at 16 sites internationally. Median follow‐up was 17.5 months (range = .0–24.0), with 54 of 58 (93.1%) followed for at least 6 months and 51 of 58 (87.9%) for 12 months. Monthly countable seizure frequency (MCSF) increased with age (median [minimum–maximum] = 1.0 in the youngest [1.0–70.0] and middle [1.0–242.0] age groups and 4.5 [.0–2647.0] in the oldest age group), and remained high, despite use of currently approved antiseizure medications. Language/communication delays were observed early, and developmental stagnation occurred after age 2 years with both instruments. In predictive modeling, chronologic age was the only significant covariate of seizure frequency (effect size = .52, p = .024). MCSF, number of antiseizure medications, age at first seizure, and convulsive status epilepticus were not predictors of language/communication raw scores.SignificanceIn infants and young children with SCN1A+ DS, language/communication delay and stagnation were independent of seizure burden. Our findings emphasize that the optimal therapeutic window to prevent language/communication delay is before 3 years of age.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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