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Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study.
Perry, M Scott; Scheffer, Ingrid E; Sullivan, Joseph; Brunklaus, Andreas; Boronat, Susana; Wheless, James W; Laux, Linda; Patel, Anup D; Roberts, Colin M; Dlugos, Dennis; Holder, Deborah; Knupp, Kelly G; Lallas, Matt; Phillips, Steven; Segal, Eric; Smeyers, Patricia; Lal, Dennis; Wirrell, Elaine; Zuberi, Sameer; Brünger, Tobias; Wojnaroski, Mary; Maru, Benit; O'Donnell, Penrose; Morton, Magda; James, Emma; Vila, Maria Candida; Huang, Norman; Gofshteyn, Jacqueline S; Rico, Salvador.
Afiliação
  • Perry MS; Cook Children's Medical Center, Fort Worth, Texas, USA.
  • Scheffer IE; University of Melbourne, Austin Health, Melbourne, Victoria, Australia.
  • Sullivan J; University of California, San Francisco, San Francisco, California, USA.
  • Brunklaus A; School of Health & Wellbeing, University of Glasgow, Glasgow, UK.
  • Boronat S; Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Wheless JW; Le Bonheur Children's Hospital, Memphis, Tennessee, USA.
  • Laux L; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Patel AD; Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Roberts CM; Doernbecher Children's Hospital, Portland, Oregon, USA.
  • Dlugos D; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Holder D; Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Knupp KG; Children's Hospital Colorado, Aurora, Colorado, USA.
  • Lallas M; Nicklaus Children's Hospital, Miami, Florida, USA.
  • Phillips S; Multicare Health System, Tacoma, Washington, USA.
  • Segal E; Northeast Regional Epilepsy Group & Hackensack University Medical Center, Hackensack Meridian School of Medicine, Hackensack, New Jersey, USA.
  • Smeyers P; Hospital Universitari i Politècnic la Fe, Valencia, Spain.
  • Lal D; UTHealth Houston, Houston, Texas, USA.
  • Wirrell E; Mayo Clinic, Rochester, Minnesota, USA.
  • Zuberi S; School of Health & Wellbeing, University of Glasgow, Glasgow, UK.
  • Brünger T; UTHealth Houston, Houston, Texas, USA.
  • Wojnaroski M; Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Maru B; SSI Strategy, London, UK.
  • O'Donnell P; Encoded Therapeutics, South San Francisco, California, USA.
  • Morton M; Encoded Therapeutics, South San Francisco, California, USA.
  • James E; Encoded Therapeutics, South San Francisco, California, USA.
  • Vila MC; Encoded Therapeutics, South San Francisco, California, USA.
  • Huang N; Encoded Therapeutics, South San Francisco, California, USA.
  • Gofshteyn JS; Encoded Therapeutics, South San Francisco, California, USA.
  • Rico S; Encoded Therapeutics, South San Francisco, California, USA.
Epilepsia ; 65(2): 322-337, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38049202
OBJECTIVE: Dravet 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. METHODS: ENVISION 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). RESULTS: Between 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. SIGNIFICANCE: In 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas Limite: Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas Limite: Child, preschool / Humans / Infant / Newborn Idioma: En Ano de publicação: 2024 Tipo de documento: Article