Literature DB >> 24405698

Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.

Nelia Zamponi1, Claudia Passamonti2, Cristina Petrelli1, Pierangelo Veggiotti3, Chiara Baldassari3, Alberto Verrotti4, Giovanni Capovilla5, Maurizio Viri6, Giangennaro Coppola7, Aglaia Vignoli8.   

Abstract

BACKGROUND: The relation between epileptic seizures and vaccinations is sometimes debated. In the present work, the impact of vaccination on seizure onset and clinical outcome of SCN1A mutation-positive patients is addressed.
METHODS: Seventy-two patients diagnosed with Dravet syndrome or generalized epilepsy with febrile seizure plus, carrying SCN1A mutations or not, were included. Details on vaccination type, temporal relationship between vaccination and seizure occurrence, seizure type at onset and during development, cognitive functioning, and vaccination completion was obtained by reviewing clinical records. Patients were divided into two groups based on the temporal window between vaccination and seizure onset (proximate group: <48 hours; distant group: >48 hours).
RESULTS: Vaccination-related seizures occurred in 25% of patients with SCN1A mutation and 18% of patients without the mutation (no significant difference). The proximate group showed an earlier age at seizure onset and a higher frequency of status epilepticus during development than did the distant group. No other significant differences were found. Subsequent vaccinations did not significantly alter the evolution of the disease.
CONCLUSIONS: Results from this relatively small series provide evidence that vaccinations do not significantly affect clinical and cognitive evolution of Dravet syndrome and generalized epilepsy with febrile seizure plus patients even if they carry SCN1A mutations.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dravet syndrome; GEFS+; SCN1A gene; cognition; seizure; vaccination

Mesh:

Substances:

Year:  2013        PMID: 24405698     DOI: 10.1016/j.pediatrneurol.2013.09.016

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  3 in total

Review 1.  KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders.

Authors:  Xinchen Teng; Abdel Aouacheria; Loïc Lionnard; Kyle A Metz; Lucian Soane; Atsushi Kamiya; J Marie Hardwick
Journal:  CNS Neurosci Ther       Date:  2019-07       Impact factor: 5.243

2.  The impact of COVID-19 in Dravet syndrome: A UK survey.

Authors:  Simona Balestrini; Galia Wilson; Claire Eldred; Helen Evans; Sanjay M Sisodiya
Journal:  Acta Neurol Scand       Date:  2021-02-11       Impact factor: 3.209

3.  Clinical spectrum and the comorbidities of Dravet syndrome in Taiwan and the possible molecular mechanisms.

Authors:  Chia-Hsuan Huang; Pi-Lien Hung; Pi-Chuan Fan; Kuang-Lin Lin; Ting-Rong Hsu; I-Jun Chou; Che-Sheng Ho; I-Ching Chou; Wei-Sheng Lin; Inn-Chi Lee; Hueng-Chuen Fan; Shyi-Jou Chen; Jao-Shwann Liang; Yi-Fang Tu; Tung-Ming Chang; Su-Ching Hu; Lee-Chin Wong; Kun-Long Hung; Wang-Tso Lee
Journal:  Sci Rep       Date:  2021-10-12       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.