IngentaConnect Epilepsy in Angelman syndrome: A questionnaire-based assessment o...

Authors: Thibert, Ronald L.¹; Conant, Kerry D.¹; Braun, Eileen K.²; Bruno, Patricia¹; Said, Rana R.³; Nespeca, Mark P.⁴; Thiele, Elizabeth A.¹

Source: Epilepsia, Volume 50, Number 11, November 2009 , pp. 2369-2376(8)

Publisher: Blackwell Publishing

Abstract:

Summary Purpose:

Angelman syndrome (AS) commonly presents with epilepsy (>80%). The goal of this study was to examine the natural history and various treatments of epilepsy in AS in a large population. Methods:

A detailed electronic survey containing comprehensive questions regarding epilepsy in AS was conducted through the Angelman Syndrome Foundation. Results:

There were responses from 461 family members of individuals with AS, of whom 86% had epilepsy (60% with multiple seizure types), the most common being atonic, generalized tonic-clonic, absence, and complex partial. Partial-onset seizures only were reported in 11% of those with epilepsy. Epilepsy was most common among those with maternal deletions and unknown subtypes, with catastrophic epilepsies present in only these two subtypes. These epilepsies were refractory to medication, with only 15% responding to the first antiepileptic drug (AED). The most commonly prescribed AED were valproic acid and clonazepam, but lamotrigine and levetiracetam appeared to have similar efficacy and tolerability. Discussion:

This is the largest study to date assessing epilepsy in AS. Although epilepsy in AS is considered a generalized epilepsy, there was a high prevalence of partial seizures. There are few previous data regarding the use of newer AED in AS, and the results of this study suggest that these newer agents, specifically levetiracetam and lamotrigine, may have efficacy similar to that of valproic acid and clonazepam, and that they appear to have similar or better side-effect profiles. Nonpharmacologic therapies such as dietary therapy and vagus nerve stimulation (VNS) also suggest favorable efficacy and tolerability, although further studies are needed.

Keywords: Epilepsy; Angelman syndrome; Chromosome 15; Antiepileptic medications

Document Type: Research article

DOI: 10.1111/j.1528-1167.2009.02108.x

Affiliations: 1: Department of Neurology, Pediatric Epilepsy Program, Massachusetts General Hospital, Boston, Massachusetts, U.S.A. 2: Angelman Syndrome Foundation, Aurora, Illinois, U.S.A. 3: Division of Pediatric Neurology, Department of Pediatrics, University of Texas Southwestern Medical Center, Children's Medical Center, Dallas, Texas, U.S.A.; 4: Neurology Division, Rady Children's Hospital/UCSD Department of Neuroscience, San Diego, California, U.S.A.

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$50.39 plus tax Refund Policy

Epilepsy in Angelman syndrome: A questionnaire-based assessment of the natural history and current treatment options