New insights highlight unmet needs for people living with Lennox-Gastaut syndrome and significant burden of the disease
- New data presented at the 15th European Epilepsy Congress highlight lengthy delays in Lennox-Gastaut syndrome (LGS) diagnosis in
Europe and significant disease burden from both seizure and non-seizure impairments[1] - LGS is a severe childhood-onset developmental and epileptic encephalopathy, a group of epilepsies associated with developmental impairment, which is characterized by several different seizure types[2]
- New treatment options are needed to improve the long-term prognosis of individuals with LGS[3]
Despite patients receiving more than three (3.4) antiseizure medications on average each day, ongoing challenges in effectively treating LGS remain[1]:
- 71% of patients (N=324/454) experienced at least 1 concomitant comorbidity, with the most frequently reported including psychomotor or cognitive impairment, attention deficit hyperactivity disorder (ADHD), sleep disorder or insomnia
- 19% and 28% of patients experienced severe or very severe physical and mental impairment, respectively, many of which persist with age
- 47% of patients were reported to have at least somewhat poor quality of life
- Daytime seizures were reported to have the greatest impact on quality of life for 39% of patients
These findings underline the need for new treatments that can target both drug-resistant seizures and the non-seizure symptoms of LGS.
Dr
LGS affects approximately one million people worldwide.[4] However, diagnosis remains complex and challenging due to the lack of specific biological markers for the condition, multiple possible causes, and varied presentation of symptoms.[2]
Although several approved drugs are available for LGS, there are still unmet needs for treatment. These drugs provide an improvement, but usually not with a sustained long-term effect, resulting in a need for novel therapies which effectively target seizures and alleviate non-seizure outcomes to enhance the prognosis for patients with LGS.[3]
Diagnostic aid for healthcare professionals
In addition, at the 15th
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References:
[1] Strzelczyk A, Gil-Nagel A, Striano P et al. Insights into Lennox-Gastaut syndrome: A European real-world study on patient profiles and unmet needs. Poster presented at: The 15th
[2] Bourgeois BFD, Douglass LM, Sankar R. et
[3] Auvin S. Lennox-Gastaut syndrome: New treatments and treatments under investigation. Rev Neurol (
[4] LGS Foundation. Factsheet: What is LGS? https://www.lgsfoundation.org/wp-content/uploads/2024/05/Updated-MAY-2024.png. Last accessed:
[5] Arzimanoglou A, Specchio N, Auvin S et al. Development of an Electronic Diagnostic Criteria Tool for Lennox-Gastaut Syndrome (LGS). Poster presented at: The 15th
[6] Specchio N, Wirrell EC, Scheffer IE, et al. ILAE Classification and Definition of Epilepsy Syndromes with Onset in Childhood: Position Paper by the
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