Increased CPA6 promoter methylation in focal epilepsy and in febrile seizures

N. Belhedi, N. Perroud, F. Karege, M. Vessaz, A. Malafosse, A. Salzmann

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

29 Citas (Scopus)

Resumen

Focal epilepsy (FE) is one of the most common forms of adult epilepsy and is usually regarded as a multifactorial disorder. Febrile seizures (FS) often appear during childhood in a subtype of FE patients, i.e. with temporal lobe epilepsy (TLE) and hippocampal sclerosis (HS). FS are the most common human convulsive event associated with fever. Genetic evidences for FS have suggested a complex mode of inheritance. Until now, to investigate genes at the genomic level, linkage analysis of familial forms and association studies have been performed, but nothing conclusive has been clearly related to FE and FS. As complex disorders, environmental factors might play a crucial role through epigenetic modification of key candidate genes such as CPA6, which encodes Carboxypeptidase A6, an extracellular protein. Therefore, we assessed DNA methylation in promoter of CPA6. In 186 FE patients and 92 FS patients compared to 93 healthy controls and 42 treated controls with antiepileptic drugs (AEDs), we found significant higher levels of methylation for epileptic patients. Methylation status were 3.4% (±3.2%) for FE cases and 4.3% (±3.5%) for FS cases, whereas healthy individuals and treated controls with AEDs showed a level of 0.8% (±2.9%) and 1.5% (±3.9%), respectively (p≤. 0.001 for all comparisons). These results let growing evidence for DNA methylation involvment in FE and FS.

Idioma originalEnglish
Páginas (desde-hasta)144-148
Número de páginas5
PublicaciónEpilepsy Research
Volumen108
N.º1
DOI
EstadoPublished - ene. 2014
Publicado de forma externa

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

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