Septal nuclei enlargement in human temporal lobe epilepsy without mesial temporal sclerosis. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: To measure the volume of basal forebrain septal nuclei in patients with temporal lobe epilepsy (TLE) as compared to patients with extratemporal epilepsy and controls. In animal models of TLE, septal lesions facilitate epileptogenesis, while septal stimulation is antiepileptic. METHOD: Subjects were recruited from 2 sites and consisted of patients with pharmacoresistant focal epilepsy (20 with TLE and mesial temporal sclerosis [MTS], 24 with TLE without MTS, 23 with extratemporal epilepsy) and 114 controls. Septal volume was measured using high-resolution MRI in association with newly developed probabilistic septal nuclei maps. Septal volume was compared between subject groups while controlling for relevant factors. RESULTS: Patients with TLE without MTS had significantly larger septal nuclei than patients with extratemporal epilepsy and controls. This was not true for patients with MTS. These results are interpreted with reference to prior studies demonstrating expansion of the septo-hippocampal cholinergic system in animal models of TLE and human TLE surgical specimens. CONCLUSION: Septal nuclei are enlarged in patients with TLE without MTS. Further investigation of septal nuclei and antiepileptic septo-hippocampal neurocircuitry could be relevant to development of new therapeutic interventions such as septal stimulation for refractory TLE.

authors

  • Butler, Tracy A.
  • Zaborszky, Laszlo
  • Wang, Xiuyuan
  • McDonald, Carrie R
  • Blackmon, Karen
  • Quinn, Brian T
  • DuBois, Jonathan
  • Carlson, Chad
  • Barr, William B
  • French, Jacqueline
  • Kuzniecky, Ruben
  • Halgren, Eric
  • Devinsky, Orrin
  • Thesen, Thomas

publication date

  • January 9, 2013

Research

keywords

  • Epilepsy, Temporal Lobe
  • Septal Nuclei

Identity

PubMed Central ID

  • PMC3590047

Scopus Document Identifier

  • 84873672279

Digital Object Identifier (DOI)

  • 10.1212/WNL.0b013e31827f0ed7

PubMed ID

  • 23303846

Additional Document Info

volume

  • 80

issue

  • 5