2007, Number 2
<< Back Next >>
Rev Mex Neuroci 2007; 8 (2)
Relationship between the epileptogenic area lateralization using Video-EEG and the functional neuroimaging evaluation: A study in pharmaco-resistant Medial Temporal Lobe Epilepsy patients submitted to surgery
Morales CLM, Sánchez CC, García ME, Bender J, García I, Lorigados L, Estupiñán DB
Language: Spanish
References: 30
Page: 127-134
PDF size: 94.42 Kb.
ABSTRACT
Objective: To evaluate the relationship between the epileptogenic area lateralization using Video-Electroencephalogram (V-EEG) with
additional extracraneal electrodes, and functional neuroimaging studies (Magnetic Resonance Espectroscopy (MRE) and Simple Photon
Emission Tomography (SPECT cerebral ) during interictal and ictal states in pharmacoresistant Medial Temporal Lobe Epilepsy patients
submitted to surgery.
Material and methods: The V-EEG results supplemented with sprectal EEG analysis, as well as the interictal and ictal
cerebral SPECT and the metabolic ratios evidenced by MRE were evaluated in 12 pharmacoresistant Medial Temporal Lobe Epilepsy patients
submitted to surgery, with normal Magnetic Resonance Imaging (MRI) or with bilateral mesial temporal sclerosis. All patients were
considered in Engel class 1 (seizure free) to the year of surgery.
Results: The biggest percent of correct lateralization were showed by the
ictal V-EEG (100%), continued by the ictal SPECT. During the interictal SPECT semiquantitative analysis, the perfution changes in the lateral
temporal region were those of more lateralization value. They were ipsilateral to the surgery side in 92.3% of the patients χ
2 (2) = 8, p <
0.0001. On the other hand, the MRE data using discriminant analysis with agrupating variable, the surgery side allowed to be statistically
significant model Wilks Lambda 0.224 F (3, 8) = 9.21 p ‹ 0.0056 whose influence variables were Cho/Cr p ‹ 0.003, NAA/Cr p ‹ 0.001 and NAA/
Cho+Cr p ‹ 0.03 indexes. The epileptogenic area was appropriately lateralized in 53.8% of the patients using MRE.
Conclusions: The
localizate/lateralize information provided by the V-EEG supplemented with the neurofunctional imaging (SPECT and MRE) allows to carry
out successful Temporal Lobe Lobectomy in TLE patients with normal MRI or bilateral morphological alterations.
REFERENCES
Wiebe S, Blume WT, Girvin JP, Eliasziw M. A randomized, controlled trial of surgery for temporal-lobe epilepsy. N Engl J Med 2001;345: 311-18.
Deacon C, WiebeS, Blume WT, McLachlan RS, Young GB, Matijevic S. Seizure identification by clinical description in temporal lobe epilepsy: how accurate are we? Neurology 2003; 61: 1686-9.
Wieser HG. Mesial temporal lobe epilepsy versus amygdalar epilepsy: late seizure recurrence after initially successful amygdalotomy and regained seizure control following hippocampectomy. Epileptic Disord 2000; 2: 141-52.
Li LM, Cendes F, Antel SB, Andermann F, Serles W, Dubeau F, Olivier A, Arnold DL. Prognostic value of proton magnetic resonance spectroscopic imaging for surgical outcome in patients with intractable temporal lobe epilepsy and bilateral hippocampal atrophy. Ann Neurol 2000; 47: 195-200.
Thivard L, Lehericy S, Krainik A, Adam C, Dormont D, Chiras J, Baulac M, Dupont S. Diffusion tensor imaging in medial temporal lobe epilepsy with hippocampal sclerosis. Neuroimage 2005; 28(3): 682-90.
Jing H, Takigawa M, Benasich AA. Relationship of nonlinear analysis, MRI and SPECT in the lateralization of temporal lobe epilepsy. Eur Neurol 2002; 48: 11-19.
Hennessy MJ, Elwes RD, Honavar M, Rabe-Hesketh S, Binnie CD, Polkey CE. Predictors of outcome and pathological considerations in the surgical treatment of intractable epilepsy associated with temporal lobe lesions. J Neurol Neurosurg Psychiatry 2001; 70: 450-8.
Salanova V, Markand O, Worth R, Garg B, Patel H, Asconape J, Park HM, Hutchins GD, Smith R, Azzarelli B. Presurgical evaluation and surgical outcome of temporal lobe epilepsy. Pediatr Neurol 1999; 20: 179-84.
Gloor P, Commentary: approaches to localization of the epileptogenic lesion. In: Engel J (ed.). Surgical treatment of the epilepsies. New York: Raven Press; 1987, p. 97-100. In: New York: Raven Press (Ed.), Surgical Treatment of the Epilepsies. 1987, p. 97-100.
Spencer SS, Spencer DD, Williamson PD. Ictal effects of anticonvulsant medication withdrawal in epileptic patients. Epilepsia 1981; 22: 297-307.
Foldvary N, Klem G, Hammel J, Bingaman W, Najm I, Luders H. The localizing value of ictal EEG in focal epilepsy. Neurology 2001; 57: 2022-8.
Blume WT, Ravindran J, Lowry NJ. Late lateralizing and localizing EEG features of scalp-recorded temporal lobe seizures. J Clin Neurophysiol 1998; 15: 514-20.
Blume WT, Kaibara M. The start-stop-start phenomenon in subdurally recorded seizures. Electroencephalography & Clinical Neurophysiology 1993; 86: 94-9.
Spencer SS. The relative contributions of MRI, SPECT, and PET imaging in epilepsy. Epilepsia 1994; 35(Suppl. 6): S72- 89.
Sperling M, O’Connor M. Auras and subclinical seizures: Characteristics and prognostic significance. Ann Neurol 1990; 28: 320-8.
Wendling F, Hernandez A, Bellanger JJ, Chauvel P, Bartolomei F. Interictal to ictal transition in human temporal lobe epilepsy: insights from a computational model of intracerebral EEG. J Clin Neurophysiol 2005; 22(5): 343- 56.
Assaf BA. Ebersole JS. Visual and quantitative ictal EEG predictors of outcome after temporal lobectomy. Epilepsia 1999; 40: 52-61.
Ergene E, Shih J, Blum D, So Nk. Frequency of bitemporal independent interictal epileptiform discharges in temporal lobe epilepsy. Epilepsia 2000; 41: 213-18.
Kotagal P, Luders H, Morris HH, III. Dystonic posturing in complex partial seizures of temporal lobe onset:a new lateralizing sign. Neurology 1989; 39: 196-201.
Dupont S, Semah F, Boon P, Saint-Hilaire JM, Adam C, Broglin D, Baulac M. Association of ipsilateral motor automatisms and contralateral dystonic posturing: a clinical feature differentiating medial from neocortical temporal lobe epilepsy. Arch Neurol 1999; 56: 927-32.
Kuba R, Rektor I, Brazdil M. Ictal limb dystonia in temporal lobe epilepsy. An invasive video-EEG finding. Eur J Neurol 2003; 10: 641-9.
Serles W, Caramanos Z, Lindinger G, Pataraia E, Baumgartner C. Combining ictal surface-electroencephalography and seizure semiology improves patient lateralization in temporal lobe epilepsy. Epilepsia 2000; 41: 1567-73.
Henry TR, Mazziotta JC, Engel J, Jr. Interictal metabolic anatomy of mesial temporal lobe epilepsy. Arch Neurol 1993; 50: 582-9.
Andraus ME, Cosenza CA, Fonseca LM, Andraus CF, D’Andrea I, Alves-Leon SV. [Interictal brain SPECT in patients with medically refractory temporal lobe epilepsy]. Arq Neuropsiquiatr 2002; 60: 779-87.
Rowe CC, Berkovic SF, Austin MC, Saling M, Kalnins RM, McKay WJ, Bladin PF. Visual and quantitative analysis of interictal SPECT with technetium-99m-HMPAO in temporal lobe epilepsy. J Nucl Med 1991; 32: 1688-94.
Markand ON, Salanova V, Whelihan E, Emsley CL. Healthrelated quality of life outcome in medically refractory epilepsy treated with anterior temporal lobectomy. Epilepsia 2000; 41: 749-59.
Lamy C, Derambure P, Josien E, Destee A, Vermesch P, Leduc V, Steinling M [Factors playing a role in the increase of localized perfusion observed by single-photon emissioncomputed tomography during an epileptic seizure] Rev Neurol (Paris) 2000; 156: 1113-19.
Cross JH, Gordon I, Connelly A, Jackson GD, Johnson CL, Neville BG, Gadian DG. Interictal 99Tc(m) HMPAO SPECT and 1H MRS in children with temporal lobe epilepsy. Epilepsia 1997; 38: 338-45.
Jackson GD, Connelly A. New NMR measurements in epilepsy. T2 relaxometry and magnetic resonance spectroscopy. Adv Neurol 1999; 79: 931-7.
Breiter SN, Arroyo S, Mathews VP, Lesser RP, Bryan RN, Barker PB. Proton MR spectroscopy in patients with seizure disorders, AJNR. Am J Neuroradiol 1994; 15: 373-84.