ROLE OF VOXEL-BASED MORPHOMETRIC ANALYSIS IN DEMONSTRATING ABNORMAL CEREBRAL STRUCTURE IN GENETIC GENERALIZED EPILEPSY: A SYSTEMATIC REVIEW
Balarabe S. A.* and Watila M. M.
ABSTRACT
Background: Quantitative Magnetic Resonance Imaging such as
Voxel-Based Morphometry (VBM) has made important contributions
to the evaluation and management of epilepsy over the last two
decades. Although VBM techniques together with histopathological
studies reveal focal cerebral abnormalities in patients with Genetic
Generalized Epilepsy (GGE); results of published studies are
sometimes contradictory thereby limiting reasonable conclusions for
effective clinical practice. This review aims to provide quantitative
summary estimates of studies on role of VBM in detecting focal
cerebral abnormalities in patients with GGE. Method: Studies were
included in the systematic review if they were full texts published in
English, with at least two groups (cases and controls) and sample size
of not less than 15 cases. Studies were identified through three electronic databases (Pubmed
EMBASE and Google scholar) from January 1995 to July 2014. Studies were systematically
searched using key words (‘‘epilepsy’’ or "Idiopathic Generalized Epilepsy" or "IGE" or
‘‘juvenile myoclonic epilepsy’’ or ‘‘JME’’ or "Absences Epilepsy" or "AE" or "Juvenile
Absence Epilepsy" or "JAE" or "Childhood Absence Epilepsy" or "CAE" or "Generalized
Tonic-clonic seizure" or "GTCS") and (‘‘voxel-based morphometry" or ‘‘VBM’’ or ‘‘voxelbased’’
or ‘‘voxel-wise’’ or ‘‘voxel’’). The references of relevant articles were also
scrutinized for additional studies. For each eligible study, data were extracted for descriptive
and diagnostic variables and summaries relating to outcome. Results: The systematic
literature search yielded six hundred and sixteen (616) published studies according to the
topic and abstracts. Eighty three (83) articles were identified as potentially eligible and were reviewed in full text. Fifteen studies (15) with a total of six hundred and forty one (641)
patients with Genetic Generalized Epilepsy [Juvenile Myoclonic Epilepsy (JME) 393
(61.3%), Epilepsy with Generalized seizure on Awakening (EGA) 194 (30.3%) and Absence
Epilepsy (AE)54 (8.4%)] and five hundred and five (505) healthy control subjects were
selected. Some studies revealed anatomical changes such as increased Gray Matter Volume
(GMV) in bilateral prefrontal cortex, while others showed decreased GMV in bilateral
thalamus in patients with GGE. Conclusion: This systematic review reveals consistent subtle
anatomical changes among patients with GGE; and support the concept of thalamocortical
circuitry involvement in the pathogenesis of GGE, particularly in JME.
Keywords: Epilepsy, voxel-based morphometry, Genetic Generalized Epilepsy, Gray matter volume.
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