Volumetric MRI, pathological, and neuropsychological progression in hippocampal sclerosis

Objective: To examine the relationships between age at onset and duration of seizure disorder with severity of hippocampal sclerosis (HS) and cognitive functioning in patients with HS and unilateral temporal lobe epilepsy. Methods: Twenty-six subjects had left temporal lobe seizure onset; 20 had right temporal onset. Measures were age at seizure onset, duration of seizure disorder divided by age (seizure duration), history of febrile convulsion (FC), ratio of the smaller hippocampal volume to the larger (HF) as determined by volumetric MRI, and pathologic HS grade. Results: Results showed that pathologic HS grade and HF were positively related to seizure duration, and negatively related to seizure onset. When subjects were divided into onset prior to age 10 versus later, subjects with earlier onset had higher mean pathologic HS grade and smaller (more asymmetric) mean HF. When subjects were divided into seizure duration <0.5 (i.e., less than half current lifetime) vs greater, subjects with seizure duration ≥0.5 had higher mean pathologic HS grade and lower mean HF. There was also evidence for earlier age at seizure onset and longer seizure duration being associated with worse performance on neuropsychological measures. FC was not related to either seizure duration or age at seizure onset, but patients with a history of FC showed higher pathologic HS grade and lower HF. A history of FC was not related to cognitive functioning. Conclusions: Unilateral HS patients with earlier seizure onset and longer duration of epilepsy have more severe HS and greater hippocampal volume asymmetry. This suggests that HS may be a progressive disorder with risk for cognitive dysfunction.

[1]  P. Gloor,et al.  Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy , 1993, Neurology.

[2]  T. Babb,et al.  The pathogenic and progressive features of chronic human hippocampal epilepsy , 1996, Epilepsy Research.

[3]  C. Cobb,et al.  Pathological grading system for hippocampal sclerosis: correlation with magnetic resonance imaging-based volume measurements of the hippocampus , 1996 .

[4]  Gregory McCarthy,et al.  Quantitative magnetic resonance imaging in temporal lobe epilepsy: Relationship to neuropathology and neuropsychological function , 1992, Annals of neurology.

[5]  Barbara Crain,et al.  Fast Spin‐Echo, Magnetic Resonance Imaging‐Measured Hippocampal Volume: Correlation with Neuronal Density in Anterior Temporal Lobectomy Patients , 1995, Epilepsia.

[6]  Frederick Andermann,et al.  Hippocampal sclerosis in temporal lobe epilepsy demonstrated by magnetic resonance imaging , 1991, Annals of neurology.

[7]  T. Sutula,et al.  Progression in mesial temporal lobe epilepsy , 1999, Annals of neurology.

[8]  J. Cavazos,et al.  Neuronal loss induced in limbic pathways by kindling: evidence for induction of hippocampal sclerosis by repeated brief seizures , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  O. Kremp [Long term intellectual and behavioral outcomes of children with febrile convulsions]. , 1998, Revue d'epidemiologie et de sante publique.

[10]  M Kokaia,et al.  Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[11]  F Cendes,et al.  Specificity of volumetric magnetic resonance imaging in detecting hippocampal sclerosis. , 1997, Archives of neurology.

[12]  G McCarthy,et al.  Diagnosis of medial temporal lobe seizure onset , 1993, Neurology.

[13]  E. Serafetinides,et al.  ETIOLOGY AND PATHOGENESIS OF TEMPORAL LOBE EPILEPSY. , 1964, Archives of neurology.

[14]  C. Jack,et al.  MRI‐Based Hippocampal Volume Measurements in Epilepsy , 1994, Epilepsia.

[15]  A. Pitkänen,et al.  Recurrent seizures may cause hippocambal damage in temporal lobe epilepsy , 1998, Neurology.

[16]  Clifford R. Jack,et al.  Quantitative MRI hippocampal volumes: association with onset and duration of epilepsy, and febrile convulsions in temporal lobectomy patients , 1993, Epilepsy Research.

[17]  C. Jack,et al.  Progressive hippocampal atrophy in chronic intractable temporal lobe epilepsy , 1999, Annals of neurology.

[18]  F Andermann,et al.  Anatomic basis of amygdaloid and hippocampal volume measurement by magnetic resonance imaging , 1992, Neurology.

[19]  A. Wyler,et al.  A grading system for mesial temporal pathology (hippocampal sclerosis) from anterior temporal lobectomy , 1992 .

[20]  W H Theodore,et al.  Hippocampal atrophy, epilepsy duration, and febrile seizures in patients with partial seizures , 1999, Neurology.

[21]  P. Gloor,et al.  Atrophy of mesial structures in patients with temporal lobe epilepsy: Cause or consequence of repeated seizures? , 1993, Annals of neurology.

[22]  Frederick Andermann,et al.  Neuroimaging evidence of progressive neuronal loss and dysfunction in temporal lobe epilepsy , 1999, Annals of neurology.

[23]  Frederick Andermann,et al.  Magnetic resonance imaging in temporal lobe epilepsy: Pathological correlations , 1987, Annals of neurology.

[24]  J. Oxbury,et al.  Hippocampal neuron loss in temporal lobe epilepsy: Correlation with early childhood convulsions , 1987, Annals of neurology.

[25]  Asla Pitkänen,et al.  A new model of chronic temporal lobe epilepsy induced by electrical stimulation of the amygdala in rat , 2000, Epilepsy Research.

[26]  S. Wang,et al.  Neurocognitive Attention and Behavior Outcome of School‐Age Children with a History of Febrile Convulsions: A Population Study , 2000, Epilepsia.

[27]  A. Wyler,et al.  Relationship of hippocampal sclerosis to duration and age of onset of epilepsy, and childhood febrile seizures in temporal lobectomy patients , 1996, Epilepsy Research.

[28]  C R Jack,et al.  Temporal lobe seizures: lateralization with MR volume measurements of the hippocampal formation. , 1990, Radiology.

[29]  C. Marescaux,et al.  Magnetic Resonance Imaging Follow‐up of Progressive Hippocampal Changes in a Mouse Model of Mesial Temporal Lobe Epilepsy , 2000, Epilepsia.

[30]  J. Zentner,et al.  Surgical treatment of epilepsies. , 2002, Acta neurochirurgica. Supplement.

[31]  C R Jack,et al.  Volumetric magnetic resonance imaging. Clinical applications and contributions to the understanding of temporal lobe epilepsy. , 1997, Archives of neurology.

[32]  C R Jack,et al.  Magnetic resonance image–based hippocampal volumentry: Correlation with outcome after temporal lobectomy , 1992, Annals of neurology.

[33]  Thomas P. Sutula,et al.  Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis , 1990, Brain Research.

[34]  E. Jolkkonen,et al.  Seizure-Induced Damage to Somatostatin-Immunoreactive Neurons in the Rat Hippocampus Is Regulated by Fimbria–Fornix Transection , 1997, Experimental Neurology.

[35]  A. Connelly,et al.  Longitudinal Quantitative Hippocampal Magnetic Resonance Imaging Study of Adults with Newly Diagnosed Partial Seizures: One‐Year Follow‐Up Results , 1998, Epilepsia.

[36]  C R Jack,et al.  Magnetic resonance imaging–based volume studies in temporal lobe epilepsy: Pathological correlations , 1991, Annals of neurology.