Skip to main content
AAN.com

Abstract

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.

Get full access to this article

View all available purchase options and get full access to this article.

References

1.
Babb TL, Brown WJ. Pathological findings in epilepsy. In: Engel J Jr, ed. Surgical treatment of the epilepsies. New York: Raven Press, 1987: 511–540.
2.
Margerison JH, Corsellis JAN. Epilepsy and the temporal lobes. Brain . 1966; 89: 499–530.
3.
Falconer MA, Serafetinides EA, Corsellis JAN. Etiology and pathogenesis of temporal lobe epilepsy. Arch Neurol . 1964; 10: 233–248.
4.
Bruton CJ. The neuropathology of temporal lobe epilepsy. New York: Oxford University Press, 1988.
5.
Sager HJ, Oxbury JM. Hippocampal neuron loss in temporal lobe epilepsy: correlation with early childhood convulsions. Ann Neurol . 1987; 22: 334–340.
6.
Cendes F, Andermann F, Dubeau F, et al. Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study. Neurology . 1993; 43: 1083–1087.
7.
Tasch E, Cendes F, Li LM, Dubeau F, Andermann F, Arnold DL. Neuroimaging evidence of progressive neuronal loss and dysfunction in temporal lobe epilepsy. Ann Neurol . 1999; 45: 569–576.
8.
Theodore WH, Bhatia S, Hatta J, et al. Hippocampal atrophy, epilepsy duration, and febrile seizures in patients with partial seizures. Neurology . 1999; 52: 132–136.
9.
Davies KG, Hermann BP, Dohan FC, Foley KT, Bush AJ, Wyler AR. Relationship of hippocampal sclerosis to duration and age of onset of epilepsy, and childhood febrile seizures in temporal lobectomy patients. Epilepsy Res . 1996; 24: 119–126.
10.
Cendes F, Andermann F, Gloor P, et al. Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures? Ann Neurol . 1993; 34: 795–801.
11.
Trenerry MR, Jack CR, Sharbrough FW, et al. Quantitative MRI hippocampal volumes: association with onset and duration of epilepsy, and febrile convulsions in temporal lobectomy patients. Epilepsy Res . 1993; 15: 247–252.
12.
Jack CR Jr., Sharbrough FW, Twomey CK, et al. Temporal lobe seizures: lateralization with MR volume measurements of the hippocampal formation. Radiology . 1990; 175: 423–429.
13.
Kuzniecky R, de la Sayette V, Ethier R, et al. Magnetic resonance imaging in temporal lobe epilepsy: pathological correlation. Ann Neurol . 1987; 22: 341–347.
14.
Berkovic SF, Andermann F, Olivier A, et al. Hippocampal sclerosis in temporal lobe epilepsy demonstrated by magnetic resonance imaging. Ann Neurol . 1991; 29: 175–182.
15.
Watson C, Jack CR, Cendes F. Volumetric magnetic resonance imaging: clinical applications and contributions to the understanding of temporal lobe epilepsy. Arch Neurol . 1997; 54: 1521–1531.
16.
Watson C, Cendes F, Fuerst D, et al. Specificity of volumetric magnetic resonance imaging in detecting hippocampal sclerosis. Arch Neurol . 1997; 54: 67–73.
17.
Jack CR Jr. MRI-based hippocampal volume measurements in epilepsy. Epilepsia . 1994; 35 (suppl 6): S21–29.
18.
Watson C, Nielsen SL, Cobb C, Burgerman R, Williamson B. Pathological grading system for hippocampal sclerosis: correlation with magnetic resonance imaging-based volume measurements of the hippocampus. J Epilepsy . 1996; 9: 56–64.
19.
Lee N, Tien RD, Lewis DV, et al. Fast spin-echo, magnetic resonance imaging-measured hippocampal volume: correlation with neuronal density in anterior temporal lobectomy patients. Epilepsia . 1995; 36: 899–904.
20.
Cascino GD, Jack CR, Parisi JE, et al. Magnetic resonance imaging-based volume studies in temporal lobe epilepsy: pathological correlations. Ann Neurol . 1991; 30: 31–36.
21.
Lencz T, McCarthy G, Bronen RA, et al. Quantitative magnetic resonance imaging in temporal lobe epilepsy: relationship to neuropathology and neuropsychological function. Ann Neurol . 1992; 31: 629–637.
22.
Jack CR, Sharbrough FW, Cascino GD, Hirschhorn KA, O’Brien PC, Marsh WR. Magnetic resonance imaged-based hippocampal volumetry: correlation with outcome after temporal lobectomy. Ann Neurol . 1992; 31: 138–146.
23.
Wenzel HJ, Born DE, Dubach MF, et al. Morphological consequences of temporal lobe seizures in immature monkey. Epilepsia . 1999; 40 (suppl 7): 80.
24.
Bouilleret V, Nehlig A, Marescaux C, Namer IJ. Magnetic resonance imaging follow-up of progressive hippocampal changes in a mouse model of mesial temporal lobe epilepsy. Epilepsia . 2000; 41: 642–650.
25.
Cavazos JE, Sutula TP. Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis. Brain Res . 1990; 527: 1–6.
26.
Cavazos JE, Das I, Sutula TP. Neuronal loss induced in limbic pathways by kindling: evidence for induction of hippocampal sclerosis by repeated brief seizures. J Neurosci . 1994; 14: 3106–3121.
27.
Bengzon J, Kokaia Z, Elmer E, Nanobashvili A, Kokaia M, Lindvall O. Apoptosis and proliferation of dentate gyrus neurons after single and intermittent limbic seizures. Proc Natl Acad Sci USA . 1997; 94: 10432–10437.
28.
Jolkkonen J, Jolkkonen E, Pitkanen A. Seizure-induced damage to somatostatin-immunoreactive neurons in the rat hippocampus is regulated by fimbria-fornix transection. Exp Neurol . 1997; 145: 141–153.
29.
Nissinen J, Halonen T, Koivisto E, Pitkanen A. A new model of chronic temporal lobe epilepsy induced by electrical stimulation of the amygdala in rat. Epilepsy Res . 2000; 38: 177–205.
30.
Sutula TP, Hermann B. Progression in mesial temporal lobe epilepsy. Ann Neurol . 1999; 45: 553–556.
31.
O’Brien TJ, So EL, Meyer FB, Parisi JE, Jack CR. Progressive hippocampal atrophy in chronic intractable temporal lobe epilepsy. Ann Neurol . 1999; 45: 526–529.
32.
Van Paesschen W, Duncan JS, Stevens JM, Connelly A. Longitudinal quantitative hippocampal magnetic resonance imaging study of adults with newly diagnosed partial seizures: one-year follow-up results. Epilepsia . 1998; 39: 633–639.
33.
Kalviainen R, Salmenpera T, Partanen K, Vainio P, Riekkinen P, Pitkanen A. Recurrent seizures may cause hippocampal damage in temporal lobe epilepsy. Neurology . 1998; 50: 1377–1382.
34.
Spencer SS, McCarthy G, Spencer DD. Diagnosis of medial temporal lobe seizure onset: relative specificity and sensitivity of quantitative MRI. Neurology . 1993; 43: 2117–2124.
35.
Watson C, Andermann F, Gloor P, et al. Anatomic basis of amygdaloid and hippocampal volume measurement by magnetic resonance imaging. Neurology . 1992; 42: 1743–1750.
36.
Wyler AR, Dohan FC, Schweitzer JB, Berry AD. A grading system for mesial temporal pathology (hippocampal sclerosis) from anterior temporal lobectomy. J Epilepsy . 1992; 5: 220–225.
37.
Mathern GW, Babb TL, Leite JP, Pretorius JK, Yeoman KM, Kuhlman PA. The pathogenic and progressive features of chronic human hippocampal epilepsy. Epilepsy Res . 1996; 26: 151–161.
38.
Verity CM, Greenwood R, Golding J. Long-term intellectual and behavioral outcomes of children with febrile convulsions. N Engl J Med . 1998; 24: 1723–1728.
39.
Chang YC, Guo NW, Huang CC, Wang ST, Tsai JJ. Neurocognitive attention and behavior outcome of school-age children with a history of febrile convulsions: a population study. Epilepsia . 2000; 41: 412–420.

Information & Authors

Information

Published In

Neurology®
Volume 57Number 2July 24, 2001
Pages: 184-188
PubMed: 11468300

Publication History

Received: March 12, 2001
Accepted: May 16, 2001
Published online: July 24, 2001
Published in print: July 24, 2001

Permissions

Request permissions for this article.

Authors

Affiliations & Disclosures

D. Fuerst, PhD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
J. Shah, MD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
W.J. Kupsky, MD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
R. Johnson, MD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
A. Shah, MD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
B. Hayman–Abello, MSc
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
T. Ergh, MA
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
Q. Poore, PhD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
A. Canady, MD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.
C. Watson, MD, PhD
From the Departments of Psychiatry and Behavioral Neurosciences (Drs. Fuerst and Poore, and B. Hayman–Abello and T. Ergh), Neurology (Drs. J. Shah, A. Shah, and Watson), Pathology (Dr. Kupsky), and Neurosurgery (Drs. Johnson and Canady), Wayne State University School of Medicine, Detroit, MI.

Notes

Address correspondence and reprint requests to Dr. Craig Watson, Department of Neurology, Wayne State University School of Medicine, 8D-UHC, 4201 St. Antoine, Detroit, MI 48201; e-mail: [email protected]

Metrics & Citations

Metrics

Citation information is sourced from Crossref Cited-by service.

Citations

Download Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Select your manager software from the list below and click Download.

Cited By
  1. Dominant, Lesional Mesial Temporal Lobe Epilepsy, Epilepsy Surgery: A Practical Case-Based Approach, (33-45), (2024).https://doi.org/10.1007/978-3-031-23828-4_2
    Crossref
  2. MANUAL TRACING QUANTIFICATION OF HIPPOCAMPI TO PREDICT THE LATERALIZATION OF THE SEIZURE FOCUS IN TEMPORAL LOBE EPILEPSY PATIENTS, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH, (83-85), (2023).https://doi.org/10.36106/ijsr/2515075
    Crossref
  3. Cognitive Impairment in MRI-Negative Epilepsy: Relationship between Neurophysiological and Neuropsychological Measures, Diagnostics, 13, 18, (2875), (2023).https://doi.org/10.3390/diagnostics13182875
    Crossref
  4. Lateralizing Characteristics of Morphometric Changes to Hippocampus and Amygdala in Unilateral Temporal Lobe Epilepsy with Hippocampal Sclerosis, Medicina, 58, 4, (480), (2022).https://doi.org/10.3390/medicina58040480
    Crossref
  5. Neurobehavioral deficits and a progressive ictogenesis in the tetrodotoxin model of epileptic spasms, Epilepsia, 63, 12, (3078-3089), (2022).https://doi.org/10.1111/epi.17428
    Crossref
  6. Epileptic discharges initiate from brain areas with elevated accumulation of α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors, Brain Communications, 4, 2, (2022).https://doi.org/10.1093/braincomms/fcac023
    Crossref
  7. Quantification of brain age using high-resolution 7 tesla MR imaging and implications for patients with epilepsy, Epilepsy & Behavior Reports, 18, (100530), (2022).https://doi.org/10.1016/j.ebr.2022.100530
    Crossref
  8. Multi-modal characterization and simulation of human epileptic circuitry, Cell Reports, 41, 13, (111873), (2022).https://doi.org/10.1016/j.celrep.2022.111873
    Crossref
  9. Diagnosis of Hippocampal Sclerosis in Children: Comparison of Automated Brain MRI Volumetry and Readers of Varying Experience, American Journal of Roentgenology, 217, 1, (223-234), (2021).https://doi.org/10.2214/AJR.20.23990
    Crossref
  10. UltraHigh Field MR Imaging in Epilepsy, Magnetic Resonance Imaging Clinics of North America, 29, 1, (41-52), (2021).https://doi.org/10.1016/j.mric.2020.09.006
    Crossref
  11. See more
Loading...

View Options

Login options

Check if you have access through your login credentials or your institution to get full access on this article.

Personal login Institutional Login
Purchase Options

The neurology.org payment platform is currently offline. Our technical team is working as quickly as possible to restore service.

If you need immediate support or to place an order, please call or email customer service:

  • 1-800-638-3030 for U.S. customers - 8:30 - 7 pm ET (M-F)
  • 1-301-223-2300 for customers outside the U.S. - 8:30 - 7 pm ET (M-F)
  • [email protected]

We appreciate your patience during this time and apologize for any inconvenience.

View options

PDF and All Supplements

Download PDF and Supplementary Material

Full Text

View Full Text

Full Text HTML

View Full Text HTML

Media

Figures

Other

Tables

Share

Share

Share article link

Share