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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1997 Oct;63(4):461–467. doi: 10.1136/jnnp.63.4.461

Bilateral reductions in hippocampal volume in adults with epilepsy and a history of febrile seizures

W Barr 1, M Ashtari 1, N Schaul 1
PMCID: PMC2169789  PMID: 9343124

Abstract

OBJECTIVES—To examine the degree and frequency of reductions in hippocampal volume in patients with temporal lobe epilepsy with and without a history of febrile seizures.
METHODS—In vivo measures of hippocampal volume were computed from three dimensional gradient echo (FLASH) images in 44 patients undergoing comprehensive evaluations for epilepsy surgery. Twenty one patients (48%) reported a history of febrile seizures. The volumes from these patients were compared with those from 23 patients without a history of febrile seizures and 34 healthy controls.
RESULTS—The febrile seizure group had significant reductions in volume, both ipsilateral (30% decrease) and contralateral (15% decrease), to the EEG seizure focus. Twelve of 18 patients with febrile seizures exhibited clinically significant ipsilateral volume reductions, defined as volumes falling 2 SD below the mean obtained from the control sample. Only four of 19 patients without febrile seizures exhibited this degree of reduction. No significant correlations were found between seizure variables (for example, duration of epilepsy, seizure frequency) and ipsilateral reductions in volume. However, a significant inverse correlation (r=−0.45, P<0.05) between seizure frequency and the volume of the hippocampus contralateral to the seizure focus was found in the febrile seizure group.
CONCLUSION—These results suggest that a history of febrile seizures is associated with the finding of a smaller hippocampus on the side ipsilateral to the subsequent temporal lobe focus whereas chronic factors seem to be be related to pathology contralateral to the seizure focus.



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Selected References

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  1. Albala B. J., Moshé S. L., Okada R. Kainic-acid-induced seizures: a developmental study. Brain Res. 1984 Mar;315(1):139–148. doi: 10.1016/0165-3806(84)90085-3. [DOI] [PubMed] [Google Scholar]
  2. Ashtari M., Barr W. B., Schaul N., Bogerts B. Three-dimensional fast low-angle shot imaging and computerized volume measurement of the hippocampus in patients with chronic epilepsy of the temporal lobe. AJNR Am J Neuroradiol. 1991 Sep-Oct;12(5):941–947. [PMC free article] [PubMed] [Google Scholar]
  3. Ashtari M., Zito J. L., Gold B. I., Lieberman J. A., Borenstein M. T., Herman P. G. Computerized volume measurement of brain structure. Invest Radiol. 1990 Jul;25(7):798–805. doi: 10.1097/00004424-199007000-00009. [DOI] [PubMed] [Google Scholar]
  4. Bogerts B., Ashtari M., Degreef G., Alvir J. M., Bilder R. M., Lieberman J. A. Reduced temporal limbic structure volumes on magnetic resonance images in first episode schizophrenia. Psychiatry Res. 1990 Apr;35(1):1–13. doi: 10.1016/0925-4927(90)90004-p. [DOI] [PubMed] [Google Scholar]
  5. CAVANAGH J. B., MEYER A. Aetiological aspects of Ammon's horn sclerosis associated with temporal lobe epilepsy. Br Med J. 1956 Dec 15;2(5006):1403–1407. doi: 10.1136/bmj.2.5006.1403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cascino G. D., Jack C. R., Jr, Parisi J. E., Sharbrough F. W., Hirschorn K. A., Meyer F. B., Marsh W. R., O'Brien P. C. Magnetic resonance imaging-based volume studies in temporal lobe epilepsy: pathological correlations. Ann Neurol. 1991 Jul;30(1):31–36. doi: 10.1002/ana.410300107. [DOI] [PubMed] [Google Scholar]
  7. Cavazos J. E., Das I., Sutula T. P. Neuronal loss induced in limbic pathways by kindling: evidence for induction of hippocampal sclerosis by repeated brief seizures. J Neurosci. 1994 May;14(5 Pt 2):3106–3121. doi: 10.1523/JNEUROSCI.14-05-03106.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cavazos J. E., Sutula T. P. Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis. Brain Res. 1990 Sep 10;527(1):1–6. doi: 10.1016/0006-8993(90)91054-k. [DOI] [PubMed] [Google Scholar]
  9. Chisholm J., Kellogg C., Franck J. E. Developmental hyperthermic seizures alter adult hippocampal benzodiazepine binding and morphology. Epilepsia. 1985 Mar-Apr;26(2):151–157. doi: 10.1111/j.1528-1157.1985.tb05399.x. [DOI] [PubMed] [Google Scholar]
  10. Cook M. J., Fish D. R., Shorvon S. D., Straughan K., Stevens J. M. Hippocampal volumetric and morphometric studies in frontal and temporal lobe epilepsy. Brain. 1992 Aug;115(Pt 4):1001–1015. doi: 10.1093/brain/115.4.1001. [DOI] [PubMed] [Google Scholar]
  11. EARLE K. M., BALDWIN M., PENFIELD W. Incisural sclerosis and temporal lobe seizures produced by hippocampal herniation at birth. AMA Arch Neurol Psychiatry. 1953 Jan;69(1):27–42. doi: 10.1001/archneurpsyc.1953.02320250033003. [DOI] [PubMed] [Google Scholar]
  12. Falconer M. A. Genetic and related aetiological factors in temporal lobe epilepsy. A review. Epilepsia. 1971 Mar;12(1):13–31. doi: 10.1111/j.1528-1157.1971.tb03912.x. [DOI] [PubMed] [Google Scholar]
  13. Falconer M. A. Mesial temporal (Ammon's horn) sclerosis as a common cause of epilepsy. Aetiology, treatment, and prevention. Lancet. 1974 Sep 28;2(7883):767–770. doi: 10.1016/s0140-6736(74)90956-8. [DOI] [PubMed] [Google Scholar]
  14. Falconer M. A., Taylor D. C. Surgical treatment of drug-resistant epilepsy due to mesial temporal sclerosis. Etiology and significance. Arch Neurol. 1968 Oct;19(4):353–361. doi: 10.1001/archneur.1968.00480040019001. [DOI] [PubMed] [Google Scholar]
  15. Free S. L., Li L. M., Fish D. R., Shorvon S. D., Stevens J. M. Bilateral hippocampal volume loss in patients with a history of encephalitis or meningitis. Epilepsia. 1996 Apr;37(4):400–405. doi: 10.1111/j.1528-1157.1996.tb00578.x. [DOI] [PubMed] [Google Scholar]
  16. French J. A., Williamson P. D., Thadani V. M., Darcey T. M., Mattson R. H., Spencer S. S., Spencer D. D. Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination. Ann Neurol. 1993 Dec;34(6):774–780. doi: 10.1002/ana.410340604. [DOI] [PubMed] [Google Scholar]
  17. Jack C. R., Jr, Sharbrough F. W., Cascino G. D., Hirschorn K. A., O'Brien P. C., Marsh W. R. Magnetic resonance image-based hippocampal volumetry: correlation with outcome after temporal lobectomy. Ann Neurol. 1992 Feb;31(2):138–146. doi: 10.1002/ana.410310204. [DOI] [PubMed] [Google Scholar]
  18. Jack C. R., Jr, Sharbrough F. W., Twomey C. K., Cascino G. D., Hirschorn K. A., Marsh W. R., Zinsmeister A. R., Scheithauer B. Temporal lobe seizures: lateralization with MR volume measurements of the hippocampal formation. Radiology. 1990 May;175(2):423–429. doi: 10.1148/radiology.175.2.2183282. [DOI] [PubMed] [Google Scholar]
  19. Jackson G. D., Kuzniecky R. I., Cascino G. D. Hippocampal sclerosis without detectable hippocampal atrophy. Neurology. 1994 Jan;44(1):42–46. doi: 10.1212/wnl.44.1.42. [DOI] [PubMed] [Google Scholar]
  20. Kim J. H., Tien R. D., Felsberg G. J., Osumi A. K., Lee N., Friedman A. H. Fast spin-echo MR in hippocampal sclerosis: correlation with pathology and surgery. AJNR Am J Neuroradiol. 1995 Apr;16(4):627–636. [PMC free article] [PubMed] [Google Scholar]
  21. King D., Spencer S. S., McCarthy G., Luby M., Spencer D. D. Bilateral hippocampal atrophy in medial temporal lobe epilepsy. Epilepsia. 1995 Sep;36(9):905–910. doi: 10.1111/j.1528-1157.1995.tb01634.x. [DOI] [PubMed] [Google Scholar]
  22. Kuks J. B., Cook M. J., Fish D. R., Stevens J. M., Shorvon S. D. Hippocampal sclerosis in epilepsy and childhood febrile seizures. Lancet. 1993 Dec 4;342(8884):1391–1394. doi: 10.1016/0140-6736(93)92754-h. [DOI] [PubMed] [Google Scholar]
  23. Lee S. S., Murata R., Matsuura S. Developmental study of hippocampal kindling. Epilepsia. 1989 May-Jun;30(3):266–270. doi: 10.1111/j.1528-1157.1989.tb05297.x. [DOI] [PubMed] [Google Scholar]
  24. Lencz T., McCarthy G., Bronen R. A., Scott T. M., Inserni J. A., Sass K. J., Novelly R. A., Kim J. H., Spencer D. D. Quantitative magnetic resonance imaging in temporal lobe epilepsy: relationship to neuropathology and neuropsychological function. Ann Neurol. 1992 Jun;31(6):629–637. doi: 10.1002/ana.410310610. [DOI] [PubMed] [Google Scholar]
  25. Lindsay J., Ounsted C., Richards P. Long-term outcome in children with temporal lobe seizures. I: Social outcome and childhood factors. Dev Med Child Neurol. 1979 Jun;21(3):285–298. doi: 10.1111/j.1469-8749.1979.tb01621.x. [DOI] [PubMed] [Google Scholar]
  26. Margerison J. H., Corsellis J. A. Epilepsy and the temporal lobes. A clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes. Brain. 1966 Sep;89(3):499–530. doi: 10.1093/brain/89.3.499. [DOI] [PubMed] [Google Scholar]
  27. Moshé S. L., Albala B. J. Maturational changes in postictal refractoriness and seizure susceptibility in developing rats. Ann Neurol. 1983 May;13(5):552–557. doi: 10.1002/ana.410130514. [DOI] [PubMed] [Google Scholar]
  28. Mouritze Dam A. Hippocampal neuron loss in epilepsy and after experimental seizures. Acta Neurol Scand. 1982 Dec;66(6):601–642. doi: 10.1111/j.1600-0404.1982.tb04528.x. [DOI] [PubMed] [Google Scholar]
  29. Nelson K. B., Ellenberg J. H. Predictors of epilepsy in children who have experienced febrile seizures. N Engl J Med. 1976 Nov 4;295(19):1029–1033. doi: 10.1056/NEJM197611042951901. [DOI] [PubMed] [Google Scholar]
  30. Nohria V., Lee N., Tien R. D., Heinz E. R., Smith J. S., DeLong G. R., Skeen M. B., Resnick T. J., Crain B., Lewis D. V. Magnetic resonance imaging evidence of hippocampal sclerosis in progression: a case report. Epilepsia. 1994 Nov-Dec;35(6):1332–1336. doi: 10.1111/j.1528-1157.1994.tb01807.x. [DOI] [PubMed] [Google Scholar]
  31. SANO K., MALAMUD N. Clinical significance of sclerosis of the cornu ammonis: ictal psychic phenomena. AMA Arch Neurol Psychiatry. 1953 Jul;70(1):40–53. doi: 10.1001/archneurpsyc.1953.02320310046003. [DOI] [PubMed] [Google Scholar]
  32. Sagar H. J., Oxbury J. M. Hippocampal neuron loss in temporal lobe epilepsy: correlation with early childhood convulsions. Ann Neurol. 1987 Sep;22(3):334–340. doi: 10.1002/ana.410220309. [DOI] [PubMed] [Google Scholar]
  33. Scheibel A. B. Are complex partial seizures a sequela of temporal lobe dysgenesis? Adv Neurol. 1991;55:59–77. [PubMed] [Google Scholar]
  34. Sloviter R. S. Permanently altered hippocampal structure, excitability, and inhibition after experimental status epilepticus in the rat: the "dormant basket cell" hypothesis and its possible relevance to temporal lobe epilepsy. Hippocampus. 1991 Jan;1(1):41–66. doi: 10.1002/hipo.450010106. [DOI] [PubMed] [Google Scholar]
  35. Sperber E. F., Haas K. Z., Stanton P. K., Moshé S. L. Resistance of the immature hippocampus to seizure-induced synaptic reorganization. Brain Res Dev Brain Res. 1991 May 20;60(1):88–93. doi: 10.1016/0165-3806(91)90158-f. [DOI] [PubMed] [Google Scholar]
  36. Sutula T. P. Experimental models of temporal lobe epilepsy: new insights from the study of kindling and synaptic reorganization. Epilepsia. 1990;31 (Suppl 3):S45–S54. doi: 10.1111/j.1528-1157.1990.tb05859.x. [DOI] [PubMed] [Google Scholar]
  37. Trenerry M. R., Jack C. R., Jr, Ivnik R. J., Sharbrough F. W., Cascino G. D., Hirschorn K. A., Marsh W. R., Kelly P. J., Meyer F. B. MRI hippocampal volumes and memory function before and after temporal lobectomy. Neurology. 1993 Sep;43(9):1800–1805. doi: 10.1212/wnl.43.9.1800. [DOI] [PubMed] [Google Scholar]
  38. Trenerry M. R., Jack C. R., Jr, Sharbrough F. W., Cascino G. D., Hirschorn K. A., Marsh W. R., Kelly P. J., Meyer F. B. Quantitative MRI hippocampal volumes: association with onset and duration of epilepsy, and febrile convulsions in temporal lobectomy patients. Epilepsy Res. 1993 Jul;15(3):247–252. doi: 10.1016/0920-1211(93)90062-c. [DOI] [PubMed] [Google Scholar]

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