Skip to main content
Log in

Diffusion tensor imaging of partial intractable epilepsy

  • Neuro
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Our aim was to assess the value of diffusion tensor imaging (DTI) in patients with partial intractable epilepsy. We used DTI (25 non-collinear directions) in 15 patients with a cortical lesion on conventional MRI. Fractional anisotropy (FA) was measured in the internal capsule, and in the normal-appearing white matter (WM), adjacent to the lesion, and away from the lesion, at a set distance of 2–3 cm. In each patient, increased or decreased FA measurements were those that varied from mirror values using an arbitrary 10% threshold. Over the whole population, ipsi- and contralateral FA measurements were also compared using a Wilcoxon test (p<0.05). Over the whole population, FA was significantly reduced in the WM adjacent to and away from the lesion, whilst being normal in the internal capsule. FA was reduced by more than 10% in the WM adjacent to and distant from the lesion in 13 and 12 patients respectively. For nine of the ten patients for whom the surgical resection encompassed the limits of the lesion on conventional MRI, histological data showed WM alterations (gliosis, axonal loss, abnormal cells). DTI often reveals WM abnormalities that are undetected on conventional MRI in patients with partial intractable epilepsy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Beaulieu C (2002) The basis of anisotropic water diffusion in the nervous system—a technical review. NMR Biomed 15:435–455

    PubMed  Google Scholar 

  2. Le Bihan D (1991) Molecular diffusion nuclear magnetic resonance imaging. Magn Reson Q 7:1–30

    PubMed  Google Scholar 

  3. Le Bihan D, Mangin JF, Poupon C, Clark CA, Pappata S, Molko N, Chabriat H (2001) Diffusion tensor imaging: concepts and applications. J Magn Reson Imaging 13:534–546

    Article  PubMed  Google Scholar 

  4. Naganawa S, Koshikawa T, Kawai H, Fukatsu H, Ishigaki T, Maruyama K, Takizawa O (2004) Optimization of diffusion-tensor MR imaging data acquisition parameters for brain fiber tracking using parallel imaging at 3 T. Eur Radiol 14:234–238

    Article  Google Scholar 

  5. Kodama F, Ogawa T, Sugihara S, Kamba M, Kohaya N, Kondo S, Kinoshita T (2003) Transneuronal degeneration in patients with temporal lobe epilepsy: evaluation by MR imaging. Eur Radiol 13:2180–2185

    Article  Google Scholar 

  6. Sundgren PC, Dong Q, Gomez-Hassan D, Mukherji SK, Maly P, Welsh R (2004) Diffusion tensor imaging of the brain: review of clinical applications. Neuroradiology 46:339–350

    Google Scholar 

  7. Oppenheim C, Rodrigo S, Poupon C, Dumas de la Roque A, Naggara O, Meder JF, Fredy D (2004) Diffusion tensor MR imaging of the brain. Clinical applications. J Radiol 85:287–296

    Google Scholar 

  8. Huisman TA (2003) Diffusion-weighted imaging: basic concepts and application in cerebral stroke and head trauma. Eur Radiol 13:2283–2297

    Article  PubMed  Google Scholar 

  9. Lythgoe MF, Busza AL, Calamante F, Sotak CH, King MD, Bingham AC, Williams SR, Gadian DG (1997) Effects of diffusion anisotropy on lesion delineation in a rat model of cerebral ischemia. Magn Reson Med 38:662–668

    Google Scholar 

  10. van Gelderen P, de Vleeschouwer MH, DesPres D, Pekar J, van Zijl PC, Moonen CT (1994) Water diffusion and acute stroke. Magn Reson Med 31:154–163

    Google Scholar 

  11. Werring DJ, Clark CA, Barker GJ, Thompson AJ, Miller DH (1999) Diffusion tensor imaging of lesions and normal-appearing white matter in multiple sclerosis. Neurology 52:1626–1632

    Google Scholar 

  12. Lim KO, Hedehus M, Moseley M, de Crespigny A, Sullivan EV, Pfefferbaum A (1999) Compromised white matter tract integrity in schizophrenia inferred from diffusion tensor imaging. Arch Gen Psychiatry 56:367–374

    Article  Google Scholar 

  13. Werring DJ, Clark CA, Barker GJ, Miller DH, Parker GJ, Brammer MJ, Bullmore ET, Giampietro VP, Thompson AJ (1998) The structural and functional mechanisms of motor recovery: complementary use of diffusion tensor and functional magnetic resonance imaging in a traumatic injury of the internal capsule. J Neurol Neurosurg Psychiatry 65:863–869

    Google Scholar 

  14. Price SJ, Pena A, Burnet NG, Jena R, Green HA, Carpenter TA, Pickard JD, Gillard JH (2004) Tissue signature characterisation of diffusion tensor abnormalities in cerebral gliomas. Eur Radiol 14:1909–1917

    Article  Google Scholar 

  15. Price SJ, Burnet NG, Donovan T, Green HA, Pena A, Antoun NM, Pickard JD, Carpenter TA, Gillard JH (2003) Diffusion tensor imaging of brain tumours at 3 T: a potential tool for assessing white matter tract invasion? Clin Radiol 58:455–462

    Article  CAS  PubMed  Google Scholar 

  16. Bozzali M, Falini A, Franceschi M, Cercignani M, Zuffi M, Scotti G, Comi G, Filippi M (2002) White matter damage in Alzheimer’s disease assessed in vivo using diffusion tensor magnetic resonance imaging. J Neurol Neurosurg Psychiatry 72:742–746

    Article  Google Scholar 

  17. Hajek M, Dezortova M, Liscak R, Vymazal J, Vladyka V (2003) 1H MR spectroscopy of mesial temporal lobe epilepsies treated with Gamma knife. Eur Radiol 13:994–1000

    Google Scholar 

  18. Rugg-Gunn FJ, Eriksson SH, Symms MR, Barker GJ, Duncan JS (2001) Diffusion tensor imaging of cryptogenic and acquired partial epilepsies. Brain 124:627–636

    Article  Google Scholar 

  19. Eriksson SH, Rugg-Gunn FJ, Symms MR, Barker GJ, Duncan JS (2001) Diffusion tensor imaging in patients with epilepsy and malformations of cortical development. Brain 124:617–626

    Article  Google Scholar 

  20. Arfanakis K, Hermann BP, Rogers BP, Carew JD, Seidenberg M, Meyerand ME (2002) Diffusion tensor MRI in temporal lobe epilepsy. Magn Reson Imaging 20:511–519

    Article  Google Scholar 

  21. Assaf BA, Mohamed FB, Abou-Khaled KJ, Williams JM, Yazeji MS, Haselgrove J, Faro SH (2003) Diffusion tensor imaging of the hippocampal formation in temporal lobe epilepsy. AJNR Am J Neuroradiol 24:1857–1862

    Google Scholar 

  22. Wieshmann UC, Clark CA, Symms MR, Franconi F, Barker GJ, Shorvon SD (1999) Reduced anisotropy of water diffusion in structural cerebral abnormalities demonstrated with diffusion tensor imaging. Magn Reson Imaging 17:1269–1274

    Article  CAS  PubMed  Google Scholar 

  23. Steens SC, Admiraal-Behloul F, Schaap JA, Hoogenraad FG, Wheeler-Kingshott CA, le Cessie S, Tofts PS, van Buchem MA (2004) Reproducibility of brain ADC histograms. Eur Radiol 14:425–430

    Article  PubMed  Google Scholar 

  24. Meencke HJ (1983) The density of dystopic neurons in the white matter of the gyrus frontalis inferior in epilepsies. J Neurol 230:171–181

    Article  Google Scholar 

  25. Hardiman O, Burke T, Phillips J, Murphy S, O’Moore B, Staunton H, Farrell MA (1988) Microdysgenesis in resected temporal neocortex: incidence and clinical significance in focal epilepsy. Neurology 38:1041–1047

    Google Scholar 

  26. Kasper BS, Stefan H, Buchfelder M, Paulus W (1999) Temporal lobe microdysgenesis in epilepsy versus control brains. J Neuropathol Exp Neurol 58:22–28

    Google Scholar 

  27. Eriksson S, Malmgren K, Rydenhag B, Jonsson L, Uvebrant P, Nordborg C (1999) Surgical treatment of epilepsy—clinical, radiological and histopathological findings in 139 children and adults. Acta Neurol Scand 99:8–15

    Google Scholar 

  28. Sisodiya SM, Free SL, Stevens JM, Fish DR, Shorvon SD (1995) Widespread cerebral structural changes in patients with cortical dysgenesis and epilepsy. Brain 118(Pt 4):1039–1050

    Google Scholar 

  29. Honavar MB, Meldrum BS (2002) Changes secondary to epilepsy. In: Graham DI, Lantos PL (eds) Greenfield’s neuropathology, pp 912–922

  30. Beaulieu C, Does MD, Snyder RE, Allen PS (1996) Changes in water diffusion due to Wallerian degeneration in peripheral nerve. Magn Reson Med 36:627–631

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Catherine Oppenheim.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dumas de la Roque, A., Oppenheim, C., Chassoux, F. et al. Diffusion tensor imaging of partial intractable epilepsy. Eur Radiol 15, 279–285 (2005). https://doi.org/10.1007/s00330-004-2578-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-004-2578-8

Keywords

Navigation