Neuroimaging and cognitive changes during déjà vu

Epilepsy and Behavior

Volumn 14, Issue 1, 2009, Pages 190-196

  Kovacs, Norbert ^a   Auer, Tibor ^a,b   Balas, Istvan ^a   Karadi, Kazmer ^a   Zambo, Katalin ^c   Schwarcz, Attila ^a   Klivenyi, Peter ^d   Jokeit, Hennric ^e   Horvath, Krisztina ^a   Nagy, Ferenc ^a   Janszky, Jozsef ^a  

^a UNIVERSITY OF PÉCS   (Hungary)

^b MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

^c UNIVERSITY OF PÉCS   (Hungary)

^d UNIVERSITY OF SZEGED   (Hungary)

^e SWISS EPILEPSY CENTER   (Switzerland)

Author keywords

Adverse reaction; Aura; D j vu; Deep brain stimulation; Dystonia; Epilepsy; Magnetic resonance imaging; Pallidum; Single photon emission computed tomography; Subtraction ictal single photon emission computed tomography co registered to magnetic resonance imaging

Indexed keywords

ADULT; ARTICLE; BRAIN DEPTH STIMULATION; BRAIN PERFUSION; CASE REPORT; COGNITIVE DEFECT; DEJA VU; DOPAMINERGIC SYSTEM; DYSTONIA; FEMALE; GLOBUS PALLIDUS; HEMIDYSTONIA; HEMIPARESIS; HIPPOCAMPUS; HUMAN; MEMORY DISORDER; NEUROANATOMY; NEUROIMAGING; NEUROPATHOLOGY; NEUROPSYCHOLOGICAL TEST; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; VERBAL MEMORY;

COGNITION; DEEP BRAIN STIMULATION; DEJA VU; EPILEPSY; FEMALE; GLOBUS PALLIDUS; HUMANS; MAGNETIC RESONANCE IMAGING; NEUROPSYCHOLOGICAL TESTS; RADIOPHARMACEUTICALS; TECHNETIUM TC 99M EXAMETAZIME; TOMOGRAPHY, EMISSION-COMPUTED, SINGLE-PHOTON; YOUNG ADULT;

EID: 58149163407     PISSN: 15255050     EISSN: 15255069     Source Type: Journal    
DOI: 10.1016/j.yebeh.2008.08.017     Document Type: Article

References (53)

1. Neppe V.M. The concept of déjá vu. Parapsychol J S Afr 4 (1983) 1-10
2. Brown A.S. A review of the deja vu experience. Psychol Bull 129 (2003) 394-413
3. Mullan S., and Penfield W. Illusions of comparative interpretation and emotion. Arch Neurol Psychiatry 81 (1959) 269-284
4. Palmini A., and Gloor P. The localizing value of auras in partial seizures: a prospective and retrospective study. Neurology 42 (1992) 801-808
5. Berkovic S.F., McIntosh A., Howell R.A., Mitchell A., Sheffield L.J., and Hopper J.L. Familial temporal lobe epilepsy: a common disorder identified in twins. Ann Neurol 40 (1996) 227-235
6. Striano P., Gambardella A., Coppola A., et al. Familial mesial temporal lobe epilepsy (FMTLE): a clinical and genetic study of 15 Italian families. J Neurol 255 (2008) 16-23
7. Sno H.N., and Linszen D.H. The deja vu experience. remembrance of things past?. Am J Psychiatry 147 (1990) 1587-1595
8. Adachi T., Adachi N., Takekawa Y., et al. Deja vu experiences in patients with schizophrenia. Compr Psychiatry 47 (2006) 389-393
9. Bancaud J., Brunet-Bourgin F., Chauvel P., and Halgren E. Anatomical origin of deja vu and vivid 'memories' in human temporal lobe epilepsy. Brain 117 Pt. 1 (1994) 71-90
10. Bartolomei F., Barbeau E., Gavaret M., et al. Cortical stimulation study of the role of rhinal cortex in deja vu and reminiscence of memories. Neurology 63 (2004) 858-864
11. Gloor P., Olivier A., Quesney L.F., Andermann F., and Horowitz S. The role of the limbic system in experiential phenomena of temporal lobe epilepsy. Ann Neurol 12 (1982) 129-144
12. Halgren E., Walter R.D., Cherlow D.G., and Crandall P.H. Mental phenomena evoked by electrical stimulation of the human hippocampal formation and amygdala. Brain 101 (1978) 83-117
13. Stevens J.R. Psychiatric consequences of temporal lobectomy for intractable seizures: a 20-30-year follow-up of 14 cases. Psychol Med 20 (1990) 529-545
14. Penfield W. The twenty-ninth Maudsley lecture: the role of the temporal cortex in certain psychical phenomena. J Ment Sci 101 (1955) 451-465
15. Neppe V.M. The psychology of déjá vu: have I been here before? (1983), Witwaterstrand University Press, Johannesburg
16. Neppe V.M. Is deja vu a symptom of temporal lobe epilepsy?. S Afr Med J 60 (1981) 907-908
17. Sengoku A., Toichi M., and Murai T. Dreamy states and psychoses in temporal lobe epilepsy: mediating role of affect. Psychiatry Clin Neurosci 51 (1997) 23-26
18. De Nayer A. Deja vu: elaboration of a hypothetical model of explanation. Psychiatr Clin (Basel) 12 (1979) 92-96
19. Gloor P. Experiential phenomena of temporal lobe epilepsy: facts and hypotheses. Brain 113 Pt. 6 (1990) 1673-1694
20. Wild E. Deja vu in neurology. J Neurol 252 (2005) 1-7
21. Taiminen T., and Jaaskelainen S.K. Intense and recurrent deja vu experiences related to amantadine and phenylpropanolamine in a healthy male. J Clin Neurosci 8 (2001) 460-462
22. Wilkerson A., and Levin E.D. Ventral hippocampal dopamine D1 and D2 systems and spatial working memory in rats. Neuroscience 89 (1999) 743-749
23. Hamani C., McAndrews M.P., Cohn M., et al. Memory enhancement induced by hypothalamic/fornix deep brain stimulation. Ann Neurol 63 (2008) 119-123
24. Kovacs N., Nagy F., Kover F., et al. Implanted deep brain stimulator and 1.0-Tesla magnetic resonance imaging. J Magn Reson Imaging 24 (2006) 1409-1412
25. Andersen A.R. 99mTc-D, L-hexamethylene-propyleneamine oxime (99mTc-HMPAO): basic kinetic studies of a tracer of cerebral blood flow. Cerebrovasc Brain Metab Rev 1 (1989) 288-318
26. O'Brien B., O'Connor M., and Mullan B.P. Subtraction ictal SPECT co-registered to MRI in partial epilepsy: description and technical validation of the method with phantom and patient studies. Nucl Med Commun 19 (1998) 31-45
27. Hodges J.R. Cognitive assessment for clinicians (1994), Oxford University Press, Oxford
28. Lezak M. Neuropsychological assessment. 4th ed. (2004), Oxford University Press, New York
29. Janszky J., Mertens M., Janszky I., Ebner A., and Woermann F.G. Left-sided interictal epileptic activity induces shift of language lateralization in temporal lobe epilepsy: an fMRI study. Epilepsia 47 (2006) 921-927
30. Schaltenbrand G., and Wahren B. Atlas for the stereotaxy of the human brain. 2nd ed. (1977), Thieme, Stuttgart
31. Degrell I., Pek G., Nagy D., Nagy E., and Hoyer S. Dementias, psychological tests, and neurotransmitters. Arch Gerontol Geriatr 4 (1985) 365-371
32. Butson C.R., Cooper S.E., Henderson J.M., and McIntyre C.C. Patient-specific analysis of the volume of tissue activated during deep brain stimulation. NeuroImage 34 (2007) 661-670
33. Butson C.R., Maks C.B., and McIntyre C.C. Sources and effects of electrode impedance during deep brain stimulation. Clin Neurophysiol 117 (2006) 447-454
34. Guridi J., and Lozano A.M. A brief history of pallidotomy. Neurosurgery 41 (1997) 1169-1180 discussion 1180-3
35. Gross C.E., Boraud T., Guehl D., Bioulac B., and Bezard E. From experimentation to the surgical treatment of Parkinson's disease: prelude or suite in basal ganglia research?. Prog Neurobiol 59 (1999) 509-532
36. Jacola L.M., Schapiro M.B., Schmithorst V.J., et al. Functional magnetic resonance imaging reveals atypical language organization in children following perinatal left middle cerebral artery stroke. Neuropediatrics 37 (2006) 46-52
37. Muller R.A., Watson C.E., Muzik O., Chakraborty P.K., and Chugani H.T. Motor organization after early middle cerebral artery stroke: a PET study. Pediatr Neurol 19 (1998) 294-298
38. Rasmussen T., and Milner B. The role of early left-brain injury in determining lateralization of cerebral speech functions. Ann NY Acad Sci 299 (1977) 355-369
39. Janszky J., Jokeit H., Heinemann D., Schulz R., Woermann F.G., and Ebner A. Epileptic activity influences the speech organization in medial temporal lobe epilepsy. Brain 126 (2003) 2043-2051
40. Weber B., Fliessbach K., Lange N., Kugler F., and Elger C.E. Material-specific memory processing is related to language dominance. NeuroImage 37 (2007) 611-617
41. Nakajima T., Nimura T., Yamaguchi K., et al. The impact of stereotactic pallidal surgery on the dopamine D2 receptor in Parkinson disease: a positron emission tomography study. J Neurosurg 98 (2003) 57-63
42. Adachi N., Adachi T., Akanuma N., et al. Deja vu experiences in schizophrenia: relations with psychopathology and antipsychotic medication. Compr Psychiatry 48 (2007) 592-596
43. Hintzman D.L., Caulton D.A., and Levitin D.J. Retrieval dynamics in recognition and list discrimination: further evidence of separate processes of familiarity and recall. Mem Cogn 26 (1998) 449-462
44. Bowles B., Crupi C., Mirsattari S.M., et al. Impaired familiarity with preserved recollection after anterior temporal-lobe resection that spares the hippocampus. Proc Natl Acad Sci USA 104 (2007) 16382-16387
45. Xiang J.Z., and Brown M.W. Differential neuronal encoding of novelty, familiarity and recency in regions of the anterior temporal lobe. Neuropharmacology 37 (1998) 657-676
46. Aggleton J.P., and Brown M.W. Episodic memory, amnesia, and the hippocampal-anterior thalamic axis. Behav Brain Sci 22 (1999) 425-444 discussion 444-89.
47. Bogacz R., and Brown M.W. Comparison of computational models of familiarity discrimination in the perirhinal cortex. Hippocampus 13 (2003) 494-524
48. Hallworth N.E., and Bland B.H. Basal ganglia-hippocampal interactions support the role of the hippocampal formation in sensorimotor integration. Exp Neurol 188 (2004) 430-443
49. Newton M.R., Berkovic S.F., Austin M.C., Reutens D.C., McKay W.J., and Bladin P.F. Dystonia, clinical lateralization, and regional blood flow changes in temporal lobe seizures. Neurology 42 (1992) 371-377
50. Miyawaki E., Perlmutter J.S., Troster A.I., Videen T.O., and Koller W.C. The behavioral complications of pallidal stimulation: a case report. Brain Cogn 42 (2000) 417-434
51. Herrmann C.S., and Demiralp T. Human EEG gamma oscillations in neuropsychiatric disorders. Clin Neurophysiol 116 (2005) 2719-2733
52. Bruns A., Eckhorn R., Jokeit H., and Ebner A. Amplitude envelope correlation detects coupling among incoherent brain signals. NeuroReport 11 (2000) 1509-1514
53. Jokeit H., and Makeig S. Different event-related patterns of gamma-band power in brain waves of fast- and slow-reacting subjects. Proc Natl Acad Sci USA 91 (1994) 6339-6343