Clinical manifestations of insular lobe seizures: a stereo-electroencephalographic study
Open accessAbstract
PURPOSE: In this study, we report the clinical features of insular lobe seizures based on data from video and stereo-electroencephalographic (SEEG) ictal recordings and direct electric insular stimulation of the insular cortex performed in patients referred for presurgical evaluation of temporal lobe epilepsy (TLE). METHODS: Since our first recordings of insular seizures, the insular cortex has been included as one of the targets of stereo-electroencephalographic (SEEG) electrode implantation in 50 consecutive patients with TLE whose seizures were suspected to originate from, or rapidly to propagate to, the perisylvian cortex. In six, a stereotyped sequence of ictal symptoms associated with intrainsular discharges could be identified. RESULTS: This ictal sequence occurred in full consciousness, beginning with a sensation of laryngeal constriction and paresthesiae, often unpleasant, affecting large cutaneous territories, most often at the onset of a complex partial seizure (five of the six patients). It was eventually followed by dysarthric speech and focal motor convulsive symptoms. The insular origin of these symptoms was supported by the data from functional cortical mapping of the insula by using direct cortical stimulations. CONCLUSIONS: This sequence of ictal symptoms looks reliable enough to characterize insular lobe epileptic seizures (ILESs). Observation of this clinical sequence at the onset of seizures on video-EEG recordings in TLE patients strongly suggests that the seizure-onset zone is located not in the temporal but in the insular lobe; recording directly from the insular cortex should occur before making any decision regarding epilepsy surgery.
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The highest prevalence of bodily self disturbances was found in the parietal cortex (primary somatosensory cortex: 27.3%) and temporo-insular cortex (24%), whereas the lowest prevalence was found for early whole-brain or temporal cortex mapping by Penfield and colleagues (0.1%−1.8%).
“The highest prevalence was found in the parietal cortex (primary somatosensory cortex: 27.3%; Sun, Zhang, Yu, et al., 2021) and temporo‐insular cortex (24%; Isnard et al., 2004), whereas the lowest prevalence was found for early whole‐brain or temporal cortex mapping by Penfield and colleagues (0.1%−1.8%; Penfield & Perot, 1963; Penfield, 1947, 1955, 1957).”
From Neural bases of the bodily self as revealed by electrical brain stimulation: A systematic review (2023) · cites this paper as Isnard et al., 2004
The Somatosensory responses section reports insular-stimulation responses involving whole-body sensations and feelings of unreality, so the paper supports an association with bodily-self disturbances. It does not report a 24% prevalence for the temporo-insular cortex; it lists each of those response types as 4% of evoked responses. The parietal and Penfield figures are attached to other citations, not Isnard et al. (LLM, conf=0.85)
Experimental — accuracy not yet measuredStudies of epileptic seizures in the insula, stroke-induced lesions to the insula, lesioning studies in rats, and direct electrical stimulation studies in primates have shown the insula is critical for perception, recognition, and working memory in taste.
“Studies of epileptic seizures in the insula (Isnard et al., 2004), stroke-induced lesions to the insula (Pritchard et al., 1999), lesioning studies in rats (DeCoteau et al., 1997; Ragozzino and Kesner, 1999; Fresquet et al., 2004), and direct electrical stimulation studies in primates (Verhagen et al., 2004) have shown the insula is critical for perception, recognition, and working memory in taste”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Isnard et al., 2004
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Cites
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798 · see citing works
EPILEPSY AND THE FUNCTIONAL ANATOMY OF THE HUMAN BRAIN
Penfield, W., & Jasper, H. (1954) · Southern Medical Journal · doi:10.1097/00007611-195407000-00024 · Cited by 4,092 · see citing works
Proposal for Revised Clinical and Electroencephalographic Classification of Epileptic Seizures
(1981) · Epilepsia · doi:10.1111/j.1528-1157.1981.tb06159.x · Cited by 3,433 · see citing works
Circuitry and functional aspects of the insular lobe in primates including humans
AUGUSTINE, J. (1996) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00011-2 · Cited by 1,776 · see citing works
Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination
French, J. A., Williamson, P. D., Thadani, V. M., Darcey, T. M., Mattson, R. H., Spencer, S. S., & Spencer, D. D. (1993) · Annals of Neurology · doi:10.1002/ana.410340604 · Cited by 874 · see citing works
THE INSULA: FURTHER OBSERVATIONS ON ITS FUNCTION
PENFIELD, W., & FAULK, M. E. (1955) · Brain · doi:10.1093/brain/78.4.445 · Cited by 606 · see citing works
Bornhövd, K., Quante, M., Glauche, V., Bromm, B., Weiller, C., & Büchel, C. (2002) · Brain · doi:10.1093/brain/awf137 · Cited by 584 · see citing works
Ostrowsky‐Coste, K. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.4.376 · Cited by 573 · see citing works
Robinson, C., & Burton, H. (1980) · The Journal of comparative neurology · doi:10.1002/cne.901920105 · Cited by 399 · see citing works
Strokes restricted to the insular cortex
Cereda, C., Ghika, J., Maeder, P., & Bogousslavsky, J. (2002) · Neurology · doi:10.1212/01.wnl.0000038905.75660.bd · Cited by 302 · see citing works
Salanova, V., Andermann, F., Rasmussen, T., Olivier, A., & QUESNEY, L. F. (1995) · Brain · doi:10.1093/brain/118.3.607 · Cited by 283 · see citing works
Reappraisal of the human vestibular cortex by cortical electrical stimulation study
Kahane, P., Hoffmann, D., Minotti, L., & Berthoz, A. (2003) · Annals of Neurology · doi:10.1002/ana.10726 · Cited by 278 · see citing works
Functional Mapping of the Insular Cortex: Clinical Implication in Temporal Lobe Epilepsy
Ostrowsky‐Coste, K., Isnard, J., Ryvlin, P., Guénot, M., Fischer, C., & Mauguı̀ere, F. (2000) · Epilepsia · doi:10.1111/j.1528-1157.2000.tb00228.x · Cited by 272 · see citing works
Self-citationBurton, H., Videen, T. O., & Raichle, M. E. (1993) · Somatosensory & Motor Research · doi:10.3109/08990229309028839 · Cited by 267 · see citing works
Weiner, H. L., Lemere, C. A., Maron, R., Spooner, E. T., Grenfell, T. J., Mori, C., Issazadeh‐Navikas, S., Hancock, W. W., & Selkoe, D. J. (2000) · Annals of Neurology · doi:10.1002/1531-8249(200010)48:4 · Cited by 261 · see citing works
An attention modulated response to disgust in human ventral anterior insula
Krolak‐Salmon, P., Hénaff, M.-A., Isnard, J., Tallon‐Baudry, C., Guénot, M., Vighetto, A., Bertrand, O., & Mauguı̀ere, F. (2003) · Annals of Neurology · doi:10.1002/ana.10502 · Cited by 251 · see citing works
Self-citationNeurophysiological Monitoring for Epilepsy Surgery: The Talairach SEEG Method
Guénot, M., Isnard, J., Ryvlin, P., et al. (2001) · Stereotactic and Functional Neurosurgery · doi:10.1159/000064595 · Cited by 233 · see citing works
Self-citationDual representation of pain in the operculo-insular cortex in humans
Frot, M. (2003) · Brain · doi:10.1093/brain/awg032 · Cited by 230 · see citing works
The insular lobe in primates including humans
Augustine, J. R. (1985) · Neurological Research · doi:10.1080/01616412.1985.11739692 · Cited by 224 · see citing works
The Role of the Insular Cortex in Dysphagia
Daniels, S. K., & Foundas, A. L. (1997) · Dysphagia · doi:10.1007/pl00009529 · Cited by 211 · see citing works
A modality-specific somatosensory area within the insula of the rhesus monkey
Schneider, R. J., Friedman, D. P., & Mishkin, M. M. (1993) · Brain Research · doi:10.1016/0006-8993(93)90305-7 · Cited by 180 · see citing works
Duffau, H., Capelle, L., Lopes, M., et al. (2002) · Acta Neurochirurgica · doi:10.1007/s00701-002-0941-6 · Cited by 154 · see citing works
GUSTATORY HALLUCINATIONS IN EPILEPTIC SEIZURES
Hausser‐Hauw, C., & Bancaud, J. (1987) · Brain · doi:10.1093/brain/110.2.339 · Cited by 147 · see citing works
Functional compensation of the left dominant insula for language
Duffau, H., Bauchet, L., Lehéricy, S., & Capelle, L. (2001) · Neuroreport · doi:10.1097/00001756-200107200-00023 · Cited by 139 · see citing works
Gustatory neural coding in the monkey cortex: stimulus intensity
Scott, T. R., Plata‐Saláman, C. R., Smith‐Swintosky, V. L., & Giza, B. K. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.1.76 · Cited by 133 · see citing works
Habib, M., Daquin, G., Milandre, L., Royère, M. L., Rey, M. F., Lanteri, A., Salamon, G., & Khalil, R. (1995) · Neuropsychologia · doi:10.1016/0028-3932(94)00108-2 · Cited by 126 · see citing works
Surgical treatment of partial epilepsy arising from the insular cortex
Roper, S. N., Levesque, M. F., Sutherling, W. W., & Engel, J. (1993) · Journal of neurosurgery · doi:10.3171/jns.1993.79.2.0266 · Cited by 125 · see citing works
Evaluation of Insular Ablation in Surgical Treatment of Temporal Lobe Epilepsy
SILFVENIUS, H., GLOOR, P., & Rasmussen, T. (1964) · Epilepsia · doi:10.1111/j.1528-1157.1964.tb03338.x · Cited by 120 · see citing works
Mauguı̀ere, F., & Courjon, J. (1978) · Brain · doi:10.1093/brain/101.2.307 · Cited by 120 · see citing works
Gustatory neural coding in the monkey cortex: stimulus quality
Smith‐Swintosky, V. L., Plata‐Saláman, C. R., & Scott, T. R. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.4.1156 · Cited by 88 · see citing works
Picard, F. (2000) · Brain · doi:10.1093/brain/123.6.1247 · Cited by 86 · see citing works
Aziz, Q., Furlong, P. L., Barlow, J. D., Hobson, A. R., ALANI, S. M., Bancewicz, J., Ribbands, M. S., Harding, G. F. A., & Thompson, D. G. (1995) · Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section · doi:10.1016/0168-5597(94)00297-r · Cited by 82 · see citing works
Kahane, P., Tassi, L., Francione, S., et al. (1993) · Neurophysiologie Clinique · doi:10.1016/s0987-7053(05)80123-6 · Cited by 78 · see citing works
Ictus emeticus and the insular cortex
Fiol, M. E., Leppik, I. E., Mireles, R., & Maxwell, R. E. (1988) · Epilepsy Research · doi:10.1016/0920-1211(88)90030-7 · Cited by 65 · see citing works
SEIZURES INVOLVING SECONDARY SENSORY AND RELATED AREAS
Blume, W. T., Jones, D. C., Young, G. B., et al. (1992) · Brain · doi:10.1093/brain/115.5.1509 · Cited by 51 · see citing works
Neural Networks Underlying Epileptic Humming
Bartoloméi, F., Wendling, F., Vignal, J., et al. (2002) · Epilepsia · doi:10.1046/j.1528-1157.2002.48501.x · Cited by 51 · see citing works
Ferro, J. M., Martins, I. P., Pinto, F., et al. (1982) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1982.tb08796.x · Cited by 43 · see citing works
Hatashita, S., Sakakibara, T., & Ishii, S. (1983) · Journal of neurosurgery · doi:10.3171/jns.1983.58.2.0300 · Cited by 42 · see citing works
Somatomotor Manifestations in Temporal Lobe Seizures
Bossi, L., Munari, C., Stoffels, C., et al. (1984) · Epilepsia · doi:10.1111/j.1528-1157.1984.tb04157.x · Cited by 40 · see citing works
[Clinical symptomatology of epileptic seizures of temporal origin].
Bancaud, J. (1987) · PubMed · Cited by 38 · see citing works
Differential Diagnosis Between Temporal and “Perisylvian” Epilepsy in a Surgical Perspective
Munari, C., Talairach, J., Bonis, A., et al. (1980) · Acta neurochirurgica. Supplementum · doi:10.1007/978-3-7091-8592-6_11 · Cited by 38 · see citing works
Cascino, G. D., & Karnes, W. E. (1990) · Journal of Epilepsy · doi:10.1016/0896-6974(90)90044-y · Cited by 33 · see citing works
[Surgical indications in so-called temporal epilepsy].
Guillaume, J., Mazars, G., & Mazars, Y. (1953) · PubMed · Cited by 28 · see citing works
Electroclinical features of the psychomotor seizure
Meinardi, H. (1983) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(83)90083-5 · Cited by 26 · see citing works
MECHANISM AND CORTICAL REPRESENTATION OF THE FEEDING PATTERN
Babkin, B. P. (1951) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1951.02320070021001 · Cited by 23 · see citing works
Pharyngeal Dysesthesia as an Aura in Temporal Lobe Epilepsy
Carmant, L., Carrazana, E. J., Kramer, U., Helmers, S. L., Holmes, G. L., Black, P. M., & Mikati, M. A. (1996) · Epilepsia · doi:10.1111/j.1528-1157.1996.tb00045.x · Cited by 21 · see citing works
Prats, J. M., Axpe, C. G., Garcia‐Nieto, M. L., et al. (1999) · Revista de Neurología · doi:10.33588/rn.2904.99028 · Cited by 10 · see citing works
Pharyngeal Dysesthesias as an Aura in Temporal Lobe Epilepsy Associated with Amygdalar Pathology
Garganis, K., Papadimitriou, C., Gymnopoulos, K., et al. (2001) · Epilepsia · doi:10.1046/j.1528-1157.2001.21100.x · Cited by 9 · see citing works
Burton, D. L. (1993) · Government Information Quarterly · doi:10.1016/0740-624x(93)90067-a · Cited by 5 · see citing works
Flagged first, then by citations
Research works printed but not linked: 8
- Guillaume MMJ, Mazars G. Technique de résection de l'insula dans les épilepsies insulaires. Rev Neurol 1949;81:900-3.
- Guillaume MMJ, Mazars G, Mazars Y. Indications chirurgicales dans les épilepsies dites "temporalis." Rev Neurol 1953;88:461-501.
- Isnard J, Guenot M, Ostrowsky K, et al. The role of the insular cortex in temporal lobe epilepsy. Ann Neurol 2000;48:614-23.
- Williamson D, Engel J, Munari C. Anatomic classification of localization-related epilepsy. In: Engel J, Pedley T, eds. Epilepsy. Philadelphia: Lippincott-Raven, 1997:2405-26.
- Prats JM, Garaizar C, Garcia-Nieto ML, et al. Opercular epileptic syndrome: an unusual form of benign partial epilepsy in childhood. Rev Neurol 1999;29:375-80.
- Kahane P, Tassi L, Francione S, et al. Electroclinical manifestations elicited by intracerebral electric stimulation "shocks" in temporal lobe epilepsy. Neurophysiol Clin 1993;23:305-26.
- Engel J, Williamson PD, Wieser HG. Mesial temporal lobe epilep- sies. In: Engel J, Pedley, eds. Epilepsy. Philadelphia: Lippincott- Raven, 1997:2417-26.
- Doyle WK, Spencer DD. Anterior temporal résections. In: Engel J, Pedley, eds. Epilepsy. Philadelphia: Lippincott-Raven, 1997:1807- 17.
Cited by
Sorted by citations
Structure and Function of the Human Insula
Uddin, L. Q., Nomi, J. S., Hébert-Seropian, B., Ghaziri, J., & Boucher, O. (2017) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000377 · Cited by 1,262 · see citing works
The hidden island of addiction: the insula
Naqvi, N. H., & Bechara, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.009 · Cited by 833 · see citing works
From the neuromatrix to the pain matrix (and back)
Iannetti, G. D., & Mouraux, A. (2010) · Experimental Brain Research · doi:10.1007/s00221-010-2340-1 · Cited by 554 · see citing works
Neural correlates of tic generation in Tourette syndrome: an event-related functional MRI study
Bohlhalter, S. (2006) · Brain · doi:10.1093/brain/awl050 · Cited by 426 · see citing works
Contributions of the insula to cognition and emotion
Gasquoine, P. G. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9246-9 · Cited by 400 · see citing works
Functional neuroanatomy of the insular lobe
Stephani, C., Fernandez-Baca Vaca, G., Maciunas, R., Koubeissi, M., & Lüders, H. O. (2011) · Brain Structure and Function · doi:10.1007/s00429-010-0296-3 · Cited by 251 · see citing works
Electrical stimulation of a small brain area reversibly disrupts consciousness.
Koubeissi, M. Z., Bartolomei, F., Beltagy, A., & Picard, F. (2014) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2014.05.027 · Cited by 216 · see citing works
Mazzola, L., Isnard, J., Peyron, R., Guénot, M., & Mauguière, F. (2009) · Pain · doi:10.1016/j.pain.2009.07.014 · Cited by 217 · see citing works
Self-citationThe insular cortex and the regulation of cardiac function
Oppenheimer, S., & Cechetto, D. (2016) · Comprehensive Physiology · doi:10.1002/cphy.c140076 · Cited by 191 · see citing works
How the insula speaks to the heart: Cardiac responses to insular stimulation in humans
Chouchou, F., Mauguière, F., Vallayer, O., Catenoix, H., Isnard, J., Montavont, A., Jung, J., Pichot, V., Rheims, S., & Mazzola, L. (2019) · Human Brain Mapping · doi:10.1002/hbm.24548 · Cited by 148 · see citing works
Self-citationIndovina, I., Riccelli, R., Chiarella, G., Petrolo, C., Augimeri, A., Giofrè, L., Lacquaniti, F., Staab, J. P., & Passamonti, L. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00334 · Cited by 140 · see citing works
The Insula: A Brain Stimulation Target for the Treatment of Addiction
Ibrahim, C., Rubin-Kahana, D. S., Pushparaj, A., Musiol, M., Blumberger, D. M., Daskalakis, Z. J., Zangen, A., & Le Foll, B. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00720 · Cited by 133 · see citing works
Spatial segregation of somato-sensory and pain activations in the human operculo-insular cortex
Mazzola, L., Faillenot, I., Barral, F.-G., Mauguière, F., & Peyron, R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.072 · Cited by 130 · see citing works
Self-citationNeural bases of the bodily self as revealed by electrical brain stimulation: A systematic review
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“…prevalence was found in the parietal cortex (primary somatosensory cortex: 27.3%; Sun, Zhang, Yu, et al., 2021) and temporo-insular cortex (24%; Isnard et al., 2004), whereas the lowest prevalence was found for early whole-brain or temporal cortex mapping by Penfield and colleagues (0.1% 1.8%;…”
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The buildup of an urge in obsessive–compulsive disorder: Behavioral and neuroimaging correlates
Stern, E. R., Brown, C., Ludlow, M., Shahab, R., Collins, K., Lieval, A., Tobe, R. H., Iosifescu, D. V., Burdick, K. E., & Fleysher, L. (2020) · Human Brain Mapping · doi:10.1002/hbm.24898 · Cited by 29 · see citing works
- Authors
- Isnard, J., Guénot, M., Sindou, M., & Mauguière, F.
- Affiliations
- Hospices Civils de Lyon (FR)
- Venue
- Epilepsia
- Publisher
- Wiley
- Published
- 2004-08-24
- Volume
- 45
- Issue
- 9
- Pages
- 1079-1090
- ISSN
- 0013-9580 (ISSN-L)
- 1528-1167
- OpenAlex
- W2052579703
- Cited by
- 504
- References
- 49
- Citations by year
- 2026: 14 · 2025: 17 · 2024: 20 · 2023: 33 · 2022: 30 · 2021: 24 · 2020: 27 · 2019: 37 · 2018: 25 · 2017: 41 · 2016: 26 · 2015: 23 · 2014: 14 · 2013: 25 · 2012: 28
- FWCI
- 7.87
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Epilepsia (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Life Sciences › Neuroscience › Cognitive Neuroscience › EEG and Brain-Computer Interfaces
- Keywords
- temporal lobe epilepsy, stereoelectroencephalography, seizure onset zone, direct cortical stimulation, insula, complex partial seizures, dysarthric speech, laryngeal constriction, preoperative assessment, epilepsy surgery
- MeSH terms
- Adult, Brain Mapping, Cerebral Cortex, Diagnosis, Differential, Electric Stimulation, Electrodes, Implanted, Electroencephalography, Epilepsy, Temporal Lobe, Female, Humans, Magnetic Resonance Imaging, Male, Monitoring, Physiologic, Neural Pathways, Preoperative Care, Seizures, Stereotaxic Techniques, Temporal Lobe, Video Recording, Treatment Outcome, Epilepsy, Rolandic
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