Reduced left amygdala volume in patients with dissociative seizures (psychogenic nonepileptic seizures)
Open accessAbstract
Purpose This study specifically investigated differences of amygdalar and hippocampal volumes between patients with dissociative seizures (DS), mesial temporal lobe sclerosis (MTS), and normal controls (NC).Methods Between 2003 and 2018, 127 patients diagnosed with DS and 278 with MTS were recruited. An additional 52 NC subjects were recruited between 2015 and 2018. We retrospectively selected 29 patients with DS (male:female, 6:23) with absence of structural confounding factors and obtained sex- and age-matched MTS and NC. We used Neuroreader to assess the volume of the amygdala and hippocampus as a percentage of total intracranial volume based on thin-slice (0.9-1.2 mm) T1-weighted images. Statistical analyses controlled for psychiatric comorbidity and logistic regression were used to evaluate efficacy of these values for individual-level diagnosis.Results The left amygdala and right hippocampus were significantly smaller in DS compared to NC (both p = 0.04), which was not explained by differences in psychiatric comorbidity. When controlling for ipsilateral hippocampal or amygdala volume, which was seen equally in all groups (Spearman, p < 0.02), these differences were no longer significant (amygdala, p = 0.16, hippocampus, p = 0.18), suggesting that amygdalar and hippocampal atrophy may reflect network or regional changes rather than focal abnormalities. The three-way accuracy for differentiating DS, MTS, and NC using these data was 64 % (95 % confidence interval: 54-74 %).Conclusion Volumetric analysis demonstrates smaller left amygdalar and right hippocampal volumes in patients with DS compared to NC, which may mirror abnormalities in functional networks seen in conversion disorders and post-traumatic stress disorder.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Contributions from sensorimotor, emotion regulation, cognitive control, and multimodal integration brain systems to FS neuropathophysiology have been identified and constitute potential targets for treatment.
“The neuropathophysiology of FS is still uncertain, but contributions from sensorimotor, 1,2 emotion regulation, 2,3 cognitive control, 4 and multimodal integration brain systems have been identified, and constitute potential targets for treatment.”
From White Matter Changes after Neurobehavioral Therapy for Functional Seizures (2023) · cites this paper as [3]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
STRESS AND HIPPOCAMPAL PLASTICITY
McEwen, B. S. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.105 · Cited by 2,087 · see citing works
Glucocorticoids and Hippocampal Atrophy in Neuropsychiatric Disorders
Sapolsky, R. M. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.10.925 · Cited by 2,016 · see citing works
Vyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06810.2002 · Cited by 1,662 · see citing works
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.7.973 · Cited by 1,610 · see citing works
Hippocampal volume and depression: a meta-analysis of MRI studies
Videbech, P., & Ravnkilde, B. (2004) · American Journal of Psychiatry · doi:10.1176/appi.ajp.161.11.1957 · Cited by 1,590 · see citing works
LaFrance, W. C., Baker, G. A., Duncan, R., Goldstein, L. H., & Reuber, M. (2013) · Epilepsia · doi:10.1111/epi.12356 · Cited by 856 · see citing works
Bremner, J. D., Vythilingam, M., Vermetten, E. H. G. J. M., Southwick, S. M., McGlashan, T. H., Nazeer, A., Khan, S., Vaccarino, V., Soufer, R., Garg, P. K., et al. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.5.924 · Cited by 721 · see citing works
Stress duration modulates the spatiotemporal patterns of spine formation in the basolateral amygdala
Mitra, R., Jadhav, S., McEwen, B. S., Vyas, A., & Chattarji, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504011102 · Cited by 663 · see citing works
Brain Magnetic Resonance Imaging of Structural Abnormalities in Bipolar Disorder
Strakowski, S. M., DelBello, M. P., Sax, K. W., Zimmerman, M. E., Shear, P. K., Hawkins, J. M., & Larson, E. R. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.3.254 · Cited by 619 · see citing works
Bernasconi, N. (2003) · Brain · doi:10.1093/brain/awg034 · Cited by 481 · see citing works
Longitudinal MRI Study of Hippocampal Volume in Trauma Survivors With PTSD
Bonne, O. B., Brandes, D., Gilboa, A., Gomori, J. M., Shenton, M. E., Pitman, R. K., & Shalev, A. Y. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.8.1248 · Cited by 430 · see citing works
Amygdala and Hippocampal Volumes in Adolescents and Adults With Bipolar Disorder
Blumberg, H. P., Kaufman, J., Martin, A., Whiteman, R. C., Zhang, J. H., Gore, J. C., Charney, D. S., Krystal, J. H., & Peterson, B. S. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.12.1201 · Cited by 396 · see citing works
An MRI study of temporal lobe structures in men with bipolar disorder or schizophrenia
Altshuler, L. L., Bartzokis, G., Grieder, T., Curran, J., Jimenez, T., Leight, K., Wilkins, J., Gerner, R., & Mintz, J. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00836-2 · Cited by 369 · see citing works
Neighborhood matters: divergent patterns of stress-induced plasticity across the brain
Chattarji, S., Tomar, A., Suvrathan, A., Ghosh, S., & Rahman, M. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4115 · Cited by 248 · see citing works
Outcome After Diagnosis of Psychogenic Nonepileptic Seizures
Walczak, T. S., Papacostas, S., Williams, D. T., Scheuer, M. L., Lebowitz, N., & Notarfrancesco, A. (1995) · Epilepsia · doi:10.1111/j.1528-1157.1995.tb00472.x · Cited by 194 · see citing works
Neuroanatomic correlates of psychogenic nonepileptic seizures: A cortical thickness and VBM study
Labate, A., Cerasa, A., Mula, M., Mumoli, L., Gioia, M. C., Aguglia, U., Quattrone, A., & Gambardella, A. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2011.03347.x · Cited by 171 · see citing works
Stress and hippocampal abnormalities in psychiatric disorders
Sala, M. (2004) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2003.12.005 · Cited by 169 · see citing works
Amygdala astrocyte reduction in subjects with major depressive disorder but not bipolar disorder
Altshuler, L. L., Abulseoud, O. A., Foland‐Ross, L. C., Bartzokis, G., Chang, S., Mintz, J., Hellemann, G., & Vinters, H. V. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2010.00838.x · Cited by 167 · see citing works
Long-Term Occupational Stress Is Associated with Regional Reductions in Brain Tissue Volumes
Blix, E., Perski, A., Berglund, H., & Savic, I. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064065 · Cited by 150 · see citing works
Self-citationWeniger, G., Lange, C., Sachsse, U., & Irle, E. (2008) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2008.01246.x · Cited by 140 · see citing works
Rogers, M. A., Yamasue, H., Abe, O., Yamada, H., Ohtani, T., Iwanami, A., Aoki, S., Kato, N., & Kasai, K. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.06.001 · Cited by 138 · see citing works
Psychogenic Nonepileptic Seizures
Tatum, W. O. (2013) · Springer eBooks · doi:10.1007/978-3-319-01366-4_29 · Cited by 114 · see citing works
The left amygdala knows fear: laterality in the amygdala response to fearful eyes
Hardee, J. E., Thompson, J. C., & Puce, A. (2008) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsn001 · Cited by 112 · see citing works
The As and Ds of stress: Metabolic, morphological and behavioral consequences
Reagan, L. P., Grillo, C. A., & Piroli, G. G. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.02.050 · Cited by 111 · see citing works
Abnormal functional connectivity density in psychogenic non-epileptic seizures
Ding, J., An, D., Liao, W., Wu, G., Xu, Q., Zhou, D., & Chen, H. (2014) · Epilepsy Research · doi:10.1016/j.eplepsyres.2014.05.006 · Cited by 101 · see citing works
Neuroimaging studies in patients with psychogenic non-epileptic seizures: A systematic meta-review
McSweeney, M., Reuber, M., & Levita, L. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.07.025 · Cited by 96 · see citing works
Comparison of Automated Brain Volume Measures obtained with NeuroQuant® and FreeSurfer
Ochs, A. L., Ross, D. E., Zannoni, M. D., Abildskov, T. J., & Bigler, E. D. (2015) · Journal of Neuroimaging · doi:10.1111/jon.12229 · Cited by 88 · see citing works
Psychogenic nonepileptic seizures: A current overview
Dickinson, P., & Looper, K. J. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03606.x · Cited by 85 · see citing works
Symptom-specific amygdala hyperactivity modulates motor control network in conversion disorder
Hassa, T., Sebastian, A., Liepert, J., Weiller, C., Schmidt, R., & Tüscher, O. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.04.004 · Cited by 79 · see citing works
Is hippocampal atrophy a future drug target?
Dhikav, V., & Anand, K. S. (2007) · Medical Hypotheses · doi:10.1016/j.mehy.2006.09.040 · Cited by 63 · see citing works
Tanpitukpongse, T. P., Mazurowski, M. A., Ikhena, J., & Petrella, J. R. (2017) · American Journal of Neuroradiology · doi:10.3174/ajnr.a5061 · Cited by 62 · see citing works
Quantitative Neuroimaging Software for Clinical Assessment of Hippocampal Volumes on MR Imaging
Ahdidan, J., Raji, C. A., DeYoe, E. A., Mathis, J. R., Noe, K. Ø., Rimestad, J., Kjeldsen, T. K., Mosegaard, J., Becker, J. T., & López, O. L. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150559 · Cited by 53 · see citing works
Naskar, S., & Chattarji, S. (2019) · eNeuro · doi:10.1523/eneuro.0338-18.2019 · Cited by 52 · see citing works
Isolated amygdala enlargement in temporal lobe epilepsy: A systematic review
Beh, S. M. J., Cook, M. J., & D'Souza, W. J. (2016) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2016.04.015 · Cited by 48 · see citing works
Minami, N., Morino, M., Uda, T., Komori, T., Nakata, Y., Arai, N., Kohmura, E., & Nakano, I. (2014) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2014-308383 · Cited by 46 · see citing works
Kim, D. W., Lee, S. K., Chung, C. K., Koh, Y.-C., Choe, G., & Lim, S. D. (2012) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2011.05.042 · Cited by 41 · see citing works
Coan, A. C., Morita, M. E., de Campos, B. M., Bergo, F. P. G., Kubota, B. Y., & Cendes, F. (2013) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2013.08.022 · Cited by 40 · see citing works
Vasta, R., Cerasa, A., Sarica, A., Bartolini, E., Martino, I., Mari, F., Metitieri, T. T., Quattrone, A., Gambardella, A., Guerrini, R., et al. (2018) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2018.09.008 · Cited by 38 · see citing works
Amygdala enlargement: Temporal lobe epilepsy subtype or nonspecific finding?
Reyes, A., Thesen, T., Kuzniecky, R., Devinsky, O., McDonald, C. R., Jackson, G. D., Vaughan, D. N., & Blackmon, K. (2017) · Epilepsy Research · doi:10.1016/j.eplepsyres.2017.02.019 · Cited by 36 · see citing works
An Overview of Psychogenic Non-Epileptic Seizures: Etiology, Diagnosis and Management
Milán-Tomás, Á., Persyko, M., del Campo, M., Shapiro, C. M., & Farcnik, K. D. (2018) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/cjn.2017.283 · Cited by 32 · see citing works
Psychogenic non‐epileptic seizures
Doss, R. C., & LaFrance, W. C., Jr. (2016) · Epileptic Disorders · doi:10.1684/epd.2016.0873 · Cited by 31 · see citing works
Reliability of reported peri-ictal behavior to identify psychogenic nonepileptic seizures
Kerr, W. T., Chau, A. M., Janio, E. A., Braesch, C. T., Le, J. M., Hori, J. M., Patel, A. B., Gallardo, N. L., Bauirjan, J., Allas, C. H., et al. (2019) · Seizure · doi:10.1016/j.seizure.2019.02.021 · Cited by 28 · see citing works
Self-citationBrain structure abnormalities in young women who presented conduct disorder in childhood/adolescence
Budhiraja, M., Savic, I., Lindner, P., Jokinen, J., Tiihonen, J., & Hodgins, S. (2017) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-017-0519-7 · Cited by 23 · see citing works
Self-citationMettenburg, J., Branstetter, B. F., Wiley, C. A., Lee, P., & Richardson, R. M. (2019) · American Journal of Neuroradiology · doi:10.3174/ajnr.a5966 · Cited by 21 · see citing works
Psychogenic nonepileptic seizures.
Gillig, P. M. (2013) · Europe PMC (PubMed Central) · Cited by 21 · see citing works
Sone, D., Ota, M., Maikusa, N., Kimura, Y., Sumida, K., Yokoyama, K., Imabayashi, E., Watanabe, M., Watanabe, Y., Okazaki, M., et al. (2016) · Epilepsy Research · doi:10.1016/j.eplepsyres.2016.09.011 · Cited by 13 · see citing works
Psychogenic Nonepileptic Seizures
(2012) · SpringerReference · doi:10.1007/springerreference_183375 · Cited by 4 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Objective score from initial interview identifies patients with probable dissociative seizures
Kerr, W. T., Janio, E. A., Chau, A. M., Braesch, C. T., Le, J. M., Hori, J. M., Patel, A. B., Gallardo, N. L., Allas, C. H., Karimi, A. H., et al. (2020) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2020.107525 · Cited by 34 · see citing works
Self-citationPredictive Processing and the Pathophysiology of Functional Neurological Disorder
Jungilligens, J., & Perez, D. L. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_473 · Cited by 34 · see citing works
Structural neuroimaging of somatoform disorders: A systematic review
Rossetti, M. G., Delvecchio, G., Calati, R., Perlini, C., Bellani, M., & Brambilla, P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.017 · Cited by 29 · see citing works
Jungilligens, J., Popkirov, S., Perez, D. L., & Diez, I. P. (2022) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2022.111533 · Cited by 22 · see citing works
Yearley, A. G., Goedmakers, C. M. W., Panahi, A., Doucette, J. A., Rana, A., Ranganathan, K., & Smith, T. R. (2023) · Artificial Intelligence in Medicine · doi:10.1016/j.artmed.2023.102607 · Cited by 21 · see citing works
White Matter Changes after Neurobehavioral Therapy for Functional Seizures
Mueller, C., Goodman, A. M., Allendorfer, J. B., Nenert, R., Gaston, T. E., Grayson, L. E., Correia, S., Philip, N. S., LaFrance, W. C., & Szaflarski, J. P. (2023) · Annals of Neurology · doi:10.1002/ana.26665 · Cited by 19 · see citing works
Kerr, W. T., Tatekawa, H., Lee, J. K., Karimi, A. H., Sreenivasan, S. S., O’Neill, J., Smith, J. M., Hickman, L. B., Savic, I., Nasrullah, N., et al. (2022) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2022.108858 · Cited by 18 · see citing works
Self-citationHassan, J., Taïb, S., & Yrondi, A. (2024) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2024.109654 · Cited by 13 · see citing works
A minority of patients with functional seizures have abnormalities on neuroimaging
Kerr, W. T., Lee, J. K., Karimi, A. H., Tatekawa, H., Hickman, L. B., Connerney, M. A., Sreenivasan, S. S., Dubey, I., Allas, C. H., Smith, J. M., et al. (2021) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2021.117548 · Cited by 12 · see citing works
Self-citationEpilepsy, dissociative seizures, and mixed: Associations with time to video-EEG
Kerr, W. T., Zhang, X., Hill, C. E., Janio, E. A., Chau, A. M., Braesch, C. T., Le, J. M., Hori, J. M., Patel, A. B., Allas, C. H., et al. (2021) · Seizure · doi:10.1016/j.seizure.2021.02.002 · Cited by 9 · see citing works
Self-citationFusunyan, M. A., Medina, M., Giambarberi, L., & Bajestan, S. N. (2024) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.20230060 · Cited by 8 · see citing works
Coebergh, J. A., Habib, S., Teodoro, T., Edwards, M. J., & Butler, M. (2024) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.20220182 · Cited by 9 · see citing works
Amygdala subfield and prefrontal cortex abnormalities in patients with functional seizures
Nasrullah, N., Kerr, W. T., Stern, J. M., Wang, Y., Tatekawa, H., Lee, J. K., Karimi, A. H., Sreenivasan, S. S., Engel, J., Eliashiv, D. E., et al. (2023) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2023.109278 · Cited by 6 · see citing works
Self-citationBiomarkers and Rehabilitation for Functional Neurological Disorder
Mark, V. W. (2024) · Journal of Personalized Medicine · doi:10.3390/jpm14090948 · Cited by 5 · see citing works
Are Functional (Psychogenic Nonepileptic) Seizures the Sole Expression of Psychological Processes?
Sojka, P., Paredes-Echeverri, S., & Perez, D. L. (2021) · Current topics in behavioral neurosciences · doi:10.1007/7854_2021_225 · Cited by 5 · see citing works
Bao, Y., Zhang, X., Fei, X., Yu, X., Tang, M., & Sun, C. (2025) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000011954 · Cited by 4 · see citing works
Neuroimaging abnormalities in functional/dissociative seizures: a meta-analysis
Homayoun, M., Lo, A. P.-K., Sinclair, B., Nazem-Zadeh, M.-R., Neal, A. J., Winton‐Brown, T., Kwan, P., & Kanaan, R. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106439 · Cited by 4 · see citing works
Lanzillotti, A. I., Sarudiansky, M., Scévola, L., Oddo, S. A., Korman, G. P., & D’Alessio, L. (2024) · Actas Españolas de Psiquiatría · doi:10.62641/aep.v52i5.1707 · Cited by 4 · see citing works
Amygdala Grey Matter Volume and Face Activation Compared to Social Network Size
Gfroerer, G. L., McGugin, R. W., Roche, A., & Gauthier, L. (2023) · Vanderbilt Undergraduate Research Journal · doi:10.15695/vurj.v13i1.5424
Higson, L. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1865708
Mega-Analysis of Structural Brain Imaging in Functional Neurological Disorder
Butler, M., Vignando, M., Allendorfer, J. B., Hassa, T., Horovitz, S. G., Jansen, J. F. A., Jungilligens, J., Kerr, W. T., Marapin, R. S., Premi, E., et al. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.06.031 · Cited by 1 · see citing works
Self-citationGalmiche, C., Tyvaert, L., Fauvé, P., Husson, C., Hologne, E., El‐Hage, W., Braun, M., Hingray, C., & Hossu, G. (2026) · Seizure · doi:10.1016/j.seizure.2026.08.025
- Authors
- Tatekawa, H., Kerr, W. T., Savic, I., Engel, J., & Salamon, N.
- Affiliations
- University of California, Los Angeles (US)
- Karolinska University Hospital (SE)
- Corresponding author
- Tatekawa, Hiroyuki
- Venue
- Seizure
- Publisher
- Elsevier BV
- Published
- 2020-02
- Volume
- 75
- Pages
- 43-48
- ISSN
- 1059-1311 (ISSN-L)
- OpenAlex
- W2994693917
- Cited by
- 22
- References
- 47
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 6 · 2023: 4 · 2022: 2 · 2021: 3 · 2020: 2
- FWCI
- 1.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Seizure (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (T32 GM08042)
- Vetenskapsrådet
- Society of Nuclear Medicine and Molecular Imaging
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
- Life Sciences › Neuroscience › Cognitive Neuroscience › Pain Management and Placebo Effect
- Keywords
- psychogenic non-epileptic seizures, amygdala volume, hippocampal volume, hippocampal sclerosis, brain atrophy, conversion disorder, post-traumatic stress disorder, neuroimaging diagnosis, volumetric analysis
- MeSH terms
- Adult, Amygdala, Female, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Organ Size, Psychophysiologic Disorders, Retrospective Studies, Seizures
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review