Detailed Information on Publication Record
2018
Hippocampal involvement in nonpathological deja vu: Subfield vulnerability rather than temporal lobe epilepsy equivalent
PEŠLOVÁ, Eva, Radek MAREČEK, Daniel Joel SHAW, Tomáš KAŠPÁREK, Martin PAIL et. al.Basic information
Original name
Hippocampal involvement in nonpathological deja vu: Subfield vulnerability rather than temporal lobe epilepsy equivalent
Authors
PEŠLOVÁ, Eva (203 Czech Republic, belonging to the institution), Radek MAREČEK (203 Czech Republic, belonging to the institution), Daniel Joel SHAW (826 United Kingdom of Great Britain and Northern Ireland, belonging to the institution), Tomáš KAŠPÁREK (203 Czech Republic, belonging to the institution), Martin PAIL (203 Czech Republic, belonging to the institution) and Milan BRÁZDIL (203 Czech Republic, guarantor, belonging to the institution)
Edition
Brain and Behavior, Hoboken, Wiley, 2018, 2162-3279
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30103 Neurosciences
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.072
RIV identification code
RIV/00216224:14110/18:00105516
Organization unit
Faculty of Medicine
UT WoS
000438495400021
Keywords in English
deja vu; hippocampal subfields; hippocampal vulnerability; mesial temporal lobe epilepsy; schizophrenia
Tags
International impact, Reviewed
Změněno: 4/3/2019 15:56, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Introduction: Morphological correlates of nonpathological deja vu (DV) have been identified recently within the human brain. Significantly reduced gray matter volume (GMV) within a set of cortical and subcortical regions reported in subjects experiencing DV seems to mirror the distribution of GMV reduction in mesial temporal lobe epilepsy (MTLE) patients but vary in terms of the hippocampus. Another condition associated with hippocampal GMV reduction and DV alike disturbance in memory processing is schizophrenia (SCH). Here, we tested the hypothesis that hippocampal involvement in nonpathological DV resembles more closely the pattern of GMV decrease observed in MTLE compared with that occurring in SCH. Methods: Using automated segmentation of the MRI data we compared the medians of GMV within 12 specific hippocampal subfields in healthy individuals that do (DV+; N = 87) and do not report deja vu experience (DV-; N = 26), and patients with MTLE (N = 47) and SCH (N = 29). By Pearson correlation, we then evaluated the similarity of MTLE and SCH groups to DV+ group with respect to spatial distribution of GMV deviation from DV- group. Results: Significant GMV decrease was found in MTLE group in most of the subfields. There were just trends in the hippocampal GMV decrease found in DV+ or SCH groups. Concerning the spatial distribution of GMV decrease, we revealed statistically significant correlation for the left hippocampus for SCH vs DV+, Otherwise there was no statistically significant correlation. Conclusions: Our findings reveal structural features of hippocampal involvement in nonpathological DV, MTLE, and SCH. Despite our expectations, the pattern of GMV reduction in the DV+ relative to the DV- group does not resemble the pattern observed in MTLE any more than that observed in SCH. The highly similar patterns of the three clinical groups rather suggest an increased vulnerability of certain hippocampal subfields; namely, Cornu Ammonis (CA)4, CA3, dentate gyrus granular cell layer (GC-DG), hippocampal-amygdaloid transition area (HATA) and subiculum.
Links
LM2015062, research and development project |
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LQ1601, research and development project |
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