Literature DB >> 31345959

Hippocampal morphometry in sudden and unexpected death in epilepsy.

Alyma Somani1, Anita-Beatrix Zborovschi1, Yan Liu1, Smriti Patodia1, Zuzanna Michalak1, Sanjay M Sisodiya1, Maria Thom2.   

Abstract

OBJECTIVE: To determine hippocampal morphometric measures, including granule cell dispersion and features of malrotation, as potential biomarkers for sudden unexpected death in epilepsy (SUDEP) from an archival postmortem series.
METHODS: In a retrospective study of 187 archival postmortems from 3 groups, SUDEP (68; 14 with hippocampal sclerosis [HS]), non-SUDEP epilepsy controls (EP-C = 66; 25 with HS), and nonepilepsy controls (NEC = 53), Nissl/hematoxylin & eosin-stained sections from left and right hippocampus from 5 coronal levels were digitized. Image analysis was carried out for granule cell layer (GCL) thickness and measurements of hippocampal dimensions (HD) for shape (width [HD1], height [HD2]) and medial hippocampal positioning in relation to the parahippocampal gyrus (PHG) length (HD3). A qualitative evaluation of hippocampal malrotational (HMAL) features, dentate gyrus invaginations (DGI), and subicular/CA1 folds (SCF) was also made.
RESULTS: GCL thickness was increased in HS more than those without (p < 0.001). In non-HS cases, increased GCL thickness was noted in EP-C compared to NEC (p < 0.05) but not between SUDEP and NEC. There was no difference in the frequency of DGI, SCF, measurements of hippocampal shape (HD1, HD2, or ratio), or medial positioning among SUDEP, EP-C, and NEC groups, when factoring in HS, coronal level, and age at death. Comparison between left and right sides within cases showed greater PHG lengths (HD3) on the right side in the SUDEP group only (p = 0.018).
CONCLUSIONS: No hippocampal morphometric features were identified in support of either excessive granule cell dispersion or features of HMAL as definitive biomarkers for SUDEP. Asymmetries in PHG measurements in SUDEP warrant further investigation as they may indicate abnormal central autonomic networks.
© 2019 American Academy of Neurology.

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Year:  2019        PMID: 31345959      PMCID: PMC6711661          DOI: 10.1212/WNL.0000000000007969

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  33 in total

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Journal:  AJNR Am J Neuroradiol       Date:  2016-09-15       Impact factor: 3.825

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Review 3.  Review: The past, present and future challenges in epilepsy-related and sudden deaths and biobanking.

Authors:  M Thom; M Boldrini; E Bundock; M N Sheppard; O Devinsky
Journal:  Neuropathol Appl Neurobiol       Date:  2018-02       Impact factor: 8.090

4.  Hippocampal malformation associated with sudden death in early childhood: a neuropathologic study: Part 2 of the investigations of The San Diego SUDC Research Project.

Authors:  Marco M Hefti; Jane B Cryan; Elisabeth A Haas; Amy E Chadwick; Laura A Crandall; Felicia L Trachtenberg; Dawna D Armstrong; Marjorie Grafe; Henry F Krous; Hannah C Kinney
Journal:  Forensic Sci Med Pathol       Date:  2016-01-19       Impact factor: 2.007

Review 5.  Unifying the definitions of sudden unexpected death in epilepsy.

Authors:  Lina Nashef; Elson L So; Philippe Ryvlin; Torbjörn Tomson
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Review 6.  Sudden unexpected death in epilepsy: epidemiology, mechanisms, and prevention.

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8.  International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: a Task Force report from the ILAE Commission on Diagnostic Methods.

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10.  Hippocampal-Brainstem Connectivity Associated with Vagal Modulation after an Intense Exercise Intervention in Healthy Men.

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  3 in total

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Journal:  Auton Neurosci       Date:  2021-07-31       Impact factor: 3.145

2.  Hippocampal granule cell dispersion: a non-specific finding in pediatric patients with no history of seizures.

Authors:  Achira Roy; Kathleen J Millen; Raj P Kapur
Journal:  Acta Neuropathol Commun       Date:  2020-04-21       Impact factor: 7.801

Review 3.  Sudden Unexplained Death in Childhood: A Neuropathology Review.

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  3 in total

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