Leukocyte expression profiles reveal gene sets with prognostic value for seizure-free outcome following stereotactic laser amygdalohippocampotomy.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
31 01 2019
Historique:
received: 25 07 2018
accepted: 13 12 2018
entrez: 2 2 2019
pubmed: 2 2 2019
medline: 15 9 2020
Statut: epublish

Résumé

Among patients with intractable epilepsy, the most commonly performed surgical procedure is craniotomy for amygdalohippocampectomy (AH). Stereotactic laser amygdalohippocampotomy (SLAH) has also been recently employed as a minimally invasive treatment for intractable temporal lobe epilepsy (TLE). Among patients treated with AH and SLAH approximately 65% and 54% of patients become seizure-free, respectively. Therefore, selection criteria for surgical candidates with improved prognostic value for post-operative seizure-free outcome are greatly needed. In this study, we perform RNA sequencing (RNA-Seq) on whole blood leukocyte samples taken from 16 patients with intractable TLE prior to SLAH to test the hypothesis that pre-operative leukocyte RNA expression profiles are prognostic for post-operative seizure outcome. Multidimensional scaling analysis of the RNA expression data indicated separate clustering of patients with seizure free (SF) and non-seizure-free (NSF) outcomes. Differential expression (DE) analysis performed on SF versus NSF groups revealed 24 significantly differentially expressed genes (≥2.0-fold change, p-value < 0.05, FDR <0.05). Network and pathway analyses identified differential activation of pathways involved in lipid metabolism, morphology of oligodendrocytes, inflammatory response, and development of astrocytes. These results suggest that pre-operative leukocyte expression profiles have prognostic value for seizure outcome following SLAH.

Identifiants

pubmed: 30705324
doi: 10.1038/s41598-018-37763-5
pii: 10.1038/s41598-018-37763-5
pmc: PMC6355811
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1086

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH065151
Pays : United States

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Auteurs

Ryan Sprissler (R)

Center for Applied Genetics and Genomic Medicine, University of Arizona, Tucson, AZ, 85721, USA.
Arizona Research Labs Division of Biotechnology, University of Arizona, Tucson, AZ, 85721, USA.

Robert Bina (R)

Division of Neurosurgery, Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

Willard Kasoff (W)

Division of Neurosurgery, Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

Marlys H Witte (MH)

Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

Michael Bernas (M)

Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.
University of North Texas Health Science Center, Fort Worth, TX, 76107, USA.

Christina Walter (C)

Division of Neurosurgery, Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

David M Labiner (DM)

Department of Neurology, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

Branden Lau (B)

Arizona Research Labs Division of Biotechnology, University of Arizona, Tucson, AZ, 85721, USA.

Michael F Hammer (MF)

Center for Applied Genetics and Genomic Medicine, University of Arizona, Tucson, AZ, 85721, USA. mfh@email.arizona.edu.
Department of Neurology, University of Arizona College of Medicine, Tucson, AZ, 85724, USA. mfh@email.arizona.edu.

Martin E Weinand (ME)

Division of Neurosurgery, Department of Surgery, University of Arizona College of Medicine, Tucson, AZ, 85724, USA.

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