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Neuronal and astrocytic tetraploidy is increased in drug-resistant epilepsy.
Sanz-García, Ancor; Sánchez-Jiménez, Patricia; Granero-Cremades, Inmaculada; de Toledo, María; Pulido, Paloma; Navas, Marta; Frade, José María; Pereboom-Maicas, Matilde Desirée; Torres-Díaz, Cristina Virginia; Ovejero-Benito, María C.
Affiliation
  • Sanz-García A; Data Analysis Unit, Hospital Universitario de la Princesa, Instituto de Investigación Sanitaria La Princesa (IIS-IP), Madrid, Spain.
  • Sánchez-Jiménez P; Department of Clinical Pharmacology, Hospital Universitario de La Princesa, Instituto de Investigaciones Sanitarias La Princesa (IIS-IP), Madrid, Spain.
  • Granero-Cremades I; NIMGenetics Genómica y Medicina S.L., Madrid, Spain.
  • de Toledo M; Department of Clinical Analysis, Hospital Universitario de La Princesa, Madrid, Spain.
  • Pulido P; Department of Neurology, Hospital Universitario de La Princesa, Madrid, Spain.
  • Navas M; Department of Neurosurgery, Hospital Universitario de La Princesa, Madrid, Spain.
  • Frade JM; Department of Neurosurgery, Hospital Universitario de La Princesa, Madrid, Spain.
  • Pereboom-Maicas MD; Department of Molecular, Cellular and Developmental Neurobiology, Instituto Cajal, CSIC, Madrid, Spain.
  • Torres-Díaz CV; Departamento de Farmacología, Fisiología y Medicina Legal y Forense, University of Zaragoza, Zaragoza, Spain.
  • Ovejero-Benito MC; Department of Neurosurgery, Hospital Universitario de La Princesa, Madrid, Spain.
Neuropathol Appl Neurobiol ; 49(1): e12873, 2023 02.
Article in En | MEDLINE | ID: mdl-36541120
AIMS: Epilepsy is one of the most prevalent neurological diseases. A third of patients with epilepsy remain drug-resistant. The exact aetiology of drug-resistant epilepsy (DRE) is still unknown. Neuronal tetraploidy has been associated with neuropathology. The aim of this study was to assess the presence of tetraploid neurons and astrocytes in DRE. METHODS: For that purpose, cortex, hippocampus and amygdala samples were obtained from patients subjected to surgical resection of the epileptogenic zone. Post-mortem brain tissue of subjects without previous records of neurological, neurodegenerative or psychiatric diseases was used as control. RESULTS: The percentage of tetraploid cells was measured by immunostaining of neurons (NeuN) or astrocytes (S100ß) followed by flow cytometry analysis. The results were confirmed by image cytometry (ImageStream X Amnis System Cytometer) and with an alternative astrocyte biomarker (NDRG2). Statistical comparison was performed using univariate tests. A total of 22 patients and 10 controls were included. Tetraploid neurons and astrocytes were found both in healthy individuals and DRE patients in the three brain areas analysed: cortex, hippocampus and amygdala. DRE patients presented a higher number of tetraploid neurons (p = 0.020) and astrocytes (p = 0.002) in the hippocampus than controls. These results were validated by image cytometry. CONCLUSIONS: We demonstrated the presence of both tetraploid neurons and astrocytes in healthy subjects as well as increased levels of both cell populations in DRE patients. Herein, we describe for the first time the presence of tetraploid astrocytes in healthy subjects. Furthermore, these results provide new insights into epilepsy, opening new avenues for future treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Epilepsy, Temporal Lobe Limits: Humans Language: En Journal: Neuropathol Appl Neurobiol Year: 2023 Document type: Article Affiliation country: Spain Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Epilepsy, Temporal Lobe Limits: Humans Language: En Journal: Neuropathol Appl Neurobiol Year: 2023 Document type: Article Affiliation country: Spain Country of publication: United kingdom