Literature DB >> 34245005

Acute thalamic damage as a prognostic biomarker for post-traumatic epileptogenesis.

Eppu Manninen1, Karthik Chary1, Niina Lapinlampi1, Pedro Andrade1, Tomi Paananen1, Alejandra Sierra1, Jussi Tohka1, Olli Gröhn1, Asla Pitkänen1.   

Abstract

OBJECTIVE: To identify magnetic resonance imaging (MRI) biomarkers for post-traumatic epilepsy.
METHODS: The EPITARGET (Targets and biomarkers for antiepileptogenesis, epitarget.eu) animal cohort completing T2 relaxation and diffusion tensor MRI follow-up and 1-month-long video-electroencephalography monitoring included 98 male Sprague-Dawley rats with traumatic brain injury and 18 controls. T2 imaging was performed on day (D) 2, D7, and D21 and diffusion tensor imaging (DTI) on D7 and D21 using a 7-Tesla Bruker PharmaScan MRI scanner. The mean and standard deviation (SD) of the T2 relaxation rate, multiple diffusivity measures, and diffusion anisotropy at each time-point within the ventroposterolateral and ventroposteromedial thalamus were used as predictor variables in multi-variable logistic regression models to distinguish rats with and without epilepsy.
RESULTS: Twenty-nine percent (28/98) of the rats with traumatic brain injury (TBI) developed epilepsy. The best-performing logistic regression model utilized the D2 and D7 T2 relaxation time as well as the D7 diffusion tensor data. The model distinguished rats with and without epilepsy (Bonferroni-corrected p-value < .001) with a cross-validated concordance statistic of 0.74 (95% confidence interval [CI] 0.60-0.84). In a cross-validated classification test, the model exhibited 54% sensitivity and 91% specificity, enriching the epilepsy rate within the study population from the expected 29% to 71%. A model using the D2 T2 data only resulted in a 73% enriched epilepsy rate (regression p-value .007, cross-validated concordance 0.70, 95% CI 0.56-0.80, sensitivity 29%, specificity 96%). SIGNIFICANCE: An MRI parameter set reporting on acute and subacute neuropathologic changes common to experimental and human TBI presents a diagnostic biomarker for post-traumatic epileptogenesis. Significant enrichment of the study population was achieved even when using a single time-point measurement, producing an expected epilepsy rate of 73%.
© 2021 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

Entities:  

Keywords:  EEG; MRI; epilepsy; traumatic brain injury

Mesh:

Substances:

Year:  2021        PMID: 34245005     DOI: 10.1111/epi.16986

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  4 in total

1.  Secondary thalamic neuroinflammation after focal cortical stroke and traumatic injury mirrors corticothalamic functional connectivity.

Authors:  Deanna Necula; Frances S Cho; Andrea He; Jeanne T Paz
Journal:  J Comp Neurol       Date:  2021-11-01       Impact factor: 3.215

2.  Enhancing GAT-3 in thalamic astrocytes promotes resilience to brain injury in rodents.

Authors:  Frances S Cho; Ilia D Vainchtein; Yuliya Voskobiynyk; Allison R Morningstar; Francisco Aparicio; Bryan Higashikubo; Agnieszka Ciesielska; Diede W M Broekaart; Jasper J Anink; Erwin A van Vliet; Xinzhu Yu; Baljit S Khakh; Eleonora Aronica; Anna V Molofsky; Jeanne T Paz
Journal:  Sci Transl Med       Date:  2022-07-06       Impact factor: 19.319

Review 3.  Novel Approaches to Prevent Epileptogenesis After Traumatic Brain Injury.

Authors:  Chris G Dulla; Asla Pitkänen
Journal:  Neurotherapeutics       Date:  2021-09-30       Impact factor: 6.088

4.  Hippocampal position and orientation as prognostic biomarkers for posttraumatic epileptogenesis: An experimental study in a rat lateral fluid percussion model.

Authors:  Riccardo De Feo; Eppu Manninen; Karthik Chary; Elina Hämäläinen; Riikka Immonen; Pedro Andrade; Xavier Ekolle Ndode-Ekane; Olli Gröhn; Asla Pitkänen; Jussi Tohka
Journal:  Epilepsia       Date:  2022-05-12       Impact factor: 6.740

  4 in total

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