Damage in thalamic projection to perilesional cortex as a prognostic biomarker for experimental post-traumatic epilepsy

丘脑投射至病灶周围皮层的损伤作为实验性创伤后癫痫的预后生物标志物

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Abstract

OBJECTIVE: To test a hypothesis that a lesion in the optic tract, a thalamocortical pathway projecting from the thalamus to the perilesional cortex, is a prognostic biomarker for the development of post-traumatic epilepsy (PTE). METHODS: A lateral fluid-percussion injury (FPI)-induced traumatic brain injury (TBI) was induced in adult male Sprague-Dawley rats. The development of PTE was assessed from 1-month-long video-electroencephalography (EEG) data acquired during the seventh post-injury month. Diffusion magnetic resonance imaging (MRI) tractography of the optic radiation was performed using data acquired at 9 days and at 5 months post-injury. The optic tract in each hemisphere was divided into segments, and tract and diffusion tensor-based metrics were obtained for use as predictor variables (a total of 451 predictors). In the training cohort, including 17 TBI rats with (TBI+) and 66 without epilepsy (TBI-) at 9 days and 18 TBI+ and 69 TBI- rats at 5 months, 20 predictor variables with the highest effect sizes (Cohen's delta) were selected. These variables were used with elastic net-regularized logistic regression to model the development of PTE. The predictor variables chosen in the training cohort were also used for model fitting in a separate validation cohort (8 TBI+ and 23 TBI- at 9 days; 9 TBI+ and 23 TBI- at 5 months). RESULTS: In the training cohort, the fitted models explained the development of PTE with (cross-validated) areas under the receiver-operating characteristic (ROC) curve (AUC) of 0.74 (p = .003) at 9 days and 0.76 (p < .001) at 5 months post-TBI. Models fitted in the validation cohort achieved AUC values of 0.50 (p = 1) at 9 days and 0.77 (p = .03) at 5 months post-TBI. SIGNIFICANCE: Our data show that white matter pathology is involved in post-traumatic epileptogenesis after lateral FPI. Moreover, imaging of thalamocortical pathway(s) to perilesional cortex could identify translational prognostic biomarkers for post-traumatic epileptogenesis.

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