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ABSTRACT: Background
There is high variability in post-stroke aphasia severity and predicting recovery remains imprecise. Standard prognostics do not include neurophysiological indicators or genetic biomarkers of neuroplasticity, which may be critical sources of variability.Objective
To evaluate whether a common polymorphism (Val66Met) in the gene for brain-derived neurotrophic factor (BDNF) contributes to variability in post-stroke aphasia, and to assess whether BDNF polymorphism interacts with neurophysiological indicators of neuroplasticity (cortical excitability and stimulation-induced neuroplasticity) to improve estimates of aphasia severity.Methods
Saliva samples and motor-evoked potentials (MEPs) were collected from participants with chronic aphasia subseque
SUBMITTER: Dresang HC
PROVIDER: S-EPMC9133188 | biostudies-literature | 2022 Jun
REPOSITORIES: biostudies-literature