Abstract
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Highlights
Highlights
● Cognitive, emotional and behavioral disorders may be induced by traumatic brain injury with all degrees of severity, and can cause them to interact with each other.
● Results showed the abnormality of the default mode network either within the network or between it, and other neural networks for a majority of cognitive, emotional and sleep disorders after traumatic brain injury.
● Traumatic brain injury-induced imbalance in neural circuits may serve as diagnostic and prognostic biomarkers of deficits after traumatic brain injury.
Plain Language Summary
Neuropsychological and neuropsychiatric deficits such as cognitive, verbal, emotional, and mental disorders may be caused Traumatic Brain Injury (TBI) under all severity levels. The most common patterns of these disorders include amnesia, executive dysfunction, verbal and nonverbal communication impairment at the pragmatic level of language, aggression, depression, different types of anxiety especially post-traumatic stress disorder, and sleep-wake cycle disorders. These deficits usually interact with each other. Various variables including age, sex, severity of injury, duration of post-traumatic amnesia, pre-injury cognitive and psychological functions, medical history, hormonal and chemical functions of brain, and genetic background may be accounted as the risk factors for development and persistence of post-TBI neuropsychological and neurological symptoms. One of the research areas in TBI is the identification of the pathogenesis of neuropsychological and neuropsychiatric deficits after TBI. Nowadays, neural circuits underlying the pathogenesis of these deficits have been partially identified using brain mapping techniques. It seems that anomalies in the neural circuits connecting the frontal lobe of brain and subcortical areas including thalamus and the basal ganglia play an important role in the development of antisocial behaviors, executive dysfunctions, and emotional deficits following TBI. Evidence-based metabolic, structural, and functional neural circuitry abnormalities, characterized by neural mapping techniques, may be useful as diagnostic, prognostic and therapeutic biomarkers, and guide clinicians in circuit-based neurotherapy.