A prospective pilot study of cognitive impairment and mood in adults with first seizure, new-onset epilepsy, and newly diagnosed epilepsy at time of initial seizure presentation

• Published in: Epilepsy & behavior 2020-11, Vol.112, p.107359-107359, Article 107359
• Main Authors: Jackson-Tarlton, Caitlin S., Whatley, Benjamin P., Kasheke, Gracious D.S., Pohlmann-Eden, Bernd, Omisade, Antonina
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Cognitive Dysfunction - complications; Cognitive Dysfunction - diagnosis; Cognitive impairment; Epilepsy - complications; Epilepsy - diagnosis; First seizure; Humans; Middle Aged; Mood; Neuropsychology; New-onset epilepsy; Newly diagnosed epilepsy; Pilot Projects; Prospective Studies; Seizures - complications; Seizures - diagnosis; Young Adult
• ISSN: 1525-5050; 1525-5069
• DOI: 10.1016/j.yebeh.2020.107359

This is an observational prospective cohort study of cognition and mood in individuals presenting to a tertiary neurology clinic with first unprovoked seizure (FS), new-onset epilepsy (NOE), and newly diagnosed epilepsy (NDE). Our aim was to understand the cognitive profile of these three diagnostic groups at the time of first presentation. Follow-up was obtained to evaluate any association between cognition at presentation and subsequent clinical course. Forty-three participants (age: 18–60 years) were recruited with FS (n = 17), NOE (n = 16), and NDE (n = 10). Clinical details, neuropsychological testing, and screening for mood disorders were obtained at the time of presentation to clinic. Seizure recurrence was evaluated at clinic follow-up at least 6–12 months following the initial presentation. In all groups, general intelligence (intelligence quotient [IQ]) was consistent with population norms, but more than half of participants (55.8%) were impaired in at least one cognitive domain. The most commonly impaired domain in all diagnostic groups was visuospatial and visuoconstruction suggesting that it may be a sensitive marker of early cognitive impairment. Those with epilepsy (NOE and NDE) at initial presentation were more likely to be impaired than those with FS, particularly on tests of attention, working memory, and processing speed. Seven participants with FS converted to NOE (FSNOE) at follow-up. They were more likely to be impaired on tests of memory than those with FS who did not convert to NOE. On mood screening, 21% of participants scored moderate or severe for depressive symptoms, and 25.6% of participants scored moderate or severe for anxiety symptoms. Cognitive impairment and mood changes are common at first seizure presentation and mirror the pattern seen in chronic epilepsy. This cooccurrence of symptomatology at disease onset prior to prolonged antiepilepsy drug exposure suggests a shared underlying disease mechanism and carries important clinical implications for effective diagnosis and management of epilepsy. Furthermore, early cognitive testing may become a clinical biomarker and enable the prediction of an individual's clinical course. •Individuals with a first unprovoked seizure demonstrate cognitive impairment.•Domain-specific impairment may predict aspects of a patient's clinical course.•Findings support a shared mechanism for cognitive impairment, mood disorders and seizures.