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Juvenile myoclonic epilepsy: evaluation of attentional and executive functions, personality traits and social adaptation

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Author(s):
Sylvie Carolina Paes Moschetta
Total Authors: 1
Document type: Master's Dissertation
Press: São Paulo.
Institution: Universidade de São Paulo (USP). Faculdade de Medicina (FM/SBD)
Defense date:
Examining board members:
Kette Dualibi Ramos Valente; Marilisa Mantovanni Guerreiro; Evelyn Kuczynski
Advisor: Kette Dualibi Ramos Valente
Abstract

Juvenile Myoclonic Epilepsy (JME) is an idiopathic generalized epilepsy usually associated with absence of structural changes. Neuropsychological studies in patients with JME, using a limited number of paradigms, show worse performance on tests assessing executive functions. In addition, the description of personality traits in patients with JME corroborates neuropsychological studies, reporting failure of impulse control in these patients, which reflects a possible frontal lobe dysfunction. These studies are either based on clinical observations or on the categorical classification criteria of DSM-IV. To moment, the correlation between executive dysfunction and impulsive personality traits in patients with JME, has not been performed, as well as neither an objective study of the social adjustment of this population. The objectives of this study were to: 1. Investigate if attentional and executive functions are impaired; 2. Investigate if there are different levels of impairment in attentional and executive functions 3. Investigate if there are alterations in personality traits using an objective instrument 4. Investigate if there is impairment of social functioning 5. Investigate if there are correlations between performance on attentional and executive functions and the expressions of personality traits related to poor impulse control, 6. Verify if there are correlations between scores on neuropsychological tests of attentional and executive functions and social functioning 7. Investigate if there are correlations between clinical variables of epilepsy and neuropsychological performance, expression of impulsive personality traits and social functioning. We evaluated 42 patients with JME by: a) a comprehensive battery of neuropsychological tests of attentional and executive functions b) a standardized assessment of personality traits (TCI) and c) a standardized scale for assessing social functioning (SAS-SR). The performances and scores on tests, of patients with JME were compared to a group of 42 control subjects without neurological or psychiatric diagnosis, matched for age, education and socioeconomic status. Patients with JME showed worse performance than controls on tests of attentional span, working memory, inhibitory control, concept formation, maintenance of goals, verbal fluency and immediate verbal memory. We also observed that 83.33% of the patients with JME had moderate or severe executive dysfunction. Patients with JME showed higher expression of personality traits associated with an impaired impulse control and worse social functioning, when compared with the control group. Attentional/ executive dysfunction was correlated with poor impulse control, but not with worse social functioning. We found correlations between the frequency of seizures and the presence of psychiatric disorders with attentional and executive dysfunction, with the highest expression of impulsive traits and with worsened social functioning. Longest duration of epilepsy and the early age of onset were respectively associated with executive dysfunction and personality. In the category analysis between groups of patients easy and difficult to control seizures, refractory patients had worse executive dysfunction with an even a greater presence of impulsive personality traits. Our study demonstrates the presence of attentional and executive dysfunction in patients with JME, as well as the presence of impulsive personality traits. Moreover, this study identified the presence of poor social functioning in these patients. We also note the existence of two distinct groups of patients, were more refractory patients appear to present broader impairment. These findings suggest that there is a need for better phenotypic characterization of patients with JME to include diverse phenotypes since our results suggest a possible existence of distinct groups of patients with JME. (AU)

FAPESP's process: 07/52110-3 - Juvenile myoclonic epilepsy: evaluation of attentional and executive functions, personality traits and social adaptation
Grantee:Sylvie Carolina Paes Moschetta
Support Opportunities: Scholarships in Brazil - Master