4.4 Article

Psychosocial complications in juvenile myoclonic epilepsy

Journal

EPILEPSY & BEHAVIOR
Volume 90, Issue -, Pages 122-128

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yebeh.2018.11.022

Keywords

Epilepsy; Frontal lobe; Executive dysfunction; Levetiracetam; Recreational drugs; ADHD

Funding

  1. Vestre Viken Hospital Trust, Norway
  2. Canadian Institutes of Health Research: Biology of Juvenile \Myoclonic Epilepsy (BIOJUME) [201503MOP-342469]
  3. European Union Seventh Framework Programme: Development of Strategies for Innovative Research to improve diagnosis, prevention and treatment in children with difficult to treat Epilepsy, DESIRE [602531]
  4. National Institute for Health Research Programme Grant for Applied Research: Changing Agendas on Sleep, Treatment and Learning in Epilepsy (CASTLE) [RP-PG-0615-20007]
  5. Medical Research Council (MRC) Centre grant [MR/N026063/1]
  6. Waterloo Foundation Project [164-3020]
  7. Charles Sykes Epilepsy Research Trust
  8. NIHR Specialist Biomedical Research Centre for Mental Health of South London and Maudsley NHS Foundation Trust
  9. MRC [MR/N026063/1] Funding Source: UKRI

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Juvenile myoclonic epilepsy (JME) constitutes about 10% of all epilepsies. Because of executive dysfunction, people with JME may be prone to impulsivity and risk-taking behavior. Our aim was to investigate whether psychosocial issues associated with impulsivity are more prominent in people with JME than in those with other types of genetic generalized epilepsy (GGE). Patients with GGE were recruited retrospectively through the Drammen Hospital records in Buskerud County, Norway, 1999-2013. They were invited to a semi-structured interview, either at the hospital or at home. Ninety-two patients with JME and 45 with other types of GGE were interviewed. Variables were evaluated in terms of their association with JME versus other GGE diagnosis using a logistic regression model. Juvenile myodonic epilepsy was associated with use of illicit recreational drugs and police charges, although with borderline significance (odds ratio [OR] 3.4, p = 0.087 and OR 4.2, p = 0.095); JME was also associated with being examined for attention-deficit hyperactivity disorder (ADHD) in females (OR 15.5, p = 0.015), a biological parent with challenges like addiction or violent behavior (OR 3.5, p = 0.032), and use of leveliracetam (OR 5.1, p = 0.014). After controlling for group differences, we found psychosocial complications to be associated with JME, potentially influencing the lives of the individuals and their families to a greater extent than the seizures per se. Thus. JME should be considered a disorder of the brain in a broader sense than a condition with seizures only. (C) 2018 Elsevier Inc. All rights reserved.

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