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Postictal Psychosis in Epilepsy: A Clinicogenetic Study.
Braatz, Vera; Martins Custodio, Helena; Leu, Costin; Agrò, Luigi; Wang, Baihan; Calafato, Stella; Rayner, Genevieve; Doyle, Michael G; Hengsbach, Christian; Bisulli, Francesca; Weber, Yvonne G; Gambardella, Antonio; Delanty, Norman; Cavalleri, Gianpiero; Foong, Jacqueline; Scheffer, Ingrid E; Berkovic, Samuel F; Bramon, Elvira; Balestrini, Simona; Sisodiya, Sanjay M.
Afiliação
  • Braatz V; Department of Neurology, Neurological and Neurosurgical Clinic of Joinville, Joinville, Brazil.
  • Martins Custodio H; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
  • Leu C; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
  • Agrò L; Chalfont Centre for Epilepsy, Buckinghamshire, UK.
  • Wang B; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
  • Calafato S; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
  • Rayner G; Stanley Center of Psychiatric Research, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA.
  • Doyle MG; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
  • Hengsbach C; Chalfont Centre for Epilepsy, Buckinghamshire, UK.
  • Bisulli F; Mental Health Neuroscience Research Department, Division of Psychiatry, University College London, London, UK.
  • Weber YG; Mental Health Neuroscience Research Department, Division of Psychiatry, University College London, London, UK.
  • Gambardella A; Melbourne School of Psychological Sciences, University of Melbourne, Parkville, Victoria, Australia.
  • Delanty N; Department of Clinical Neuropsychology, Austin Health, Melbourne, Victoria, Australia.
  • Cavalleri G; Epilepsy Programme, Department of Neurology, Beaumont Hospital, Dublin, Ireland.
  • Foong J; FutureNeuro Research Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.
  • Scheffer IE; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Berkovic SF; IRCCS Istituto delle Scienze Neurologiche di Bologna, Full Member of the ERN EpiCARE, delle Scienze Neurologiche di Bologna (EpiCARE reference center), Bologna, Italy.
  • Bramon E; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy.
  • Balestrini S; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Sisodiya SM; Department of Epileptology and Neurology, University of Aachen, Aachen, Germany.
Ann Neurol ; 90(3): 464-476, 2021 09.
Article em En | MEDLINE | ID: mdl-34288049
ABSTRACT

OBJECTIVE:

Psychoses affecting people with epilepsy increase disease burden and diminish quality of life. We characterized postictal psychosis, which comprises about one quarter of epilepsy-related psychoses, and has unknown causation.

METHODS:

We conducted a case-control cohort study including patients diagnosed with postictal psychosis, confirmed by psychiatric assessment, with available data regarding epilepsy, treatment, psychiatric history, psychosis profile, and outcomes. After screening 3,288 epilepsy patients, we identified 83 with psychosis; 49 had postictal psychosis. Controls were 98 adults, matched by age and epilepsy type, with no history of psychosis. Logistic regression was used to investigate clinical factors associated with postictal psychosis; univariate associations with a p value < 0.20 were used to build a multivariate model. Polygenic risk scores for schizophrenia were calculated.

RESULTS:

Cases were more likely to have seizure clustering (odds ratio [OR] = 7.59, p < 0.001), seizures with a recollected aura (OR = 2.49, p = 0.013), and a family history of psychiatric disease (OR = 5.17, p = 0.022). Cases showed predominance of right temporal epileptiform discharges (OR = 4.87, p = 0.007). There was no difference in epilepsy duration, neuroimaging findings, or antiseizure treatment between cases and controls. Polygenic risk scores for schizophrenia in an extended cohort of postictal psychosis cases (n = 58) were significantly higher than in 1,366 epilepsy controls (R2  = 3%, p = 6 × 10-3 ), but not significantly different from 945 independent patients with schizophrenia (R2  = 0.1%, p = 0.775).

INTERPRETATION:

Postictal psychosis occurs under particular circumstances in people with epilepsy with a heightened genetic predisposition to schizophrenia, illustrating how disease biology (seizures) and trait susceptibility (schizophrenia) may interact to produce particular outcomes (postictal psychosis) in a common disease. ANN NEUROL 2021;90464-476.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Polimorfismo de Nucleotídeo Único / Epilepsia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Polimorfismo de Nucleotídeo Único / Epilepsia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article