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Genomic and clinical predictors of lacosamide response in refractory epilepsies.
Heavin, Sinéad B; McCormack, Mark; Wolking, Stefan; Slattery, Lisa; Walley, Nicole; Avbersek, Andreja; Novy, Jan; Sinha, Saurabh R; Radtke, Rod; Doherty, Colin; Auce, Pauls; Craig, John; Johnson, Michael R; Koeleman, Bobby P C; Krause, Roland; Kunz, Wolfram S; Marson, Anthony G; O'Brien, Terence J; Sander, Josemir W; Sills, Graeme J; Stefansson, Hreinn; Striano, Pasquale; Zara, Federico; Depondt, Chantal; Sisodiya, Sanjay; Goldstein, David; Lerche, Holger; Cavalleri, Gianpiero L; Delanty, Norman.
Afiliação
  • Heavin SB; School of Pharmacy and Biomolecular Sciences Royal College of Surgeons Dublin Ireland.
  • McCormack M; School of Pharmacy and Biomolecular Sciences Royal College of Surgeons Dublin Ireland.
  • Wolking S; Luxembourg Centre for Systems Biomedicine University of Luxembourg Esch-sur-Alzette Luxembourg.
  • Slattery L; Department of Neurology and Epileptology Hertie Institute for Clinical Brain Research University of Tübingen Tübingen Germany.
  • Walley N; School of Pharmacy and Biomolecular Sciences Royal College of Surgeons Dublin Ireland.
  • Avbersek A; Centre for Human Genome Variation Duke University Durham NC USA.
  • Novy J; Department of Clinical and Experimental Epilepsy UCL Queen Square Institute of Neurology London UK.
  • Sinha SR; Chalfont Centre for Epilepsy Buckinghamshire UK.
  • Radtke R; Department of Clinical and Experimental Epilepsy UCL Queen Square Institute of Neurology London UK.
  • Doherty C; Chalfont Centre for Epilepsy Buckinghamshire UK.
  • Auce P; Centre for Human Genome Variation Duke University Durham NC USA.
  • Craig J; Centre for Human Genome Variation Duke University Durham NC USA.
  • Johnson MR; School of Medicine Trinity College Dublin Dublin Ireland.
  • Koeleman BPC; Department of Neurology St James's Hospital Dublin Ireland.
  • Krause R; Department of Molecular and Clinical Pharmacology Institute of Translational Medicine University of Liverpool Liverpool UK.
  • Kunz WS; Department of Neurosciences Belfast Health and Social Care Trust Belfast UK.
  • Marson AG; Division of Brain Sciences Imperial College Faculty of Medicine London UK.
  • O'Brien TJ; Center of Molecular Medicine University Medical Center Utrecht Utrecht The Netherlands.
  • Sander JW; Luxembourg Centre for Systems Biomedicine University of Luxembourg Esch-sur-Alzette Luxembourg.
  • Sills GJ; Institute of Experimental Epileptology and Cognition Research and Department of Epileptology University of Bonn Bonn Germany.
  • Stefansson H; Department of Molecular and Clinical Pharmacology Institute of Translational Medicine University of Liverpool Liverpool UK.
  • Striano P; The Departments of Neuroscience and Neurology The Alfred Hospital Monash University Victoria Australia.
  • Zara F; Department of Clinical and Experimental Epilepsy UCL Queen Square Institute of Neurology London UK.
  • Depondt C; Department of Molecular and Clinical Pharmacology Institute of Translational Medicine University of Liverpool Liverpool UK.
  • Sisodiya S; deCODE Genetics/Amgen Inc Reykjavik Iceland.
  • Goldstein D; Pediatric Neurology and Muscular Diseases Unit DINOGMI-Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health Institute "G. Gaslini" University of Genova Genova Italy.
  • Lerche H; Laboratory of Neurogenetics and Neuroscience Institute G. Gaslini Genova Italy.
Epilepsia Open ; 4(4): 563-571, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31819912
ABSTRACT

OBJECTIVE:

Clinical and genetic predictors of response to antiepileptic drugs (AEDs) are largely unknown. We examined predictors of lacosamide response in a real-world clinical setting.

METHODS:

We tested the association of clinical predictors with treatment response using regression modeling in a cohort of people with refractory epilepsy. Genetic assessment for lacosamide response was conducted via genome-wide association studies and exome studies, comprising 281 candidate genes.

RESULTS:

Most patients (479/483) were treated with LCM in addition to other AEDs. Our results corroborate previous findings that patients with refractory genetic generalized epilepsy (GGE) may respond to treatment with LCM. No clear clinical predictors were identified. We then compared 73 lacosamide responders, defined as those experiencing greater than 75% seizure reduction or seizure freedom, to 495 nonresponders (<25% seizure reduction). No variants reached the genome-wide significance threshold in our case-control analysis.

SIGNIFICANCE:

No genetic predictor of lacosamide response was identified. Patients with refractory GGE might benefit from treatment with lacosamide.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article