Literature DB >> 28608234

Genomics-Guided Precise Anti-Epileptic Drug Development.

Norman Delanty1,2, Gianpiero Cavalleri3.   

Abstract

Traditional antiepileptic drug development approaches have yielded many important clinically valuable anti-epileptic drugs. However, the screening of promising compounds has been naturally agnostic to epilepsy etiology in individual human patients. Now, genomic medicine is changing the way we view human disease. International collaborations are unraveling the many molecular genetic causes of the epilepsies, including the early onset epileptic encephalopathies, and some of the familial focal epilepsies. Further advances in precision diagnostics will be facilitated by ongoing large collaborations and the wider availability of whole exome and whole genome sequencing in clinical practice. Securing a precise molecular diagnosis in some individual patients will pave the way for the advent of precision therapeutics of new and re-purposed compounds in the treatment of the epilepsies. This new approach is already beginning, e.g., with the use of everolimus in patients with tuberous sclerosis complex (and perhaps other mTORopathies), the use of quinidine in some children with KCNT1 mutations, and the use of the ketogenic diet in individuals with GLUT-1 deficiency. This article explores the promise of genomics guided drug development as an approach to complement the more traditional model.

Entities:  

Keywords:  Anti-epileptic drug development; Epilepsy; Genomics; Precision therapeutics

Mesh:

Substances:

Year:  2017        PMID: 28608234     DOI: 10.1007/s11064-017-2312-y

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  26 in total

1.  Ineffective quinidine therapy in early onset epileptic encephalopathy with KCNT1 mutation.

Authors:  Pin Fee Chong; Ryoko Nakamura; Hirotomo Saitsu; Naomichi Matsumoto; Ryutaro Kira
Journal:  Ann Neurol       Date:  2016-02-12       Impact factor: 10.422

Review 2.  Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies.

Authors:  Ryan S Dhindsa; David B Goldstein
Journal:  Curr Neurol Neurosci Rep       Date:  2015-10       Impact factor: 5.081

Review 3.  Precision medicine in genetic epilepsies: break of dawn?

Authors:  Philipp Sebastian Reif; Meng-Han Tsai; Ingo Helbig; Felix Rosenow; Karl Martin Klein
Journal:  Expert Rev Neurother       Date:  2016-11-10       Impact factor: 4.618

Review 4.  TSC1/TSC2 signaling in the CNS.

Authors:  Juliette M Han; Mustafa Sahin
Journal:  FEBS Lett       Date:  2011-02-15       Impact factor: 4.124

5.  Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study.

Authors:  Jacqueline A French; John A Lawson; Zuhal Yapici; Hiroko Ikeda; Tilman Polster; Rima Nabbout; Paolo Curatolo; Petrus J de Vries; Dennis J Dlugos; Noah Berkowitz; Maurizio Voi; Severine Peyrard; Diana Pelov; David N Franz
Journal:  Lancet       Date:  2016-09-06       Impact factor: 79.321

6.  Quinidine in the treatment of KCNT1-positive epilepsies.

Authors:  Mohamad A Mikati; Yong-Hui Jiang; Michael Carboni; Vandana Shashi; Slave Petrovski; Rebecca Spillmann; Carol J Milligan; Melody Li; Annette Grefe; Allyn McConkie; Samuel Berkovic; Ingrid Scheffer; Saul Mullen; Melanie Bonner; Steven Petrou; David Goldstein
Journal:  Ann Neurol       Date:  2015-11-18       Impact factor: 10.422

Review 7.  A roadmap for precision medicine in the epilepsies.

Authors: 
Journal:  Lancet Neurol       Date:  2015-09-20       Impact factor: 44.182

8.  Epi4K: gene discovery in 4,000 genomes.

Authors: 
Journal:  Epilepsia       Date:  2012-05-29       Impact factor: 5.864

9.  Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.

Authors:  Scott C Baraban; Matthew T Dinday; Gabriela A Hortopan
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

Review 10.  Genetics of tuberous sclerosis complex: implications for clinical practice.

Authors:  Carolina Caban; Nubaira Khan; Daphne M Hasbani; Peter B Crino
Journal:  Appl Clin Genet       Date:  2016-12-21
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  1 in total

Review 1.  Individualizing Treatment Approaches for Epileptic Patients with Glucose Transporter Type1 (GLUT-1) Deficiency.

Authors:  Armond Daci; Adnan Bozalija; Fisnik Jashari; Shaip Krasniqi
Journal:  Int J Mol Sci       Date:  2018-01-05       Impact factor: 5.923

  1 in total

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