Literature DB >> 26369628

Quinidine in the treatment of KCNT1-positive epilepsies.

Mohamad A Mikati1, Yong-Hui Jiang2, Michael Carboni3, Vandana Shashi2, Slave Petrovski4, Rebecca Spillmann4, Carol J Milligan5, Melody Li5, Annette Grefe6, Allyn McConkie2, Samuel Berkovic7, Ingrid Scheffer7, Saul Mullen5, Melanie Bonner8, Steven Petrou7, David Goldstein4.   

Abstract

We report 2 patients with drug-resistant epilepsy caused by KCNT1 mutations who were treated with quinidine. Both mutations manifested gain of function in vitro, showing increased current that was reduced by quinidine. One, who had epilepsy of infancy with migrating focal seizures, had 80% reduction in seizure frequency as recorded in seizure diaries, and partially validated by objective seizure evaluation on EEG. The other, who had a novel phenotype, with severe nocturnal focal and secondary generalized seizures starting in early childhood with developmental regression, did not improve. Although quinidine represents an encouraging opportunity for therapeutic benefits, our experience suggests caution in its application and supports the need to identify more targeted drugs for KCNT1 epilepsies.
© 2015 American Neurological Association.

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Year:  2015        PMID: 26369628      PMCID: PMC4811613          DOI: 10.1002/ana.24520

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  18 in total

1.  Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.

Authors:  Sarah E Heron; Katherine R Smith; Melanie Bahlo; Lino Nobili; Esther Kahana; Laura Licchetta; Karen L Oliver; Aziz Mazarib; Zaid Afawi; Amos Korczyn; Giuseppe Plazzi; Steven Petrou; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Nat Genet       Date:  2012-10-21       Impact factor: 38.330

Review 2.  Long-term efficacy of low doses of quinidine on malignant arrhythmias in Brugada syndrome with an implantable cardioverter-defibrillator: a case series and literature review.

Authors:  Manlio F Márquez; Aimé Bonny; Eduardo Hernández-Castillo; Antonio De Sisti; Jorge Gómez-Flores; Santiago Nava; Françoise Hidden-Lucet; Pedro Iturralde; Manuel Cárdenas; Joelci Tonet
Journal:  Heart Rhythm       Date:  2012-08-28       Impact factor: 6.343

3.  Targeted treatment of migrating partial seizures of infancy with quinidine.

Authors:  David Bearden; Alanna Strong; Jessica Ehnot; Marissa DiGiovine; Dennis Dlugos; Ethan M Goldberg
Journal:  Ann Neurol       Date:  2014-07-26       Impact factor: 10.422

4.  Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability.

Authors:  Christopher P Derry; Sarah E Heron; Fiona Phillips; Stephen Howell; Jacinta MacMahon; Hilary A Phillips; John S Duncan; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer
Journal:  Epilepsia       Date:  2008-05-09       Impact factor: 5.864

5.  Excitatory effects of gap junction blockers on cerebral cortex seizure-like activity in rats and mice.

Authors:  Logan J Voss; Gregory Jacobson; James W Sleigh; Alistair Steyn-Ross; Moira Steyn-Ross
Journal:  Epilepsia       Date:  2009-04-19       Impact factor: 5.864

6.  KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine.

Authors:  Carol J Milligan; Melody Li; Elena V Gazina; Sarah E Heron; Umesh Nair; Chantel Trager; Christopher A Reid; Anu Venkat; Donald P Younkin; Dennis J Dlugos; Slavé Petrovski; David B Goldstein; Leanne M Dibbens; Ingrid E Scheffer; Samuel F Berkovic; Steven Petrou
Journal:  Ann Neurol       Date:  2014-04-14       Impact factor: 10.422

7.  Effects of gap junction blockers on human neocortical synchronization.

Authors:  S Gigout; J Louvel; H Kawasaki; M D'Antuono; V Armand; I Kurcewicz; A Olivier; J Laschet; B Turak; B Devaux; R Pumain; M Avoli
Journal:  Neurobiol Dis       Date:  2006-02-14       Impact factor: 5.996

8.  Inhibition of desipramine hydroxylation (Cytochrome P450-2D6) in vitro by quinidine and by viral protease inhibitors: relation to drug interactions in vivo.

Authors:  L L von Moltke; D J Greenblatt; S X Duan; J P Daily; J S Harmatz; R I Shader
Journal:  J Pharm Sci       Date:  1998-10       Impact factor: 3.534

9.  De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.

Authors:  Giulia Barcia; Matthew R Fleming; Aline Deligniere; Valeswara-Rao Gazula; Maile R Brown; Maeva Langouet; Haijun Chen; Jack Kronengold; Avinash Abhyankar; Roberta Cilio; Patrick Nitschke; Anna Kaminska; Nathalie Boddaert; Jean-Laurent Casanova; Isabelle Desguerre; Arnold Munnich; Olivier Dulac; Leonard K Kaczmarek; Laurence Colleaux; Rima Nabbout
Journal:  Nat Genet       Date:  2012-10-21       Impact factor: 38.330

10.  The impact of P-gp functionality on non-steady state relationships between CSF and brain extracellular fluid.

Authors:  Joost Westerhout; Jean Smeets; Meindert Danhof; Elizabeth C M de Lange
Journal:  J Pharmacokinet Pharmacodyn       Date:  2013-03-29       Impact factor: 2.745

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  44 in total

Review 1.  The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.

Authors:  Davide Mei; Elena Parrini; Carla Marini; Renzo Guerrini
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

Review 2.  Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.

Authors:  Feng Wei; Li-Min Yan; Tao Su; Na He; Zhi-Jian Lin; Jie Wang; Yi-Wu Shi; Yong-Hong Yi; Wei-Ping Liao
Journal:  Neurosci Bull       Date:  2017-05-09       Impact factor: 5.203

3.  An Epilepsy-Associated KCNT1 Mutation Enhances Excitability of Human iPSC-Derived Neurons by Increasing Slack KNa Currents.

Authors:  Imran H Quraishi; Shani Stern; Kile P Mangan; Yalan Zhang; Syed R Ali; Michael R Mercier; Maria C Marchetto; Michael J McLachlan; Eugenia M Jones; Fred H Gage; Leonard K Kaczmarek
Journal:  J Neurosci       Date:  2019-07-26       Impact factor: 6.167

4.  Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.

Authors:  Allyn McConkie Rosell; Loren D M Pena; Kelly Schoch; Rebecca Spillmann; Jennifer Sullivan; Stephen R Hooper; Yong-Hui Jiang; Nicolas Mathey-Andrews; David B Goldstein; Vandana Shashi
Journal:  J Genet Couns       Date:  2016-02-12       Impact factor: 2.537

Review 5.  Therapy in Sleep-Related Hypermotor Epilepsy (SHE).

Authors:  Gian Maria Asioli; Simone Rossi; Francesca Bisulli; Laura Licchetta; Paolo Tinuper; Federica Provini
Journal:  Curr Treat Options Neurol       Date:  2020-01-30       Impact factor: 3.598

Review 6.  Drug development in the era of precision medicine.

Authors:  Sarah A Dugger; Adam Platt; David B Goldstein
Journal:  Nat Rev Drug Discov       Date:  2017-12-08       Impact factor: 84.694

7.  Treatment Responsiveness in KCNT1-Related Epilepsy.

Authors:  Mark P Fitzgerald; Martina Fiannacca; Douglas M Smith; Tracy S Gertler; Boudewijn Gunning; Steffen Syrbe; Nienke Verbeek; Hannah Stamberger; Sarah Weckhuysen; Berten Ceulemans; An-Sofie Schoonjans; Massimiliano Rossi; Geneviève Demarquay; Gaetan Lesca; Kern Olofsson; D A Koolen; Frauke Hornemann; Stephanie Baulac; Guido Rubboli; Kelly Q Minks; Bohoon Lee; Ingo Helbig; Dennis Dlugos; Rikke S Møller; David Bearden
Journal:  Neurotherapeutics       Date:  2019-07       Impact factor: 7.620

Review 8.  Stiripentol in the Management of Epilepsy.

Authors:  Katherine C Nickels; Elaine C Wirrell
Journal:  CNS Drugs       Date:  2017-05       Impact factor: 5.749

9.  GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.

Authors:  Dong Li; Hongjie Yuan; Xilma R Ortiz-Gonzalez; Eric D Marsh; Lifeng Tian; Elizabeth M McCormick; Gabrielle J Kosobucki; Wenjuan Chen; Anthony J Schulien; Rosetta Chiavacci; Anel Tankovic; Claudia Naase; Frieder Brueckner; Celina von Stülpnagel-Steinbeis; Chun Hu; Hirofumi Kusumoto; Ulrike B S Hedrich; Gina Elsen; Konstanze Hörtnagel; Elias Aizenman; Johannes R Lemke; Hakon Hakonarson; Stephen F Traynelis; Marni J Falk
Journal:  Am J Hum Genet       Date:  2016-09-08       Impact factor: 11.025

10.  Epilepsy-causing sequence variations in SIK1 disrupt synaptic activity response gene expression and affect neuronal morphology.

Authors:  Christoph Pröschel; Jeanne N Hansen; Adil Ali; Emily Tuttle; Michelle Lacagnina; Georgia Buscaglia; Marc W Halterman; Alex R Paciorkowski
Journal:  Eur J Hum Genet       Date:  2016-12-14       Impact factor: 4.246

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