Literature DB >> 29196578

Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidine.

Saul A Mullen1, Patrick W Carney1, Annie Roten1, Michael Ching1, Paul A Lightfoot1, Leonid Churilov1, Umesh Nair1, Melody Li1, Samuel F Berkovic1, Steven Petrou1, Ingrid E Scheffer2.   

Abstract

OBJECTIVE: To evaluate quinidine as a precision therapy for severe epilepsy due to gain of function mutations in the potassium channel gene KCNT1.
METHODS: A single-center, inpatient, order-randomized, blinded, placebo-controlled, crossover trial of oral quinidine included 6 patients with severe autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) due to KCNT1 mutation. Order was block randomized and blinded. Four-day treatment blocks were used with a 2-day washout between. Dose started at 900 mg over 3 divided doses then, in subsequent participants, was reduced to 600 mg, then 300 mg. Primary outcome was seizure frequency measured on continuous video-EEG in those completing the trial.
RESULTS: Prolonged QT interval occurred in the first 2 patients at doses of 900 and 600 mg quinidine per day, respectively, despite serum quinidine levels well below the therapeutic range (0.61 and 0.51 μg/mL, reference range 1.3-5.0 μg/mL). Four patients completed treatment with 300 mg/d without adverse events. Patients completing the trial had very frequent seizures (mean 14 per day, SD 7, median 13, interquartile range 10-18). Seizures per day were nonsignificantly increased by quinidine (median 2, 95% confidence interval -1.5 to +5, p = 0.15) and no patient had a 50% seizure reduction.
CONCLUSION: Quinidine did not show efficacy in adults and teenagers with ADNFLE. Dose-limiting cardiac side effects were observed even in the presence of low measured serum quinidine levels. Although small, this trial suggests use of quinidine in ADNFLE is likely to be ineffective coupled with considerable cardiac risks. CLINICAL TRIALS REGISTRATION: Australian Therapeutic Goods Administration Clinical Trial Registry (trial number 2015/0151). CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that for persons with severe epilepsy due to gain of function mutations in the potassium channel gene KCNT1, quinidine does not significantly reduce seizure frequency.
Copyright © 2017 American Academy of Neurology.

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Year:  2017        PMID: 29196578     DOI: 10.1212/WNL.0000000000004769

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  25 in total

Review 1.  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

2.  Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy.

Authors:  Robertino Dilena; Jacopo C DiFrancesco; Maria Virginia Soldovieri; Antonella Giacobbe; Paolo Ambrosino; Ilaria Mosca; Maria Albina Galli; Sophie Guez; Monica Fumagalli; Francesco Miceli; Dario Cattaneo; Francesca Darra; Elena Gennaro; Federico Zara; Pasquale Striano; Barbara Castellotti; Cinzia Gellera; Costanza Varesio; Pierangelo Veggiotti; Maurizio Taglialatela
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

Review 3.  Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.

Authors:  Julia Oyrer; Snezana Maljevic; Ingrid E Scheffer; Samuel F Berkovic; Steven Petrou; Christopher A Reid
Journal:  Pharmacol Rev       Date:  2018-01       Impact factor: 25.468

Review 4.  [Advances in sleep-related hypermotor epilepsy].

Authors:  Jiahui Xu; Bo Jin; Lisan Zhang; Shuang Wang
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2020-08-25

Review 5.  The Functional Properties, Physiological Roles, Channelopathy and Pharmacological Characteristics of the Slack (KCNT1) Channel.

Authors:  Qi Zhang; Ye Liu; Jie Xu; Yue Teng; Zhe Zhang
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

6.  The phenotypic spectrum of KCNT1: a new family with variable epilepsy syndromes including mild focal epilepsy.

Authors:  Christina Cherian; Juan P Appendino; Setareh Ashtiani; Paolo Federico; Christine P Molnar; Marina Kerr; Aneal Khan; Ping Yee Billie Au; Karl Martin Klein
Journal:  J Neurol       Date:  2021-09-19       Impact factor: 4.849

7.  The Slack Channel Regulates Anxiety-Like Behaviors via Basolateral Amygdala Glutamatergic Projections to Ventral Hippocampus.

Authors:  Qi Zhang; Shun-Heng Gao; Zhong-Shan Shen; Yun Wang; Su-Wan Hu; Guang-Bing Duan; Ye Liu; Dan-Ya Zhong; Jing Liu; Meng-Han Sun; Xin Zhang; Tian-Yu Cao; Jun-Li Cao; Qiong-Yao Tang; Zhe Zhang
Journal:  J Neurosci       Date:  2022-02-23       Impact factor: 6.709

Review 8.  Electrophysiological Biomarkers in Genetic Epilepsies.

Authors:  Caren Armstrong; Eric D Marsh
Journal:  Neurotherapeutics       Date:  2021-10-12       Impact factor: 6.088

9.  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

10.  Discovery of the First Orally Available, Selective KNa1.1 Inhibitor: In Vitro and In Vivo Activity of an Oxadiazole Series.

Authors:  Andrew M Griffin; Kristopher M Kahlig; Robert John Hatch; Zoë A Hughes; Mark L Chapman; Brett Antonio; Brian E Marron; Marion Wittmann; Gabriel Martinez-Botella
Journal:  ACS Med Chem Lett       Date:  2021-03-09       Impact factor: 4.345

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