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Precision therapy with quinidine of KCNT1-related epileptic disorders: A systematic review

期刊

BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
卷 88, 期 12, 页码 5096-5112

出版社

WILEY
DOI: 10.1111/bcp.15479

关键词

epilepsy; KCNT1; quinidine

资金

  1. National Natural Science Foundation of China [82171315]

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The clinical utility of quinidine therapy for KCNT1-related epileptic disorders is still uncertain, as contradictory results were found in similar patients. Age, seizure types, genotypes of KCNT1 mutations, and brain MRI did not significantly influence the therapeutic effects of quinidine.
Aims Despite numerous studies on quinidine therapies for epilepsies associated with KCNT1 gene mutations, there is no consensus on its clinical utility. Thus, we reviewed studies evaluating the efficacy and safety of quinidine in KCNT1-related epileptic disorders. Methods Electronic databases were queried for in vivo and in vitro studies on quinidine therapy in KCNT1-related epilepsies published on or before 1 May 2022. The evaluation of evidence was done as per the American Academy of Neurology's classification scheme. Identification of significant factors that possibly influenced therapeutic effects of quinidine were performed using chi(2) tests. Results Twenty-seven studies containing 82 patient records were reviewed. Records of 80 patients with 33 KCNT1 mutations were analysed, of which 20 patients had gained >= 50% seizure reduction due to quinidine therapy. However, quinidine therapy often had different effects on patients with the same KCNT1 mutation. Age, genotypes of KCNT1 mutations, seizure types and brain MRI did not significantly influence the therapeutic effect of quinidine. Prolonged QTc was the most common among all adverse events with quinidine. Notably, results of in vitro quinidine tests did not correspond with in vivo tests. Conclusions Therapeutic effects of quinidine on KCNT1-related epilepsies remained indefinite as contradictory results were detected in similar patients. Age, seizure types, genotypes of KCNT1 mutations and brain MRI did not influence the therapeutic effects of quinidine. Insensitivity to quinidine by a certain Kcnt1 genotype in molecular tests is predictive of its inefficacy in human populations of the respective mutation.

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