Electrophysiological features of sleep in children with Kir4.1 channel mutations and Autism–Epilepsy phenotype: a preliminary study. Issue 4 (13th November 2019)

• Record Type: Journal Article
• Authors: Cucchiara, Federico; Frumento, Paolo; Banfi, Tommaso; Sesso, Gianluca; Di Galante, Marco; D'Ascanio, Paola; Valvo, Giulia; Sicca, Federico; Faraguna, Ugo
• Is Part Of: Sleep. Volume 43:Issue 4(2020)
• Publication Date: 2019-11-13
• Subjects: children -- autism -- epilepsy -- EEG -- nap -- sleep homeostasis -- tripartite synapse -- K+ buffering -- Kir4.1 -- KCNJ10; Sleep -- Physiological aspects -- Periodicals; Sleep disorders -- Periodicals; Sommeil -- Aspect physiologique -- Périodiques; Sommeil, Troubles du -- Périodiques; Sleep disorders; Sleep -- Physiological aspects; Sleep -- physiological aspects; Sleep Wake Disorders; Psychophysiology; Electronic journals; Periodicals; 616.8498
• DOI: 10.1093/sleep/zsz255
• Languages: English
• ISSNs: 0161-8105

Abstract

Abstract: Study Objectives: Recently, a role for gain-of-function (GoF) mutations of the astrocytic potassium channel Kir4.1 ( KCNJ10 gene) has been proposed in subjects with Autism–Epilepsy phenotype (AEP). Epilepsy and autism spectrum disorder (ASD) are common and complexly related to sleep disorders. We tested whether well characterized mutations in KCNJ10 could result in specific sleep electrophysiological features, paving the way to the discovery of a potentially relevant biomarker for Kir4.1-related disorders. Methods: For this case–control study, we recruited seven children with ASD either comorbid or not with epilepsy and/or EEG paroxysmal abnormalities (AEP) carrying GoF mutations of KCNJ10 and seven children with similar phenotypes but wild-type for the same gene, comparing period-amplitude features of slow waves detected by fronto-central bipolar EEG derivations (F3-C3, F4-C4, and Fz-Cz) during daytime naps. Results: Children with Kir4.1 mutations displayed longer slow waves periods than controls, in Fz-Cz (mean period = 112, 617 ms ± SE = 0.465 in mutated versus mean period = 105, 249 ms ± SE = 0.375 in controls, p < 0.001). An analog result was found in F3-C3 (mean period = 125, 706 ms ± SE = 0.397 in mutated versus mean period = 120, 872 ms ± SE = 0.472 in controls, p < 0.001) and F4-C4 (mean period = 127, 914 ms ± SE = 0.557 in mutated versus mean period = 118, 174 ms ± SE = 0.442 in controls, p < 0.001). Conclusion: This preliminary finding suggests that period-amplitude slow wave features are modified in subjects carrying Kir4.1 GoF mutations. Potential clinical applications of this finding are discussed.