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Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies

Suppression‐burst (SB) is an electroencephalographic pattern observed in neonatal‐ and infantile‐onset developmental and epileptic encephalopathies (DEEs), which are associated with high mortality in early life. However, the relation of SB electroencephalogram (SB‐EEG) with autonomic function requir...

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Autores principales: Yamamoto, Kaoru, Baba, Shimpei, Saito, Takashi, Nakagawa, Eiji, Sugai, Kenji, Iwasaki, Masaki, Fujita, Atsushi, Fukuda, Hiromi, Mizuguchi, Takeshi, Kato, Mitsuhiro, Matsumoto, Naomichi, Sasaki, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235550/
https://www.ncbi.nlm.nih.gov/pubmed/36740266
http://dx.doi.org/10.1002/epi4.12705
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author Yamamoto, Kaoru
Baba, Shimpei
Saito, Takashi
Nakagawa, Eiji
Sugai, Kenji
Iwasaki, Masaki
Fujita, Atsushi
Fukuda, Hiromi
Mizuguchi, Takeshi
Kato, Mitsuhiro
Matsumoto, Naomichi
Sasaki, Masayuki
author_facet Yamamoto, Kaoru
Baba, Shimpei
Saito, Takashi
Nakagawa, Eiji
Sugai, Kenji
Iwasaki, Masaki
Fujita, Atsushi
Fukuda, Hiromi
Mizuguchi, Takeshi
Kato, Mitsuhiro
Matsumoto, Naomichi
Sasaki, Masayuki
author_sort Yamamoto, Kaoru
collection PubMed
description Suppression‐burst (SB) is an electroencephalographic pattern observed in neonatal‐ and infantile‐onset developmental and epileptic encephalopathies (DEEs), which are associated with high mortality in early life. However, the relation of SB electroencephalogram (SB‐EEG) with autonomic function requires clarification. We investigated the relationship between heart rate (HR) and phasic transition during SB‐EEG in DEEs to explore the mechanism of early death. Seven patients (two with KCNT1‐DEE) with neonatal‐ and infantile‐onset DEE who presented with SB‐EEG were retrospectively identified. Five‐minute SB‐EEGs were analyzed with simultaneous recording of electrocardiograms. Mean HR, suppression duration, and burst period were calculated by measuring RR intervals. Two patients with KCNT1‐DEE exhibited synchronous HR fluctuations, with an HR decrease during suppression and an increase during burst. The HR decrease was larger (−6.1% and −7.7%) and the median duration of suppression was longer (4.0 and 8.2 s) in patients with KCNT1‐DEE than the other five (range: −2.9% to 0.9% and 0.7‐1.7s, respectively). A strong negative correlation was confirmed between suppression duration and HR reduction rates in one patient with KCNT1‐DEE. SB phases may influence HR regulation in patients with KCTN1‐DEE.
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spelling pubmed-102355502023-06-03 Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies Yamamoto, Kaoru Baba, Shimpei Saito, Takashi Nakagawa, Eiji Sugai, Kenji Iwasaki, Masaki Fujita, Atsushi Fukuda, Hiromi Mizuguchi, Takeshi Kato, Mitsuhiro Matsumoto, Naomichi Sasaki, Masayuki Epilepsia Open Short Research Articles Suppression‐burst (SB) is an electroencephalographic pattern observed in neonatal‐ and infantile‐onset developmental and epileptic encephalopathies (DEEs), which are associated with high mortality in early life. However, the relation of SB electroencephalogram (SB‐EEG) with autonomic function requires clarification. We investigated the relationship between heart rate (HR) and phasic transition during SB‐EEG in DEEs to explore the mechanism of early death. Seven patients (two with KCNT1‐DEE) with neonatal‐ and infantile‐onset DEE who presented with SB‐EEG were retrospectively identified. Five‐minute SB‐EEGs were analyzed with simultaneous recording of electrocardiograms. Mean HR, suppression duration, and burst period were calculated by measuring RR intervals. Two patients with KCNT1‐DEE exhibited synchronous HR fluctuations, with an HR decrease during suppression and an increase during burst. The HR decrease was larger (−6.1% and −7.7%) and the median duration of suppression was longer (4.0 and 8.2 s) in patients with KCNT1‐DEE than the other five (range: −2.9% to 0.9% and 0.7‐1.7s, respectively). A strong negative correlation was confirmed between suppression duration and HR reduction rates in one patient with KCNT1‐DEE. SB phases may influence HR regulation in patients with KCTN1‐DEE. John Wiley and Sons Inc. 2023-02-14 /pmc/articles/PMC10235550/ /pubmed/36740266 http://dx.doi.org/10.1002/epi4.12705 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Short Research Articles
Yamamoto, Kaoru
Baba, Shimpei
Saito, Takashi
Nakagawa, Eiji
Sugai, Kenji
Iwasaki, Masaki
Fujita, Atsushi
Fukuda, Hiromi
Mizuguchi, Takeshi
Kato, Mitsuhiro
Matsumoto, Naomichi
Sasaki, Masayuki
Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title_full Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title_fullStr Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title_full_unstemmed Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title_short Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
title_sort synchronous heart rate reduction with suppression‐burst pattern in kcnt1‐related developmental and epileptic encephalopathies
topic Short Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235550/
https://www.ncbi.nlm.nih.gov/pubmed/36740266
http://dx.doi.org/10.1002/epi4.12705
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