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

Author:

Yamamoto Kaoru1ORCID,Baba Shimpei1ORCID,Saito Takashi1ORCID,Nakagawa Eiji12,Sugai Kenji13,Iwasaki Masaki4ORCID,Fujita Atsushi5,Fukuda Hiromi56,Mizuguchi Takeshi5,Kato Mitsuhiro7ORCID,Matsumoto Naomichi5ORCID,Sasaki Masayuki1

Affiliation:

1. Department of Child Neurology, National Center Hospital National Center of Neurology and Psychiatry (NCNP) Tokyo Japan

2. Department of Epileptology, National Center Hospital NCNP Tokyo Japan

3. Division of Pediatrics Soleil Kawasaki Medical Center for the Handicapped Kawasaki Japan

4. Department of Neurosurgery, National Center Hospital NCNP Tokyo Japan

5. Department of Human Genetics Yokohama City University Graduate School of Medicine Yokohama Japan

6. Department of Neurology and Stroke Medicine Yokohama City University Graduate School of Medicine Yokohama Japan

7. Department of Pediatrics, Showa University School of Medicine and Epilepsy Medical Center Showa University Hospital Tokyo Japan

Abstract

AbstractSuppression‐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.

Funder

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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