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High-amplitude fast activity in EEG: An early diagnostic marker in children with beta-propeller protein-associated neurodegeneration (BPAN)

Authors :
Kyoko Takano
Tetsuo Kubota
Yu Okai
Masahiro Kawaguchi
Masaharu Tanaka
Hiroyuki Yamamoto
Yuki Maki
Mitsuo Motobayashi
Takeshi Suzuki
Tomohiko Nakata
Naoko Shiba
Yusaku Miyamoto
Kazuhiro Muramatsu
Jun Natsume
Yoko Sakaguchi
Hiroyuki Kidokoro
Source :
Clinical Neurophysiology. 131:2100-2104
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Objective The early diagnosis of beta-propeller protein-associated neurodegeneration (BPAN) before distinct brain magnetic resonance imaging (MRI) findings of iron deposition occur remains challenging. This study examined whether children with BPAN have characteristic high-amplitude (>50 μV) fast activity (HAFA) on electroencephalography (EEG). Methods We conducted a retrospective analysis of EEG performed during childhood in five patients with BPAN. We also examined 143 EEGs from 59 patients with different etiologies, including epilepsy (n = 33), acute encephalopathy (n = 6), neurodevelopmental disorders (n = 5), non-epileptic events (n = 4), and others (n = 11). Trained electroencephalographers reviewed all of the EEGs. When excessive fast activity was observed, the amplitude, frequency, and locality were assessed. Results All five patients with BPAN underwent initial EEGs at 12–21 months old, and diffuse continuous HAFA (range 20–50 Hz) was observed on both awake and sleep EEGs. In the awake records, there was no clear posterior dominant rhythm in 4 of the 5 patients. Although 28% of the 143 EEGs had continuous excessive fast activity, mainly in the sleep records, only two (1.4%) exhibited HAFA when asleep, and their awake EEGs had clear posterior dominant rhythm. Conclusions The EEGs of children with BPAN showed diffuse HAFA continuously when both awake and asleep, which is uncommon in children with other etiologies. Significance This study provides an important clue for the early diagnosis of BPAN.

Details

ISSN :
13882457
Volume :
131
Database :
OpenAIRE
Journal :
Clinical Neurophysiology
Accession number :
edsair.doi.dedup.....77c37cd272b47a357cd9c2cb47e145df
Full Text :
https://doi.org/10.1016/j.clinph.2020.06.006