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Infantile Epileptic Spasms Syndrome Complicated by Leigh Syndrome and Leigh-Like Syndrome: A Retrospective, Nationwide, Multicenter Case Series.

Authors :
Sasaki, Michiru
Okanishi, Tohru
Matsuoka, Tsuyoshi
Yoshimura, Ayumi
Maruyama, Shinsuke
Shiohama, Tadashi
Hoshino, Hiroki
Mori, Tatsuo
Majima, Hisakazu
Matsumoto, Hiroshi
Kobayashi, Satoru
Chiyonobu, Tomohiro
Matsushige, Takeshi
Nakamura, Kazuyuki
Kubota, Kazuo
Tanaka, Ryuta
Fujita, Takako
Enoki, Hideo
Suzuki, Yasuhiro
Nakamura, Sadao
Source :
Pediatric Neurology. Aug2024, Vol. 157, p29-38. 10p.
Publication Year :
2024

Abstract

Six percent of patients with Leigh syndrome (LS) present with infantile epileptic spasms syndrome (IESS). However, treatment strategies for IESS with LS remain unclear. This retrospective study aimed to evaluate the efficacy and safety of treatment strategies in patients with IESS complicated by LS and Leigh-like syndrome (LLS). We distributed questionnaires to 750 facilities in Japan, and the clinical data of 21 patients from 15 hospitals were collected. The data comprised treatment strategies, including adrenocorticotropic hormone (ACTH) therapy, ketogenic diet (KD) therapy, and antiseizure medications (ASMs); effectiveness of each treatment; and the adverse events. The median age at LS and LLS diagnosis was 7 months (range: 0 to 50), whereas that at the onset of epileptic spasms was 7 (range: 3 to 20). LS was diagnosed in 17 patients and LLS in four patients. Seven, two, five, and seven patients received ACTH + ASMs, ACTH + KD + ASMs, KD + ASMs, and ASMs only, respectively. Four (44%) of nine patients treated with ACTH and one (14%) of seven patients treated with KD achieved electroclinical remission within one month of treatment. No patients treated with only ASMs achieved electroclinical remission. Seven patients (33%) achieved electroclinical remission by the last follow-up. Adverse events were reported in four patients treated with ACTH, none treated with KD therapy, and eight treated with ASMs. ACTH therapy shows the best efficacy and rapid action in patients with IESS complicated by LS and LLS. The effectiveness of KD therapy and ASMs in this study was insufficient. • Infantile epileptic spasms syndrome with Leigh and Leigh-like syndromes case series. • Four of 9 patients treated with ACTH achieved electroclinical remission < 1 month. • One of seven treated with ketogenic diet (KD) achieved electroclinical remission. • No patients treated with only ASMs achieved electroclinical remission. • Adverse events were reported in 4 with ACTH, none with KD, and 8 with ASMs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08878994
Volume :
157
Database :
Academic Search Index
Journal :
Pediatric Neurology
Publication Type :
Academic Journal
Accession number :
178464159
Full Text :
https://doi.org/10.1016/j.pediatrneurol.2024.05.007