Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
Hiroshima Journal of Medical Sciences Volume 71 Issue 1-2
Page 31-38
published_at 2022-06
アクセス数 : 401 件
ダウンロード数 : 202 件
今月のアクセス数 : 7 件
今月のダウンロード数 : 3 件
この文献の参照には次のURLをご利用ください : https://ir.lib.hiroshima-u.ac.jp/00052902
File |
HiroshimaJMedSci_71_31.pdf
549 KB
種類 :
fulltext
|
Title ( eng ) |
Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
|
Creator |
MORINO Hiroyuki
NAKAMURA Ryuji
KAWAMOTO Masashi
|
Source Title |
Hiroshima Journal of Medical Sciences
|
Volume | 71 |
Issue | 1-2 |
Start Page | 31 |
End Page | 38 |
Journal Identifire |
[PISSN] 0018-2052
[EISSN] 2433-7668
[NCID] AA00664312
|
Abstract |
Malignant hyperthermia (MH) is an anaesthetic complication that causes an abnormal hypermetabolic state. RYR1 encoding ryanodine receptors of the sarcoplasmic reticulum and CACNA1S encoding α subunits of dihydropyridine receptors are known to be associated with MH pathogenicity. We performed genetic screening using next-generation sequencing to evaluate the prevalence of genes associated with MH pathogenicity and clinical symptoms. This was a retrospective cohort study wherein next-generation sequencing data of 77 families diagnosed with MH predisposition by calcium-induced calcium release (CICR) tests from 1995 to 2019 was used to search for RYR1 and CACNA1S variants. Furthermore, the clinical symptoms and predisposition tests in participants with RYR1 and CACNA1S variants were compared. In the 77 families, 44.2%, 7.8%, and 48.1% individuals had RYR1, CACNA1S, and neither RYR1 nor CACNA1S variants, respectively. Clinically significant differences were found in the maximum body temperature, maximum elevated body temperature for 15 min, creatinine kinase level, and CICR rate between the RYR1 and CACNA1S groups. The prevalence of pathogenic CACNA1S variants appears to be prominent in Japan. The severity of clinical symptoms and the CICR rate were greater in individuals with RYR1 variants than in those with CACNA1S variants, likely due to more direct regulation of calcium levels by ryanodine receptors than by dihydropyridine receptors. Genetic analysis of MH in future studies may help identify other genes associated with MH, which will further clarify the relationship between genotypes and MH symptoms and contribute to safer anaesthesia practice.
|
Keywords |
Malignant hyperthermia
Next Generation Sequencing
RYR1
CACNA1S
|
Descriptions |
This study was supported by a Grant-in-Aid for Young Scientists (grant number: 17K16733 to Y.N. and 20K17783 to R.K.) from the Japan Society for the Promotion of Science and by the Takeda Science Foundation (H.K.).
|
Language |
eng
|
Resource Type | departmental bulletin paper |
Publisher |
Hiroshima University Medical Press
|
Date of Issued | 2022-06 |
Rights |
Copyright (c) 2022 Hiroshima University Medical Press
|
Publish Type | Version of Record |
Access Rights | open access |
Source Identifier |
[ISSN] 0018-2052
[ISSN] 2433-7668
[NCID] AA00664312
[DOI] 10.24811/hjms.71.1-2_31
|