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Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study

Authors :
Shigekazu Sugino
Daisuke Konno
Yosuke Kawai
Masao Nagasaki
Yasuhiro Endo
Tomo Hayase
Misako Yamazaki-Higuchi
Yukihiro Kumeta
Shunsuke Tachibana
Katsuhiko Saito
Jun Suzuki
Kanta Kido
Nahoko Kurosawa
Akiyoshi Namiki
Masanori Yamauchi
Source :
Human Genomics, Vol 14, Iss 1, Pp 1-10 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Background Genetic factors such as single-nucleotide polymorphisms (SNPs) play a key role in the development of postoperative nausea and vomiting (PONV). However, previous findings are not widely applicable to different populations because of population-specific genetic variation. We developed a Japanese-specific DNA microarray for high-throughput genotyping. The aim of the current study was to identify SNPs associated with PONV on a genome-wide scale using this microarray in a sample of Japanese surgical patients. Methods Associations between 659,636 SNPs and the incidence of PONV 24 h after surgery in a limited sample of 24 female patients were assessed using the microarray. After imputation of genotypes at 24,330,529 SNPs, 78 SNPs were found to be associated with the incidence of PONV. We chose 4 of the 78 SNPs to focus on by in silico functional annotation. Finally, we genotyped these 4 candidate SNPs in 255 patients using real-time PCR to verify association with the incidence of PONV. Results The T > C variant of rs11232965 in the long non-coding RNA MIR4300HG was significantly associated with reduced incidence of PONV among genotypes and between alleles (p = 0.01 and 0.007). Conclusions We identified a novel SNP (rs11232965) in the long non-coding RNA MIR4300HG that is associated with PONV. The rs11232965-SNP variant (T > C) is protective against the incidence of PONV. Trial registration This study was registered at the UMIN Clinical Trials Registry (Identifier: UMIN000022903 , date of registration: June 27, 2016, retrospectively registered.

Details

Language :
English
ISSN :
14797364
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Human Genomics
Publication Type :
Academic Journal
Accession number :
edsdoj.2a1d43d1cba2498d94f37b05c8bdbede
Document Type :
article
Full Text :
https://doi.org/10.1186/s40246-020-00282-4