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Published on: November 30, 2016
Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide
Shigekazu Sugino1,2, Daisuke Konno3, Yosuke Kawai4
1Department of Anesthesiology and Perioperative Medicine, Tohoku University School of Medicine, Seiryo-machi 2-1, Sendai, Miyagi, 980-8575, Japan. shigekazu.sugino.d3@tohoku.ac.jp.
A novel single-nucleotide polymorphism (SNP) in MIR4300HG, rs11232965, was identified as protective against postoperative nausea and vomiting (PONV) in Japanese patients. This genetic variant may help predict PONV risk in surgical patients.
Area of Science:
- Genetics
- Pharmacogenomics
- Molecular Biology
Background:
- Postoperative nausea and vomiting (PONV) is influenced by genetic factors, including single-nucleotide polymorphisms (SNPs).
- Previous genetic studies on PONV lack broad applicability due to population-specific genetic variations.
- A Japanese-specific DNA microarray was developed for high-throughput genotyping to address these limitations.
Purpose of the Study:
- To identify SNPs associated with PONV on a genome-wide scale in a Japanese surgical patient cohort.
- To investigate population-specific genetic variations contributing to PONV susceptibility.
- To validate candidate SNPs associated with PONV using real-time PCR.
Main Methods:
- Genome-wide association study (GWAS) using a Japanese-specific DNA microarray on 24 female patients.
- Imputation of genotypes for over 24 million SNPs.
- Selection of 4 candidate SNPs based on in silico functional annotation.
- Validation of 4 candidate SNPs in 255 patients using real-time PCR.
Main Results:
- Genome-wide analysis identified 78 SNPs associated with PONV incidence.
- The T > C variant of rs11232965 in the long non-coding RNA MIR4300HG showed a significant association with reduced PONV incidence (p = 0.01 and 0.007).
Conclusions:
- A novel SNP, rs11232965, in MIR4300HG is significantly associated with PONV.
- The rs11232965 T > C variant acts as a protective factor against PONV incidence.
- This finding contributes to understanding the genetic basis of PONV in the Japanese population.
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Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

