Genome-Wide Association Study Identifies Novel Candidate Variants Associated with Postoperative Nausea and Vomiting

Author:

Nishizawa Daisuke1ORCID,Morino Ryozo2,Inoue Rie13,Ohka Seii1,Kasai Shinya1,Hasegawa Junko1,Ebata Yuko1,Nakayama Kyoko1,Sumikura Hiroyuki3,Hayashida Masakazu13,Yokota Miyuki45,Ikeda Kazutaka1ORCID

Affiliation:

1. Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan

2. Division of Anesthesiology, Koujinkai Daiichi Hospital, Tokyo 125-0041, Japan

3. Department of Anesthesiology and Pain Medicine, Juntendo University School of Medicine, Tokyo 113-8421, Japan

4. Department of Anesthesiology, Cancer Institute Hospital, Tokyo 135-8550, Japan

5. Department of Anesthesiology, East Hokkaido Hospital, Kushiro 085-0036, Japan

Abstract

Considerable individual differences are widely observed in the incidence of postoperative nausea and vomiting (PONV). We conducted a genome-wide association study (GWAS) to identify potential candidate single-nucleotide polymorphisms (SNPs) that contribute to PONV by utilizing whole-genome genotyping arrays with more than 950,000 markers. The subjects were 806 patients who provided written informed consent and underwent elective surgery under general anesthesia with propofol or desflurane. The GWAS showed that two SNPs, rs2776262 and rs140703637, in the LOC100506403 and CNTN5 gene regions, respectively, were significantly associated with the frequency of nausea. In another GWAS conducted only on patients who received propofol, rs7212072 and rs12444143 SNPs in the SHISA6 and RBFOX1 gene regions, respectively, were significantly associated with the frequency of nausea as well as the rs2776262 SNP, and the rs45574836 and rs1752136 SNPs in the ATP8B3 and LOC105370198 gene regions, respectively, were significantly associated with vomiting. Among these SNPs, clinical and SNP data were available for the rs45574836 SNP in independent subjects who underwent laparoscopic gynecological surgery, and the association was replicated in these subjects. These results indicate that these SNPs could serve as markers that predict the vulnerability to PONV. Our findings may provide valuable information for achieving satisfactory prophylactic treatment for PONV.

Funder

Japan Society for the Promotion of Science

Ministry of Health, Labour, and Welfare

Japan Agency for Medical Research and Development

Smoking Research Foundation

Japan Research Foundation for Clinical Pharmacology

Asahi Kasei Pharma Open Innovation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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