TMEM132C rs7296262 Single-Nucleotide Polymorphism Is Significantly Associated with Nausea Induced by Opioids Administered for Cancer Pain and Postoperative Pain.
Yuna KangDaisuke NishizawaSeii OhkaTakeshi TeruiKunihiko IshitaniRyozo MorinoMiyuki YokotaJunko HasegawaKyoko NakayamaYuko EbataKyotaro KoshikaTatsuya IchinoheAnd Kazutaka IkedaPublished in: International journal of molecular sciences (2024)
Opioids are almost mandatorily used for analgesia for cancer pain and postoperative pain. Opioid analgesics commonly induce nausea as a side effect. However, the genetic factors involved are still mostly unknown. To clarify the genetic background of individual differences in the occurrence of nausea during opioid administration, the incidence of nausea was investigated in 331 patients (Higashi-Sapporo Hospital [HS] group) who received morphine chronically for cancer pain treatment and in 2021 patients (Cancer Institute Hospital [CIH] group) who underwent elective surgery under general anesthesia. We conducted a genome-wide association study of nausea in HS samples. Among the top 20 candidate single-nucleotide polymorphisms (SNPs), we focused on the TMEM132C rs7296262 SNP, which has been reportedly associated with psychiatric disorders. The rs7296262 SNP was significantly associated with nausea in both the HS and CIH groups (TT+TC vs. CC; HS group, p = 0.0001; CIH group, p = 0.0064). The distribution of nausea-prone genotypes for the rs7296262 SNP was reversed between HS and CIH groups. These results suggest that the TMEM132C rs7296262 SNP is significantly associated with nausea during opioid use, and the effect of the SNP genotype on nausea is reversed between chronic and acute phases of opioid use.
Keyphrases
- postoperative pain
- chemotherapy induced
- chronic pain
- pain management
- genome wide
- papillary thyroid
- end stage renal disease
- squamous cell
- newly diagnosed
- ejection fraction
- neuropathic pain
- minimally invasive
- prognostic factors
- dna methylation
- peritoneal dialysis
- risk assessment
- gene expression
- high density
- lymph node metastasis
- genome wide association study
- patients undergoing
- liver failure
- acute coronary syndrome
- hepatitis b virus
- copy number
- risk factors
- young adults
- atrial fibrillation
- genetic diversity
- respiratory failure
- atomic force microscopy
- mechanical ventilation