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OPRM1 A118G Polymorphism and Ondansetron Efficacy for Postoperative Nausea and Vomiting in Laparoscopic
Xu Zhao1, Qingqing Yu2, Guanling Yu2
1Department of Anesthesiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, People's Republic of China.
Background:
The OPRM1 A118G polymorphism has been implicated in modulating susceptibility to postoperative nausea and vomiting (PONV). Ondansetron, a 5-HT3 receptor antagonist, is widely utilized for PONV prophylaxis; however, whether its efficacy is influenced by OPRM1 A118G polymorphism remains unclear.
Methods:
We conducted a retrospective cohort study including patients undergoing laparoscopic gynecological surgery between January 2019 and December 2024; propensity score matching was used to adjust for confounders. OPRM1 A118G genotypes (AA, AG, GG) were analyzed through polymerase chain reaction and sequencing. PONV incidence and severity were assessed using the Visual Analog Scale (VAS) at various postoperative time points.
Results:
The Ondansetron group had significantly lower PONV incidence within 2 hours (38.82% vs 56.98%, p = 0.0174) and 2 ~ 24 hours (8.24% vs 19.77%, p = 0.0300). The OPRM1 A118G polymorphism was associated with higher PONV risk, particularly in patients with the AG/GG genotypes in the control group. In the Ondansetron group, the association was significant only within 2 hours (p = 0.0460).
Conclusion:
The OPRM1 A118G polymorphism is associated with an increased risk of early PONV, particularly in patients with the G allele, which has been related to reduced μ-opioid receptor sensitivity and increased opioid requirements, thereby predisposing patients to a higher PONV risk. Ondansetron significantly reduces PONV incidence and severity, especially in patients with higher genetic susceptibility.
Insights
The OPRM1 A118G gene variant increases the risk of postoperative nausea and vomiting (PONV). Ondansetron effectively reduces PONV, particularly in patients with this genetic susceptibility.
Area of Science:
- Pharmacogenetics
- Anesthesiology
- Gastroenterology
Background:
- Postoperative nausea and vomiting (PONV) is a common complication.
- The OPRM1 A118G polymorphism may influence PONV susceptibility.
- Ondansetron is a standard PONV prophylaxis, but its efficacy relative to OPRM1 A118G is unclear.
Purpose of the Study:
- To investigate the impact of the OPRM1 A118G polymorphism on PONV risk.
- To evaluate the efficacy of Ondansetron in patients with varying OPRM1 A118G genotypes.
Main Methods:
- Retrospective cohort study of patients undergoing laparoscopic gynecological surgery.
- Propensity score matching for confounder adjustment.
- Genotyping for OPRM1 A118G polymorphism via PCR and sequencing.
- Assessment of PONV incidence and severity using Visual Analog Scale (VAS).
Main Results:
- Ondansetron significantly reduced PONV incidence compared to controls within 2 hours (38.82% vs 56.98%) and 2-24 hours (8.24% vs 19.77%).
- The OPRM1 A118G polymorphism, particularly AG/GG genotypes, was linked to higher PONV risk in the control group.
- In the Ondansetron group, the genetic association with PONV was significant within the first 2 hours.
Conclusions:
- The OPRM1 A118G polymorphism increases early PONV risk, especially with the G allele, potentially due to reduced μ-opioid receptor sensitivity.
- Ondansetron effectively mitigates PONV incidence and severity, demonstrating particular benefit in genetically susceptible individuals.
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