Polymorphisms contribute to differences in the effect of rocuronium in Chinese patients
Authors:
- 4 November 2021
- journal article
- research article
- Published by Wiley in Basic & Clinical Pharmacology & Toxicology
- Vol. 130 (1) , 141-150
Abstract
Rocuronium is widely utilized in clinical general anaesthesia, and individual differences in pharmacology and clearance have been observed. Two hundred thirty‐six Chinese patients undergoing selective thyroid/breast mass resection were studied. Total intravenous anaesthesia was induced with a single dose of propofol (2 mg·kg−1), sufentanil (0.5 μg·kg−1), and rocuronium (0.6 mg·kg−1) and maintained with propofol (3–5 mg·kg−1·h−1) and remifentanil (0.2–0.4 μg·kg−1·min−1). Intubation conditions and a train‐of‐four index of patients were utilized to assess the effects and duration of rocuronium. The data from 228 patients were analysed and reported. Genotypes NR1I2 rs2472677 C > T, NR1I2 rs6785049 G > A, SLCO1B1 rs4363657 T > C, SLCO1A2 rs4762699 T > C, and UGT1A1 rs4148323 G > A contributed to individual variation in rocuronium. Of the clinical variables tested, age, BMI, total dose of propofol, NR1I2 rs2472677, and SLCO1A2 rs4762699 correlated significantly (P < 0.05 for all) with the clinical duration or total clinical action time of rocuronium in a multiple linear regression model. No significant interactions were observed in intubation conditions. Genetic variations in NR1I2 rs2472677, NR1I2 rs6785049, SLCO1B1 rs4363657, SLCO1A2 rs4762699, and UGT1A1 rs4148323 were related to extensive interindividual variability in the clinical duration and total clinical action time of rocuronium.Keywords
Funding Information
- National Natural Science Foundation of China (82071251)
- National Key Research and Development Program of China (2018YFC2001802)
This publication has 36 references indexed in Scilit:
- A Genome‐Wide Association Study for Serum Bilirubin Levels and Gene‐Environment Interaction in a Chinese PopulationGenetic Epidemiology, 2013
- Nuclear-receptor–mediated regulation of drug– and bile-acid–transporter proteins in gut and liverDrug Metabolism Reviews, 2013
- PXR and CAR single nucleotide polymorphisms influence plasma efavirenz levels in South African HIV/AIDS patientsBMC Medical Genetics, 2012
- Impact of OATP transporters on pharmacokineticsBritish Journal of Pharmacology, 2009
- PXR, CAR and HNF4α genotypes and their association with pharmacokinetics and pharmacodynamics of docetaxel and doxorubicin in Asian patientsThe Pharmacogenomics Journal, 2007
- Good clinical research practice in pharmacodynamic studies of neuromuscular blocking agents II: the Stockholm revisionActa Anaesthesiologica Scandinavica, 2007
- Regulation of the UGT1A1 bilirubin-conjugating pathway: Role of a new splicing event at the UGT1A locusHepatology, 2006
- ROLE OF ORGANIC ANION TRANSPORTER OATP1B1 (OATP-C) IN HEPATIC UPTAKE OF IRINOTECAN AND ITS ACTIVE METABOLITE, 7-ETHYL-10-HYDROXYCAMPTOTHECIN: IN VITRO EVIDENCE AND EFFECT OF SINGLE NUCLEOTIDE POLYMORPHISMSDrug Metabolism and Disposition, 2005
- Polymorphisms in Human Organic Anion-transporting Polypeptide 1A2 (OATP1A2)Journal of Biological Chemistry, 2005
- The pharmacokinetics and pharmacodynamics of rocuronium in patients with hepatic cirrhosisBritish Journal of Clinical Pharmacology, 1997