Literature DB >> 23313934

Effect of CYP3A4*18B polymorphisms and interactions with OPRM1 A118G on postoperative fentanyl requirements in patients undergoing radical gastrectomy.

Qin Liao1, Dao-Jin Chen, Fan Zhang, Li Li, Rong Hu, Yong-Zhong Tang, Wen Ou-Yang, Dong Huang.   

Abstract

The present study aimed to investigate the effect of cytochrome P450 3A4 (CYP3A4)*18B polymorphisms and the interaction of the µ opioid receptor gene (OPRM1) A118G and CYP3A4*18B polymorphisms on postoperative fentanyl analgesia in Chinese Han patients undergoing radical gastrectomy. In total, 97 patients scheduled to undergo radical gastrectomy under general anesthesia were enrolled in this study. Post‑operative patient‑controlled intravenous analgesia of fentanyl was administered as analgesia up to 48 h following surgery. Venous blood (2 ml) was obtained from each patient to measure the OPRM1 A118G and CYP3A4*18B genotypes. The differences in fentanyl consumption and adverse effects were compared among the genotypes at 24 and 48 h following surgery. In the first 48 h following surgery, patients in the CYP3A4*18B/*18B group consumed significantly less fentanyl compared with patients in the *1/*1 group (P=0.032). With regards to the joint genetic effect, during the 48‑h period, patients with AA and *1*18B polymorphisms received fewer fentanyl doses compared with those with AG and *1*1 (P=0.049), while patients with AG and *1*18B polymorphisms received significantly fewer fentanyl doses compared with those with AG and *1*1 (P=0.010), and patients with *18B*18B polymorphisms received significantly fewer fentanyl doses compared with those with AA and *1*1 (P=0.024) or those with AG and *1*1 polymorphisms (P=0.006). No correlation between OPRM1 A118G and CYP3A4*18B and postoperative nausea, vomiting and dizziness was found. Results demonstrated that 48 h following surgery, patients with the CYP3A4*18B/*18B genotype required less fentanyl than patients with the CYP3A4*1/*1 genotype to control pain. Additionally, the combined genotype of CYP3A4*18B and OPRM1 A118G may affect fentanyl doses administered for pain control, but not postoperative nausea, vomiting and dizziness.

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Year:  2013        PMID: 23313934     DOI: 10.3892/mmr.2013.1270

Source DB:  PubMed          Journal:  Mol Med Rep        ISSN: 1791-2997            Impact factor:   2.952


  4 in total

1.  Genetic Factors Associated with Postoperative Nausea and Vomiting: a Systematic Review.

Authors:  Pedro López-Morales; Diego Flores-Funes; Elena González Sánchez-Migallón; Ramón José Lirón-Ruiz; José Luis Aguayo-Albasini
Journal:  J Gastrointest Surg       Date:  2018-05-03       Impact factor: 3.452

2.  Effect of CYP3A41G and CYP3A53 Polymorphisms on Pharmacokinetics and Pharmacodynamics of Ticagrelor in Healthy Chinese Subjects.

Authors:  Shuaibing Liu; Xiangfen Shi; Xin Tian; Xiaojian Zhang; Zhiyong Sun; Liyan Miao
Journal:  Front Pharmacol       Date:  2017-03-31       Impact factor: 5.810

Review 3.  Interplay of Vitamin D and CYP3A4 Polymorphisms in Endocrine Disorders and Cancer.

Authors:  Siva Swapna Kasarla; Vannuruswamy Garikapati; Yashwant Kumar; Sujatha Dodoala
Journal:  Endocrinol Metab (Seoul)       Date:  2022-06-03

Review 4.  Nature and nurture of human pain.

Authors:  Inna Belfer
Journal:  Scientifica (Cairo)       Date:  2013-04-02
  4 in total

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