Jelena Lilic, Vesna G Marjanovic, Ivana Budic, Nikola Stefanovic, Dragana Stokanovic, Goran T Marjanovic, Tatjana Jevtovic-Stoimenov, Mladjan Golubovic, Maja Zecevic, Radmila Velickovic-Radovanovic
{"title":"阿片受体基因多态性对小儿围手术期芬太尼和阿芬太尼镇痛效果的影响","authors":"Jelena Lilic, Vesna G Marjanovic, Ivana Budic, Nikola Stefanovic, Dragana Stokanovic, Goran T Marjanovic, Tatjana Jevtovic-Stoimenov, Mladjan Golubovic, Maja Zecevic, Radmila Velickovic-Radovanovic","doi":"10.2147/pgpm.s443035","DOIUrl":null,"url":null,"abstract":"<strong>Introduction:</strong> The polymorphism of the gene coding mu-opioid receptor (<em>OPRM1</em>) is one of the factors contributing to the variability in the response to opioid analgesics in children. The goal of this study is to investigate its role in association with postoperative acute pain in children of various ages.<br/><strong>Methods:</strong> This prospective study analyzed 110 pediatric patients, after plastic or orthopedic surgery, who were genotyped and randomly assigned to receive fentanyl or alfentanil. Postoperative pain was rated using Numerical Rating Scale (0– 10). All the patients were genotyped for<em>OPRM1 118A>G</em> (<em>rs1799971</em>) gene polymorphism.<br/><strong>Results:</strong> School children under the age of 11 with the <em>OPRM1 AA</em> genotype were shown to have a higher BMI (p< 0.05). Children over the age of 12 carrying G allele <em>OPRM1</em>, had increased postoperative pain sensitivity and intensity (3.28± 1.95 vs 4.91± 2.17; p< 0.05), as compared to <em>AA</em> allele carriers.<br/><strong>Discussion:</strong> <em>OPRM1 118A>G</em> polymorphism may explain the variation in the perception of postoperative pain in children over the age of 12 and may be a useful predictor for adjusting the dose of analgesics, but the dose is relative to the patient’s needs regardless of his genetic characteristics. In younger children, carriers of polymorphic <em>OPRM1 118G</em> allele may be protected from obesity, due to diminished <em>MOP</em> expression.<br/><br/><strong>Keywords:</strong> polymorphism, <em>OPRM1</em>, opioid, pain, children<br/>","PeriodicalId":501056,"journal":{"name":"Pharmacogenomics and Personalized Medicine","volume":"138 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Impact of Opioid Receptor Gene Polymorphism on Fentanyl and Alfentanil’s Analgesic Effects in the Pediatric Perioperative Period\",\"authors\":\"Jelena Lilic, Vesna G Marjanovic, Ivana Budic, Nikola Stefanovic, Dragana Stokanovic, Goran T Marjanovic, Tatjana Jevtovic-Stoimenov, Mladjan Golubovic, Maja Zecevic, Radmila Velickovic-Radovanovic\",\"doi\":\"10.2147/pgpm.s443035\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<strong>Introduction:</strong> The polymorphism of the gene coding mu-opioid receptor (<em>OPRM1</em>) is one of the factors contributing to the variability in the response to opioid analgesics in children. The goal of this study is to investigate its role in association with postoperative acute pain in children of various ages.<br/><strong>Methods:</strong> This prospective study analyzed 110 pediatric patients, after plastic or orthopedic surgery, who were genotyped and randomly assigned to receive fentanyl or alfentanil. Postoperative pain was rated using Numerical Rating Scale (0– 10). All the patients were genotyped for<em>OPRM1 118A>G</em> (<em>rs1799971</em>) gene polymorphism.<br/><strong>Results:</strong> School children under the age of 11 with the <em>OPRM1 AA</em> genotype were shown to have a higher BMI (p< 0.05). Children over the age of 12 carrying G allele <em>OPRM1</em>, had increased postoperative pain sensitivity and intensity (3.28± 1.95 vs 4.91± 2.17; p< 0.05), as compared to <em>AA</em> allele carriers.<br/><strong>Discussion:</strong> <em>OPRM1 118A>G</em> polymorphism may explain the variation in the perception of postoperative pain in children over the age of 12 and may be a useful predictor for adjusting the dose of analgesics, but the dose is relative to the patient’s needs regardless of his genetic characteristics. In younger children, carriers of polymorphic <em>OPRM1 118G</em> allele may be protected from obesity, due to diminished <em>MOP</em> expression.<br/><br/><strong>Keywords:</strong> polymorphism, <em>OPRM1</em>, opioid, pain, children<br/>\",\"PeriodicalId\":501056,\"journal\":{\"name\":\"Pharmacogenomics and Personalized Medicine\",\"volume\":\"138 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacogenomics and Personalized Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2147/pgpm.s443035\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacogenomics and Personalized Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/pgpm.s443035","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
简介编码μ阿片受体(OPRM1)基因的多态性是导致儿童对阿片类镇痛药反应差异的因素之一。本研究的目的是调查其在不同年龄儿童术后急性疼痛中的作用:这项前瞻性研究分析了 110 名整形外科或骨科手术后的儿童患者,对他们进行了基因分型,并随机分配他们接受芬太尼或阿芬太尼治疗。术后疼痛采用数字评分量表(0-10)进行评分。所有患者都进行了OPRM1 118A>G(rs1799971)基因多态性的基因分型:结果显示:OPRM1 AA 基因型的 11 岁以下学龄儿童的体重指数较高(p< 0.05)。与 AA 等位基因携带者相比,12 岁以上携带 G 等位基因 OPRM1 的儿童术后疼痛敏感性和疼痛强度增加(3.28± 1.95 vs 4.91± 2.17;p< 0.05):讨论:OPRM1 118A>G多态性可能解释了12岁以上儿童对术后疼痛感受的差异,也可能是调整镇痛剂剂量的有用预测指标,但剂量是相对于患者的需求而言的,与患者的遗传特征无关。在年龄较小的儿童中,多态性OPRM1 118G等位基因的携带者可能会因澳门巴黎人娱乐官网表达的减少而免受肥胖的影响。关键词:多态性、OPRM1、阿片类、疼痛、儿童
The Impact of Opioid Receptor Gene Polymorphism on Fentanyl and Alfentanil’s Analgesic Effects in the Pediatric Perioperative Period
Introduction: The polymorphism of the gene coding mu-opioid receptor (OPRM1) is one of the factors contributing to the variability in the response to opioid analgesics in children. The goal of this study is to investigate its role in association with postoperative acute pain in children of various ages. Methods: This prospective study analyzed 110 pediatric patients, after plastic or orthopedic surgery, who were genotyped and randomly assigned to receive fentanyl or alfentanil. Postoperative pain was rated using Numerical Rating Scale (0– 10). All the patients were genotyped forOPRM1 118A>G (rs1799971) gene polymorphism. Results: School children under the age of 11 with the OPRM1 AA genotype were shown to have a higher BMI (p< 0.05). Children over the age of 12 carrying G allele OPRM1, had increased postoperative pain sensitivity and intensity (3.28± 1.95 vs 4.91± 2.17; p< 0.05), as compared to AA allele carriers. Discussion:OPRM1 118A>G polymorphism may explain the variation in the perception of postoperative pain in children over the age of 12 and may be a useful predictor for adjusting the dose of analgesics, but the dose is relative to the patient’s needs regardless of his genetic characteristics. In younger children, carriers of polymorphic OPRM1 118G allele may be protected from obesity, due to diminished MOP expression.
Keywords: polymorphism, OPRM1, opioid, pain, children