Giacon Martina, Cargnin Sarah, Talmon Maria, Terrazzino Salvatore
Department of Pharmaceutical Sciences, University of Piemonte Orientale "A. Avogadro", Largo Donegani 2, 28100, Novara, Italy.
Department of Health Sciences, Università del Piemonte Orientale (UPO), 28100, Novara, Italy.
Eur J Clin Pharmacol. 2025 Mar;81(3):403-417. doi: 10.1007/s00228-024-03798-z. Epub 2025 Jan 7.
Several studies have attempted to identify genetic determinants of clinical response to opioids administered during labor or after cesarean section. However, their results were often contrasting. A systematic review and meta-analysis was conducted to quantitatively assess the association between gene polymorphisms and clinical outcomes of opioid administration in the treatment of labor pain and post-cesarean pain.
A comprehensive search was performed up to December 2023 using PubMed, Web of Knowledge, Cochrane Library, and OpenGrey databases. The clinical endpoints of interest were pain score after opioid treatment, total opioid consumption, patient's analgesic satisfaction, and incidence of opioid side effects. Random-effects meta-analyses were conducted when data were available in at least three studies.
Twenty-six studies enrolling 7765 patients were included in the systematic review. Overall, a total of 12 candidate polymorphic genes (OPRM1, COMT, CYP2D6, CYP3A4, ABCB1, ABCC3, UGT2B7, CGRP, OPRK1, OPRD1, KCNJ6, KCNJ9) were considered by the included studies, among which the most investigated variant was OPRM1 rs1799971. Overall pooled results indicated that individuals carrying the G allele of OPRM1 rs1799971 required higher opioid doses for pain management in comparison to rs1799971 AA subjects (standardized mean difference: 0.26; 95% CI: 0.09-0.44; P = 0.003). Such an association was confirmed in the subgroups of patients with labor pain and post-cesarean pain.
The present meta-analysis provides strong evidence of an association between OPRM1 rs1799971 and opioid dose requirement for relief of labor pain or post-cesarean pain. However, given the insufficient evidence for other polymorphic gene variants, large studies are still needed to investigate the impact of genetic variability on the efficacy and safety of opioid medications for relief of labor pain and post-cesarean pain (INPLASY Registration No. 202410040).
多项研究试图确定分娩期间或剖宫产术后使用阿片类药物的临床反应的遗传决定因素。然而,它们的结果往往相互矛盾。进行了一项系统评价和荟萃分析,以定量评估基因多态性与阿片类药物治疗分娩疼痛和剖宫产后疼痛的临床结局之间的关联。
截至2023年12月,使用PubMed、Web of Knowledge、Cochrane图书馆和OpenGrey数据库进行了全面检索。感兴趣的临床终点是阿片类药物治疗后的疼痛评分、阿片类药物总消耗量、患者的镇痛满意度以及阿片类药物副作用的发生率。当至少三项研究中有可用数据时,进行随机效应荟萃分析。
系统评价纳入了26项研究,共7765例患者。总体而言,纳入的研究共考虑了12个候选多态性基因(OPRM1、COMT、CYP2D6、CYP3A4、ABCB1、ABCC3、UGT2B7、CGRP、OPRK1、OPRD1、KCNJ6、KCNJ9),其中研究最多的变体是OPRM1 rs1799971。总体汇总结果表明,与rs1799971 AA受试者相比,携带OPRM1 rs1799971 G等位基因的个体在疼痛管理中需要更高剂量的阿片类药物(标准化平均差:0.26;95% CI:0.09 - 0.44;P = 0.003)。这种关联在分娩疼痛和剖宫产后疼痛患者亚组中得到证实。
本荟萃分析提供了强有力的证据,证明OPRM1 rs1799971与缓解分娩疼痛或剖宫产后疼痛所需的阿片类药物剂量之间存在关联。然而,鉴于其他多态性基因变体的证据不足,仍需要大型研究来调查基因变异性对阿片类药物缓解分娩疼痛和剖宫产后疼痛的疗效和安全性的影响(INPLASY注册号:202410040)。