The Effect of OPRM1 and COMT Genotypes on the Analgesic Response to Intravenous Fentanyl Labor Analgesia

被引:32
|
作者
Landau, Ruth [1 ]
Liu, Shih-Kai [2 ,3 ]
Blouin, Jean-Louis [4 ]
Carvalho, Brendan [5 ]
机构
[1] Univ Washington, Dept Anesthesiol & Pain Med, Med Ctr, Seattle, WA 98195 USA
[2] Univ Washington, Dept Anesthesiol, Seattle, WA 98195 USA
[3] China Med Univ Hosp, Dept Anesthesia Pain Serv & Crit Care Med, Taichung, Taiwan
[4] Univ Hosp Geneva, Geneva, Switzerland
[5] Stanford Univ, Med Ctr, Dept Anesthesiol, Palo Alto, CA 94304 USA
来源
ANESTHESIA AND ANALGESIA | 2013年 / 116卷 / 02期
关键词
CATECHOL-O-METHYLTRANSFERASE; INTRATHECAL FENTANYL; CANCER PAIN; MORPHINE; GENE; REQUIREMENTS; POLYMORPHISM;
D O I
10.1213/ANE.0b013e318273f2c7
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BACKGROUND: IV fentanyl is used as a labor analgesic; however, few studies have reported the effects of IV fentanyl for early labor analgesia. We evaluated the analgesic response to IV fentanyl according to the combined effect of the single-nucleotide polymorphisms rs1799971 (c.118A/G, p. 40Asn/Asp) of the mu-opioid receptor gene (OPRM1) and rs4680 (c.472G/A, p.158Val/Met) of the catechol-O-methyltransferase (COMT) gene in women requesting labor analgesia. METHODS: Labor analgesia was initiated with IV fentanyl 1.5 mu g/kg. The primary outcome was analgesic success, defined as Numerical Verbal Pain Scale score <= 10/100 15 minutes after the dose of fentanyl. Analgesic and side effect outcomes were compared according to OPRM1 and COMT genotypes. RESULTS: One hundred six women were enrolled and received IV fentanyl. IV analgesic success was 6% in women with the combination Asn/Asn-Met/Met (n = 17) versus 20% in all other women combined (not Asn/Asn-Met/Met; P = 0.30; difference = 14%; 95% confidence interval [CI], -10% to 26%). IV analgesic success was 20% in women 118A/A (Asn/Asn) versus 21% for A/G and G/G of OPRM1 (P = 0.82; difference = 2%; 95% CI, -17% to 19%), and 10% in women 472A (Met/Met) versus 22% for A/G (Met/Val) and GIG (Val/Val) of COMT (P = 0.24; difference = 12%; 95% CI, -6% to 26%). Met/Met158 (n = 31) versus Met/Val or Val/Val of COMT was associated with a smaller decrease in Numerical Verbal Pain Scale (24 +/- 18 vs 37 +/- 23; P = 0.005; mean difference = -13; 99% Cl, -25 to -1). CONCLUSION: This study was underpowered to draw firm conclusions on the influence of OPRM1 and COMT genotypes on labor analgesia with IV fentanyl. Further larger studies are needed to evaluate whether genotyping COMT alone or in combination with OPRM1 may have potentially useful clinical implications, such as not offering IV fentanyl in early labor to women who will most likely not benefit from it. (Anesth Analg 2013;116:386-91)
引用
收藏
页码:386 / 391
页数:6
相关论文
共 50 条
  • [21] Lack of association between DRD2 and OPRM1 genotypes and adiposity
    Hardman, C. A.
    Rogers, P. J.
    Timpson, N. J.
    Munafo, M. R.
    INTERNATIONAL JOURNAL OF OBESITY, 2014, 38 (05) : 730 - 736
  • [22] Polymorphism of the μ-Opioid Receptor Gene (OPRM1 118A>G) Affects Fentanyl-Induced Analgesia During Anesthesia and Recovery
    Wei Dong Wu
    Yi Wang
    Yong Ming Fang
    Hai Yan Zhou
    Molecular Diagnosis & Therapy, 2009, 13 (5) : 331 - 337
  • [23] Effect of OPRM variant on labor analgesia and post-cesarean delivery analgesia
    Tan, E. C.
    Sia, A. T.
    INTERNATIONAL JOURNAL OF OBSTETRIC ANESTHESIA, 2010, 19 (04) : 458 - 459
  • [24] COMT and OPRM1 genotype associations with daily knee pain variability and activity induced pain
    Martire, Lynn M.
    Wilson, Stephanie J.
    Small, Brent J.
    Conley, Yvette P.
    Janicki, Piotr K.
    Sliwinski, Martin J.
    SCANDINAVIAN JOURNAL OF PAIN, 2016, 10 : 6 - 12
  • [25] Lack of association between DRD2 and OPRM1 genotypes and adiposity
    C A Hardman
    P J Rogers
    N J Timpson
    M R Munafò
    International Journal of Obesity, 2014, 38 : 730 - 736
  • [26] Genetic Influences of OPRM1, OPRD1 and COMT on Morphine Analgesia in a Multi-Modal, Multi-Tissue Human Experimental Pain Model
    Nielsen, Lecia M.
    Christrup, Lona L.
    Sato, Hiroe
    Drewes, Asbjorn M.
    Olesen, Anne E.
    BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2017, 121 (01) : 6 - 12
  • [27] Genetic polymorphisms of OPRM1 on the efficacy and safety of anesthetic and analgesic agents: a systematic review
    Yee, Liew
    Capule, Francis R.
    Makmor-Bakry, Mohd
    PHARMACOGENOMICS, 2022, 23 (10) : 609 - 617
  • [28] Effect of intravenous versus epidural fentanyl on the minimum local analgesic concentration of epidural bupivacaine in labor
    Polley, LS
    Columb, MO
    Naughton, NN
    Wagner, DS
    Dorantes, DM
    van de Ven, CJM
    ANESTHESIOLOGY, 2000, 93 (01) : 122 - 128
  • [29] Minimum analgesic doses of fentanyl and sufentanil for epidural analgesia in the first stage of labor
    Capogna, G
    Camorcia, M
    Columb, MO
    ANESTHESIA AND ANALGESIA, 2003, 96 (04): : 1178 - 1182
  • [30] Association of single nucleotide polymorphisms of ABCB1, OPRM1 and COMT with pain perception in cancer patients
    Wang, Xu-shi
    Song, Hai-bin
    Chen, Si
    Zhang, Wei
    Liu, Jia-qi
    Huang, Chao
    Wang, Hao-ran
    Chen, Yuan
    Chu, Qian
    JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2015, 35 (05) : 752 - 758