Continuing war on pain: a personalized approach to the therapy with nonsteroidal anti-inflammatory drugs and opioids

被引:13
作者
Bach-Rojecky, Lidija [1 ]
Vadunec, Dalia [1 ]
Zunic, Katarina [1 ]
Kurija, Jelena [1 ]
Sipicki, Sara [1 ]
Gregg, Ryan [2 ]
Mikula, Ivan [3 ,4 ,5 ]
Primorac, Dragan [3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11 ]
机构
[1] Univ Zagreb, Dept Pharmacol, Fac Pharm & Biochem, A Kovacica 1, Zagreb 10000, Croatia
[2] OneOme LLC, 807 Broadway St NE 100, Minneapolis, MN 55413 USA
[3] St Catherine Specialty Hosp, Zagreb 10000, Croatia
[4] St Catherine Specialty Hosp, Zagreb 10000, Croatia
[5] St Catherine Specialty Hosp, Zabok 49210, Croatia
[6] Penn State Univ, Eberly Coll Sci, Dept Forens Sci, 517 Thomas St, State Coll, PA 16803 USA
[7] Univ Split, Dept Pediat, Sch Med, Soltanska 2, Split 21000, Croatia
[8] Univ Osijek, Dept Pediat, Sch Med, Ul Cara Hadrijana 10, Osijek 31000, Croatia
[9] Univ Osijek, Fac Dent Med & Hlth, Dept Pediat, Crkvena 21, Osijek 31000, Croatia
[10] Univ Rijeka, Sch Med, Dept Biotechnol, Brce Branchetta 20-1, Rijeka 51000, Croatia
[11] Childrens Hosp Srebrnjak, Srebrnjak 100, Zagreb 10000, Croatia
关键词
analgesic effect; epigenetics; genes; nonsteroidal anti-inflammatory drugs; opioids; pain treatment; pharmacogenetics; side effects; toxicity; CLINICAL PHARMACOKINETICS; INDIVIDUAL-DIFFERENCES; EPIGENETIC REGULATION; MORPHINE; METABOLISM; PHARMACOGENETICS; BIOAVAILABILITY; PHARMACOLOGY; POLYMORPHISM; CYP2C9;
D O I
10.2217/pme-2018-0116
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Successful pain management requires the delivery of analgesia with minimal risk of adverse drug reactions. Nonsteroidal anti-inflammatory drugs and opioids remain the mainstay of treatment for the majority of patients. Unfortunately, almost 50% of all patients experience inadequate pain relief and serious side effects. Allelic variants in genes coding for target proteins, transporters and enzymes, which govern analgesic drugs action and their fate in the organism, might explain inter-individual variability in pain severity and in drug-induced pain relief and toxicities. Additionally, it seems that epigenetic changes contribute to the highly variable response to pain treatment. Therefore, pharmacogenomic testing might be a valuable tool for personalization of pain treatment, with a multidisciplinary team approach involved.
引用
收藏
页码:171 / 184
页数:14
相关论文
共 89 条
  • [31] Bluprenorphine - Clinical pharmacokinetics in the treatment of opioid dependence
    Elkader, A
    Sproule, B
    [J]. CLINICAL PHARMACOKINETICS, 2005, 44 (07) : 661 - 680
  • [32] Comparative pharmacology and toxicology of tramadol and tapentadol
    Faria, J.
    Barbosa, J.
    Moreira, R.
    Queiros, O.
    Carvalho, F.
    Dinis-Oliveira, R. J.
    [J]. EUROPEAN JOURNAL OF PAIN, 2018, 22 (05) : 827 - 844
  • [33] CYP2C9 variants as a risk modifier of NSAID-related gastrointestinal bleeding: a case-control study
    Figueiras, Adolfo
    Estany-Gestal, Ana
    Aguirre, Carmelo
    Ruiz, Borja
    Vidal, Xavier
    Carvajal, Alfonso
    Salado, Ines
    Salgado-Barreira, Angel
    Rodella, Luca
    Moretti, Ugo
    Ibanez, Luisa
    [J]. PHARMACOGENETICS AND GENOMICS, 2016, 26 (02) : 66 - 73
  • [34] Individual differences in pain: understanding the mosaic that makes pain personal
    Fillingim, Roger B.
    [J]. PAIN, 2017, 158 (04) : S11 - S18
  • [35] CLINICAL PHARMACOKINETICS OF PARACETAMOL
    FORREST, JAH
    CLEMENTS, JA
    PRESCOTT, LF
    [J]. CLINICAL PHARMACOKINETICS, 1982, 7 (02) : 93 - 107
  • [36] Oxycodone:: a pharmacological and clinical review
    Gallego, A. Ordonez
    Baron, M. Gonzalez
    Arranz, E. Espinosa
    [J]. CLINICAL & TRANSLATIONAL ONCOLOGY, 2007, 9 (05) : 298 - 307
  • [37] CLINICAL PHARMACOKINETICS OF MORPHINE
    GLARE, PA
    WALSH, TD
    [J]. THERAPEUTIC DRUG MONITORING, 1991, 13 (01) : 1 - 23
  • [38] Comparative pharmacokinetics and bioavailability of tapentadol following oral administration of immediate- and prolonged-release formulations
    Goehler, Karin
    Brett, Martin
    Smit, Johan W.
    Rengelshausen, Jens
    Terlinden, Rolf
    [J]. INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2013, 51 (04) : 338 - 348
  • [39] Celecoxib, a selective cyclooxygenase-2 inhibitor for the treatment of rheumatoid arthritis and osteoarthritis
    Goldenberg, MM
    [J]. CLINICAL THERAPEUTICS, 1999, 21 (09) : 1497 - 1513
  • [40] HALMED, 2017, IZVJ POTR LIJ REP HR