Towards personalized treatment of pain using a quantitative systems pharmacology approach

被引:14
作者
Goulooze, Sebastiaan C. [1 ]
Krekels, Elke H. J. [1 ]
Van Dijk, Monique [2 ,3 ,4 ]
Tibboel, Dick [2 ,3 ]
van der Graaf, Piet H. [1 ,7 ]
Hankemeier, Thomas [5 ]
Knibbe, Catherijne A. J. [1 ,6 ]
Van Hasselt, J. G. Coen [1 ]
机构
[1] Leiden Univ, Leiden Acad Ctr Drug Res, Cluster Syst Pharmacol, Div Pharmacol, Leiden, Netherlands
[2] Erasmus MC Sophia Childrens Hosp, Intens Care, Rotterdam, Netherlands
[3] Erasmus MC Sophia Childrens Hosp, Dept Pediat Surg, Rotterdam, Netherlands
[4] Erasmus MC Sophia Childrens Hosp, Dept Pediat, Div Neonatol, Rotterdam, Netherlands
[5] Leiden Univ, Leiden Acad Ctr Drug Res, Cluster Syst Pharmacol, Div Analyt Biosci, Leiden, Netherlands
[6] St Antonius Hosp, Dept Clin Pharm, Nieuwegein, Netherlands
[7] Canterbury Innovat Ctr, Certara QSP, Canterbury, Kent, England
关键词
Pain; Personalized medicine; Quantitative systems pharmacology; Biomarker; Analgesia; POSTOPERATIVE PAIN; PRECISION MEDICINE; DRUG DISCOVERY; PSYCHOLOGICAL PREDICTORS; OPIOID ANALGESIA; BIOMARKERS; MORPHINE; PLACEBO; PERCEPTION; EXPERIENCE;
D O I
10.1016/j.ejps.2017.05.027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pain is a complex biopsychosocial phenomenon of which the intensity, location and duration depends on various underlying components. Treatment of pain is associated with considerable inter-individual variability, and as such, requires a personalized approach. However, a priori prediction of optimal analgesic treatment for individual patients is still challenging. Another challenge is the assessment and treatment of pain in patients unable to self-report pain. In this mini-review, we first provide a brief overview of the various components underlying pain, and their associated biomarkers. These include clinical, psychosocial, neurophysiological, and biochemical components. We then discuss the use of empirical and mechanism-based pharmacokinetic-pharmacodynamic modelling to support personalized treatment of pain. Finally, we propose how these concepts can be extended to a quantitative systems pharmacology (QSP) approach that integrates the components of clinical pain and treatment response. This integrative approach can support predictions of optimal pharmacotherapy of pain, compared with approaches that focus on single components of pain. Moreover, combination of QSP modelling with state-of-the-art metabolomics approaches may offer unique possibilities to identify novel pain biomarkers. Such biomarkers could support both the personalized treatment of pain and translational drug development of novel analgesic agents. In conclusion, a QSP approach will likely improve our ability to predict pain and treatment response, paving the way for personalized treatment of pain.
引用
收藏
页码:S32 / S38
页数:7
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