Hall Kathryn T, Loscalzo Joseph, Kaptchuk Ted J
Department of Medicine, Brigham & Women's Hospital, Boston, MA 02115, USA.
Division of Preventive Medicine, Brigham & Women's Hospital, Boston, MA 02215, USA.
Pharmacogenomics. 2019 May;20(7):529-551. doi: 10.2217/pgs-2019-0001.
Disease, drugs and the placebos used as comparators are inextricably linked in the methodology of the double-blind, randomized controlled trial. Nonetheless, pharmacogenomics, the study of how individuals respond to drugs based on genetic substrate, focuses primarily on the link between genes and drugs, while the link between genes and disease is often overlooked and the link between genes and placebos is largely ignored. Herein, we use the example of the enzyme catechol-O-methyltransferase to examine the hypothesis that genes can function as pharmacogenomic hubs across system-wide regulatory processes that, if perturbed in andomized controlled trials, can have primary and combinatorial effects on drug and placebo responses.
在双盲随机对照试验的方法学中,疾病、药物以及用作对照的安慰剂紧密相连。尽管如此,药物基因组学,即研究个体基于遗传底物如何对药物作出反应的学科,主要关注基因与药物之间的联系,而基因与疾病之间的联系常常被忽视,基因与安慰剂之间的联系在很大程度上也被忽略。在此,我们以儿茶酚-O-甲基转移酶为例,来检验这样一个假说:基因可作为跨全系统调节过程的药物基因组学枢纽,若在随机对照试验中受到干扰,可能会对药物和安慰剂反应产生主要及组合效应。