Genetics and the placebo effect: the placebome

被引:170
作者
Hall, Kathryn T. [1 ,2 ]
Loscalzo, Joseph [3 ]
Kaptchuk, Ted J. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Program Placebo Studies, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med,Div Gen Med & Primary Care, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med, Boston, MA 02215 USA
关键词
placebo; RCT; COMT; no treatment control; pharmacogenomics; CATECHOL-O-METHYLTRANSFERASE; MAJOR DEPRESSIVE DISORDER; MONOAMINE-OXIDASE; CLINICAL-TRIALS; MORPHINE REQUIREMENTS; ANTAGONIST NALOXONE; NEUROTROPHIC FACTOR; DOPAMINE RELEASE; COMT GENE; POLYMORPHISM;
D O I
10.1016/j.molmed.2015.02.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Placebos are indispensable controls in randomized clinical trials (RCTs), and placebo responses significantly contribute to routine clinical outcomes. Recent neurophysiological studies reveal neurotransmitter pathways that mediate placebo effects. Evidence that genetic variations in these pathways can modify placebo effects raises the possibility of using genetic screening to identify placebo responders and thereby increase RCT efficacy and improve therapeutic care. Furthermore, the possibility of interaction between placebo and drug molecular pathways warrants consideration in RCT design. The study of genomic effects on placebo response, 'the placebome', is in its infancy. Here, we review evidence from placebo studies and RCTs to identify putative genes in the placebome, examine evidence for placebo-drug interactions, and discuss implications for RCTs and clinical care.
引用
收藏
页码:285 / 294
页数:10
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