Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome

被引:139
作者
Hall, Kathryn T. [1 ,2 ]
Lembo, Anthony J. [2 ,3 ]
Kirsch, Irving [2 ,4 ]
Ziogas, Dimitrios C. [5 ]
Douaiher, Jeffrey [6 ]
Jensen, Karin B. [2 ,7 ]
Conboy, Lisa A. [2 ]
Kelley, John M. [2 ,7 ,8 ]
Kokkotou, Efi [2 ,3 ]
Kaptchuk, Ted J. [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Gen Med & Primary Care, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Program Placebo Studies, Boston, MA 02215 USA
[3] Beth Israel Deaconess Med Ctr, Dept Gastroenterol, Boston, MA 02215 USA
[4] Univ Plymouth, Sch Psychol, Plymouth PL4 8AA, Devon, England
[5] Univ Athens, Dept Internal Med, Athens, Greece
[6] Dept Surg, Baltimore, MD USA
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat, Boston, MA USA
[8] Endicott Coll, Beverly, MA USA
来源
PLOS ONE | 2012年 / 7卷 / 10期
关键词
COMT VAL(158)MET POLYMORPHISM; PREFRONTAL CORTEX; INDIVIDUAL-DIFFERENCES; CLINICAL-TRIALS; END-POINT; GENOTYPE; DOPAMINE; METAANALYSIS; IMPROVEMENT; RESPONSES;
D O I
10.1371/journal.pone.0048135
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Identifying patients who are potential placebo responders has major implications for clinical practice and trial design. Catechol-O-methyltransferase (COMT), an important enzyme in dopamine catabolism plays a key role in processes associated with the placebo effect such as reward, pain, memory and learning. We hypothesized that the COMT functional val158met polymorphism, was a predictor of placebo effects and tested our hypothesis in a subset of 104 patients from a previously reported randomized controlled trial in irritable bowel syndrome (IBS). The three treatment arms from this study were: no-treatment ("waitlist"), placebo treatment alone ("limited") and, placebo treatment "augmented" with a supportive patient-health care provider interaction. The primary outcome measure was change from baseline in IBS-Symptom Severity Scale (IBS-SSS) after three weeks of treatment. In a regression model, the number of methionine alleles in COMT val158met was linearly related to placebo response as measured by changes in IBS-SSS (p = .035). The strongest placebo response occurred in met/met homozygotes treated in the augmented placebo arm. A smaller met/met associated effect was observed with limited placebo treatment and there was no effect in the waitlist control. These data support our hypothesis that the COMT val158met polymorphism is a potential biomarker of placebo response.
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页数:6
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