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

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 l...

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Autores principales: Hall, Kathryn T., Lembo, Anthony J., Kirsch, Irving, Ziogas, Dimitrios C., Douaiher, Jeffrey, Jensen, Karin B., Conboy, Lisa A., Kelley, John M., Kokkotou, Efi, Kaptchuk, Ted J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479140/
https://www.ncbi.nlm.nih.gov/pubmed/23110189
http://dx.doi.org/10.1371/journal.pone.0048135
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author Hall, Kathryn T.
Lembo, Anthony J.
Kirsch, Irving
Ziogas, Dimitrios C.
Douaiher, Jeffrey
Jensen, Karin B.
Conboy, Lisa A.
Kelley, John M.
Kokkotou, Efi
Kaptchuk, Ted J.
author_facet Hall, Kathryn T.
Lembo, Anthony J.
Kirsch, Irving
Ziogas, Dimitrios C.
Douaiher, Jeffrey
Jensen, Karin B.
Conboy, Lisa A.
Kelley, John M.
Kokkotou, Efi
Kaptchuk, Ted J.
author_sort Hall, Kathryn T.
collection PubMed
description 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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spelling pubmed-34791402012-10-29 Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome Hall, Kathryn T. Lembo, Anthony J. Kirsch, Irving Ziogas, Dimitrios C. Douaiher, Jeffrey Jensen, Karin B. Conboy, Lisa A. Kelley, John M. Kokkotou, Efi Kaptchuk, Ted J. PLoS One Research Article 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. Public Library of Science 2012-10-23 /pmc/articles/PMC3479140/ /pubmed/23110189 http://dx.doi.org/10.1371/journal.pone.0048135 Text en © 2012 Hall et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hall, Kathryn T.
Lembo, Anthony J.
Kirsch, Irving
Ziogas, Dimitrios C.
Douaiher, Jeffrey
Jensen, Karin B.
Conboy, Lisa A.
Kelley, John M.
Kokkotou, Efi
Kaptchuk, Ted J.
Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title_full Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title_fullStr Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title_full_unstemmed Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title_short Catechol-O-Methyltransferase val158met Polymorphism Predicts Placebo Effect in Irritable Bowel Syndrome
title_sort catechol-o-methyltransferase val158met polymorphism predicts placebo effect in irritable bowel syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479140/
https://www.ncbi.nlm.nih.gov/pubmed/23110189
http://dx.doi.org/10.1371/journal.pone.0048135
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