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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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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. |
format | Online Article Text |
id | pubmed-3479140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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