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On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials

Previous research reports suggest greater baseline variability is associated with greater pain relief in those who receive a placebo. However, studies that evidence this association do not control for confounding effects from regression to the mean and natural history. In this report, we analyzed da...

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Autores principales: Tiwari, Siddharth R., Vigotsky, Andrew D., Apkarian, A. Vania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024103/
https://www.ncbi.nlm.nih.gov/pubmed/35465296
http://dx.doi.org/10.3389/fpain.2022.844309
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author Tiwari, Siddharth R.
Vigotsky, Andrew D.
Apkarian, A. Vania
author_facet Tiwari, Siddharth R.
Vigotsky, Andrew D.
Apkarian, A. Vania
author_sort Tiwari, Siddharth R.
collection PubMed
description Previous research reports suggest greater baseline variability is associated with greater pain relief in those who receive a placebo. However, studies that evidence this association do not control for confounding effects from regression to the mean and natural history. In this report, we analyzed data from two randomized clinical trials (Placebo I and Placebo II, total N = 139) while adjusting for the effects of natural history and regression to the mean via a no treatment group. Results agree between the two placebo groups in each study: both placebo groups showed negligible semi-partial correlations between baseline variability and adjusted response [r(sp) (CI(95%)) = 0.22 (0.03, 0.42) and 0 (−0.07, 0.07) for Placebo I and II, respectively]. The no treatment group in Placebo I showed a negative correlation [−0.22 (−0.43, −0.02)], but the no treatment and drug groups in Placebo II's correlations were negligible [−0.02 (−0.08, 0.02) and 0.00 (−0.10, 0.12) for the no treatment and drug groups, respectively]. When modeled as a linear covariate, baseline pain variability accounted for <1% of the variance in post-intervention pain across both studies. Even after adjusting for baseline pain and natural history, the inability of baseline pain variability to account for substantial variance in pain response highlights that previous results concerning pain variability and treatment response may be inconsistent. Indeed, the relationship appears to be neither consistently specific nor sensitive to improvements in the placebo group. More work is needed to understand and establish the prognostic value of baseline pain variability—especially its placebo specificity and generalizability across patient populations.
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spelling pubmed-90241032022-04-23 On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials Tiwari, Siddharth R. Vigotsky, Andrew D. Apkarian, A. Vania Front Pain Res (Lausanne) Pain Research Previous research reports suggest greater baseline variability is associated with greater pain relief in those who receive a placebo. However, studies that evidence this association do not control for confounding effects from regression to the mean and natural history. In this report, we analyzed data from two randomized clinical trials (Placebo I and Placebo II, total N = 139) while adjusting for the effects of natural history and regression to the mean via a no treatment group. Results agree between the two placebo groups in each study: both placebo groups showed negligible semi-partial correlations between baseline variability and adjusted response [r(sp) (CI(95%)) = 0.22 (0.03, 0.42) and 0 (−0.07, 0.07) for Placebo I and II, respectively]. The no treatment group in Placebo I showed a negative correlation [−0.22 (−0.43, −0.02)], but the no treatment and drug groups in Placebo II's correlations were negligible [−0.02 (−0.08, 0.02) and 0.00 (−0.10, 0.12) for the no treatment and drug groups, respectively]. When modeled as a linear covariate, baseline pain variability accounted for <1% of the variance in post-intervention pain across both studies. Even after adjusting for baseline pain and natural history, the inability of baseline pain variability to account for substantial variance in pain response highlights that previous results concerning pain variability and treatment response may be inconsistent. Indeed, the relationship appears to be neither consistently specific nor sensitive to improvements in the placebo group. More work is needed to understand and establish the prognostic value of baseline pain variability—especially its placebo specificity and generalizability across patient populations. Frontiers Media S.A. 2022-04-08 /pmc/articles/PMC9024103/ /pubmed/35465296 http://dx.doi.org/10.3389/fpain.2022.844309 Text en Copyright © 2022 Tiwari, Vigotsky and Apkarian. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pain Research
Tiwari, Siddharth R.
Vigotsky, Andrew D.
Apkarian, A. Vania
On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title_full On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title_fullStr On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title_full_unstemmed On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title_short On the Relationship Between Pain Variability and Relief in Randomized Clinical Trials
title_sort on the relationship between pain variability and relief in randomized clinical trials
topic Pain Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9024103/
https://www.ncbi.nlm.nih.gov/pubmed/35465296
http://dx.doi.org/10.3389/fpain.2022.844309
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