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Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial

Emerging evidence suggests that interleukin (IL)-8 has a protective role in the context of depression. Higher levels of IL-8 are associated with lower depressive symptom severity among depressed patients, and treatment-related increases in IL-8 correlate with a positive response in depressed patient...

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Autores principales: Kruse, Jennifer L., Boyle, Chloe C., Olmstead, Richard, Breen, Elizabeth C., Tye, Susannah J., Eisenberger, Naomi I., Irwin, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309160/
https://www.ncbi.nlm.nih.gov/pubmed/35871638
http://dx.doi.org/10.1038/s41598-022-16364-3
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author Kruse, Jennifer L.
Boyle, Chloe C.
Olmstead, Richard
Breen, Elizabeth C.
Tye, Susannah J.
Eisenberger, Naomi I.
Irwin, Michael R.
author_facet Kruse, Jennifer L.
Boyle, Chloe C.
Olmstead, Richard
Breen, Elizabeth C.
Tye, Susannah J.
Eisenberger, Naomi I.
Irwin, Michael R.
author_sort Kruse, Jennifer L.
collection PubMed
description Emerging evidence suggests that interleukin (IL)-8 has a protective role in the context of depression. Higher levels of IL-8 are associated with lower depressive symptom severity among depressed patients, and treatment-related increases in IL-8 correlate with a positive response in depressed patients. This study (a secondary analysis of a completed randomized controlled trial) aimed to examine whether higher levels of IL-8 mitigate increases in depressed mood in response to an experimental model of inflammation induced depression. Given epidemiologic relationships identified between IL-6, tumor necrosis factor (TNF)- α, and subsequent depression, levels of these pro-inflammatory cytokines were also explored as potential moderators of depressed mood response to endotoxin. Secondary analyses were completed on data from healthy adults (n = 114) who completed a double-blind, placebo-controlled randomized trial in which participants were randomly assigned to receive either a single infusion of low-dose endotoxin (derived from Escherichia coli; 0.8 ng/kg of body weight) or placebo (same volume of 0.9% saline). IL-8, as well as IL-6 and TNF- α, were measured at baseline prior to infusion, and depressed mood and feelings of social disconnection were assessed approximately hourly. Baseline levels of IL-8, but not IL-6 or TNF-α, moderated depressed mood (β = − 0.274, p = .03) and feelings of social disconnection (β = − 0.307, p = .01) responses, such that higher baseline IL-8 was associated with less increase in depressed mood and feelings of social disconnection in the endotoxin, but not placebo, condition. IL-8 had threshold effects, in which highest quartile IL-8 (≥ 2.7 pg/mL) attenuated increases in depressed mood in response to endotoxin as compared to lower IL-8 quartiles (p = .02). These findings suggest that IL-8 may be a biological factor that mitigates risk of inflammation-associated depression. Clinical trials registration: ClinicalTrials.gov NCT01671150, registration date 23/08/2012.
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spelling pubmed-93091602022-07-26 Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial Kruse, Jennifer L. Boyle, Chloe C. Olmstead, Richard Breen, Elizabeth C. Tye, Susannah J. Eisenberger, Naomi I. Irwin, Michael R. Sci Rep Article Emerging evidence suggests that interleukin (IL)-8 has a protective role in the context of depression. Higher levels of IL-8 are associated with lower depressive symptom severity among depressed patients, and treatment-related increases in IL-8 correlate with a positive response in depressed patients. This study (a secondary analysis of a completed randomized controlled trial) aimed to examine whether higher levels of IL-8 mitigate increases in depressed mood in response to an experimental model of inflammation induced depression. Given epidemiologic relationships identified between IL-6, tumor necrosis factor (TNF)- α, and subsequent depression, levels of these pro-inflammatory cytokines were also explored as potential moderators of depressed mood response to endotoxin. Secondary analyses were completed on data from healthy adults (n = 114) who completed a double-blind, placebo-controlled randomized trial in which participants were randomly assigned to receive either a single infusion of low-dose endotoxin (derived from Escherichia coli; 0.8 ng/kg of body weight) or placebo (same volume of 0.9% saline). IL-8, as well as IL-6 and TNF- α, were measured at baseline prior to infusion, and depressed mood and feelings of social disconnection were assessed approximately hourly. Baseline levels of IL-8, but not IL-6 or TNF-α, moderated depressed mood (β = − 0.274, p = .03) and feelings of social disconnection (β = − 0.307, p = .01) responses, such that higher baseline IL-8 was associated with less increase in depressed mood and feelings of social disconnection in the endotoxin, but not placebo, condition. IL-8 had threshold effects, in which highest quartile IL-8 (≥ 2.7 pg/mL) attenuated increases in depressed mood in response to endotoxin as compared to lower IL-8 quartiles (p = .02). These findings suggest that IL-8 may be a biological factor that mitigates risk of inflammation-associated depression. Clinical trials registration: ClinicalTrials.gov NCT01671150, registration date 23/08/2012. Nature Publishing Group UK 2022-07-24 /pmc/articles/PMC9309160/ /pubmed/35871638 http://dx.doi.org/10.1038/s41598-022-16364-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kruse, Jennifer L.
Boyle, Chloe C.
Olmstead, Richard
Breen, Elizabeth C.
Tye, Susannah J.
Eisenberger, Naomi I.
Irwin, Michael R.
Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title_full Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title_fullStr Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title_full_unstemmed Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title_short Interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
title_sort interleukin-8 and depressive responses to an inflammatory challenge: secondary analysis of a randomized controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309160/
https://www.ncbi.nlm.nih.gov/pubmed/35871638
http://dx.doi.org/10.1038/s41598-022-16364-3
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