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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.
Afiliação
  • Kruse JL; Norman Cousins Center for Psychoneuroimmunology, Los Angeles, USA. jkruse@mednet.ucla.edu.
  • Boyle CC; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, Jane and Terry Semel Institute for Neuroscience and Human Behavior at UCLA, 300 UCLA Medical Plaza, Room 2273, Los Angeles, CA, 90095, USA. jkruse@mednet.ucla.edu.
  • Olmstead R; Norman Cousins Center for Psychoneuroimmunology, Los Angeles, USA.
  • Breen EC; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, Jane and Terry Semel Institute for Neuroscience and Human Behavior at UCLA, 300 UCLA Medical Plaza, Room 2273, Los Angeles, CA, 90095, USA.
  • Tye SJ; Norman Cousins Center for Psychoneuroimmunology, Los Angeles, USA.
  • Eisenberger NI; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, Jane and Terry Semel Institute for Neuroscience and Human Behavior at UCLA, 300 UCLA Medical Plaza, Room 2273, Los Angeles, CA, 90095, USA.
  • Irwin MR; Norman Cousins Center for Psychoneuroimmunology, Los Angeles, USA.
Sci Rep ; 12(1): 12627, 2022 07 24.
Article em En | MEDLINE | ID: mdl-35871638
ABSTRACT
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 (ß = - 0.274, p = .03) and feelings of social disconnection (ß = - 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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Interleucina-8 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citocinas / Interleucina-8 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
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