Sleep disturbance is associated with perturbations in immune-inflammatory pathways in oncology outpatients undergoing chemotherapy

被引:3
|
作者
Calvo-Schimmel, Alejandra [1 ]
Kober, Kord M. [1 ]
Paul, Steven M. [1 ]
Cooper, Bruce A. [1 ]
Harris, Carolyn [1 ]
Shin, Joosun [1 ]
Hammer, Marilyn J. [2 ]
Conley, Yvette P. [3 ]
Dokiparthi, Vasuda [1 ]
Olshen, Adam [4 ]
Levine, Jon D. [5 ]
Miaskowski, Christine [1 ]
机构
[1] Univ Calif San Francisco, Dept Physiol Nursing, 2 Koret Waye N631Y, San Francisco, CA 94143 USA
[2] Dana Farber Canc Inst, Boston, MA USA
[3] Univ Pittsburgh, Sch Nursing, Pittsburgh, PA USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
关键词
Cancer; Chemotherapy; Inflammation; Immune mechanisms; Insomnia; Pathway impact analysis; Sleep disturbance; DIFFERENTIAL EXPRESSION ANALYSIS; GENE-EXPRESSION; T-CELLS; DEPRIVATION; VALIDATION; DISORDER; BIOLOGY; NUMBER; HEALTH;
D O I
10.1016/j.sleep.2022.11.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective/background: Sleep disturbance is a common problem in patients receiving chemotherapy. Purpose was to evaluate for perturbations in immune-inflammatory pathways between oncology patients with low versus very high levels of sleep disturbance. Patients/methods: Sleep disturbance was evaluated using the General Sleep Disturbance Scale six times over two cycles of chemotherapy. Latent profile analysis was used to identify subgroups of patients with distinct sleep disturbance profiles. Pathway impact analyses were performed in two independent samples using gene expression data obtained from RNA sequencing (n = 198) and microarray (n = 162) technologies. Fisher's combined probability test was used to identify significantly perturbed pathways between Low versus Very High sleep disturbance classes. Results: In the RNA sequencing and microarray samples, 59.1% and 51.9% of patients were in the Very High sleep disturbance class, respectively. Thirteen perturbed pathways were related to immuneinflammatory mechanisms (i.e., endocytosis, phagosome, antigen processing and presentation, natural killer cell mediated cytotoxicity, cytokine-cytokine receptor interaction, apoptosis, neutrophil extracellular trap formation, nucleotide-binding and oligomerization domain-like receptor signaling, Th17 cell differentiation, intestinal immune network for immunoglobulin A production, T-cell receptor signaling, complement and coagulation cascades, and tumor necrosis factor signaling). Conclusions: First study to identify perturbations in immune-inflammatory pathways associated with very high levels of sleep disturbance in oncology outpatients. Findings suggest that complex immuneinflammatory interactions underlie sleep disturbance. (c) 2022 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:305 / 315
页数:11
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