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Stimulated Production of Proinflammatory Cytokines Covaries Inversely With Heart Rate Variability

Bibliographic Data

ID19302043
AuthorsAnna L Marsland (0000-0001-8951-7513, Behavioral Pharma (United States), corresponding author), Peter J Gianaros (0000-0003-2313-5277, Behavioral Pharma (United States)), Aric A Prather (0000-0003-1302-8283, University of Pittsburgh), J Richard Jennings (0000-0001-6988-3348, Behavioral Pharma (United States)), Serina A Neumann (0000-0002-8035-1518, Behavioral Pharma (United States)), Stephen B Manuck (0000-0003-0484-7324, University of Pittsburgh)
Year2007
Volume69
Issue8
Pages709-716
Publication date2007-10-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenuePsychosomatic Medicine (JOURNAL)
Journal identifiersISSN: 0033-3174 • E-ISSN: 1534-7796
PublisherOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/psy.0b013e3181576118
PMID17942840
OpenAlexW2092466452
LanguageEN
Citations received7
References cited46

OBJECTIVE: To examine whether high-frequency heart rate variability, an indirect measure of parasympathetic (vagal) control over variations in heart rate, is associated with immune reactivity to an in vitro inflammatory challenge. Convergent evidence from the animal literature shows that the autonomic nervous system plays a key role in regulating the magnitude of immune responses to inflammatory stimuli. Signaling by the parasympathetic system inhibits the production of proinflammatory cytokines by activated monocytes/macrophages and thus decreases local and systemic inflammation. As yet, no direct human evidence links parasympathetic activity to inflammatory competence. METHODS: We examined the relationship of variations in heart rate, recorded during paced respiration, to lipopolysaccharide-induced production of the inflammatory cytokines interleukin (IL)-1beta, IL-6, tumor necrosis factor (TNF)-alpha, and IL-10 among a community sample of 183 healthy adults (mean age = 45 years; 59% male; 92% White, 7% African-American). RESULTS: Consistent with animal findings, higher derived estimates of vagal activity measured during paced respiration were associated with lower production of the proinflammatory cytokines TNF-alpha and IL-6 (r = -.18 to -.30), but were not related to production of the anti-inflammatory cytokine IL-10. These associations persisted after controlling for demographic and health characteristics, including age, gender, race, years of education, smoking, hypertension, and white blood cell count. CONCLUSIONS: These data provide initial human evidence that vagal activity is inversely related to inflammatory competence, raising the possibility that vagal regulation of immune reactivity may represent a pathway linking psychosocial factors to risk for inflammatory disease

Blood pressure · Cytokine · Heart rate · Heart rate variability · Immune system · Inflammation · Interleukin 6 · Lipopolysaccharide · Proinflammatory cytokine · Sickness behavior · Tumor necrosis factor alpha · Vagal tone · Endocrinology · Heart rate and cardiovascular health · Heart Rate Variability and Autonomic Control · Immunology · Internal Medicine · Medicine · Vagus Nerve Stimulation Research

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Unique citing works7
Citations per year0.41
Citation span2009 - 2026 (18)
Citation velocitycurrent
Highly citedNo
Citation typesNeutral: 6

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