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Inflammatory cytokine response and reduced heart rate variability in newborns with hypoxic ischemic encephalopathy

OBJECTIVE: To determine whether systemic inflammation-modulating cytokine expression is related to heart rate variability (HRV) in newborns with hypoxic ischemic encephalopathy (HIE). STUDY DESIGN: Data from 30 newborns with HIE were analyzed. Cytokine levels (IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, I...

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Detalles Bibliográficos
Autores principales: Al-Shargabi, Tareq, Govindan, R. B., Dave, Rhiya, Metzler, Marina, Wang, Yunfei, du Plessis, Adre, Massaro, An N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446303/
https://www.ncbi.nlm.nih.gov/pubmed/28252659
http://dx.doi.org/10.1038/jp.2017.15
Descripción
Sumario:OBJECTIVE: To determine whether systemic inflammation-modulating cytokine expression is related to heart rate variability (HRV) in newborns with hypoxic ischemic encephalopathy (HIE). STUDY DESIGN: Data from 30 newborns with HIE were analyzed. Cytokine levels (IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, IL-1β, TNF-α, IFN-λ) were measured either at 24 hours of cooling (n=5), 72 hours of cooling (n=4), or at both timepoints (n=21). The following HRV metrics were quantified in the time domain: alpha_S, alpha_L, root mean square (RMS) at short time scales (RMS_S), RMS at long time scales (RMS_L), while low frequency power (LF) and high frequency power (HF) were quantified in the frequency domain. The relationships between HRV metrics and cytokines were evaluated using mixed-models. RESULTS: IL-6, IL-8, IL-10, and IL-13 levels were inversely related to selected HRV metrics. CONCLUSION: Inflammation-modulating cytokines may be important mediators in the autonomic dysfunction observed in newborns with HIE.