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Cytokine Profiles of Preterm Neonates with Fungal and Bacterial Sepsis

BACKGROUND: Information on cytokine profiles in fungal sepsis (FS), an important cause of mortality in extremely low birthweight infants (ELBW), is lacking. We hypothesized that cytokine profiles in the 1(st) 21 days of life in ELBW with FS differ from those with bacterial sepsis (BS) or no sepsis (...

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Detalles Bibliográficos
Autores principales: Sood, Beena G., Shankaran, Seetha, Schelonka, Robert L., Saha, Shampa, Benjamin, Danny K., Sánchez, Pablo J., Adams-Chapman, Ira, Stoll, Barbara J., Thorsen, Poul, Skogstrand, Kristin, Ehrenkranz, Richard A., Hougaard, David M., Goldberg, Ronald N., Tyson, Jon E., Das, Abhik, Higgins, Rosemary D., Carlo, Waldemar A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629907/
https://www.ncbi.nlm.nih.gov/pubmed/22562288
http://dx.doi.org/10.1038/pr.2012.56
Descripción
Sumario:BACKGROUND: Information on cytokine profiles in fungal sepsis (FS), an important cause of mortality in extremely low birthweight infants (ELBW), is lacking. We hypothesized that cytokine profiles in the 1(st) 21 days of life in ELBW with FS differ from those with bacterial sepsis (BS) or no sepsis (NS). METHODS: In a secondary analyses of the NICHD Cytokine study, three groups were defined - FS (≥1 episode of FS), BS (≥1 episode of BS without FS), and NS. Association between 11 cytokines assayed in dried blood spots obtained on days 0-1, 3±1, 7±2, 14±3, and 21±3 and sepsis group was explored. RESULTS: Of 1066 infants, 89 had FS and 368 had BS. Compared to BS, FS was more likely to be associated with lower birthweight, vaginal delivery, patent ductus arteriosus, postnatal steroids, multiple central lines, longer respiratory support and hospital stay, and higher mortality (p<0.05). Analyses controlling for covariates showed significant group differences over time for IFN-γ, IL-10, IL-18, TGF-β and TNF-α (p<0.05). CONCLUSION: Significant differences in profiles for IFN-γ, IL-10, IL-18, TGF-β and TNF-α in FS, BS or NS in this hypothesis-generating secondary study require validation in rigorously designed prospective studies and may have implications for diagnosis and treatment.