Post-natal age is a critical determinant of the neonatal host response to sepsis - GSE69686

Neonates manifest a unique host response to sepsis even among other children. Preterm neonates may experience sepsis soon after birth or during often protracted birth hospitalizations as they attain physiologic maturity. We examined the transcriptome using genome-wide expression profiling on prospectively collected peripheral blood samples from infants evaluated for sepsis within 24 hours after clinical presentation. Simultaneous plasma samples were examined for alterations in inflammatory mediators. Group designation (sepsis or uninfected) was determined retrospectively based on clinical exam and laboratory results over the next 72 hours from the time of evaluation. Unsupervised analysis showed the major node of separation between groups was timing of sepsis episode relative to birth (early, <3 days or late, >3 days). Principal component analyses revealed significant differences between patients with early or late sepsis despite the presence of similar key immunologic pathway aberrations in both groups. Unique to neonates, the uninfected state and host response to sepsis is significantly affected by timing relative to birth. Future therapeutic approaches may need to be tailored to the timing of the infectious event based on post-natal age.

We used human microarrays to detail the molecular profile of the events that occur following sepsis in hospitalized neonates. Please note that 'uninfected chorio' represents babies who were not infected but had chorioamnionitis exposure.

Infants were retrospectively classified as having sepsis on the basis of the presence of all three criteria: (a) persistently abnormal clinical examination (at least 2 d of clinical signs [Supplementary Table S1]), (b) positive culture results (blood) and (c) presence of abnormal laboratory studies supporting systemic inflammation (C-reactive protein [CRP] within 48 h of evaluation >45 mg/L). Infants with negative cultures but persistently abnormal exams and systemic inflammation were classified as having clinical sepsis. Uninfected patients had serial (at least two values 24 h apart) CRP <10 mg/dL and sterile cultures and had antimicrobial treatment discontinued <48 h after empiric initiation without subsequent clinical impact.

Sepsis (2021 ICD-10-CM code* = A41)

The data was normalized using RMA. Analyzed using BRB array tools

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE69686