PEDIATRICS · 2003 · 74 citations · 28 references
MedicineImmunologyPediatricsInflammationPediatric ImmunologySepsisInfection In Preterm BirthNeonatal ImmunologyNeonatal InfectionsNeonatal SepsisPediatric SepsisSepsis PathophysiologyGenotype DistributionInflammation In NewbornsInflammatory Response To InfectionInterleukin-6 Gene PolymorphismsInterleukin-6 Gene VariantsNeonatal Host Defense Against InfectionNeonatal SepticemiaNeonatal Susceptibility To Infection
OBJECTIVE: Systemic infection affects one quarter of preterm infants. Defense from infection is in part mediated by the cytokine interleukin-6 (IL-6). We tested the hypothesis that the IL-6 -174 GG genotype, associated with lower IL-6 response to inflammation, is also associated with the development of septicemia in preterm infants. METHODS: The study group comprised 157 infants who were born at < or =32 weeks. Genotype distribution (34% [54] GG, 46% [72] GC, 20% [31] CC) and C allele frequency (0.43; 95% confidence interval [CI]: 0.37-0.48) were similar to the UK adult population. Among the patients who developed bacterially confirmed septicemia (n = 51 [33%]), there was a significantly higher prevalence of the IL-6 -174 GG genotype than that observed in those who did not develop infection (47% vs 28% for GG: odds ratio [OR]: 2.3; 95% CI: 1.1-4.5). This association remained statistically significant (OR: 2.7; 95% CI: 1.2-6.3) after multiple binary logistic regression adjustment for other significant predictors of the development of septicemia. Late infection alone was similarly associated with GG genotype (septicemia 47% vs no septicemia 29% for GG: OR: 2.2; 95% CI: 1.1-4.3). CONCLUSIONS: Variation in the IL-6 gene seems to influence the defense against bacterial pathogens in the very preterm infant.
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Daniel Fishman, Gary Faulds, Rachel Jeffery et al. · Journal of Clinical Investigation · 1998 · 2.2K citations · Full text
David Brull, Hugh Montgomery, Julie Sanders et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2001 · 409 citations · Full text
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