Am J Perinatol 2017; 34(07): 684-692
DOI: 10.1055/s-0036-1597132
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Systematic Review and Meta-analysis: Gene Association Studies in Neonatal Sepsis

Lakshmi Srinivasan
1   Division of Neonatology, Department of Pediatrics, The Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
,
Daniel T. Swarr
1   Division of Neonatology, Department of Pediatrics, The Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
,
Megha Sharma
2   Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin
,
C. Michael Cotten
3   Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina
,
Haresh Kirpalani
1   Division of Neonatology, Department of Pediatrics, The Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
› Author Affiliations
Further Information

Publication History

25 April 2016

25 October 2016

Publication Date:
13 December 2016 (online)

Abstract

Background Association studies of various gene variants in neonatal sepsis show conflicting results.

Objective We performed a systematic review of candidate gene association studies in neonatal sepsis to provide pooled estimates of risk for selected gene variants.

Methods We performed a search using MeSH terms “infection,” “sepsis,” “infant,” “genetic variation,” “polymorphism,” and “genetic association studies.” We included studies evaluating associations between neonatal sepsis and genetic variants (2000–2015). We excluded case reports/series, commentaries, narrative reviews, and nonhuman research. We assessed quality of studies using STREGA guidelines. Following estimation of odds ratios (ORs), data were pooled using random effects models.

Results Twenty eight of 1,404 identified studies were included. Meta-analyses were performed for interleukin (IL)-6, tumor necrosis factor-α (TNF-α), and IL-10 as these gene variants were tested in multiple studies. TNF-α 308GG genotype demonstrated trends toward increased sepsis risk in the primary analysis of culture-proven sepsis (OR 1.18, 95% confidence interval [CI] 0.97–1.44). IL-10 1082GG genotype was associated with lower sepsis odds in very low-birth-weight (VLBW) infants (OR 0.51, 95% CI 0.29–0.91).

Conclusion We uncovered an association between IL-10 1082 gene variation and sepsis in VLBW infants but did not identify associations between neonatal sepsis and TNF-α 308 or IL-6 gene variation. Larger cohort replication studies are required to validate these findings.

Authors' Contributions

L.S. and H.K. conceptualized and designed the study. L.S. drafted the initial manuscript and approved the final manuscript as submitted. L.S., D.T.S., and M.S. performed the initial review of article, data extraction, data analyses, reviewed and revised the manuscript, and approved the final manuscript as submitted. H.K. and M.C. critically reviewed the manuscript and approved the final manuscript as submitted. All authors approved the final manuscript as submitted and agreed to be accountable for all aspects of the work.


 
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