Journal article
Role of Polymorphic Variants as Genetic Modulators of Infection in Neonatal Sepsis
Pediatric research, Vol.68(4), pp.323-329
2010
DOI: 10.1203/PDR.0b013e3181e6a068
PMCID: PMC2940937
PMID: 20463618
Abstract
This study is a retrospective, case control study involving 535 preterm infants examining the roles of sequence polymorphisms in genes that mediate host immune responses to bacterial infection in newborn infants. A total of 49 single nucleotide polymorphisms (SNPs) in 19 candidate genes including inflammatory cytokines (IL6, IL10, IL1B, and TNF), cytokine receptors (IL1RN), toll-like receptors (TLR2, TLR4, and TLR5), and cell surface receptors (CD14) were genotyped. Subjects were stratified into three groups (sepsis, suspected sepsis, and control). The data were analyzed using a family-based transmission disequilibrium test. We found that birth weight, gestational age, duration of rupture of membranes, and presence of clinical chorioamnionitis were strongly associated with sepsis. Polymorphisms in TLR2 (rs3804099), TLR5 (rs5744105), IL10 (rs1800896), and PLA2G2A (rs1891320) genes were associated with sepsis. Allelic variants in PLA2G2A and TLR2 were associated with Gram-positive infections, whereas IL10 was associated with Gram-negative infections (p < 0.05). We conclude allelic variations in PLA2G2A, TLR2, TLR5, and IL10 may moderate the predisposition to sepsis in preterm infants.
Details
- Title: Subtitle
- Role of Polymorphic Variants as Genetic Modulators of Infection in Neonatal Sepsis
- Creators
- Asmaa ABU-MAZIAD - Department of Pediatrics University of Iowa, Children's Hospital, Iowa City, Iowa 52242, United StatesKendra SCHAA - Department of Pediatrics University of Iowa, Children's Hospital, Iowa City, Iowa 52242, United StatesEdward F BELL - Department of Pediatrics University of Iowa, Children's Hospital, Iowa City, Iowa 52242, United StatesJohn M DAGLE - Department of Pediatrics University of Iowa, Children's Hospital, Iowa City, Iowa 52242, United StatesMargaret COOPER - Center for Craniofacial and Dental Genetics , University of Pittsburgh, Pittsburgh, Pennsylvania 15219, United StatesMary L MARAZITA - Center for Craniofacial and Dental Genetics , University of Pittsburgh, Pittsburgh, Pennsylvania 15219, United StatesJeffrey C MURRAY - Department of Pediatrics University of Iowa, Children's Hospital, Iowa City, Iowa 52242, United States
- Resource Type
- Journal article
- Publication Details
- Pediatric research, Vol.68(4), pp.323-329
- DOI
- 10.1203/PDR.0b013e3181e6a068
- PMID
- 20463618
- PMCID
- PMC2940937
- NLM abbreviation
- Pediatr Res
- ISSN
- 0031-3998
- eISSN
- 1530-0447
- Publisher
- Lippincott Williams & Wilkins; Hagerstown, MD
- Language
- English
- Date published
- 2010
- Academic Unit
- Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Biochemistry and Molecular Biology; Dental Research; Neonatology
- Record Identifier
- 9984024512502771
Metrics
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