Faculty Collaboration Database

A TIR domain receptor-associated protein (TIRAP) variant SNP (rs8177374) confers protection against premature birth. J Perinatol 2013 May;33(5):341-6

Date

10/11/2012

Pubmed ID

23047423

DOI

10.1038/jp.2012.120

Scopus ID

2-s2.0-84877582305 (requires institutional sign-in at Scopus site)   7 Citations

Abstract

OBJECTIVE: To investigate whether single nucleotide polymorphisms (SNPs) in genes encoding the Toll-like receptor (TLR) signaling pathway modulate susceptibility to preterm birth (PTB).

STUDY DESIGN: Prospective case-control study examining the contribution of nine TLR SNPs to PTB (<37 weeks) and PTB <32 weeks. Genotyping was done on neonatal blood using a multiplexed single-base extension assay. Chi-square test, Fischer's exact test and classification trees were used for data analysis.

RESULT: Preterm infants (n=177) were more likely to be African American (P=0.02), and were more likely to be born to mothers who smoked (P=0.007), had pregnancy-induced hypertension (PIH; P=0.002) and placental abruption (P=0.0004) when compared with term infants (n=146). The TLR2, TLR4, TLR5, TLR9, nuclear factor-kappa B1 (NFκB1), NFκBIA and IRAK1 variants were not associated with PTB whereas the TIR domain receptor-associated protein (TIRAP) variant was more prevalent in term infants when compared with preterm infants born <32 weeks (P=0.004). PTB <32 weeks was more prevalent in infants without the TIRAP variant whose mothers had PIH and did not smoke (P=0.001). Presence of the TIRAP variant protected against PTB <32 weeks (P=0.015) in Caucasian infants.

CONCLUSION: In our study, a TLR pathway adapter variant (TIRAP (rs8177374)) protected against PTB<32 weeks, supporting our hypothesis that genetic variation in the innate immune signaling pathway contributes to altered risk of PTB.

Author List

Karody VR, Le M, Nelson S, Meskin K, Klemm S, Simpson P, Hines R, Sampath V

Authors

Vijender R. Karody MD Associate Professor in the Pediatrics department at Medical College of Wisconsin
Pippa M. Simpson PhD Adjunct Professor in the Pediatrics department at Medical College of Wisconsin

MESH terms used to index this publication - Major topics in bold

Case-Control Studies
Female
Genotype
Humans
Infant, Newborn
Male
Membrane Glycoproteins
Polymorphism, Single Nucleotide
Pregnancy
Premature Birth
Receptors, Interleukin-1
Signal Transduction
Toll-Like Receptors