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PREGNANCY

Polymorphisms in the tumor necrosis factor alpha and interleukin 1-beta promoters with possible gene regulatory functions increase the risk of preterm birth

, , , , , , , , , & show all
Pages 1285-1290 | Received 12 May 2008, Published online: 03 Aug 2009
 

Abstract

Objective. To investigate the relation between 19 selected single nucleotide polymorphisms in three cytokine genes, tumor necrosis factor alpha (TNFA), interleukin 1-beta (IL1B) and interleukin 6 (IL6) and preterm birth (<37 weeks’ gestation). Design. Case-control association study. Sample. A total of 117 singleton pregnant Danish Caucasian women, including 62 preterm birth cases and 55 controls (birth ≥37 weeks). Methods. Genotyping was performed using TaqMan probes and traditional sequencing. Descriptive statistics were carried out with Fisher's exact test and Wilcoxon rank-sum test. All genetic data were tested for Hardy–Weinberg equilibrium and analyzed using logistic regression, 2×2 proportions or χ2. Haplotypes were estimated for each gene and permutation used for association testing. Results. Women carrying the TNFA -857 C>T rare allele (T) and those homozygous for the IL1B -31 T>C and IL1B -511 C>T rare alleles (C and T) have an increased risk of preterm birth with OR 3.1 (95% CI: 1.0-10.3) and OR 6.4 (95% CI: 1.3-60.5), respectively. Two estimated TNFA haplotypes were associated with preterm birth with OR 3.1 (p=0.037) and OR 2.7 (p=0.045). Conclusion. Polymorphisms in the cytokine genes TNFA and IL1B may increase the risk of preterm birth, possibly by a dysregulation of the immune system in pregnancy.

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