Premium
TNF‐238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population
Author(s) -
Elhawary Nasser A.,
Tayeb Mohammed T.,
AbdelGhafar Shereen,
Rashad Mona,
Alkhotani AbdelAziz
Publication year - 2013
Publication title -
pediatric pulmonology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.866
H-Index - 106
eISSN - 1099-0496
pISSN - 8755-6863
DOI - 10.1002/ppul.22748
Subject(s) - bronchopulmonary dysplasia , medicine , birth weight , gestational age , pediatrics , population , low birth weight , genotype , allele , sepsis , gastroenterology , pregnancy , genetics , environmental health , gene , biology
Bronchopulmonary dysplasia (BPD) remains as a major and increasing burden in Egypt. Rationale To determine whether alleles of TNFα‐238G > A affect the risk of BPD or the severity of BPD in preterm infants in Egypt. Study Design We prospectively genotyped 220 premature neonates (birth weight <1,500 g and gestational age 26–32 weeks) for the −238 polymorphism, and assessed the clinical risk factors for BPD in our study populations. Infants with BPD were mechanically ventilated. Results Infants who developed BPD (n = 120) had a younger gestational age (31.0 ± 2.1 weeks vs. 34.3 ± 1.5 weeks) and lower birth weight (1,490 ± 360 g vs. 1,880 ± 520 g) than infants who did not develop BPD (n = 100). Results of antenatal steroid supplementation, surfactant therapy, or sepsis might affect the genetic modulation of BPD. The −238G > A polymorphism was associated with a twofold risk of BPD (OR = 2.86; 95% confidence interval, 1.35–3.83). Despite the dominance of the G allele in the Egyptian population, the −238A allele was more common among infants with BPD (23%) than among infants without BPD (15%). The A allele occurred less often in infants with mild BPD (9%) than in infants with severe (39%) or moderate (52%). The AA genotype occurred in 15% of cases but in none of the controls. Conclusion The TNFα −238G > A polymorphism—particularly the presence of an A allele—should be evaluated as a biomarker to predict the clinical outcome of preterm infants with BPD in Egypt. Even the presence of one copy of this mutant allele appears to be sufficient to influence the severity of disease. Pediatr Pulmonol. 2013; 48:699–706. © 2012 Wiley Periodicals, Inc.