Abstract
Objective
To study the relationship between SP-A2 and SP-B gene polymorphisms and respiratory distress syndrome in preterm neonates.
Design
Cross-sectional.
Setting
Neonatal intensive care unit and the Molecular Biology unit of the Chemical Pathology Department, Kasr Alainy hospital, Cairo University.
Participants
Sixty-five preterm infants with respiratory distress syndrome and 50 controls. The genomic DNA was isolated using DNA extraction kits. SYBR Greenbased real-time PCR was used to determine the variant genotypes of SP-A2 c.751 G<A and SP-B c.8714 G<C single nucleotide polymorphisms.
Results
Homozygosity of SP-A (OR 46, 95% CI 14–151) and SP-B (OR 5.2, 95% CI 2.3–11.4) alleles increased the risk of respiratory distress syndrome. The logistic regression model showed that genotypes SP-A2 (OR 164) and SP-B (OR 18) were directly related to the occurrence of respiratory distress syndrome, whereas gestational age (OR 0.57) and 5-minute Apgar score (OR 0.19) were inversely related to its occurrence.
Conclusions
There is a possible involvement of SP-A2 and SP-B genes polymorphisms in the genetic predisposition to respiratory distress syndrome.
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Abuelhamed, W.A., Zeidan, N., Shahin, W.A. et al. Human surfactant proteins A2 (SP-A2) and B (SP-B) genes as determinants of respiratory distress syndrome. Indian Pediatr 52, 391–394 (2015). https://doi.org/10.1007/s13312-015-0643-9
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DOI: https://doi.org/10.1007/s13312-015-0643-9