scholarly journals Mucosal Tumor Necrosis Factor-α Production and Extensive Disruption of Sulfated Glycosaminoglycans Begin within Hours of Birth in Neonatal Respiratory Distress Syndrome

1996 ◽  
Vol 40 (3) ◽  
pp. 484-489 ◽  
Author(s):  
Simon H Murch ◽  
Kate Costeloe ◽  
Nigel J Klein ◽  
Helene Rees ◽  
Neil McIntosh ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Abolfazl Khoshdel ◽  
Soleiman Kheiri ◽  
Peyman Omidvari ◽  
Fahimeh Moradi ◽  
Majid Hamidi ◽  
...  

Cytokine polymorphisms may contribute to the prevalence of respiratory distress syndrome. The present study was done to investigate the frequency of interleukin- (IL-) 10 and tumor necrosis factor- (TNF-) α gene polymorphisms and their association with the risk of RDS in preterm infants. One-hundred and nineteen patients with RDS and 119 healthy preterm infants were enrolled. PCR restriction fragment length polymorphism was used to determine the frequency of IL-10 and TNF-α genotypes at -1082 A and -308 A, respectively. One-hundred and nineteen out of 238 infants had RDS (50%). The age of the mothers and gestational age ranged 17–45 (mean: 28.6±5.3) years and 24–34 (mean: 34.3±2.38) weeks, respectively. Totally, 23 deaths were recorded in the RDS group. Incidence of TNF-α-308 A/A and TNF-α-308 G/A was 84% and 16%, respectively. TNF-a-308 G/G was not found in both groups. Prevalence of IL-10-1082 G/G and IL-10-1082 G/A variants was 65.5% and 34.5%, respectively. IL-10-1082 A/A was not found in both groups. The incidence of the allele G in the IL-10-1082 polymorphism was lower in RDS group (P<0.05). We found that the risk of RDS was correlated to sex, gestational age, and IL-10-1082.


1992 ◽  
Vol 146 (3) ◽  
pp. 694-700 ◽  
Author(s):  
P. E. Parsons ◽  
F. A. Moore ◽  
E. E. Moore ◽  
D. N. Iklé ◽  
P. M. Henson ◽  
...  

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