Endothelial Nitric Oxide Synthase (NOS3) Genotype in Pulmonary Artery Hypertension

2005 ◽  
Vol 11 (6) ◽  
pp. S97
Keyword(s):  
Nitric Oxide ◽  
Nitric Oxide Synthase ◽  
Pulmonary Artery ◽  
Endothelial Nitric Oxide Synthase ◽  
Pulmonary Artery Hypertension ◽  
Oxide Synthase ◽  
Endothelial Nitric Oxide

Estrogen Upregulates Endothelial Nitric Oxide Synthase Gene Expression in Fetal Pulmonary Artery Endothelium

1997 ◽  
Vol 81 (3) ◽  
pp. 355-362 ◽  
Author(s):  
Amy N. MacRitchie ◽  
Sandy S. Jun ◽  
Zhong Chen ◽  
Zohre German ◽  
Ivan S. Yuhanna ◽  
...  
Keyword(s):  
Gene Expression ◽  
Nitric Oxide ◽  
Nitric Oxide Synthase ◽  
Pulmonary Artery ◽  
Endothelial Nitric Oxide Synthase ◽  
Oxide Synthase ◽  
Endothelial Nitric Oxide

Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) and acute pulmonary hypertension post cardiopulmonary bypass in children with congenital cardiac diseases

2010 ◽  
Vol 21 (2) ◽  
pp. 161-169 ◽  
Author(s):  
Tsvetomir Loukanov ◽  
Katharina Hoss ◽  
Pentcho Tonchev ◽  
Homa Klimpel ◽  
Raul Arnold ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Pulmonary Hypertension ◽  
Cardiopulmonary Bypass ◽  
Nitric Oxide Synthase ◽  
Pulmonary Artery ◽  
Pulmonary Artery Pressure ◽  
Endothelial Nitric Oxide Synthase ◽  
Cardiac Diseases ◽  
Oxide Synthase ◽  
Endothelial Nitric Oxide

AbstractBackgroundIntra-cardiac repair of congenital cardiac diseases in children with left–right shunt is often associated with acute elevation of pulmonary artery pressure following cardiopulmonary bypass. We studied the correlation between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and pulmonary hypertension in children with congenital cardiac diseases.Methods and resultsA total of 80 children with congenital cardiac diseases at a median age of 3.8 years, ranged 0.1–36.2 years, and 136 controls were enrolled. Most patients presented with significant left-to-right shunt – pulmonary-to-systemic blood flow of 2.8, with a range from 0.6 to 7.5. In all, 40 out of 80 children showed pulmonary hypertension with mean pressure of 42, ranged 26–82, millimetres of mercury. Thirty-one out of 40 children underwent intra-cardiac repair and 15 out of 31 operated patients were found to have an acute elevation of pulmonary artery pressure after cardiopulmonary bypass. The Glu298Asp polymorphism was identified using polymerase chain reaction and restriction fragment length polymorphism. Both in patients and in controls, the genotype distribution corresponded to the Hardy–Weinberg equilibrium. The gene frequency for Glu298Glu, Glu298Asp and Asp298Asp was not different in the control group compared to the patients (Armitage trend test: p = 0.37). The endothelial nitric oxide synthase polymorphism was related to acute post-operative elevation of pulmonary artery pressure (genotypic frequency 53.3 versus 25%; Armitage trend test: p = 0.038). In addition, the allelic frequency of the Glu298Asp was related to post-operative pulmonary hypertension (Fischer’s exact test: p = 0.048). The positive predictive value was 71.43%.ConclusionPatients with left-to-right shunt are more likely to develop acute elevation of pulmonary artery pressure after cardiopulmonary bypass when presenting with the Glu298Asp polymorphism of the gene endothelial nitric oxide synthase. This could be used as a genetic marker for the predisposition for the development of pulmonary hypertension after intra-cardiac repair.

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