Key result
The bb genotype of ecNOS was significantly more common in patients with asthma compared to healthy controls, whereas ACE genotype distribution did not differ significantly.
Why the study?
Nitric oxide and ACE may influence airway homeostasis and asthma pathogenesis, but the genetic involvement of ecNOS and ACE polymorphisms in asthma was unclear.
Are polymorphisms of the ecNOS and ACE genes associated with the development and severity of bronchial asthma?
Case-Control (n=431)
Are polymorphisms of the ecNOS and ACE genes associated with the development and severity of bronchial asthma?
Polymorphisms of the ecNOS gene, but not the ACE gene, may be associated with the development of bronchial asthma, though neither appears to influence disease severity.
ecNOS bb genotype may link to asthma susceptibility; leaves open causal role and clinical relevance pending replication.
BACKGROUND: Nitric oxide, including that produced by endothelial constitutive nitric oxide synthase (ecNOS), may regulate vascular and airway tone in the lungs and may influence various aspects of airway homeostasis. Angiotensin-converting enzyme (ACE) is expressed at high levels in the lungs and plays a role in the metabolism of angiotensin II, bradykinin, and substance P, all of which are potentially involved in the pathogenesis of asthma. An insertion-deletion polymorphism of the ACE gene has been shown to be associated with enzyme activity levels of ACE. To examine the possible involvement of the ecNOS and/or ACE genes as the genetic basis of bronchial asthma, we investigated whether there was any association between bronchial asthma and polymorphisms of the ecNOS and/or ACE genes. METHODS: A total of 310 patients with bronchial asthma and 121 healthy subjects took part in this study. The ecNOS and ACE genotypes were determined in all subjects by polymerase chain reaction. RESULTS: 1) The distribution of one genotype (bb) of ecNOS was significantly higher in the asthma group than in the control population. 2) The ACE genotype distribution was not significantly different between the control and the asthma groups. 3) In asthmatic patients, the ACE and ecNOS genotype distribution did not differ significantly among groups of patients with different severities of asthma. CONCLUSIONS: These results suggest that polymorphisms of the ecNOS gene, but not the ACE gene, may be associated with the development of asthma. However, the severity of asthma may not be influenced by polymorphisms of the ecNOS and ACE genes.
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Lee et al. (2000) conducted a case-control in Bronchial asthma (n=431). Polymorphisms of the ecNOS and ACE genes vs. Healthy subjects was evaluated on Association between bronchial asthma and polymorphisms of the ecNOS and/or ACE genes. The bb genotype of ecNOS was significantly more common in patients with asthma compared to healthy controls, whereas ACE genotype distribution did not differ significantly.
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