Endothelial nitric oxide synthase genotype is associated with pulmonary hypertension severity in left heart failure patients. (1st May 2018)

• Record Type: Journal Article
• Authors: Duarte, Julio D.; Kansal, Mayank; Desai, Ankit A.; Riden, Katherine; Arwood, Meghan J.; Yacob, Alex A.; Stamos, Thomas D.; Cavallari, Larisa H.; Zamanian, Roham T.; Shah, Sanjiv J.; Machado, Roberto F.
• Is Part Of: Pulmonary circulation. Volume 8:Number 2(2018)
• Page Start: 1
• Page End: 8
• Publication Date: 2018-05-01
• Subjects: genetics/genomics -- nitric oxide synthase -- clinical studies; Pulmonary circulation -- Periodicals; Pulmonary circulation; Electronic journals -- Sciences; Periodicals; 616.24005
• DOI: 10.1177/2045894018773049
• Languages: English
• ISSNs: 2045-8932

Abstract

Abstract : The biological mechanisms behind the development of pulmonary hypertension in the setting of left heart failure (HF‐PH), including combined pre‐ and post‐capillary pulmonary hypertension (Cpc‐PH), remains unclear. This study aimed to use candidate polymorphisms in nitric oxide synthase (NOS) genes to explore the role of NOS in HF‐PH. DNA samples from 118 patients with HF‐PH were genotyped for the NOS3 rs1799983 and NOS2 rs3730017 polymorphisms. A multiple regression model was used to compare hemodynamic measurements between genotype groups. Patients with the T/T genotype at rs1799983 possessed a nearly 10 mmHg increased transpulmonary gradient (TPG) compared to those with other genotypes ( P = 0.006). This finding was replicated in an independent cohort of 94 HF‐PH patients ( P = 0.005). However, when tested in a cohort of 162 pre‐capillary pulmonary arterial hypertension patients, no association was observed. In a combined analysis of both HF‐PH cohorts, mean pulmonary artery pressure (mPAP), diastolic pulmonary gradient (DPG), and CpcPH status were also associated with rs1799983 genotype ( P = 0.005, P = 0.03, and P = 0.02, respectively). In patients with HF‐PH, the NOS3 rs1799983 polymorphism is associated with TPG, and potentially mPAP and DPG as well. These findings suggest that endothelial NOS (encoded by NOS3 ) may be involved in the pulmonary vascular remodeling observed in Cpc‐PH and warrants further study.