Abstract
Pulmonary arterial hypertension (PAH) is a life-threatening condition, characterized by an imbalance of vasoactive substances and remodeling of pulmonary vasculature. Nitric oxide, formed from l-arginine, is essential for homeostasis and smooth muscle cell relaxation in PAH. Our aim was to compare plasma concentrations of l-arginine, asymmetric dimethylarginine (ADMA), and symmetric dimethylarginine (SDMA) in PAH compared to left ventricular systolic dysfunction (LVSD) and healthy subjects. This was an observational, multicenter study comparing 21 patients with PAH to 14 patients with LVSD and 27 healthy subjects. Physical examinations were obtained and blood samples were collected. Plasma levels of ADMA, SDMA, l-arginine, l-ornithine, and l-citrulline were analyzed using liquid chromatography–tandem mass spectrometry (LC–MS/MS). Plasma levels of ADMA and SDMA were higher, whereas l-arginine and l-arginine/ADMA ratio were lower in PAH patients compared to healthy subjects (p < 0.001). Patients with PAH also had lower levels of l-arginine than patients with LVSD (p < 0.05). l-Arginine correlated to 6 min walking distance (6MWD) (rs = 0.58, p = 0.006) and l-arginine/ADMA correlated to WHO functional class (rs = −0.46, p = 0.043) in PAH. In conclusion, l-arginine levels were significantly lower in treatment naïve PAH patients compared to patients with LVSD. Furthermore, l-arginine correlated with 6MWD in PAH. l-arginine may provide useful information in differentiating PAH from LVSD.
Highlights
Pulmonary arterial hypertension (PAH) is a rare disease characterized by endothelial dysfunction and pulmonary vascular remodeling, leading to elevated pulmonary vascular resistance, right ventricular heart failure, and premature death [1]
nitric oxide (NO) is formed in the course of transformation of l-arginine to citrulline, a reaction catalyzed by the enzyme NO synthase (NOS) (Fig. 1) [3]
These findings strongly indicate an association between asymmetric dimethylarginine (ADMA) plasma levels and PAH/pulmonary hypertension (PH) pathogenesis [22]
Summary
Pulmonary arterial hypertension (PAH) is a rare disease characterized by endothelial dysfunction and pulmonary vascular remodeling, leading to elevated pulmonary vascular resistance, right ventricular heart failure, and premature death [1]. Elevated ADMA levels can lead to decreased NO production and endothelial dysfunction [7]. Oxidative stress and/or inhibition of DDAH lead to increased ADMA levels in endothelial cells and inhibit NO-mediated endothelium-dependent relaxation of blood vessels [10,11,12]. Elevated plasma ADMA levels have been reported in several types of pulmonary hypertension (PH) [14,15,16,17,18,19,20,21]. Together, these findings strongly indicate an association between ADMA plasma levels and PAH/PH pathogenesis [22]. ADMA levels may predict cardiovascular outcome and mortality in PAH [14]
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