Open AccessExhaled Nitric Oxide in Pulmonary Arterial Hypertension Associated with Systemic Sclerosis
Author(s) -
Cao Zeling,
Mathai Stephen C.,
Hummers Laura K.,
Shah Ami A.,
Wigley Fredrick M.,
Lechtzin Noah,
Hassoun Paul M.,
Girgis Reda E.
Publication year - 2016
Publication title -
pulmonary circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.791
H-Index - 40
ISSN - 2045-8940
DOI - 10.1086/688768
Subject(s) - medicine , exhaled nitric oxide , nitric oxide , gastroenterology , cardiology , pulmonary hypertension , lung , lung function
The fractional exhaled concentration of nitric oxide (FE NO ) has been shown to be reduced in idiopathic pulmonary arterial hypertension (PAH) but has not been adequately studied in PAH associated with systemic sclerosis (SSc). We measured FE NO at an expiratory flow rate of 50 mL/s in 21 treatment‐naive patients with SSc‐associated PAH (SSc‐PAH), 94 subjects with SSc without pulmonary involvement, and 84 healthy volunteers. Measurements of FE NO at additional flow rates of 100, 150, and 250 mL/s were obtained to derive the flow‐independent nitric oxide exchange parameters of maximal airway flux (J′aw NO ) and steady‐state alveolar concentration (CA NO ). FE NO at 50 mL/s was similar ( P = 0.22) in the SSc‐PAH group (19 ± 12 parts per billion [ppb]) compared with the SSc group (17 ± 12 ppb) and healthy control group (21 ± 11 ppb). No change was observed after 4 months of targeted PAH therapy in 14 SSc‐PAH group patients ( P = 0.9). J′aw NO was modestly reduced in SSc group subjects without lung disease (1.2 ± 0.5 nl/s) compared with healthy controls (1.64 ± 0.9; P < 0.05) but was similar to that in the SSc‐PAH group. CA NO was elevated in individuals with SSc‐PAH (4.8 ± 2.6 ppb) compared with controls with SSc (3.3 ± 1.4 ppb) and healthy subjects (2.6 ± 1.5 ppb; P < 0.001 for both). However, after adjustment for the diffusing capacity of CO, there was no significant difference in CA NO between individuals with SSc‐PAH and controls with SSc. We conclude that FE NO is not useful for the diagnosis of PAH in SSc. Increased alveolar nitric oxide in SSc‐PAH likely represents impaired diffusion into pulmonary capillary blood.