Pulmonary arterial hypertension in systemic lupus erythematosus based on a CSTAR-PAH study: Baseline characteristics and risk factors.

Abstract

Pulmonary arterial hypertension (PAH) is a complex and devastating complication of systemic lupus erythematosus (SLE). We sought to describe the baseline characteristics of right heart catheterization (RHC)-confirmed SLE-associated PAH and identify risk factors for PAH in SLE patients. A multicenter, cross-sectional study was conducted using the Chinese SLE Treatment and Research group (CSTAR) registry. Baseline data for patients with SLE-associated PAH and SLE patients without PAH were collected and compared. Risk factors for PAH among patients with SLE were identified. A total of 292 patients with SLE-associated PAH were enrolled. RHC was used to reveal hemodynamic features, including mean pulmonary arterial pressure (46.2±12.0mmHg), pulmonary arterial wedge pressure (7.84±3.92mmHg), pulmonary vascular resistance (10.86±5.57 Wood units), and cardiac index (2.77±0.91L/min×m2 ). A multivariate logistic regression analysis showed that serositis (odds ratio [OR]=5.524, 95% CI 3.605-8.465, P<0.001), anti-ribonucleoprotein (RNP) antibody positivity (OR=13.332, 95% CI 9.500-18.710, P<0.001), and diffusion capacity of carbon monoxide in the lung (DLCO)/%Pred <70% (OR=10.018, 95% CI 6.619-15.162, P<0.001) were independent predictors of PAH. We recommend using transthoracic echocardiography (TTE) to perform early screening of SLE patients who have serositis, anti-RNP antibody positivity, or DLCO/%Pred <70%. RHC is suggested for patients suspected of having PAH. Once a diagnosis of SLE-PAH is confirmed, evaluation and treatment should immediately begin. Overall, we recommend performing early screening using TTE in SLE patients with serositis, anti-RNP antibodies, or a DLCO/%Pred <70%, even for patients in a relatively stable condition according to SLE disease activity index.