Pulmonary hypertension in Takayasu arteritis with pulmonary artery involvement: risk factors and impact on mortality

BACKGROUND: Pulmonary artery involvement (PAI) in Takayasu arteritis (TAK) can cause pulmonary hypertension (PH). We aimed to compare clinical and imaging features between TAK patients with and without PH, identify factors associated with PH and describe long-term outcomes. METHODS: A prospective cohort of 147 TAK patients was studied from 2016 to 2024. Eligibility required fulfilment of established TAK criteria or multidisciplinary confirmation of CT-proven PAI after exclusion of other causes. Baseline demographics, clinical symptoms, laboratory and imaging findings, haemodynamic parameters and treatments were collected. The primary endpoint was all-cause mortality. Logistic regression identified factors associated with PH, and Cox proportional hazards regression evaluated predictors of mortality. RESULTS: Among 87 TAK-PAI patients, 40 (46%) had PH. Compared with non-PH patients, those with PH had higher Qanadli scores, longer diagnostic delay (median 20.5 vs 6.0 months, p=0.011), more severe symptoms, worse cardiopulmonary function, and higher N-terminal pro-B-type natriuretic peptide and right ventricular dimension (all p