Why the study?
PA stiffness affects RV function in PAH, and prognosis depends on RV function in patients with ASD-PAH, but PA remodelling and its link to RV function had not been characterized using 4D flow MRI.
4D flow MRI demonstrates that pulmonary artery stiffness is increased and compliance decreased in ASD-PAH, with more severe impairment seen in patients with preserved RV function.
Background Pulmonary artery (PA) stiffness plays a significant role on right ventricular (RV) function, as evidenced in pulmonary arterial hypertension (PAH). In patients with atrial septal defect–related PAH (ASD-PAH), prognosis is dependent on RV function. We aimed to characterize PA remodelling and its relationship with RV function using 4-dimensional flow magnetic resonance imaging (4D flow MRI) in patients with ASD-PAH. Methods We prospectively included 24 adults with ASD-PAH. They underwent 4D flow MRI and right heart catheterization within 24-48 hours. Remodelling of PA was analysed (stiffness, compliance, distensibility, elastance, and pulsatility) and PA vortex was evaluated. RV adaptation was measured by RV ejection fraction and RV-PA coupling. Results The median age was 50 [41-55] years, and the median mean PA pressure and pulmonary vascular resistance were 50 [39-58] mm Hg and 8.0 [6.8-11.3] WU, respectively. Fourteen patients (58.3%) had RV dysfunction (RV ejection fraction <45%). All presented PA dilation (median main PA diameter: 42 [37-48] mm) and an increase in PA stiffness (10 [7.4-15.3]), whereas compliance and distensibility were decreased (2.1 [1.8-4.1] mm 2 /mm Hg and 0.19 [0.13-0.29] %/mm Hg). No correlation was found between PA dilation and indexes of PA remodelling. PA remodelling parameters were more severely impaired in patients with preserved RV function, with an increased stiffness ( P = 0.01) and a decreased compliance and distensibility ( P = 0.02). Conclusions PA stiffness parameters characterized by 4D flow MRI were impaired in the population with ASD-PAH, and PA remodelling appears to be influenced by volumetric overload from the left-to-right shunt through the ASD.
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Valdeolmillos et al. (2025) studied this question.
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