Key result
High RV diastolic stiffness is linked to worse clinical progression and survival in PAH.
Why the study?
Does high right ventricular diastolic stiffness predict clinical progression in patients with pulmonary arterial hypertension?
Cohort (n=123)
No
Does high right ventricular diastolic stiffness predict clinical progression in patients with pulmonary arterial hypertension?
Right ventricular diastolic stiffness measured by single-beat pressure-volume analysis is significantly associated with disease severity and poorer clinical progression in pulmonary arterial hypertension.
RV diastolic stiffness >0.53 mmHg·mL-1 may identify higher-risk PAH; hypothesis-generating and requires prospective validation before clinical use.
Right ventricular (RV) diastolic stiffness is increased in pulmonary arterial hypertension (PAH) patients. We investigated whether RV diastolic stiffness is associated with clinical progression and assessed the contribution of RV wall thickness to RV systolic and diastolic stiffness. Using single-beat pressure-volume analyses, we determined RV end-systolic elastance (Ees), arterial elastance (Ea), RV--arterial coupling (Ees/Ea), and RV end-diastolic elastance (stiffness, Eed) in controls (n=15), baseline PAH patients (n=63) and treated PAH patients (survival >5 years n=22 and survival <5 years n=23). We observed an association between Eed and clinical progression, with baseline Eed >0.53 mmHg·mL(-1) associated with worse prognosis (age-corrected hazard ratio 0.27, p=0.02). In treated patients, Eed was higher in patients with survival <5 years than in patients with survival >5 years (0.91±0.50 versus 0.53±0.33 mmHg·mL(-1), p<0.01). Wall-thickness-corrected Eed values in PAH patients with survival >5 years were not different from control values (0.76±0.47 versus 0.60±0.41 mmHg·mL(-1), respectively, not significant), whereas in patients with survival <5 years, values were significantly higher (1.52±0.91 mmHg·mL(-1), p<0.05 versus controls). RV diastolic stiffness is related to clinical progression in both baseline and treated PAH patients. RV diastolic stiffness is explained by the increased wall thickness in patients with >5 years survival, but not in those surviving <5 years. This suggests that intrinsic myocardial changes play a distinctive role in explaining RV diastolic stiffness at different stages of PAH.
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Trip et al. (2015) conducted a cohort in Idiopathic and heritable pulmonary arterial hypertension (n=123). High right ventricular end-diastolic elastance (>0.53 mmHg·mL-1) vs. Low right ventricular end-diastolic elastance (≤0.53 mmHg·mL-1) was evaluated on Clinical progression (all-cause mortality or lung transplantation) (HR 0.27, 95% CI 0.09-0.80, p=0.02). Baseline right ventricular diastolic stiffness >0.53 mmHg·mL-1 was associated with worse clinical progression and survival (HR 0.27) in patients with pulmonary arterial hypertension.
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