Why the study?
PAH and CTEPH cause right ventricular dysfunction with extrapulmonary sequelae including renal dysfunction, but the characteristics of renal dysfunction and the effect of pulmonary hypertension treatment on renal function needed assessment.
Does pulmonary hypertension treatment improve renal function in patients with PAH and CTEPH?
Does pulmonary hypertension treatment improve renal function in patients with PAH and CTEPH?
Renal dysfunction is prevalent in PAH and CTEPH and predicts mortality, but pulmonary hypertension therapies provide only minimal short-term improvement in eGFR.
PH treatment yields only minimal short-term eGFR gains despite renal dysfunction predicting mortality; extends cardiorenal risk observations in PAH/CTEPH but leaves open clinical impact.
Background Pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) cause right ventricular dysfunction with extrapulmonary sequelae including renal dysfunction. We sought to characterise renal dysfunction in PAH and CTEPH and to assess the effect of pulmonary hypertension treatment on renal function. Methods We performed an individual participant data meta-analysis of 6694 participants from 18 phase III randomised clinical trials of pulmonary hypertension therapies. We calculated estimated glomerular filtration rate (eGFR) using the race-agnostic 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Results The mean± sd age was 49.6±15.5 years, 78% were female and 58% had idiopathic PAH. A total of 907 (13.5%) participants had a baseline eGFR <60 mL·min −1 ·1.73 m −2 . Lower baseline eGFR correlated with higher mean right atrial pressure (mRAP) and lower cardiac index. At 12–16 weeks, a 10 mmHg decrease in mRAP from baseline or a 1 L·min −1 ·m −2 increase in cardiac index was associated with only a 1.7 mL·min −1 ·1.73 m −2 (95% CI −2.9–−0.5 mL·min −1 ·1.73 m −2 ; p=0.006) or a 1.4 mL·min −1 ·1.73 m −2 (95% CI 0.5–2.4 mL·min −1 ·1.73 m −2 ; p=0.003) increase in eGFR, respectively. A 10 mL·min −1 ·1.73 m −2 lower baseline eGFR was associated with an increased risk of all-cause mortality (adjusted hazard ratio 1.16, 95% CI 1.08–1.23; p<0.001). Interestingly, pulmonary hypertension treatment was associated with only a small improvement in eGFR at 12–16 weeks (adjusted β 2.0 mL·min −1 ·1.73 m −2 , 95% CI 1.4–2.6 mL·min −1 ·1.73 m −2 ; p<0.001). Conclusion Renal dysfunction remains highly prevalent in PAH and CTEPH and is associated with worse haemodynamics and worse clinical outcomes. In this cohort with relatively preserved renal function, pulmonary hypertension treatment was associated with only a minimal improvement in eGFR.
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Meservey et al. (2025) studied this question.
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