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Aims: The haemodynamic response to exercise is prognostic in pulmonary hypertension (PH). However, little is known about right ventricular (RV) adaptation in this context. We analysed the patterns and prognostic relevance of RV adaptation to exercise in PH.
Methods And Results: We prospectively analysed 46 patients with PH and 19 disease controls with invasive exclusion of PH. All underwent three-dimensional echocardiography, pressure-volume catheterization, and right heart catheterization at rest and during stepwise exercise on a semi-supine ergometer. Patients with PH were classified as homeometric if they had increased RV end-systolic elastance and preserved RV-pulmonary arterial coupling (end-systolic/arterial elastance) during exercise (18 patients); otherwise, they were classified as heterometric (28 patients). The mean pulmonary arterial pressure/cardiac output (mPAP/CO) slope was similar in the homeometric and heterometric groups (8.8 [6.5-13.1] vs. 8.6 [4.8-18.8] mmHg·min/L), and lower in disease controls (2.1 [1.1-4.0] mmHg/L). Multivariable logistic regression identified systolic pulmonary arterial pressure change during exercise (ΔsPAP) (odds ratio [OR] 0.93, 95% confidence interval [CI] 0.87-0.99; p = 0.019) and peak exercise cardiac index (OR 0.42, 95% CI 0.18-0.97; p = 0.042) as key differentiators of homeometric/heterometric adaptation. Heterometric adaptation was significantly associated with clinical worsening and all-cause mortality (log-rank p = 0.0006 and p = 0.0246, respectively) and independently predicted clinical worsening (hazard ratio [HR] 6.52, 95% CI 2.16-19.63; p = 0.001); the HR for all-cause mortality was 6.96 (95% CI 0.87-55.66; p = 0.067).
Conclusions: Pulmonary hypertension can present with two RV patterns under stress: homeometric with increased contractile reserve and heterometric with poorer outcome. While the mPAP/CO slope does not differentiate the two, ΔsPAP and peak cardiac index offer potential for RV adaptation pattern identification and thus prognostication.
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http://dx.doi.org/10.1002/ejhf.3802 | DOI Listing |
Am J Physiol Heart Circ Physiol
September 2025
Division of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, USA.
Right ventricular (RV) failure is the primary cause of death among patients with pulmonary arterial hypertension (PAH). Patients with congenital heart disease-associated PAH (CHD-PAH) demonstrate improved outcomes compared to patients with other forms of PAH, which is related to the maintenance of an adaptively hypertrophied RV. In an ovine model of CHD-PAH, we aimed to elucidate the cellular, microvascular, and transcriptional adaptations to congenital pressure overload that support RV function.
View Article and Find Full Text PDFEur J Heart Fail
September 2025
Institute for Exercise and Environmental Medicine, Texas Health Presbyterian Hospital Dallas, Dallas, TX, USA.
Aims: Obesity is commonly hypothesized to lead to the development of heart failure (HF) in part due to increases in blood volume (BV) and left ventricular (LV) remodelling. Whether adiposity and obesity severity are associated with BV expansion and subsequent LV remodelling in middle-aged individuals at increased risk (IR) prior to the onset of HF is unknown.
Methods And Results: We analysed data from 96 middle-aged (40-64 years) non-obese (25.
Open Heart
September 2025
Division of Pulmonary Circulation, Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan
Background: Balloon pulmonary angioplasty (BPA) improves haemodynamics in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH). Previous studies on BPA have set the treatment objective to achieve a mean pulmonary arterial pressure (mPAP) of <30 mm Hg. However, the clinical impact of mPAP after BPA remains unclear.
View Article and Find Full Text PDFOpen Heart
September 2025
Department of Cardiology, Aalborg University Hospital, Aalborg, Denmark.
Background: Evidence regarding cardiovascular adaptation to pregnancy in women with pregestational diabetes is limited. Our study aimed to describe left ventricular (LV) remodelling and vascular adaptation to pregnancy in women with type 1 diabetes.
Methods: In this prospective cohort study, three consecutive cardiac MRI scans were conducted on age-matched and BMI-matched pregnant women with pregestational type 1 diabetes and pregnant women without diabetes.
Herz
September 2025
Universitätsklinik für Herzchirurgie, Herzzentrum Leipzig, Leipzig, Deutschland.
In recent years the treatment for heart failure (HF) has become much more complex. This development has highlighted the importance of a multidisciplinary HF team to ensure the best possible individually adapted treatment decisions, taking the patient's personal wishes into account and to achieve optimal results. In Germany, specialized HF practices, clinics and tertiary bespoke HF unit centers were established to ensure qualified care for HF patients.
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