» Articles » PMID: 37587582

Right Atrial Adaptation to Precapillary Pulmonary Hypertension: Pressure-Volume, Cardiomyocyte, and Histological Analysis

Abstract

Background: Precapillary pulmonary hypertension (precPH) patients have altered right atrial (RA) function and right ventricular (RV) diastolic stiffness.

Objectives: This study aimed to investigate RA function using pressure-volume (PV) loops, isolated cardiomyocyte, and histological analyses.

Methods: RA PV loops were constructed in control subjects (n = 9) and precPH patients (n = 27) using magnetic resonance and catheterization data. RA stiffness (pressure rise during atrial filling) and right atrioventricular coupling index (RA minimal volume / RV end-diastolic volume) were compared in a larger cohort of patients with moderate (n = 39) or severe (n = 41) RV diastolic stiffness. Cardiomyocytes were isolated from RA tissue collected from control subjects (n = 6) and precPH patients (n = 9) undergoing surgery. Autopsy material was collected from control subjects (n = 6) and precPH patients (n = 4) to study RA hypertrophy, capillarization, and fibrosis.

Results: RA PV loops showed 3 RA cardiac phases (reservoir, passive emptying, and contraction) with dilatation and elevated pressure in precPH. PrecPH patients with severe RV diastolic stiffness had increased RA stiffness and worse right atrioventricular coupling index. Cardiomyocyte cross-sectional area was increased 2- to 3-fold in precPH, but active tension generated by the sarcomeres was unaltered. There was no increase in passive tension of the cardiomyocytes, but end-stage precPH showed reduced number of capillaries per mm accompanied by interstitial and perivascular fibrosis.

Conclusions: RA PV loops show increased RA stiffness and suggest atrioventricular uncoupling in patients with severe RV diastolic stiffness. Isolated RA cardiomyocytes of precPH patients are hypertrophied, without intrinsic sarcomeric changes. In end-stage precPH, reduced capillary density is accompanied by interstitial and perivascular fibrosis.

Citing Articles

Atrial Fibrosis in Atrial Fibrillation: Mechanistic Insights, Diagnostic Challenges, and Emerging Therapeutic Targets.

Karakasis P, Theofilis P, Vlachakis P, Korantzopoulos P, Patoulias D, Antoniadis A Int J Mol Sci. 2025; 26(1.

PMID: 39796066 PMC: 11720255. DOI: 10.3390/ijms26010209.


Translation of pathophysiological mechanisms of atrial fibrosis into new diagnostic and therapeutic approaches.

Schotten U, Goette A, Verheule S Nat Rev Cardiol. 2024; .

PMID: 39443702 DOI: 10.1038/s41569-024-01088-w.


Four-dimensional automated quantitative echocardiography assessment of right heart remodeling in patients with functional tricuspid regurgitation.

Cai Y, Zhang X, Huang T, Luo X, Zeng D, Chang S Quant Imaging Med Surg. 2024; 14(10):7318-7329.

PMID: 39429598 PMC: 11485358. DOI: 10.21037/qims-24-676.


Pathophysiology of the right ventricle and its pulmonary vascular interaction.

Hemnes A, Celermajer D, DAlto M, Haddad F, Hassoun P, Prins K Eur Respir J. 2024; 64(4).

PMID: 39209482 PMC: 11525331. DOI: 10.1183/13993003.01321-2024.


Right ventricular diastolic adaptation to pressure overload in different rat strains.

Axelsen J, Andersen S, Ringgaard S, Smal R, Llucia-Valldeperas A, Nielsen-Kudsk J Physiol Rep. 2024; 12(13):e16132.

PMID: 38993022 PMC: 11239975. DOI: 10.14814/phy2.16132.