Cellular Communication Network Protein 2 in the Right Ventricle of Pulmonary Arterial Hypertension
Year: 2025
Type: article
Study design: Observational Study
Abstract: ABSTRACT Cellular communication network 2 (CCN2) is a secreted matricellular protein associated with pulmonary arterial hypertension (PAH) but has not been studied relative to PAH severity, outcomes, or right ventricle (RV) structure and function in a large human cohort and preclinical animal model. This study assessed the associations between CCN2 and PAH severity, survival, hemodynamic measurements, and cardiovascular dysfunction. Serum CCN2 levels were compared in 2548 adults with PAH and 216 controls. CCN2 levels in PAH patients were compared to functional and hemodynamic measurements, and survival outcomes. RV‐pulmonary artery coupling and RV morphology were also assessed in a small subset of patients via pressure–volume loops and cardiac magnetic resonance imaging. In a preclinical PAH model, plasma CCN2 levels were compared between ventricles with PAH progression. CCN2 mRNA levels in both ventricles in the preclinical model were measured to compare with morphologic histologic variables. CCN2 serum levels were significantly higher in PAH compared to controls (p < 0.0001). Higher CCN2 levels were associated with reduced RV contractility (p = 0.003). Higher CCN2 levels were associated with worse 6MWD (p = 0.035), and higher risk of mortality or transplant (p = 0.025). In the preclinical model, prepulmonary CCN2 plasma levels increased with the progression of disease. CCN2 mRNA levels in the RV were associated with decreased RV capillary density (p = 0.015) and increased RV fibrosis (p = 0.045). Though more investigation is needed, it appears that CCN2 plays a role in the development of PAH and potentially in RV maladaptation in PAH.
Source: Pulmonary Circulation
DOI: 10.1002/pul2.70067
Authors: Carly E. Byrd, Jennifer E. Schramm, Jun Yang, Allan E. Barnes, Megan Griffiths, Anjira S. Ambade, Darin T. Rosen, Ilton M. Cubero Salazar, Catherine E. Simpson, Ryan J. Tedford, Steven Hsu, Dhananjay Vaidya, Todd M. Kolb, Michael W. Pauciulo, William C. Nichols, David D. Ivy, Eric D. Austin, Paul M. Hassoun, Rachel L. Damico, Allen D. Everett
Institutions: Johns Hopkins University, The University of Texas Southwestern Medical Center, Medical University of South Carolina, Johns Hopkins Medicine, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Children's Hospital Colorado, Vanderbilt University Medical Center, University of Miami
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,310
Awards: G1441675580, Mechanisms of Right Ventricular Dysfunction in Scleroderma-associated PAH, G1932362413, G2841533278, G3265250566, G4206978221, The role of xanthine oxidoreductase activity and altered metabolism in scleroderma-associated pulmonary arterial hypertension, G5033267147, G5950203795, Multidisciplinary Training Program in Lung Disease
OpenAlex ID: W4409125385
