Defining the molecular signatures of human right heart failure

• Published in: Life sciences (1973) Vol. 196; pp. 118 - 126
• Main Authors: Williams, Jordan L., Cavus, Omer, Loccoh, Emefah C., Adelman, Sara, Daugherty, John C., Smith, Sakima A., Canan, Benjamin, Janssen, Paul M.L., Koenig, Sara, Kline, Crystal F., Mohler, Peter J., Bradley, Elisa A.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-03-2018; Elsevier BV
• Subjects: Adult; Aged; Biomarkers - analysis; Cardiac arrhythmia; Connective tissue growth factor; Familial Primary Pulmonary Hypertension - pathology; Female; Gene expression; Gene Expression Regulation - drug effects; Heart diseases; Heart failure; Heart Failure - genetics; Heart Failure - pathology; Heart Ventricles - metabolism; Humans; Hypertension; Implantation; Inflammation; Lung diseases; Male; Middle Aged; Molecular mechanisms; Pulmonary hypertension; Right heart failure; Right ventricular failure; RNA, Messenger - biosynthesis; RNA, Messenger - genetics; Signal Transduction - genetics; Transcription; Ventricle; Ventricular Dysfunction, Left - genetics; Ventricular Dysfunction, Left - pathology; Ventricular Dysfunction, Right - genetics; Ventricular Dysfunction, Right - pathology; Ventricular Function, Right; Right ventricular failure; Right heart failure; Pulmonary hypertension; Molecular mechanisms
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2018.01.021

Right ventricular failure (RVF) varies significantly from the more common left ventricular failure (LVF). This study was undertaken to determine potential molecular pathways that are important in human right ventricular (RV) function and may mediate RVF.
We analyzed mRNA of human non-failing LV and RV samples and RVF samples from patients with pulmonary arterial hypertension (PAH), and post-LVAD implantation. We then performed transcript analysis to determine differential expression of genes in the human heart samples. Immunoblot quantification was performed followed by analysis of non-failing and failing phenotypes.
Inflammatory pathways were more commonly dysregulated in RV tissue (both non-failing and failing phenotypes). In non-failing human RV tissue we found important differences in expression of FIGF, TRAPPAC, and CTGF suggesting that regulation of normal RV and LV function are not the same. In failing RV tissue, FBN2, CTGF, SMOC2, and TRAPP6AC were differentially expressed, and are potential targets for further study.
This work provides some of the first analyses of the molecular heterogeneity between human RV and LV tissue, as well as key differences in human disease (RVF secondary to pulmonary hypertension and LVAD mediated RVF). Our transcriptional data indicated that inflammatory pathways may be more important in RV tissue, and changes in FIGF and CTGF supported this hypothesis. In PAH RV failure samples, upregulation of FBN2 and CTGF further reinforced the potential significance that altered remodeling and inflammation play in normal RV function and failure.