Key result
Ischemic heart disease is associated with substantial differences in gene expression across all cell types in the right atrium, leading to inflammatory microvascular dysfunction.
Why the study?
Ischemic heart disease plays a central role in electrical and structural remodeling of the right atrium, predisposing to arrhythmias, heart failure, and sudden death.
Observational
Findings hypothesis-generating only; leaves open targeted therapies for right atrial remodeling in ischemic heart disease.
Ischemic heart disease is globally the leading cause of death. It plays a central role in the electrical and structural remodeling of the right atrium, predisposing to arrhythmias, heart failure, and sudden death. Here, we provide the first dissection of the gene expression changes in the live right atrial tissue, using single-nuclei RNA-seq and spatial transcriptomics. We investigate matched samples of the tissue and pericardial fluid and reveal substantial differences in disease- associated gene expression in all cell types, leading to inflammatory microvascular dysfunction and changes in the tissue composition. Our study demonstrates the importance of creating high- resolution cellular maps and partitioning disease signals beyond epicardial coronary arteries and ischemic left ventricle to identify candidate mechanisms leading to more severe types of human cardiovascular disease. One-Sentence Summary Single-cell dissection of ex vivo heart biopsies and pericardial fluid in ischemic heart disease and heart failure
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Linna-Kuosmanen et al. (2021) conducted an observational in Ischemic heart disease and heart failure. Ischemic heart disease was evaluated on Gene expression changes in live right atrial tissue and pericardial fluid. Ischemic heart disease is associated with substantial differences in gene expression across all cell types in the right atrium, leading to inflammatory microvascular dysfunction.
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