Cardiac chamber-specific genetic alterations suggest candidate genes and pathways implicating the left ventricle in the pathogenesis of atrial fibrillation.

Herrera-Rivero M, Gandhi S, Witten A, Ghalawinji A, Schotten U, Stoll M

Research article (journal) | Peer reviewed

Abstract

It is believed that the atria play a predominant role in the initiation and maintenance of atrial fibrillation (AF), while the role of left ventricular dysfunction in the pathophysiology remains enigmatic. We sought to dissect chamber specificity of AF-associated transcriptional changes using RNA-sequencing. We performed intra- and inter-chamber differential expression analyses comparing AF against sinus rhythm to identify genes specifically dysregulated in human left atria, right atria, and left ventricle (LV), and integrated known AF genetic associations with expression quantitative trait loci datasets to inform the potential for disease causal contributions within each chamber. Inter-chamber patterns changed drastically. Vast AF-associated transcriptional changes specific to LV, enriched for biological pathway terms implicating mitochondrial function, developmental processes and immunity, were supported at the genetic level, but no major enrichments for candidate genes specific to the atria were found. Our observations suggest an active role of the LV in the pathogenesis of AF.

Details about the publication

JournalGenomics
Volume114
Issue2
Page range110320-110320
StatusPublished
Release year2022 (01/05/2022)
Language in which the publication is writtenEnglish
DOI10.1016/j.ygeno.2022.110320
KeywordsAtrial Fibrillation; Heart Atria; Heart Ventricles; Humans

Authors from the University of Münster

Ghalawinji, MHD Amer
Humangenetik, Abt. für Genetische Epidemiologie
Herrera Rivero, Marisol
Humangenetik, Abt. für Genetische Epidemiologie
Stoll, Monika
Humangenetik, Abt. für Genetische Epidemiologie
Witten, Anika
Humangenetik, Abt. für Genetische Epidemiologie