Cardiac resynchronization therapy corrects dyssynchrony-induced regional gene expression changes on a genomic level

Andreas S. Barth, Takeshi Aiba, Victoria Halperin, Deborah DiSilvestre, Khalid Chakir, Carlo Colantuoni, Richard S. Tunin, Victoria Lea Dimaano, Wayne Yu, Theodore P. Abraham, David A. Kass, Gordon F. Tomaselli

Research output: Contribution to journalArticle

64 Citations (Scopus)

Abstract

Background-Cardiac electromechanical dyssynchrony causes regional disparities in workload, oxygen consumption, and myocardial perfusion within the left ventricle. We hypothesized that such dyssynchrony also induces region-specific alterations in the myocardial transcriptome that are corrected by cardiac resynchronization therapy (CRT). Methods and Results-Adult dogs underwent left bundle branch ablation and right atrial pacing at 200 bpm for either 6 weeks (dyssynchronous heart failure, n=12) or 3 weeks, followed by 3 weeks of resynchronization by biventricular pacing at the same pacing rate (CRT, n=10). Control animals without left bundle branch block were not paced (n=13). At 6 weeks, RNA was isolated from the anterior and lateral left ventricular (LV) walls and hybridized onto canine-specific 44K microarrays. Echocardiographically, CRT led to a significant decrease in the dyssynchrony index, while dyssynchronous heart failure and CRT animals had a comparable degree of LV dysfunction. In dyssynchronous heart failure, changes in gene expression were primarily observed in the anterior LV, resulting in increased regional heterogeneity of gene expression within the LV. Dyssynchrony-induced expression changes in 1050 transcripts were reversed by CRT to levels of nonpaced hearts (false discovery rate =5%). CRT remodeled transcripts with metabolic and cell signaling function and greatly reduced regional heterogeneity of gene expression as compared with dyssynchronous heart failure. Conclusions-Our results demonstrate a profound effect of electromechanical dyssynchrony on the regional cardiac transcriptome, causing gene expression changes primarily in the anterior LV wall. CRT corrected the alterations in gene expression in the anterior wall, supporting a global effect of biventricular pacing on the ventricular transcriptome that extends beyond the pacing site in the lateral wall.

Original languageEnglish (US)
Pages (from-to)371-378
Number of pages8
JournalCirculation: Cardiovascular Genetics
Volume2
Issue number4
DOIs
StatePublished - Aug 1 2009
Externally publishedYes

Fingerprint

Cardiac Resynchronization Therapy
Gene Expression
Heart Failure
Transcriptome
Bundle-Branch Block
Left Ventricular Dysfunction
Workload
Oxygen Consumption
Heart Ventricles
Canidae
Perfusion
Dogs
RNA

Keywords

  • Cardiac resynchronization therapy
  • Conduction
  • Electrical stimulation
  • Heart failure
  • Remodeling

ASJC Scopus subject areas

  • Genetics
  • Cardiology and Cardiovascular Medicine
  • Genetics(clinical)

Cite this

Cardiac resynchronization therapy corrects dyssynchrony-induced regional gene expression changes on a genomic level. / Barth, Andreas S.; Aiba, Takeshi; Halperin, Victoria; DiSilvestre, Deborah; Chakir, Khalid; Colantuoni, Carlo; Tunin, Richard S.; Dimaano, Victoria Lea; Yu, Wayne; Abraham, Theodore P.; Kass, David A.; Tomaselli, Gordon F.

In: Circulation: Cardiovascular Genetics, Vol. 2, No. 4, 01.08.2009, p. 371-378.

Research output: Contribution to journalArticle

Barth, AS, Aiba, T, Halperin, V, DiSilvestre, D, Chakir, K, Colantuoni, C, Tunin, RS, Dimaano, VL, Yu, W, Abraham, TP, Kass, DA & Tomaselli, GF 2009, 'Cardiac resynchronization therapy corrects dyssynchrony-induced regional gene expression changes on a genomic level', Circulation: Cardiovascular Genetics, vol. 2, no. 4, pp. 371-378. https://doi.org/10.1161/CIRCGENETICS.108.832345
Barth, Andreas S. ; Aiba, Takeshi ; Halperin, Victoria ; DiSilvestre, Deborah ; Chakir, Khalid ; Colantuoni, Carlo ; Tunin, Richard S. ; Dimaano, Victoria Lea ; Yu, Wayne ; Abraham, Theodore P. ; Kass, David A. ; Tomaselli, Gordon F. / Cardiac resynchronization therapy corrects dyssynchrony-induced regional gene expression changes on a genomic level. In: Circulation: Cardiovascular Genetics. 2009 ; Vol. 2, No. 4. pp. 371-378.
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