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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Circ Cardiovasc Genet. Author manuscript; available in PMC 2010 August 1.
Published in final edited form as:
PMCID: PMC2801868
NIHMSID: NIHMS131309

Cardiac Resynchronization Therapy Corrects Dyssynchrony-induced Regional Gene Expression Changes on a Genomic Level

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 (CRT).

Methods and Results

Adult dogs underwent left bundle branch ablation (LBBB) and right atrial pacing at 200 bpm for either 6 weeks (dyssynchronous heart failure, DHF, n=12) or 3 weeks followed by 3 weeks of resynchronization by bi-ventricular pacing at the same pacing rate (CRT, n=10). Control animals without LBBB were not paced (NF, n=13). At 6 weeks, RNA was isolated from the anterior and lateral LV walls and hybridized onto canine-specific 44K microarrays. Echocardiographically, CRT led to a significant decrease in the dyssynchrony index, while DHF and CRT animals had a comparable degree of LV dysfunction. In DHF, changes in gene expression were primarily observed in the anterior LV, resulting in increased regional heterogeneity of gene expression within the left ventricle. Dyssynchrony-induced expression changes in 1050 transcripts were reversed by CRT to levels of NF hearts (false discovery rate <5%). CRT remodeled transcripts with metabolic and cell signaling function and greatly reduced regional heterogeneity of gene expression compared with DHF.

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.

Keywords: Cardiac Resynchronization Therapy, Heart Failure, Gene Expression, Microarray

Introduction

Nearly 5 million Americans suffer from heart failure (HF) and more than 250,000 die annually.1 Asymmetrical contraction resulting from an intraventricular conduction delay is present in ~30% of patients with HF2 and has been identified as an independent predictor of mortality in HF patients.3-5 A left bundle branch block (LBBB) decreases regional loading, contractile work, myocardial blood flow and oxygen consumption in the early-activated anterior myocardium, while these parameters are increased in the late-activated lateral LV.6, 7 Bi-ventricular stimulation, or cardiac resynchronization therapy (CRT) has been developed to treat this disorder. It improves contractile synchrony, systolic function, re-homogenizes regional work load, and in patients, improves clinical symptoms and survival.8, 9

We first reported that dyssynchronous HF also leads to regional disparities of protein expression, notably in stress-response kinases and cytokines,10, 11 with enhanced levels in the higher stress (late-activated) lateral wall. More recently, we showed that CRT can re-homogenize these changes.10 However, our previous analysis was focused on individual proteins, and most likely missed a much broader impact of dyssynchrony and CRT on regional molecular expression patterns. To test this, we used a global gene expression profiling approach in a recently developed canine model of dyssynchronous HF and CRT,10 examining regional disparities in the cardiac transcriptome in dyssynchronous HF, and determining the capacity of CRT to ameliorate these abnormalities.

Methods

Cardiac Resynchronization in a Canine Tachypacing-Induced Heart Failure Model

Details of the animal model have been described previously.10, 12-14 Briefly, adult male mongrel dogs (n=22) underwent left bundle branch radiofrequency ablation, and later received bipolar epicardial leads (Medtronic, Minneapolis, MN) implanted on the right atrium, right ventricular free wall, and lateral LV. For 3 weeks, all dogs were subjected to rapid atrial pacing (200 min-1) to induce dyssynchronous heart failure (DHF). Dogs were subsequently divided into two groups for an additional pacing period of three weeks: While DHF animals (n=12) continued to receive atrial tachypacing, CRT dogs (n=10) received bi-ventricular tachypacing at the same rate during the latter half of the pacing protocol. Control animals without LBBB were not paced (NF, n=13). All protocols followed USDA and NIH guidelines, and were approved by our institution's Animal Care and Use Committee.

Echocardiography and Hemodynamic Recordings

Chamber function was assessed by two-dimensional echocardiography with tissue Doppler imaging (at 3 and 6 week time points), and by invasive catheterization at the time of sacrifice. The details have been previously reported.10

Microarray Hybridization and Statistical Analysis

Total RNA was isolated with TRIzol reagent from the subendocardium of the anterior and lateral LV walls in the distribution of the LAD and left circumflex artery, respectively. Following a one-color design in 11 NF, 10 DHF and 9 CRT animals, RNA was labeled with Cy3 and hybridized onto Agilent 44K canine-specific microarrays. Agilent's RNA spike-ins were mixed with the sample and co-hybridized to the arrays following the manufacturer's instructions. The quality of the microarray hybridizations was verified by controlling for the dynamic range, saturation, pixel noise, grid misalignment and signal-to-noise ratio.

To validate results from one-color microarray experiments where RNA isolated from the anterior and lateral walls from the same heart was hybridized onto two separate arrays, experiments were also performed using a two-color design in a subset of animals (6 NF, 5 DHF and 5 CRT dogs), partially overlapping those used for the one-color design. In these experiments, corresponding anterior and lateral samples from the same LV were labeled with Cy3 and Cy5 (including dye swap experiments) and hybridized onto the same array to achieve a direct comparison of the relative gene expression in different regions of the same heart. Additional validation included comparison of the data from this study to two publicly available datasets of dyssynchronous heart failure in dogs with RV pacing-induced LV dysfunction (Gene Expression Omnibus accession numbers GSE5247 and GSE9794).15, 16

Preprocessing and most of the statistical analysis were done using R (www.r-project.org) and Bioconductor (www.bioconductor.org). Microarray data were normalized using quantile normalization implemented in Bioconductor's “affy”-package (for one-color data) or loess normalization implemented in Bioconductor's “limma”-package (for two-color microarray data). Complying with MIAME standards (Minimum Information about a Microarray Experiment),17 microarray data has been submitted to a public repository (Gene Expression Omnibus, GEO; the SuperSeries accession number GSE14661 includes GSE14327 (1-color design) and GSE14338 (2-color design data)).

To determine differentially expressed genes, multiclass and unpaired two-class Significance Analysis of Microarrays (SAM) was used.18 Differences in gene expression were regarded as statistically significant if a false discovery rate (FDR) of q<0.05 was achieved. Functional annotation of differentially expressed genes was based on the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways database. Overrepresentation of specific KEGG pathways in a gene set was statistically analyzed by “FatiGO+”19 and the Database for Annotation, Visualization and Integrated Discovery (DAVID).20

An on-line data supplement containing one figure and two tables appears at http://circ.ahajournals.org. The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.

Results

Dyssynchronous Heart Failure and Biventricular Pacing

The hemodynamic features of the canine DHF and CRT model have been reported previously,10 and results obtained more recently from a larger cohort are summarized in Table 1. Compared with normal controls, DHF ventricles display marked dyssynchrony that was restored to normal levels with CRT. Significant differences were observed in ejection fraction (increase of ~10%), stroke volume, and left ventricular contractility assessed by dP/dTmax normalized to instantaneous developed pressure. End-diastolic pressure was similarly elevated, and both DHF and CRT hearts remained dilated and had evidence of failure.

Table 1
Phenotypic characterization. Echocardiographic and invasive hemodynamic measurements of DHF (n=17), CRT (n=15) and non-failing (n=6) dogs

Regional regulation of gene expression in DHF

Figure 1 shows the relative distribution of significantly up- and down-regulated transcripts for eleven KEGG pathways in the anterior myocardium comparing non-failing and paced (DHF) animals. Energy-deriving processes including oxidative phosphorylation, tricarboxylic acid cycle (TCA), fatty acid and amino acid metabolism were concomitantly down-regulated in failing myocardium, while various cell signaling pathways and extracellular matrix components were up-regulated. To validate the reproducibility of the results obtained with the Agilent microarray platform, we compared our results to two publicly available datasets of pacing-induced (single site, and also dyssynchronous) HF in dogs, generated with Affymetrix microarrays with tissue from the anterior LV wall (FDR<5% for all studies).15, 16 The high concordance of gene expression patterns between these three studies underscores the reproducibility of our findings and highlights the robust genomic fingerprint of DHF in the anterior myocardium.

Figure 1
KEGG pathway analysis in tachycardia-pacing induced heart failure

Dyssynchronous contraction of the LV associated with LBBB imposes greater stress on the lateral wall compared to the anterior LV. To test the hypothesis that DHF alters gene expression patterns in a region-specific fashion, samples from anterior and lateral LV myocardium were examined separately in non-failing and DHF animals. Separate analysis of the regional transcriptome from the same hearts (NF n=11, DHF n=10), identified over six-times as many genes that were differentially expressed between NF and DHF hearts in anterior compared to lateral LV myocardium (2173 vs. 346 transcripts, respectively; SAM with FDR<5%; Table 2 and Online Figure 1). Besides these quantitative differences, important qualitative differences were evident for DHF-induced gene expression changes in the anterior and lateral myocardium. While down-regulation of energy-deriving processes including oxidative phosphorylation and TCA cycle was more pronounced in the anterior compared to the lateral wall, regulation of cell signaling pathways and extracellular matrix components displayed a different pattern in the lateral and anterior LV myocardium in dyssynchronous HF. For instance, cell signaling pathways were up-regulated in the anterior LV wall, but predominantly down-regulated in the lateral LV wall (Figure 2, upper panel). The small number of regulated genes found in lateral myocardium of DHF hearts limited the statistical power of the KEGG pathway analysis, thus an additional analysis was performed where KEGG pathways of the first 1000 up- and down-regulated transcripts were compared in both regions, irrespective of the significance level. This approach was employed to determine if the changes in gene expression in the lateral wall differ only quantitatively from those in the anterior LV wall. The metabolic gene classes were still down-regulated; however, the pattern of gene expression in cell signaling pathways and extracellular matrix components differed considerably from the robust genomic fingerprint observed in anterior myocardium in DHF (Figure 1 and lower panel of Figure 2), suggesting a quantitatively and qualitatively different transcriptomic response to electromechanical dyssynchrony in the anterior and lateral LV.

Figure 2
Regional KEGG pathway analysis in tachycardia-pacing induced heart failure
Table 2
Results of Statistical Analysis of Microarrays (SAM), False Discovery Rate (FDR) <5%

Biventricular Pacing Reverses Gene Expression Changes

Separate analysis of gene expression in anterior and lateral LV samples identified only 7 differentially expressed transcripts between DHF and CRT hearts (Table 2 and Online Table 1). However, when anterior and lateral samples from the same hearts were paired by examining the difference in gene expression between the two regions (anterior minus lateral LV wall), a large number of transcripts were found to be differentially expressed between DHF and CRT hearts (Table 2). An unsupervised clustering of 1050 transcripts, identified by SAM multiclass analysis of regional differences in gene expression between anterior and lateral wall for NF, DHF and CRT hearts, revealed that CRT hearts clustered with NF, rather than with gene expression patterns from DHF samples (Figure 3A; the gene list is provided in Online Table 2). An identical picture emerged when data from the two-color microarray design were clustered (Figure 3B). The latter experiments also revealed few gene expression changes between the anterior and lateral regions in the NF myocardium (Figure 4). This was substantiated by SAM, with only 2 transcripts being differentially expressed between anterior and lateral regions in non-failing myocardium (LIM domain only protein 3 in anterior myocardium and glutathione S-transferase P in lateral myocardium, FDR5% in two-color array data). In contrast, there was a marked heterogeneity in gene expression between anterior and lateral LV regions in DHF that was reduced by CRT to levels comparable to NF hearts (Figure 4). Moreover, CRT partially reversed DHF-induced gene expression changes (Figure 5), as evidenced by KEGG pathway analysis; transcripts of metabolic activity were up-regulated in the anterior wall while transcripts encoding for cell signaling pathways and extracellular matrix components were down-regulated. Therefore, CRT restored the relative balance of gene expression between the anterior and lateral LV, e.g. expression of MAPK pathway signaling and extracellular matrix components was reduced in the anterior wall but increased in lateral LV (Figure 5).

Figure 3
Clustering of regional differences between anterior and lateral myocardium
Figure 4
Dyssynchrony leads to increased regional heterogeneity in gene expression that is partially reduced with CRT
Figure 5
Partial correction of pacing-induced gene expression changes by CRT

Discussion

Using an unbiased and global assessment of transcriptional activity in a large animal model of dyssynchronous heart failure, we found that dyssynchrony-induced changes in gene expression were more pronounced in the anterior compared with the lateral LV. The genes that showed significant heterogeneity in regional expression with dyssynchrony are involved in important processes such as metabolic pathways, extracellular matrix remodeling, and myocardial stress responses. The disparity in the number of regulated transcripts between the early- and late-activated LV regions gave rise to an increased regional heterogeneity of gene expression within the dyssynchronously contracting myocardium. Remarkably, dyssynchrony-induced expression changes were reversed by CRT to levels in NF hearts, as evident by a reduced regional heterogeneity of gene expression and prominent reverse remodeling of transcripts with metabolic and cell signaling function.

A number of factors have been shown to regulate transcriptional activity in the heart, including contractile activity, stretch, myocardial perfusion and metabolism.21-23 As all these parameters are altered in a region-specific fashion in DHF, they could account for the differential transcriptional response of the anterior and lateral walls. It is well known that cardiac dyssynchrony, whether due to a LBBB or right ventricular free wall pacing, decreases regional loading, contractile work, myocardial blood flow and oxygen consumption in the early-activated anterior myocardium. For instance, the regional pressure-strain loop area which corresponds to the external work performed, is reduced to a greater extent in the anterior compared to the lateral wall in DHF hearts.13 In line with this finding, down-regulation of metabolic transcripts was significantly greater in anterior compared with lateral LV regions. Biventricular pacing improves contractile timing, thereby increasing regional work in the anterior wall, while reducing work in the lateral LV region. Experimentally, this has been shown to couple with rebalancing of glucose metabolism24 and myocardial blood flow25 (rising in the anterior and declining in lateral walls), and such findings are consistent with CRT-associated increases in transcripts levels encoding oxidative phosphorylation and various metabolic pathways in anterior samples observed in this study. In another study performed in these models, we have observed up-regulation of proteins in various metabolic pathways in CRT by examining the myocardial mitochondrial proteome.26 Indeed, nearly 50% of the protein changes involved subunits of the oxidative phosphorylation chain, the majority of which displayed marked up-regulation with CRT. Additionally, key enzymes in anaplerotic pathways such as branched chain amino acid oxidation and pyruvate carboxylation were increased, suggesting that CRT may increase the pool of Krebs cycle intermediates to fuel oxidative phosphorylation.26

While CRT effectively restored dyssynchrony-induced gene expression changes in this model, it did not correct overall HF-induced transcriptomic alterations. The changes in gene expression levels brought about by CRT were only significant when a paired design for anterior and lateral LV region of each heart was employed, i.e. influencing heterogeneity of expression, but far less when anterior and lateral regions in DHF and CRT hearts were compared separately (Table 2). In our view, two main findings suggest that even this small yet significant effect of CRT on the cardiac transcriptome likely has global effects on heart function. First, dyssynchrony-induced gene expression changes tended to aggravate the HF-related transcriptomic signature (Figures 2 and and5).5). In DHF for example, various cell signaling and extracellular matrix remodeling pathways were up-regulated in the early-activated anterior but down-regulated in the late-activated lateral LV wall. In contrast, biventricular pacing partially reversed cell signaling and extracellular matrix remodeling changes by restoring the relative balance in gene expression levels between anterior and lateral wall (down-regulation in anterior regions with concomitant up-regulation of mRNA levels of these pathways in the lateral wall). Thus, dyssynchrony-induced expression changes could well contribute to the decline in EF in DHF animals between 3 and 6 weeks of pacing, while CRT animals showed a modest increase in EF during the same period (Table 1). Second, dyssynchrony-induced gene expression changes significantly increased the heterogeneity of gene expression within early- and late-activated LV wall regions. It is tempting to speculate that this increased heterogeneity within the LV wall also reflects regionally heterogeneous remodeling of ion channels that exists in this HF model,12 and possibly increased QT dispersion.27, 28 In a study that examined QT interval duration in relation to CRT, Berger et al. found that QT dispersion increased during right ventricular, and decreased during biventricular pacing,29 thus paralleling changes observed for action potential duration with DHF and CRT in isolated cardiomyocytes.12

In summary, we demonstrate a profound effect of electrical activation on the regional cardiac transcriptome and provide unique insights into transcriptome-wide molecular processes underlying transcriptomic remodeling in CRT. The dyssynchronous failing heart is not simply worse heart failure, but a form of disease with profound regional gene expression disparities. Moreover, we show for the first time that by re-coordinating contraction, such expression heterogeneity can be essentially returned to normal, even in a failing heart, on a genome-wide level. This may point to a more biological method to assess the impact of CRT.

Study Limitations

Pacing-induced heart failure is a widely-used animal model of non-ischemic heart failure that shares major electrophysiological (APD prolongation, high incidence of sudden cardiac death, atrial arrhythmias), morphological (biventricular dilatation) and functional (depressed contractility) hallmarks of human heart failure. However, tachypacing-induced HF does not mimic all features of human heart failure, as the changes in myocardial structure occurring with tachypacing are dissimilar to clinical forms of HF due to chronic ischemia or hypertensive disease. Thus, extrapolation of the findings from this heart failure model to clinical forms of HF should be done with caution, as this model will not fully represent the complex clinical spectrum of HF. Additionally, pharmacological interventions known to disrupt the neurohormonal dysfunction in HF (e.g. beta-blockade or ACE-inhibition) were not employed in this model. As this study was designed to examine the effects of CRT with ongoing HF, tachypacing was maintained throughout the study. Thus, if anything, this model might be predicted to delay benefits that might come from re-synchronization itself, though improvement was still clearly documented. Given the higher heart rate necessary to induce and maintain HF in this model, the processes of remodeling and reverse remodeling may differ from the clinical HF syndrome. Additional studies will be needed to differentiate transcriptional changes associated with altered electrical activation of the ventricles and dyssynchronous mechanical contraction independent of heart failure.

Supplementary Material

Acknowledgments

Funding Sources The work was supported by NIH P01 HL 077180, HL 072488 and R33 HL087345 to D.A.K. and G.F.T, NIH T32 HL007227 to A.S.B. and the Abraham and Virginia Weiss Professorship (D.A.K.). G.F.T. is the Michel Mirowski M.D. Professor of Cardiology.

Footnotes

Conflict of Interest Disclosures None.

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