Key result
LVAD implantation significantly decreased the expression of genes involved in cellular immune response and T cell activation at 7 days, which partially recovered by 6 months post-implant.
Why the study?
Does continuous-flow LVAD implantation alter peripheral blood gene expression pathways in patients with end-stage heart failure?
Observational (n=9)
No
Does continuous-flow LVAD implantation alter peripheral blood gene expression pathways in patients with end-stage heart failure?
p-value: p=<0.05
Genomic analysis reveals that LVAD implantation in end-stage heart failure is associated with an acute decrease in immune response gene expression at 7 days, which partially recovers by 6 months.
INTRODUCTION: Continuous-flow left ventricular assist devices (LVADs) are an established therapy for patients with end-stage heart failure. The short- and long-term impact of these devices on peripheral blood gene expression has not been characterized, and may provide insight into the molecular pathways mediated in response to left ventricular remodeling and an improvement in overall systemic circulation. We performed RNA sequencing to identify genes and pathways influenced by these devices. METHODS: RNA was extracted from blood of 9 heart failure patients (8 male) prior to LVAD implantation, and at 7 and 180 days postoperatively. Libraries were sequenced on an Illumina HiSeq2000 and sequences mapped to the human Ensembl GRCh37.67 genome assembly. RESULTS: A specific set of genes involved in regulating cellular immune response, antigen presentation, and T cell activation and survival were down-regulated 7 days after LVAD placement. 6 months following LVAD placement, the expression levels of these genes were significantly increased; yet importantly, remained significantly lower than age and sex-matched samples from healthy controls. CONCLUSIONS: In summary, this genomic analysis identified a significant decrease in the expression of genes that promote a healthy immune response in patients with heart failure that was partially restored 6 months following LVAD implant.
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Mitchell et al. (2013) conducted an observational in End-stage heart failure (Stage D) (n=9). Left Ventricular Assist Device (LVAD) implantation vs. Pre-LVAD baseline was evaluated on Differential expression of genes regulating cellular immune response, antigen presentation, and T cell activation (p=<0.05). LVAD implantation significantly decreased the expression of genes involved in cellular immune response and T cell activation at 7 days, which partially recovered by 6 months post-implant.
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