End-stage heart failure (HF) patients are refractory to usual medical therapies and face a risk of death that is greater than most cancers.1 At present, the most effective therapy is cardiac transplantation, but this option is limited by the lack of suitable donor organs and strict eligibility criteria.2 Left ventricular assist devices (LVADs) provide an alternative means of treatment and are increasingly being used as either a bridge to transplantation or destination therapy. Even though it provides circulatory support for the failing heart, LVAD therapy also exposes the body to pathophysiologic changes that are unprecedented in human evolution: continuous blood flow, an external power source, and univentricular support. As a result, patients supported with VADs experience a unique variety of clinical conditions such as gastrointestinal bleeding, strokes, right ventricular failure, and infections, the pathobiology of which remains imprecisely understood.3 Because of the limitations of usual cardiovascular assessments such as imaging in VAD patients, biomarker assessments have the potential to uncover the unique pathophysiologic changes that occur with VAD support.4
MicroRNAs (miRNAs) have emerged as bona fide regulators of physiologic and pathologic cardiovascular function.5 MicroRNAs are 22–23 nucleotide single-stranded noncoding RNAs that bind messenger RNAs at their 3′ untranslated regions and negatively regulate their expression through translational repression or messenger RNA degradation. The importance of miRNAs comes from their ability to repress hundreds of target genes, often regulating biologic networks entirely.6,7 MicroRNAs are stable and readily detectable in peripheral circulation and amenable to silencing; therefore, they have been postulated to play an important role as circulating biomarkers and potential therapeutic targets in HF.8,9 Therefore, we sought to examine baseline levels and long-term changes in the expression of 23 distinct miRNAs in 40 patients who underwent LVAD placement at Duke University Medical Center (DUMC).
Details outlining the patient population have been previously outlined.4 From January 1, 2011 to October 30, 2012, a total of 40 patients aged 18 and older who required mechanical circulatory support with continuous-flow LVAD as a bridge to transplantation or destination therapy were enrolled at DUMC. Patients agreed to collection and banking of peripheral blood samples for the purpose of research and had paired long-term (>60 days) samples available. Blood samples were collected within 24 hours before LVAD implantation and at >60 days postimplant via peripheral vein into ethylenediaminetetraacetic acid containing tubes, centrifuged immediately, and stored at −80°C before analysis. Both miRNA and biomarker levels were measured from blood samples at the time points specified above. Clinical data at baseline, including demographics, medications, comorbidities, and laboratory data, were collected up to 24 hours before LVAD implantation. Data on more detailed assessments performed before LVAD placement for clinical purposes, such as cardiopulmonary exercise testing, invasive hemodynamics, echocardiographic parameters, and usual laboratories, were evaluated. As a control, plasma was collected from seven healthy control subjects. This study was approved by the DUMC Institutional Review Board, performed in accordance with the ethical guidelines of the declaration of Helsinki, and all patients provided written informed consent.
Reverse transcription reactions were performed using the Life Technologies TaqMan MicroRNA Reverse Transcription Kit (Part number 4366596) (Thermo Fischer Scientific). An Applied Biosystems 9700 PCR System (Thermo Fischer Scientific) was used to carry out the reverse transcription polymerase chain reactions. An a priori list of 23 miRNAs purported to be associated with the pathogenesis of HF were selected for investigation: miRNA-1, miRNA-10a, miRNA-15b, miRNA-16, miRNA-21, miRNA-24, miRNA-27a, miRNA-27b, miRNA-29a, miRNA-92a, miRNA-103, miRNA-126, miRNA-133a, miRNA-146a, miRNA-146b, miRNA-155, miRNA-159a, miRNA-195, miRNA-221, miRNA-222, miRNA-320, miRNA-423, and miRNA-872. Nineteen miRNAs (miR-15b, miR-16, miR-21, miR-24, miR-27a, miR-29a, miR-92a, miR-103, miR-126, miR-133a, miR-146a, miR-146b, miR-155, miR-159a, miR-195, miR-221, miR-222, miR-320, and miR-423) were ultimately included for further analysis as they demonstrated adequate expression in >80% of patient samples. Quantitative real-time polymerase chain reactions were performed in quadruplicate for all samples, and threshold cycle (Ct values) were detected. Ct values were computed with Life Technologies/Applied Biosystems ExpressionSuite Software (version 1.0.3) (Thermo Fischer Scientific). The data were analyzed with automatic settings for assigning the baseline. The Ct was defined as the fractional cycle number at which the fluorescence exceeded the given threshold. MicroRNA expression levels were normalized to a global normalization value, defined as the mean of all Ct values computed. Relative quantification (RQ) was obtained using the 2−ΔΔCt method,10 by which the normalized fold change was determined as follows: 1) normalization of the Ct of the target miRNA to that of the global normalization value for all pre- and post-LVAD samples. To compute the pre-LVAD RQ ratios, we calculated 2) ΔCtpre = Ctpre, target − Ctglobal, and ΔCtcontrol = Ctcontrol, target − Ctglobal for all pre-LVAD samples, 3) differential expression (ΔΔCtpre) of each miRNA was calculated (and expressed as a 2−ΔΔCt ratio) by subtracting mean ΔCtcontrol from mean ΔCtpre. To compute the post-LVAD RQ ratios, we calculated 4) ΔCtpost = Ctpost, target − Ctglobal, and ΔCtcontrol = Ctcontrol, target − Ctglobal for all post-LVAD samples, 5) differential expression (ΔΔCtpost) of each miRNA was calculated (and expressed as a 2−ΔΔCt ratio) by subtracting mean ΔCtcontrol from mean ΔCtpost. In the formulas above, “control” refers to the samples of the seven healthy patients, “global” is the global normalization value, and “target” is that of the target miRNA of interest.
Baseline characteristics of the study cohort are expressed as medians (interquartile ranges [IQRs]) for continuous variables and percentages for categorical variables. We examined miR levels in several ways: 1) baseline levels stratified by pre-LVAD N-terminal pro-brain natriuretic peptide (NT-proBNP) tertile levels, 2) changes in miRs via median pre/post ratio overall, and 3) changes in miRs via median pre/post ratio according to improvement in levels of three validated HF biomarkers after LVAD placement: galectin-3, NT-proBNP, and soluble ST2 (sST2). In the absence of clear guidelines for clinically important degrees of improvement in biomarker levels after LVAD placement, we a priori defined this as a >25% decrease from baseline levels for each of these markers, as this degree of change approximates the suggested threshold for biologic variation in established HF.4,11 We used Wilcoxon signed-rank tests to compare differences in miRNA levels before and after LVAD placement. Two-tailed p values were computed for all statistical tests. We applied a Bonferroni correction by dividing the original critical value (p = 0.05) by the number of hypotheses being tested (the number of candidate miRs: n = 19). This created a new critical value of p = 0.0026, which was used to determine statistical significance. Statistical analysis was performed using SAS version 9.3 statistical software (SAS Institute Inc., Cary, NC).
Table 1 shows the baseline characteristics of the entire cohort of 40 individuals who underwent LVAD placement. The median age was 67 years (IQR: 51–74); N = 26 patients (65%) were Caucasian, and N = 29 (72.5%) were male. The majority of patients (62.5%) were implanted with a Heartmate II LVAD, with the remaining implanted with a HeartWare LVAD. Overall, median left ventricular ejection fraction was 20% (15–20), left ventricular end diastolic dimension was 6.9 cm (6.3–7.3), right atrial pressure was 12 mm Hg (7–19), pulmonary capillary wedge pressure was 25 mm Hg (19–31), and cardiac index was 1.9 L/min/m2 (1.7–2.2). Cardiopulmonary exercise testing parameters also revealed a high degree of exercise intolerance, with median peak measured maximal oxygen uptake (VO2) of 12.7 (11.6–13.7) ml/kg/min and minute ventilation-carbon dioxide production relationship (VeVCO2) slope of 42 (34.6–47.3). Median concentrations of commonly measured electrolytes were within normal limits. Blood urea nitrogen, creatinine levels, and red cell distribution width were slightly elevated (28 mg/dl, 1.4 mg/dl, 16.7%, respectively), whereas albumin levels were slightly decreased (3.3 g/dl). As compared with the expected ranges, HF biomarkers were markedly elevated as follows: NT-proBNP (3162 pg/ml [upper limit of normal 1200]), galectin-3 (24 ng/ml [25.9]), sST2 (67 ng/ml ), growth differentiation factor (GDF)-15 (3232 ng/L ), C-reactive protein (22 mg/L ), copeptin (101 pmol/L ), and neutrophil gelatinase-associated lipocalin (NGAL) (132 ng/ml ).
Baseline MicroRNA Levels Stratified by Brain Natriuretic Peptide Levels
Given the predominance of natriuretic peptides as the objective biochemical measure of HF, we examined miRNA levels shown in Table 2, stratified by tertiles of NT-proBNP. Subjects in the highest tertile of NT-proBNP had quantitatively longer length of stay (16 vs. 11 days), higher degrees of renal insufficiency (creatinine 1.8 vs. 1.4mg/dl), and poorer cardiac index (1.9 vs. 2.1 L/min/m2). Additionally, the highest tertile cohort had greater elevations in plasma concentrations of biomarkers measured, including galectin-3, sST2, GDF-15, and NGAL. Differences in the baseline miRNA levels of the highest tertile of patients compared with that of the lowest tertile were not statistically significant.
Changes in MicroRNA Levels with left Ventricular Assist Device Support
Serial blood draws were performed at a median of 96.5 (72–150) days post-LVAD placement. Table 3 and Figure 1 show the change in RQ ratios from pre- to post-LVAD implantation, demonstrated as a median pre/post ratio. After LVAD implantation, seven miRNAs (miR-21, miR-92a, miR-103, miR-159a, miR-195, miR-320, and miR-423) were downregulated, represented by a pre/post ratio >1. The largest reductions (i.e., highest median pre/post ratio >1) were demonstrated by miR-103 (ratio 1.40 [IQR: 0.76–1.91]) and miR-159a (ratio 1.28 [0.48–2.02]). However, these differences did not reach statistical significance (miR-103, p = 0.12; miR-159a, p = 0.21). Twelve miRNAs (miR-15b, miR-16, miR-24, miR-27a, miR-29a, miR-126, miR-133a, miR-146a, miR-146b, miR-155, miR-221, and miR-222) were found to be upregulated as shown by a pre/post ratio <1. The largest increase in miRNA levels occurred with miR-126 (ratio 0.82 [0.54–1.32]) and miR-155 (ratio 0.78 [0.54–1.01]). Notably, the change in plasma miRNA level with LVAD implantation was only statistically significant for miR-155 (p < 0.002).
MicroRNA Levels According to Biomarker Change
Last, we examined changes in plasma miRNA levels with LVAD implantation according to prespecified changes in serial biomarker (galectin-3, NT-proBNP, and sST2) levels. Median pre/post ratios are shown for individuals with a ≤25% decrease (no improvement, Table 4) versus a >25% decrease (improvement, Table 5) in each of serial galectin-3, NT-proBNP, and sST2 levels. Approximately 1/3 of individuals demonstrated an improvement in biomarker levels with LVAD implantation; in this group, a majority of miRs (N = 11) showed an overall upregulation of levels. Notably, miR-155 along with four other miRs (27a, 126, 133a, and 146b) were upregulated in both cohorts of patients with and without improvement in prespecified biomarker levels. Smaller sample size limited formal statistical analysis.
Our study evaluated baseline levels and long-term changes in the expression of circulating miRNAs in patients with end-stage HF supported by LVADs. We found that, after correcting for multiple testing, plasma levels of 18 of the 19 cardiac miRNAs previously shown to play a role in HF pathophysiology remained unchanged with LVAD support; only expression of miR-155 was upregulated. This appeared to occur regardless of improvement in serial levels of HF biomarkers. MicroRNA-155 has been recently shown to play a fundamental role in the axis between inflammation and arteriogenesis (formation of collateral arteries), both processes of which are aberrant in LVAD patients.5,12 It is entirely plausible that increases in expression of miR-155 after VAD support may explain the untoward predisposition toward neovascularization, and therefore gastrointestinal bleeding. If supported by further study, this hypothesis lends itself to testing via selective inhibition of miR-155 in subgroups of LVAD patients.
MicroRNAs have emerged as key regulators of multiple biologic pathways; their dominance arising from an ability to control hundreds of target genes, turning on or off the entire pathways simultaneously.13 Furthermore, they are stable, readily detectable in peripheral circulation, and amenable to silencing; therefore, they have generated considerable excitement as circulating biomarkers and potential therapeutic targets in cardiovascular disease.7 As a result, over just a brief period of time, several miRNAs have been found to modulate expression levels of genes that govern the process of adaptive or maladaptive cardiac remodeling in HF, viral myocarditis, arrhythmias, and coronary heart disease.14–21
There is a significant body of literature in support of miR-155 being a proinflammatory miRNA, serving as a key regulator of both the innate and adaptive immune systems. It has subsequently been implicated in several disease states with an inflammatory undertone, ranging from alcoholic liver disease to arthritis to several malignancies.22–24 In the realm of cardiology, miR-155 has been extensively studied in terms of its role in vascular dysfunction.25 A recently published study appears to bridge this gap between inflammation and vascular disease, as it relates to miR-155. In a murine model of neovascularization, Pankratz et al.5 found that miR-155 was a key driver of macrophage-mediated collateral artery formation (arteriogenesis), and mice deficient in miR-155 had attenuated arteriogenesis after femoral artery ligation.12 This effect was mediated via miR-155 modulation of the leukocyte-enriched feedback regulator gene suppressor of cytokine signaling 1 (SOCS1) that antagonizes Jak/Stat activation of chemokines and cytokines.26 Moreover, Yang et al.27 found that miR-155 mediated angiogenesis and endothelial cell maturation by targeting E2F transcription factor 2 (E2F2) transcription factor. In light of these findings and our previous report of high degrees of inflammation after long-term LVAD support, it is plausible that miR-155 over-activation might be playing a role in neovascularization in the gastrointestinal tract and contribute to the high rates of bleeding seen in this patient population.4 Furthermore, dysregulation of the innate immune system might contribute to increased risk of infection seen after LVAD placement.
Given the seemingly ubiquitous functions of miR-155 in basic cellular functions, the clinical implications of our findings will require careful validation and study. Indeed, there remains a large gap in translating miR-155 from our study into a clinically relevant and valid tool, and we recognize that larger sample sizes, correlation to clinical parameters, and long-term follow-up will be of the utmost importance. If future studies show that miR-155 is indeed upregulated after LVAD support, and more so in patients with excessive gastrointestinal bleeding, it may represent a diagnostic predictive tool to identify patients at risk of development of arteriovenous malformation and a therapeutic target for prevention of unwanted arteriogenesis. Moreover, given the heterogeneity of patients receiving LVADs, it would be useful to stratify miR-155 levels according to HF etiology, especially given that hypoxia is a chief feature of ischemic cardiomyopathy and presumably enhances angiogenesis and endothelial cell maturation. Indeed, inhibitors of miR-155 are already in late stages of clinical development for hematologic malignancies and amyotrophic lateral sclerosis; they may be readily testable in patients with LVADs who represent a unique population that may be particularly amenable to early phase clinical research.28
Several potential study limitations require consideration. First, and foremost, as previously mentioned, these findings are strictly hypothesis generating, and although buttressed by numerous prior studies, will need validation in other LVAD cohorts. Our study hypothesis was broad in that the miRs measured could change in either direction; thus, even with the Bonferroni correction, we are limited in drawing conclusions based on statistical outcome alone. Second, we did not have granular information about clinical outcomes in our patient population, limiting our ability to demonstrate clear-cut associations between miR-155 and neovascularization. Moreover, our clinical correlation included all patients regardless of HF etiology, duration of HF, or concomitant therapy with HF medications, contributing to greater heterogeneity of our clinical dataset. Third, our measurements of Ct values in the reverse transcription polymerase chain reactions utilized a “global normalization” number as the reference value. However, to date, there is no consensus with respect to miR reference genes that can be used as internal controls for biologic variability.29
In summary, we found that plasma levels of 18 of the 19 miRNAs previously associated with cardiovascular pathophysiology remained unchanged with long-term LVAD support; only expression of miR-155 was upregulated. This appeared to occur regardless of improvement in serial levels of HF biomarkers. MicroRNA-155 has been recently shown to play a fundamental role in the axis between inflammation and formation of collateral arteries, both processes of which are aberrant in LVAD patients. If corroborated by further study, miR-155 might represent a mechanism by which untoward neovascularization occurs in LVAD patients and a potential target for therapeutic intervention.
1. Braunwald E. The war against heart failure: the Lancet lecture. Lancet 2015.385: 812–824.
2. Ahmad T, Patel CB, Milano CA, Rogers JG. When the heart runs out of heartbeats: Treatment options for refractory end-stage heart failure. Circulation 2012.125: 2948–2955.
3. Caccamo M, Eckman P, John R. Current state of ventricular assist devices. Curr Heart Fail Rep 2011.8: 91–98.
4. Ahmad T, Wang T, O’Brien EC, et al. Effects of left ventricular assist device
support on biomarkers of cardiovascular stress, fibrosis, fluid homeostasis, inflammation, and renal injury. JACC Heart Fail 2015.3: 30–39.
5. Rayner KJ. MicroRNA
-155 in the heart: The right time at the right place in the right cell. Circulation 2015.131: 1533–1535.
6. Divakaran V, Mann DL. The emerging role of microRNAs in cardiac remodeling and heart failure. Circ Res 2008.103: 1072–1083.
7. Mann DL. MicroRNAs and the failing heart. N Engl J Med 2007.356: 2644–2645.
8. Di Stefano V, Zaccagnini G, Capogrossi MC, Martelli F. microRNAs as peripheral blood biomarkers of cardiovascular disease. Vascul Pharmacol 2011.55: 111–118.
9. Schipper ME, van Kuik J, de Jonge N, Dullens HF, de Weger RA. Changes in regulatory microRNA
expression in myocardium of heart failure patients on left ventricular assist device
support. J Heart Lung Transplant 2008.27: 1282–1285.
10. Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 2008.3: 1101–1108.
11. Araújo JP, Azevedo A, Lourenço P, Rocha-Gonçalves F, Ferreira A, Bettencourt P. Intraindividual variation of amino-terminal pro-B-type natriuretic peptide levels in patients with stable heart failure. Am J Cardiol 2006.98: 1248–1250.
12. Pankratz F, Bemtgen X, Zeiser R, et al. MicroRNA
-155 exerts cell-specific antiangiogenic but proarteriogenic effects during adaptive neovascularization. Circulation 2015.131: 1575–1589.
13. Braunwald E. Cardiovascular science: Opportunities for translating research into improved care. J Clin Invest 2013.123: 6–10.
14. Zhu GF, Yang LX, Guo RW, et al. microRNA
-155 is inversely associated with severity of coronary stenotic lesions calculated by the Gensini score. Coron Artery Dis 2014.25: 304–310.
15. Nazari-Jahantigh M, Wei Y, Noels H, et al. MicroRNA
-155 promotes atherosclerosis by repressing Bcl6 in macrophages. J Clin Invest 2012.122: 4190–4202.
16. Seok HY, Chen J, Kataoka M, et al. Loss of MicroRNA
-155 protects the heart from pathological cardiac hypertrophy. Circ Res 2014.114: 1585–1595.
17. Heymans S, Corsten MF, Verhesen W, et al. Macrophage microRNA
-155 promotes cardiac hypertrophy and failure. Circulation 2013.128: 1420–1432.
18. Corsten MF, Papageorgiou A, Verhesen W, et al. MicroRNA
profiling identifies microRNA
-155 as an adverse mediator of cardiac injury and dysfunction during acute viral myocarditis. Circ Res 2012.111: 415–425.
19. De Rosa S, Curcio A, Indolfi C. Emerging role of microRNAs in cardiovascular diseases. Circ J 2014.78: 567–575.
20. Martinez-Fernandez A. MicroRNA
therapy for the failing heart. Circ Cardiovasc Genet 2014.7: 393–394.
21. Tijsen AJ, Creemers EE, Moerland PD, et al. MiR423-5p as a circulating biomarker for heart failure. Circ Res 2010.106: 1035–1039.
22. Thai TH, Calado DP, Casola S, et al. Regulation of the germinal center response by microRNA
-155. Science 2007.316: 604–608.
23. O’Connell RM, Taganov KD, Boldin MP, Cheng G, Baltimore D. MicroRNA
-155 is induced during the macrophage inflammatory response. Proc Natl Acad Sci U S A 2007.104: 1604–1609.
24. Rodriguez A, Vigorito E, Clare S, et al. Requirement of bic/microRNA
-155 for normal immune function. Science 2007.316: 608–611.
25. Du F, Yu F, Wang Y, et al. MicroRNA
-155 deficiency results in decreased macrophage inflammation and attenuated atherogenesis in apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol 2014.34: 759–767.
26. Morita Y, Naka T, Kawazoe Y, et al. Signals transducers and activators of transcription (STAT)-induced STAT inhibitor-1 (SSI-1)/suppressor of cytokine signaling-1 (SOCS-1) suppresses tumor necrosis factor alpha-induced cell death in fibroblasts. Proc Natl Acad Sci U S A 2000.97: 5405–5410.
27. Yang D, Wang J, Xiao M, Zhou T, Shi X. Role of Mir-155 in controlling HIF-1α level and promoting endothelial cell maturation. Sci Rep 2016.6: 35316.
29. Evans S, Mann DL. Circulating p53-responsive microRNAs as predictive biomarkers in heart failure after acute myocardial infarction: The long and arduous road from scientific discovery to clinical utility. Circ Res 2013.113: 242–244.
Keywords:Copyright © 2017 by the American Society for Artificial Internal Organs
ventricular assist device; microRNA