Key result
Preoperative myocardial levels of ubiquitin ligases, including atrogin-1 (r=0.71, p=0.005) and Muscle Ring Finger 1 (r=-0.68, p=0.005), were significantly associated with postoperative hypertrophy.
Why the study?
Reverse remodeling after aortic valve replacement is variable and may depend on how the ubiquitin-proteasome system tackles hypertrophy, but its association with myocardial ubiquitin ligases was unknown.
Are preoperative myocardial levels of E3 ubiquitin ligases associated with the degree of postoperative reverse remodeling in patients with severe aortic stenosis undergoing valve replacement?
Observational
Are preoperative myocardial levels of E3 ubiquitin ligases associated with the degree of postoperative reverse remodeling in patients with severe aortic stenosis undergoing valve replacement?
Preoperative myocardial levels of specific ubiquitin ligases correlate with postoperative hypertrophy markers in patients undergoing aortic valve replacement, highlighting the potential role of the ubiquitin-proteasome system in reverse remodeling.
Should not yet alter AVR decisions; leaves open ubiquitin ligases as remodeling biomarkers.
Currently, aortic valve replacement is the only treatment capable of relieving left ventricle pressure overload in patients with severe aortic stenosis. It aims to improve cardiac function and revert hypertrophy, by triggering myocardial reverse remodeling. Despite immediately relieving afterload, reverse remodeling turns out to be extremely variable. Among other factors, the extent of reverse remodeling may depend on how well ubiquitin-proteasome system tackle hypertrophy. Therefore, we assessed tagged ubiquitin and ubiquitin ligases in the left ventricle collected from patients undergoing valve replacement and tested their association to the degree of reverse remodeling. Patients were classified according to the regression of left ventricle mass (ΔLVM) and assigned to complete (ΔLVM≥15%) or incomplete (ΔLVM≤5%) reverse remodeling groups. No direct inter-group differences were observed. Nevertheless, correlation analysis supports a fundamental role of the ubiquitin-proteasome system during reverse remodeling. Indeed, total protein ubiquitination was associated to hypertrophic indexes such as interventricular septal thickness (r = 0.55, p = 0.03) and posterior wall thickness (r = 0.65, p = 0.009). No significant correlations were observed for Muscle Ring Finger 3. Surprisingly, though, higher levels of atrogin-1 were associated to postoperative interventricular septal thickness (r = 0.71, p = 0.005). In turn, Muscle Ring Finger 1 correlated negatively with this postoperative hypertrophy marker (r = -0.68, p = 0.005), suggesting a cardioprotective role during reverse remodeling. No significant correlations were found with left ventricle mass regression, although a trend for a negative association between the ligase Murine Double Minute 2 and mass regression (r = -0.44, p = 0.10) was found. Animal studies will be necessary to understand whether this ligase is protective or detrimental. Herein, we show, for the first time, an association between the preoperative myocardial levels of ubiquitin ligases and postoperative hypertrophy, highlighting the therapeutic potential of targeting ubiquitin ligases in incomplete reverse remodeling.
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Trindade et al. (2020) conducted an observational in Severe aortic stenosis. Preoperative myocardial expression of E3 ubiquitin ligases vs. Complete vs incomplete reverse remodeling was evaluated on Postoperative hypertrophy (interventricular septal thickness) and left ventricle mass regression (r = 0.71, p=0.005). Preoperative myocardial levels of ubiquitin ligases, including atrogin-1 (r=0.71, p=0.005) and Muscle Ring Finger 1 (r=-0.68, p=0.005), were significantly associated with postoperative hypertrophy.
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