Why the study?
To explore why bicuspid aortic stenosis has certain clinical differences from the tricuspid morphology, by evaluating metabolomics profiles before and after TAVR.
Does the metabolomic profile differ between bicuspid and tricuspid aortic stenosis in patients undergoing TAVR?
Does the metabolomic profile differ between bicuspid and tricuspid aortic stenosis in patients undergoing TAVR?
Bicuspid aortic stenosis exhibits distinct metabolic profiles compared to tricuspid morphology, with altered arginine/proline metabolism and arachidonic acid pathways correlating with disease severity and LV recovery post-TAVR.
Background To explore why bicuspid aortic stenosis has certain clinical differences from the tricuspid morphology, we evaluated the metabolomics profile involved in bicuspid aortic valve (BAV) aortic stenosis prior to and after transcatheter aortic valve replacement (TAVR) in comparison with tricuspid aortic valve (TAV). Methods In this TAVR cohort with prospectively collected data, blood samples were obtained before TAVR valve deployment and at the 7th day after TAVR, which were then sent for liquid and gas chromatography-mass spectrometry detection. Besides comparisons between BAV and TAV, BAV patients were also divided in subgroups according to baseline hemodynamics (i.e. maximal transaortic velocity, V max ) and post-procedural reverse left ventricular (LV) remodeling (i.e. the change in LV mass index from baseline, ∆LVMI) for further analysis. Metabolic differences between groups were identified by integrating univariate test, multivariate analysis and weighted correlation network analysis algorithm. Results A total of 57 patients were enrolled including 33 BAV patients. The BAV group showed lower arginine and proline metabolism both before and post TAVR than TAV represented by decreased expression of L-Glutamine. In BAV subgroup analysis, patients with baseline V max > 5 m/s ( n = 11) or the 4 th quartile of change in ∆LVMI at one-year follow-up (i.e. poorly-recovered LV, n = 8) showed elevated arachidonic acid metabolism compared with V max < 4.5 m/s ( n = 12) or the 1 st quartile of ∆LVMI (i.e. well-recovered LV, n = 8) respectively. Conclusions Difference in arginine and proline metabolism was identified between BAV and TAV in TAVR recipients. Elevated arachidonic acid metabolism may reflect more severe baseline hemodynamics and worse LV reserve remodeling after TAVR in BAV.
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Xiong et al. (2020) studied this question.
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