1. Calcific Aortic Valve Disease 'Omics' Is Timely, But Are We Looking Too Late?
- Author
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Samantha K. Atkins, Sasha A Singh, and Elena Aikawa
- Subjects
Aortic valve disease ,CV, correlation of variation ,medicine.medical_specialty ,AS, aortic stenosis ,TAV, tricuspid aortic valve ,BAV, bicuspid aortic valve ,targeted lipidomics ,MPG, mean pressure gradient ,AVA, aortic valve area ,PC, phosphatidylcholine ,Clinical Research ,CAVS, calcific aortic valve stenosis ,valvular calcification ,Internal medicine ,medicine ,AV, aortic valve ,LysoPC, lysophosphatidylcholine ,ATX, autotaxin ,Valvular calcification ,business.industry ,aortic stenosis ,Calcific aortic valve stenosis ,calcific aortic valve stenosis ,Lp(a), lipoprotein(a) ,Omics ,nontargeted metabolomics ,QC, quality control ,MG, monoglyceride ,LysoPA, lysophosphatidic acid ,Cardiology ,lysophosphatidic acids ,Cardiology and Cardiovascular Medicine ,business ,LysoPE, lysophosphatidylethanolamine ,Vmax, peak aortic jet velocity - Abstract
Visual Abstract, Highlights • This study is the first step towards the creation of a metabolomic map of calcified human aortic valves. • The study highlights an independent association of LysoPA with CAVS severity. • The study demonstrates that LysoPA levels are associated with faster CAVS progression rate., Summary This study outlines the first step toward creating the metabolite atlas of human calcified aortic valves by identifying the expression of metabolites and metabolic pathways involved at various stages of calcific aortic valve stenosis progression. Untargeted analysis identified 72 metabolites and lipids that were significantly altered (p
- Published
- 2020
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