Interaction of Autotaxin With Lipoprotein(a) in Patients With Calcific Aortic Valve Stenosis

JACC Basic Transl Sci. 2020 Aug 26;5(9):888-897. doi: 10.1016/j.jacbts.2020.06.012. eCollection 2020 Sep.

Abstract

Our objectives were to determine whether autotaxin (ATX) is transported by lipoprotein(a) [Lp(a)] in human plasma and if could be used as a biomarker of calcific aortic valve stenosis (CAVS). We first found that ATX activity was higher in Lp(a) compared to low-density lipoprotein fractions in isolated fractions of 10 healthy participants. We developed a specific assay to measure ATX-Lp(a) in 88 patients with CAVS and 144 controls without CAVS. In a multivariable model corrected for CAVS risk factors, ATX-Lp(a) was associated with CAVS (p = 0.003). We concluded that ATX is preferentially transported by Lp(a) and might represent a novel biomarker for CAVS.

Keywords: ALR, adiponectin-to-leptin ratio; ATX, autotaxin; ATX-apo(a), ATX carried by Lp(a); ATX-apoB, ATX carried by apoB-containing lipoproteins; BMI, body mass index; CAD, coronary artery disease; CAVS, calcific aortic valve stenosis; HDL, high-density lipoprotein; LDL, low-density lipoprotein; Lp(a), lipoprotein(a); LysoPA, lysophosphatidic acid; LysoPC, lysophosphatidylcholine; OxPLs, oxidized phospholipids; apo(a), apolipoprotein(a); apoB, apolipoprotein B; autotaxin; calcific aortic valve stenosis; lipoprotein(a); low-density lipoproteins; obesity.