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. 2017 Dec 25;2(6):646–654. doi: 10.1016/j.jacbts.2017.07.007

Table 1.

Gradients Detected Across Atherosclerotic Plaques

HUGO Designation Molecule Δ Concentration (NPX) p(FDR) Δ(%)/Sampling Length
Before balloon dilation
 OLR1 Oxidized LDL receptor 1 (LOX-1) 20.01 (−5.2 to 137.1) <0.05 53.2
 EGF Epidermal growth factor 23.9 (−19.3 to 62.0) <0.005 47.8
 IL-16 Interleukin-16 2.8 (−3.2 to 30.0) <0.05 39.0
 CD40LG sCD40 ligand 1.6 (−1.3 to 5.6) <0.005 27.6
 CXCL1 C-X-C motif chemokine 1 (Gro-a, GRO1, NAP-3, KC) 12.3 (1.3 to 60.1) <0.005 26.7
 TNFSF14 Tumor necrosis factor ligand superfamily member 14 0.4 (−0.3 to 4.7) <0.05 26.5
 CXCL5/6 C-X-C motif chemokine 6 (GCP2) 6.1 (0.6 to 23.1) <0.005 24.7
 PDGFB Platelet-derived growth factor subunit B 12.9 (−4.0 to 41.6) <0.005 24.5
 IL-8 Interleukin-8 3.3 (−1.3 to 51.4) <0.05 24.1
 IL1RN Interleukin-1 receptor antagonist protein 1.8 (0.2 to 7.0) <0.005 15.5
 RETN Resistin 10.6 (−3.9 to 16.5) <0.05 12.9
 DKK1 Dickkopf-related protein 1 2.9 (0.2 to 12.0) <0.005 10.5
 PLAUR Urokinase plasminogen activator surface receptor 20.9 (−7.0 to 106.1) <0.05 6.9
 CCL4 C-C motif chemokine-4 (MIP-1β) 4.5 (−1.3 to 10.9) <0.05 6.4
 HBEGF Heparin-binding EGF-like growth factor 2.6 (−1.2 to 0.1) <0.05 5.4
After balloon dilation
 HSPB1 Heat shock 27-kDa protein 1.1 (−4.5 to 54.2) <0.05 26.11
 EGF Epidermal growth factor 10.1 (−35.2 to 67.4) <0.05 21.05
 PDGFB Platelet-derived growth factor subunit B 8.6 (−35.6 to 81.0) <0.05 18.26
 CXCL5/6 C-X-C motif chemokine 6 (GCP2) 3.2 (−7.3 to 39.2) <0.05 16.59
 MMP-12 Matrix metalloproteinase-12 8.7 (−20.3 to 153.2) <0.05 14.48
 IL-8 Interleukin-8 1.8 (−6.1 to 14.6) <0.05 10.19
 DKK1 Dickkopf-related protein 1 2.8 (−9.4 to 11.2) <0.05 8.60
 CCL2 Monocyte chemotactic protein 1 (MCP-1) 14.9 (−88.5 to 119.9) <0.05 6.39
 HBEGF Heparin-binding EGF-like growth factor 2.5 (−12.7 to 10.3) <0.05 4.44

Blood sampling across coronary plaques was achieved using the Liquid Biopsy System before balloon dilation and after balloon dilation. Proximal and distal measurements of the biomolecules, identified by their HUGO designations, were used to calculate the change in concentration across plaques, which are shown as median values (range), measured by proximity extension assay multiplex assays and expressed in ΔNPX units. The significance of gradients is indicated by p(FDR) values. To aid comparison between different analytes, NPX values were further used to calculate the median percentage change in concentration across the sampling distance.

p(FDR) = false discovery rate p values; HUGO = Human Genome Organization; LDL = low-density lipoprotein; NPX = normalized protein expression.