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Table 3 Nine proteins that optimally differentiated patients with IPF from control participants. Proteins selected by the linear discriminant function with recursive feature elimination and the respective model coefficient

From: Peripheral blood proteomic profiling of idiopathic pulmonary fibrosis biomarkers in the multicentre IPF-PRO Registry

Gene

Aptamer ID

Protein

Model coefficienta

APOA1

2750–3

Apolipoprotein A-I

0.38

C1R

3285–23

Complement C1r subcomponent

−0.41

MMP3

2788–55

Stromelysin-1

−0.30

SFN

4829–43

14–3-3 protein sigma

0.43

CCL18

3044–3

C-C motif chemokine 18

0.36

ICAM5

5124–69

Intercellular adhesion molecule 5

−0.06

SHH

2743–5

Sonic hedgehog protein

0.46

OLR1

3636–37

Oxidised low-density ipoprotein receptor 1

−0.32

CAPG

4968–50

Macrophage-capping protein

0.28

  1. aThe sign of the coefficient indicates whether the subject’s linear discriminant analysis score increases or decreases as values of the protein change. Higher scores are associated with IPF, as opposed to control, status