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. 2018 Apr 4;5:87. doi: 10.3389/fmed.2018.00087

Table 2.

Summary of gene signatures that classify interstitial lung diseases.

# Genes Tissue origin Disease comparison Sample size Year Reference
407 Lung Idiopathic pulmonary fibrosis (IPF) vs HP 15 (IPF)12 (HP) 2006 (5)
332/6 Lung Sporadic IPF vs familial, IPF vs non-specific interstitial pneumonitis (NSIP) 16 sporadic IPF (2 NSIP)10 familial (4 NSIP) 2007 (8)
242/335 Lung, fibroblasts CTRL vs (SScPF; SScPAH; iPAH; IPF) 33 (15 severe PF, 6 moderate/severe PF and PAH, 4 moderate PF with PAH, 7 PAH), 10 IPF 2011 (75)
<50 Lung SSc/IFP; IPF vs NSIP ≤10 2007, 2011 (8, 75)
22 Lung IUP vs (non-IUP, sarc, HP) 77 training set (39 IUP, 38 non-IUP), validation set 48 (22 IUP, 26 non-IUP) 2015 (19)
4,734 Lung PH-IPF and PAH vs CTRL 18 (PAH), 8 (PH-IPF) 2010 (76)
74 Lung Chronic lung disease 13 data sets 2015 (77)
>1,500/32a LCM lung PH-IPF vs CTRL, PH-chronic obstructive pulmonary disease (COPD) vs CTRL, PH-IPF vs PH-COPD LCM pulmonary arterioles (n = 8) 2014 (78)
255 LCM lung PH-IPF vs NPH-IPF 8 PH-IPF, 8 NPH-IPF 2013 (79)
2,490b337c214d Lung IPF vs COPD vs CTRL 19 IPF, 49 COPD 2016 (18)
3 Gene clusters Lung IPF vs COPD vs CTRL 319 (3 data sets)e 2015 (15)

a32 small DEGs overlap between PH-IPF and PH-COPD.

b2,490 DEGs between IPF and CTRL.

cDEGs between COPD and CTRL.

dDEGs overlap between IPF and COPD.

e4,259 mRNA and 438 microRNA and also includes 669 clinical variables.