Table 2.
Author | Year | Patient groups (n=) | Technique | Comparison | Discriminative compounds (n=) | Performance (AUC/accuracy) |
Plantier et al.[19▪▪] | 2022 | IPF (53) CTD-ILD (51) HC (51) |
GC-tof-MS | IPF vs. HC CTD-ILD vs. HC IPF vs. CTD-ILD |
34 11 16 |
0.91/84.6% 0.84/77.5% 0.84/76.9% |
Yamada et al.[20] | 2017 | IPF (40) HC (55) |
MCC-IMS | IPF vs. HC | 5 | -/76.8–83.2%a |
Yang et al.[17] | 2017 | Pneumoconiosis (25) Stone workers (154) |
GC-MS | Pneumoconiosis vs. exposed | 9 | 0.90/– c |
Fijten et al.[16] | 2017 | Sarcoidosis (87)b HC (26) |
GC-tof-MS | Sarcoidosis vs. HC | 9 | 0.76/74.1%c |
Jalali et al.[18] | 2016 | Silicosis (4) HC (45)d Silica exposed (20) |
GC-MS | Silicosis vs. exposed Silicosis vs. HC |
Multiple results | Not reported |
Westhoff et al.[15] | 2007 | Sarcoidosis (5)e Sarcoidosis suspected (4)f |
MCC-IMS | Sarcoidosis vs. suspected | 13 | No statistical test results reported |
Hayton et al.[21] | 2020 | IPF (46) | GC-MS | Stable vs. disease progression at 6 months | 1 | N/A |
Guiot et al.[22] | 2020 | SSc (27, of which 17 with SSc-ILD) | Unknown | SSc-ILD vs. SSc without ILD | 0 | N/A |
Main results of the cited articles are displayed. Conference abstracts are shown in italic.
A separate accuracy for each of the discriminative VOCs was calculated. AUC, area-under-the-curve; CTD, connective tissue disease; GC, gas chromatography; HC, healthy control; ILD, interstitial lung disease; IMS, ion mobility spectrometry; IPF, idiopathic pulmonary fibrosis; MCC, multicapillary column (i.e. variation of a capillary gas chromatograph); MS, mass spectrometry; SSc, systemic sclerosis; tof, time of flight (i.e. type of mass analyzer).
n = 18 had Scadding stage 0.
Results of test/validation cohorts or cross-validation analyses are displayed here.
Group was split in 20 nonsmoking and 25 smoking individuals.
Not all patients had ILD.
Sarcoidosis excluded after biopsy of mediastinal lymphadenopathy.