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. 2019 Aug 3;8(8):1163. doi: 10.3390/jcm8081163

Table 1.

Candidate and established biomarkers of acute lung injury.

Pathophysiological Entity for Biomarker Biomarker Established and Validated Clinical Use Potential Implemented Broadly Included in This Review
Alveolar damage (Pneumocytes type I and II) SPD Yes Risk stratification in mechanically ventilated patients No Yes
s-RAGE (yes) ? No Yes
KL-6 (yes) ? No Yes
FGF-7 No No No No
Airway (conductive) damage CC16 Yes Possibly not in acute lung injury No Yes
Endothelial VEGF Yes + No No
Gelsolin (yes) * ? No Yes
sTM (yes) - No No
Syndecan-1 No - No No
Inflammation/Infection PCT Yes Antibiotic reduction Yes Yes
Eosinophilic granulocyte Yes Reduction of corticosteroid use Yes Yes
IL-1β Yes No No No
TNFα Yes No No No
Mitochondrial DNA No Yes—possibly No No

SPD: surfactant protein D; s-RAGE: soluble receptor for advanced glycation end-products (sRAGE); KL-6: Krebs von Lungen-6; FGF-7: fibroblast growth factor-7; CC16: club cell secretory protein 16; VEGF: vascular endothelial growth factor; sTM: soluble thrombomodulin; PCT: procalcitonin; IL-1β: interleukin-1β; TNFα. * only one large study.