Pneumoconiosis was diagnosed by open lung biopsy in two dental technicians who had interstitial lung disease. Mineralogical analysis was performed to investigate the origin of the dust that had been inhaled. A marked accumulation of silicon and phosphorus was found in both cases. The hard metals chromium and cobalt were also found. Dental technician's pneumoconiosis is a complex pneumoconiosis in which such dust and hard metals may play a role.
Adult ; *Dental Technicians ; Human ; Lung/pathology ; Lung Diseases, Interstitial/*diagnosis/metabolism ; Male ; Minerals/metabolism ; Occupational Diseases/*diagnosis/metabolism ; Pneumoconiosis/*diagnosis/metabolism ; Radiography, Thoracic ; Tomography, X-Ray Computed

OBJECTIVETo explore the significance of intercellular adhesion molecule -1 (CD54 or ICAM-1), epidermal growth factor receptor (EGFR) and platelet-derived factor (PDGF) in sputum cells of workers exposed to dust and patients with pneumoconiosis for the early diagnosis of pneumoconiosis.

METHODSThe subjects included 62 workers exposed to dusts, 51 workers not exposed to dusts, 22 patients with pneumoconiosis and 10 healthy controls. The respiratory sputum technique was used to collect the sputum samples and the biomarkers (ICAM-1, EGFR and PDGF) of the sputum samples were detected with the sputum samples.

RESULTSWhen the exposure group was compared with non-exposure group, there were no significant differences of surface biomarkers (ICAM-1, EGFR and PDGF) in sputum cells (neutrophil leucocytes, macrophages, lymphocytes and acidophilic/basophil leucocytes). As compared with other workers exposed to dusts, the surface CD54 and EGFR expression levels increased significantly and the surface PDGF expression level decreased significantly in workers exposed to dusts for 10 years (P<0.05). As compared with controls, the CD54 and EGFR expression levels of sputum cells increased significantly and the PDGF expression level of sputum cells decreased significantly in patients with pneumoconiosis at the stages of I and II + mI (P<0.05).

CONCLUSIONThe expression levels of the surface CD54, EGFR and PDGF of sputum cells in workers exposed to dusts and patients with pneumoconiosis changed, which may be useful for early detecting pneumoconiosis.and patients is changed, which may be meaningful for early detection of pneumoconiosis.

Adult ; Aged ; Biomarkers ; metabolism ; Case-Control Studies ; Coal Mining ; Dust ; Humans ; Intercellular Adhesion Molecule-1 ; metabolism ; Middle Aged ; Occupational Exposure ; Platelet-Derived Growth Factor ; metabolism ; Pneumoconiosis ; diagnosis ; metabolism ; Receptor, Epidermal Growth Factor ; metabolism ; Sputum ; metabolism ; Young Adult

OBJECTIVETo evaluate the alterations of biomarkers in the development and progression of coal workers' pneumoconiosis (CWP).

METHODSThe type and number of cells, and the levels of tumor necrosis factor-alpha (TNF-alpha), pulmonary surfactant protein, phospholipids and fibronectin in bronchoalveolar lavage fluid were assayed in 14 health active coal miners, 21 coal miners without CWP and 13 miners with CWP of 0/1 to 1/1.

RESULTSCompared to active coal miners without CWP (8.23 microg/mL), TNF-alpha concentration was gradually decreased when dust exposure was stopped (5.90 microg/mL). Elevated surfactant protein A (SP-A) level and phosphatidylglycerol (PG) to phosphatidylinositol (PI) ratio were found in miners actively exposed to coal dust (6528 ng/mL for SP-A and 10. for PG/PI), and both parameters decreased when CWP progressed from CWP (0/1) (3419 microg/mL for SP-A and 5.9 for PG/PI) to CWP (1/1) (1654 microg/mL for SP-A and 5.5 for PG/PI).

CONCLUSIONBiomarkers in bronchoalveolar lavage fluid can be used to screen coal miners at high risk of developing coal workers' pneumoconiosis.

Adult ; Animals ; Biomarkers ; analysis ; Bronchoalveolar Lavage Fluid ; chemistry ; Coal Mining ; Disease Progression ; Humans ; L Cells (Cell Line) ; Mice ; Middle Aged ; Phospholipids ; metabolism ; Pneumoconiosis ; diagnosis ; metabolism ; physiopathology ; Pulmonary Surfactant-Associated Protein A ; metabolism ; Tumor Necrosis Factor-alpha ; metabolism