TABLE 2

Demographic data of cases in the validation study

CharacteristicsaPAPsPAPhPAPOther lung diseases
Subjects n213405162
Male/female n122/6019/210/586/75
Age years mean±sd52.6±14.757.6±13.356.4±14.566.2±12.0
Asian/Caucasian n213/040/05/0162/0
Serum GMAb concentration U·mL−1
 Mean±sd103.6±127.50.191±0.3020.148±0.1410.517±.818
 Maximum899.91.90.3848.57
 Minimum5.590.040.020.01
Diagnostic procedures n
 BAL213365144
 VATS04017
 Autopsy0001
Other lung diseases n
 CTD45
 DIPD20
 IIPs60
  IPF8
  Other IIPs52
 Infectious disease19
 Miscellaneous18

Connective tissue disease (CTD) cases included five amyopathic dermatomyositis cases, 11 polymyositis/dermatomyositis interstitial lung diseases, 11 rheumatoid arthritis cases, four Sjögren syndromes, five systemic scleroses and nine other diseases. Infectious disease cases included eight Pneumocystis pneumonias, four bacterial pneumonias, three influenza pneumonias and four other infectious diseases. Miscellaneous diseases included four alveolar haemorrhages, three chronic eosinophilic pneumonias, two acute respiratory distress syndromes, two chronic hypersensitivity pneumonias and seven other diseases. aPAP: autoimmune pulmonary alveolar proteinosis; sPAP: secondary pulmonary alveolar proteinosis; hPAP: hereditary pulmonary alveolar proteinosis; GMAb: granulocyte–macrophage colony-stimulating factor autoantibody; BAL: bronchoalveolar lavage; VATS: video-assisted thoracic surgery; DIPD: drug-induced pulmonary disease; IIP: idiopathic interstitial pneumonia; IPF: idiopathic pulmonary fibrosis.