Idiopathic pulmonary fibrosis disease diagnosis marker and application thereof in preparing diagnosis or prognosis tool
A technology for pulmonary fibrosis and disease diagnosis, which is applied in the field of medical diagnosis and can solve the problems of lack of specificity, confusing diagnosis, and unclear etiology.
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Embodiment 1
[0058] Screening for genes differentially expressed in patients with idiopathic pulmonary fibrosis and normal controls
[0059] 1. Clinical research objects:
[0060] A total of 30 patients with idiopathic pulmonary fibrosis were selected, including 21 males and 9 females, with an age range of 30-83 years old. The diagnostic criteria were in accordance with the "Special Pulmonary Disease" revised by the Chinese Respiratory Society for Interstitial Lung Disease and the American Thoracic Society (ATS). Guidelines for the diagnosis and treatment of paroxysmal pulmonary fibrosis.
[0061]Exclusion criteria: (1) Patients with other lung diseases, such as bronchial asthma, pulmonary interstitial fibrosis, lung cancer, etc.; (2) Patients with infection in other parts; (3) Patients with severe cardiovascular and cerebrovascular diseases, diabetes, blood system Diseases, malignant tumors, organ failure, and hepatitis; (4) Those who suffer from immune system diseases or have recently u...
Embodiment 2
[0070] Validation of differentially expressed genes in idiopathic pulmonary fibrosis patients and normal controls
[0071] 4. Detection of COX5B by ELISA
[0072] Example 2 Verification of COX5B differentially expressed in idiopathic pulmonary fibrosis patients and normal subjects.
[0073] 5. Blood total peptide extraction, mass spectrometry detection
[0074] Using LC-MS / MS mass spectrometry Example 2 to verify the content of COX5B in the blood of patients with idiopathic pulmonary fibrosis and normal people.
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