Pleural fluid markers for malignant pleural effusions
AssigneeThe University of Hong Kong
InventorChing-Wan Lam
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Abstract
Methods of diagnosis and/or prognosis of malignant disease from pleural effusion samples are disclosed. The methods typically include determining the normalized intensity of one or more biomarkers, such as acetone and 3-hydroxybutyate, in pleural effusion samples using nuclear magnetic resonance (NMR), such as proton NMR (1H-NMR) spectroscopy. Reference values for malignant disease diagnosis using the disclosed biomarkers are provided. Reference values for prognosis of median survival time based on the disclosed biomarkers are also provided.
Claims17
A method of diagnosing a malignant disease or survival term thereof, comprising
- obtaining samples of effusions from a subject in need of diagnosis,
- measuring the normalized intensity of a biomarker selected from the group consisting of acetone, 3-hydroxybutyrate, 1-methylhistamine, 1-methylnicotinamide, 2-methylglutarate, 2-oxoglutarate, 3-OH-3-methylglutarate, 3-methyladipate, 4-aminohippurate, acetone, adenine, alanine, creatine, dimethylamine, formate, fumarate, glucose, glycolate, imidazole, lactate, methylamine, O-acetylcarnitine, oxalacetate, phenylacetylglycine, phenylalanine, tryptophan, tyrosine, cis-aconitate, myo-inositol, trans-aconitate, leucine, valine, acetate, acetoacetate, creatinine, and trimethylalanine-N-oxide in the effusions, and
- comparing the normalized intensity of the biomarker in the effusions of the subject in need of diagnosis and the normalized intensity in a normal or non-diseased subject,
- wherein the subject is diagnosed with a malignant disease when the normalized intensity of the biomarker in the effusion of the subject in need of diagnosis is at least 1.5 fold greater than the normalized intensity of the biomarker in the effusion of the normal or non-diseased subject.
Dependencies are inferred from the claim text.