Serum metabolism marker for diagnosing benign and malignant pulmonary nodules and application of the metabolic marker
A technology of metabolic markers and metabolites, which is applied in the diagnosis of benign and malignant pulmonary nodules, serum metabolic markers and its screening, can solve the problems of single sample source, metabolites with low disease specificity, and limited clinical significance. Achieve the effect of reducing trauma and radiation risk
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Embodiment 1
[0034] This embodiment provides a screening method for serum metabolic markers, comprising the following steps:
[0035] S1, collecting samples
[0036] In this study, after obtaining the consent of the patients, peripheral venous blood was collected from 140 patients with benign pulmonary nodules (benign pulmonary nodules group) and 143 patients with malignant pulmonary nodules (malignant pulmonary nodules group) in Shanghai Chest Hospital. Serum samples. All patients with pulmonary malignant nodules had no history of other malignant tumors, other major systemic diseases, and no chronic medical history of long-term medication. The time of blood collection was in the morning on an empty stomach. All serum samples were centrifuged and stored in a -80°C refrigerator. During the study, serum samples were taken out and thawed for subsequent analysis.
[0037] S2, Extensive targeted metabolomics analysis of serum
[0038] (1) Sample pretreatment
[0039] Take out the sample co...
Embodiment 2
[0076] The research objects of this example included 70 serum samples of patients with benign pulmonary nodules and 71 serum samples of malignant pulmonary nodules from 2 independent medical centers. All patients with benign and malignant pulmonary nodules had no other history of malignant tumors, other major systemic diseases, and no chronic medical history of long-term medication. The time of blood collection was in the morning on an empty stomach. All serum samples were centrifuged and stored in a -80°C refrigerator. During the study, serum samples were taken out and thawed for subsequent analysis.
[0077] The detection conditions and data analysis methods of this example are the same as those of Example 1, and the differential metabolites detected and analyzed are the following 12 kinds: 4-hydroxy-L-proline, hyodeoxycholic acid, xanthine, 2-hydroxy- 6-aminopurine, 5,6-dihydrothymine, isobutyrylcarnitine, guanine, glutamic acid, asparagine, formononetin, alanine, kynuric ...
Embodiment 3
[0095] This embodiment provides a detection kit, comprising:
[0096] (1) Standards for metabolic markers: hydroxy-L-proline, hyodeoxycholic acid, xanthine, 2-hydroxy-6-aminopurine, 5,6-dihydrothymine, isobutyrylcarnitine, Guanine, glutamic acid, asparagine, formononetin, alanine, kynuuric acid, individually packaged or mixed packaged.
[0097] (2) Solvent:
[0098] Pure methanol and 50% acetonitrile in water for sample extraction.
[0099] 50% acetonitrile in water can be used as a solvent to dissolve the standards.
[0100] (3) Internal standard: L-phenylalanine.
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