Marker composition and detection kit for liver cancer detection
A technology of markers and kits, applied in the field of marker combinations and detection kits for liver cancer detection, to achieve the effect of improving sensitivity and specificity, high sensitivity and specificity
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Embodiment 1
[0079] Example 1: Collection and processing of serum from different groups of people
[0080] In the Cancer Hospital of Tianjin Medical University, 60-300 cases of peripheral blood were collected from liver cancer patients, hepatitis B patients and normal subjects respectively. In the experiment, the serum of 288 patients with liver cancer, 87 patients with hepatitis B, 80 patients with liver cirrhosis and 241 normal patients were collected.
[0081] Within 1 hour of peripheral blood collection, centrifuge at 3000g for 5-10 minutes, transfer the serum into a new centrifuge tube, and store in a -80°C refrigerator.
Embodiment 2
[0082] Example 2: Diagnostic application of markers of the present invention or combinations thereof
[0083] The concentrations of AFP, AFU, GPC3, GGT2, and HGF in the serum to be tested were detected by ELISA using a commercially available kit (details are shown below) according to the manufacturer's instructions.
[0084]
[0085] 1) Evaluation indicators and selection of diagnostic tests
[0086] Sensitivity (true positive rate, Sensitivity), specificity (true negative rate, Specificity), positive predictive value (PPV), negative predictive value (NPV) were used to evaluate the diagnostic effect of the tested indicators:
[0087] Sensitivity=TP / (TP+FN)×100%
[0088] Specificity=TN / (TN+FP)×100%
[0089] Positive predictive value = TP / (TP+FP) × 100%
[0090] Negative predictive value = TN / (TN+FN) × 100%
[0091] Correct index (Youden index) = (sensitivity + specificity) - 100%
[0092] Among them, TN (true negative) = true negative; FP (false positive) = false positi...
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