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出 处:《现代检验医学杂志》2012年第3期57-58,61,共3页Journal of Modern Laboratory Medicine
摘 要:目的建立血清和肽素ELISA法定量测定的改良法,并探讨其应用价值。方法用定量ELISA法测定患者和健康者的血清和肽素。结果该法检出限为0.018pmol/L,线性为0.075~24.0pmol/L,平均回收率为98.8%,批内CV为3.39%,批间CV为5.58%,参考区间为2.1~12.3pmol/L。21例脓毒症和31例获得性肺炎及33例急性心肌梗死与52例心力衰竭患者的血清和肽素值分别为48.96±5.80,32.82±5.02,68.51±5.63和23.14±5.47pmol/L,它们之间的差异具有统计学意义(F=501.542,P=0.000)。结论该法灵敏、特异和准确,血清和肽素定量测定是诊断脓毒症、获得性肺炎、急性心肌梗死和心力衰竭的较好实验指标。Objective To establish enzyme-linked immuneosorbent assay (ELISA) of improvement for the quantitative determination of a C-terminal portion of pro-vasopressin(copeptin) in serum and to investigate its clinical application. Methods Serum copeptin of patients and of normal controls were measured by ELISA. Results The limit of detection (LOD) was 0. 018 pmol/L. The linearity was 0. 075 - 24. 0 pmol/L. The average rate of recovery was 98.8%. Within-run CV was 3.39 % and between-run CV was 5.58 %. The reference interval were 2. 1 -1 2. 3 pmol/L. The serum copeptin concentrations of 21 patients with sepsis were 48. 96±5.80 pmol/L,of 31 patients with acquired pneumonia were 32. 82±5. 02 pmol/L of 33 patients with acute myocardial infarction were 68.51± 5.63 pmol/L and of 52 patients with chronic heart failure were 23.14±5.47 pmol/L. Significant differences were observed in them (F=501. 542, P=0. 000). Conclusion This method is sensitive,specific and accurate. Quantitative detection of eopeptin is now better laboratory test for patients of sepsis of ac- quired pneumonia of acute myocardial infarction and of Chronic heart failure.
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