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使用达德拜耳N乳胶CRP单试剂检测法测定健康献血者血清C反应蛋白的参考区间。

Reference interval for serum C-reactive protein in healthy blood donors using the Dade Behring N Latex CRP mono assay.

作者信息

Erlandsen E J, Randers E

机构信息

Department of Clinical Biochemistry, Viborg County Hospital, Viborg, Denmark.

出版信息

Scand J Clin Lab Invest. 2000 Feb;60(1):37-43. doi: 10.1080/00365510050185029.

Abstract

Measurement of the serum concentration of the acute-phase reactant C-reactive protein (CRP) provides an useful objective marker in clinical practice, both in screening for diseases and in monitoring disease activity and response to therapy. The aim of this study was to evaluate the analytical performance of the assay in the concentration range from 0.2 to 15 mg/L, and to determine a reference interval for serum CRP in healthy blood donors using the Dade Behring N Latex CRP mono assay on the Dade Behring Nephelometer II. The assay is a particle-enhanced nephelometric immunoassay with a measuring range of 0.2-1100 mg/L. The sample volume is 40 microL, and the assay time is 6 min. The coefficients of variation for within-run and between-run imprecision studies were between 2.2 and 5.4% in serum pools with CRP concentrations between 1.29 and 11.98 mg/L. Linearity studies showed excellent correlation between the theoretical and the measured values. No interferences were detected from hemoglobin <1.0 mmol/L, bilirubin <512 micromol/L and Intralipid <20 g/L. Blood samples were collected from 268 healthy blood donors (107 females and 161 males) between 20 and 65 years old. The non-parametric reference intervals for serum CRP was calculated to be <0.2-14.7 mg/L in females and <0.2-9.16 mg/L in males. The Mann-Whitney U-test revealed no gender-related difference for serum CRP (p-value=0.72). A common reference interval for serum CRP for both genders was calculated to be <0.2-10.5 mg/L (median 0.98 mg/L, range <0.2-17.3 mg/L).

摘要

测定急性期反应物C反应蛋白(CRP)的血清浓度在临床实践中是一种有用的客观指标,可用于疾病筛查、监测疾病活动及评估治疗反应。本研究的目的是评估在0.2至15 mg/L浓度范围内该检测方法的分析性能,并使用Dade Behring Nephelometer II上的Dade Behring N Latex CRP单克隆检测法确定健康献血者血清CRP的参考区间。该检测方法是一种颗粒增强散射比浊免疫测定法,测量范围为0.2 - 1100 mg/L。样本体积为40微升,检测时间为6分钟。在CRP浓度为1.29至11.98 mg/L的血清混合液中,批内和批间不精密度研究的变异系数在2.2%至5.4%之间。线性研究表明理论值与测量值之间具有良好的相关性。未检测到血红蛋白<1.0 mmol/L、胆红素<512 μmol/L和脂肪乳剂<20 g/L的干扰。收集了268名年龄在20至65岁之间的健康献血者(107名女性和161名男性)的血样。计算得出女性血清CRP的非参数参考区间为<0.2 - 14.7 mg/L,男性为<0.2 - 9.16 mg/L。曼-惠特尼U检验显示血清CRP无性别差异(p值 = 0.72)。计算得出男女血清CRP的共同参考区间为<0.2 - 10.5 mg/L(中位数0.98 mg/L,范围<0.2 - 17.3 mg/L)。

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