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首页> 外文期刊>Clinical Laboratory >Comparison Of High-sensitivity C-reactive Protein Serum Assayresults Obtained Using Dade-behring Bnii Nephelometer Andrnortho Vitros Fs 5.1 Clinical Analyzer In Respect Of Crp-related Riskrnassessment Of Chronic Metabolic Diseases
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Comparison Of High-sensitivity C-reactive Protein Serum Assayresults Obtained Using Dade-behring Bnii Nephelometer Andrnortho Vitros Fs 5.1 Clinical Analyzer In Respect Of Crp-related Riskrnassessment Of Chronic Metabolic Diseases

机译:使用Dade-behring Bnii浊度计Andrnortho Vitros Fs 5.1临床分析仪获得的针对Crp相关的慢性代谢性疾病风险评估的高灵敏度C反应蛋白血清测定结果的比较

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Background: Serum concentration of high sensitive C-reactive protein (hsCRP) can predict the risk of chronic metabolic and cardiovascular diseases but it is unclear whether turbidimetric high sensitive assays of CRP are adequate.rnMethods: Concentrations of serum CRP in 126 samples of serum were measured with high-sensitivity methods using nephelometry (BN II Nephelometer) and turbidimetry (Ortho Vitros FS 5.1).rnResults: For CRP concentrations measured by nephelometry and turbidimetry intra-assay CVs were 3.2 and 0.9% at mean CRP concentrations of 1.4 and 2.1 mg/l, inter-assay CVs for commercial controls were 3.1% and 3.6% at mean concentrations of 1.3 and 1.7 mg/1, and mean biases were 7.62% and 2.26%, respectively. Measurements were strongly, linearly correlated (r=0.99; CRP_(Vitros)=0.03 + 1.03CRP_(BNII)). When disease risk was assessed by nephelometry and turbidimetry, results were similar. If the risk of disease was classified as moderate (1.0 < CRP ≤ 3.0 mg/l) or high (CRP > 3.0 mg/l), the frequency of misclassified cases was only 2.3 and 2.1%, respectively. The classification agreement weighted k coefficient was 0.94 (95% C.I.: 0.89-0.98).rnConclusions: turbidimetric high sensitive CRP assays can properly classify CRP-related prediction of chronic metabolic diseases with special consideration on cardiovascular risk.
机译:背景:高敏C反应蛋白(hsCRP)的血清浓度可以预测慢性代谢和心血管疾病的风险,但尚不清楚浊度高敏CRP检测是否足够。用浊度法(BN II比浊法)和比浊法(Ortho Vitros FS 5.1)用高灵敏度方法测定。结果:对于浊度法和比浊法测定的CRP浓度,在1.4和2.1 mg的平均CRP浓度下,测定内CV分别为3.2和0.9% / l,在平均浓度为1.3和1.7 mg / 1时,商业对照的批间CV为3.1%和3.6%,平均偏差分别为7.62%和2.26%。测量值呈强线性相关(r = 0.99; CRP_(Vitros)= 0.03 + 1.03CRP_(BNII))。当通过比浊法和比浊法评估疾病风险时,结果相似。如果将疾病风险分类为中度(1.0 3.0 mg / l),则错误分类病例的发生率分别仅为2.3%和2.1%。分类协议加权k系数为0.94(95%C.I .: 0.89-0.98)。结论:浊度法高灵敏度CRP分析可以对CRP相关的慢性代谢疾病预测进行适当分类,并特别考虑心血管风险。

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