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一种基于敏感定量测试条的即时白蛋白尿筛选检测法。

A sensitive quantitative test strip based point-of-care albuminuria screening assay.

机构信息

Department of Clinical Chemistry, Ghent University Hospital, Ghent, Belgium.

出版信息

Clin Chem Lab Med. 2012 Jan 6;50(4):673-8. doi: 10.1515/cclm.2012.0849.

Abstract

BACKGROUND

Chronic kidney disease is a major health problem and the global guidelines require screening of albuminuria. Therefore, affordable and sensitive albuminuria screening tests are needed. We explored the potential of urine strips, generally reported in the ordinal scale, measured on an automatic strip reader for reporting quantitative and sensitive albumin results.

METHODS

We compared reflectance data of Combur-Test® strips obtained from the Cobas U411 reader (Roche) with albuminuria data from a nephelometer BNII (Siemens) and with protein concentrations from the pyrogallol red method (Modular P, Roche) for 389/328 non-pathologic and pathologic urine samples, respectively.

RESULTS

Imprecision of the reflectance signal of the Cobas U411 was measured with commercial control material (Bio-Rad). Inter-run coefficients of variations (CVs) for reflectance for levels 1 and 2 were 1.7%/4.9%, respectively, and intra-run CVs were 1.8%/4.2%, respectively. Good agreement was obtained between the albumin concentration of the BNII and the protein strip reflectance data (n=389): Y (10,000/protein reflectance, 1/%)=160+0.132·X (albuminuria BNII, mg/L)-0.0000111·X2 (albuminuria BNII, mg/L); r2=0.921. Lower agreement was found between the protein assay (n=328) and the reflectance (r2=0.831). A calibration curve was made between 11.5 mg/L and 121.5 mg/L. The limit of blank (LOB) was 44.7 mg/L.

CONCLUSIONS

The present study demonstrates that reflectance data generated by a test strip reader allows for quantitative analysis of albumin. Although the lower limit of the microalbumin range (30 mg/L) cannot be achieved with the dye-binding method, the results are satisfactory for screening purposes.

摘要

背景

慢性肾脏病是一个主要的健康问题,全球指南要求筛查白蛋白尿。因此,需要负担得起且敏感的白蛋白尿筛查试验。我们探讨了尿液试纸的潜力,这些试纸通常以序数量表报告,在自动试纸阅读器上测量,以报告定量和敏感的白蛋白结果。

方法

我们将 Cobas U411 阅读器(罗氏)上获得的 Combur-Test®试纸的反射率数据与来自比浊计 BNII(西门子)的白蛋白尿数据以及来自焦酚红法(罗氏 Modular P)的蛋白浓度进行比较,分别为 389/328 份非病理和病理尿液样本。

结果

使用商业质控品(伯乐)测量 Cobas U411 反射率信号的不精密度。水平 1 和 2 的反射率批内变异系数(CV)分别为 1.7%/4.9%,批间 CV 分别为 1.8%/4.2%。在 BNII 的白蛋白浓度和蛋白试纸反射率数据之间(n=389)获得了良好的一致性:Y(10000/蛋白反射率,1%)=160+0.132·X(BNII 白蛋白尿,mg/L)-0.0000111·X2(BNII 白蛋白尿,mg/L);r2=0.921。在蛋白检测(n=328)和反射率之间的一致性较低(r2=0.831)。在 11.5mg/L 至 121.5mg/L 之间制作了校准曲线。空白限(LOB)为 44.7mg/L。

结论

本研究表明,试纸阅读器产生的反射率数据可用于白蛋白的定量分析。虽然染料结合法无法达到微量白蛋白范围(30mg/L)的下限,但结果足以满足筛查目的。

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