Diagnostic value of random urine protein/creatinine ratio for preeclampsia

IF 1.7 Q3 MEDICAL LABORATORY TECHNOLOGY Practical Laboratory Medicine Pub Date : 2023-12-13 DOI:10.1016/j.plabm.2023.e00351
Jingjing Guo, Lianlian Zhou, Suzhen Pan, Baoqing Li
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Abstract

Objective

The 24-h urine protein remains the gold standard to diagnose proteinuria in suspected preeclamptic patients. However, this test is time consuming and sometimes inaccurate. In this study, we aimed to analyse the correlation between the random urine protein/creatinine ratio (UPCR) and 24-h urine protein and to explore the clinical value of UPCR in the diagnosis of preeclampsia.

Method

We retrospectively evaluated 109 pregnant women from our hospital who had hypertensive diseases. They were grouped according to time of urine collection and disease severity to compare differences in random urine protein, urine creatinine, and UPCR. The correlation between the UPCR and 24-h urine protein was determined by Pearson's linear correlation.

Results

We found no statistically significant differences in random urine protein, urine creatinine, or UPCR among the four time of sampling groups. Further, random urine protein, UPCR, and 24-h urine protein between the gestational hypertension and preeclampsia groups differed significantly (P < 0.001). Correlation analysis showed significant positive correlation between random urine protein, and 24-h urine protein, and UPCR and 24-h urine protein, with r values of 0.789 and 0.810, respectively. According to the receiver operating characteristic (ROC) curve, the optimal threshold, sensitivity, specificity, and area under the curve of UPCR for the diagnosis of preeclampsia were 0.456 g/mmol, 67.8 %, 78.3 %, and 0.747, respectively (95 % confidence interval [CI], 0.65–0.844).

Conclusion

This study indicated that UPCR is significantly correlated with 24-h urine protein and is expected to replace the 24-h urine protein test as a diagnostic indicator of preeclampsia.

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随机尿蛋白/肌酐比值对子痫前期的诊断价值
目的 24 小时尿蛋白仍是诊断疑似先兆子痫患者蛋白尿的金标准。然而,这种检测耗时较长,有时还不准确。本研究旨在分析随机尿蛋白/肌酐比值(UPCR)与 24 小时尿蛋白之间的相关性,并探讨 UPCR 在诊断子痫前期中的临床价值。根据尿液采集时间和疾病严重程度对她们进行分组,比较随机尿蛋白、尿肌酐和 UPCR 的差异。结果 我们发现随机尿蛋白、尿肌酐和 UPCR 在四个取尿时间组之间没有统计学差异。此外,妊娠高血压组和子痫前期组的随机尿蛋白、尿肌酐和 24 小时尿蛋白差异显著(P < 0.001)。相关分析表明,随机尿蛋白与 24 小时尿蛋白、UPCR 与 24 小时尿蛋白之间存在明显的正相关,r 值分别为 0.789 和 0.810。根据接收者操作特征曲线(ROC),UPCR 诊断子痫前期的最佳阈值、敏感性、特异性和曲线下面积分别为 0.456 g/mmol、67.8%、78.3% 和 0.747(95% 置信区间 [CI],0.65-0.844)。
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来源期刊
Practical Laboratory Medicine
Practical Laboratory Medicine Health Professions-Radiological and Ultrasound Technology
CiteScore
3.50
自引率
0.00%
发文量
40
审稿时长
7 weeks
期刊介绍: Practical Laboratory Medicine is a high-quality, peer-reviewed, international open-access journal publishing original research, new methods and critical evaluations, case reports and short papers in the fields of clinical chemistry and laboratory medicine. The objective of the journal is to provide practical information of immediate relevance to workers in clinical laboratories. The primary scope of the journal covers clinical chemistry, hematology, molecular biology and genetics relevant to laboratory medicine, microbiology, immunology, therapeutic drug monitoring and toxicology, laboratory management and informatics. We welcome papers which describe critical evaluations of biomarkers and their role in the diagnosis and treatment of clinically significant disease, validation of commercial and in-house IVD methods, method comparisons, interference reports, the development of new reagents and reference materials, reference range studies and regulatory compliance reports. Manuscripts describing the development of new methods applicable to laboratory medicine (including point-of-care testing) are particularly encouraged, even if preliminary or small scale.
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