Protein-to-creatinine ratio in spot urine samples as a predictor of quantitation of proteinuria

被引:44
作者
Xin, G
Wang, M [1 ]
Jiao, LL
Xu, GB
Wang, HY
机构
[1] Peking Univ, Hosp 1, Dept Nephrol, Beijing 100034, Peoples R China
[2] Peking Univ, Hosp 1, Dept Clin Lab, Beijing 100034, Peoples R China
关键词
proteinuria; urinary protein excretion; urine protein-to-creatinine ratio;
D O I
10.1016/j.cccn.2004.06.019
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Normal individuals usually excrete very small amounts of protein in the urine. Persistently increased protein excretion is usually a marker of kidney damage. Quantifying protein in urine is commonly used in the diagnosis of kidney diseases, detection of treatment effects and evaluation of prognosis. We evaluated the use of the total protein-to-creatinine ratio (P/C) in spot urine specimens as a predictor of urine protein excretion in 24-h collections. Methods: The correlation between P/C in first morning and random urine specimens and urinary protein excretion in 24-h collections were analyzed. The cutoff value of P/C in first morning urine specimens for screening urinary protein excretion of I and 3 g in 24-h collections was determined by receiver operating characteristics (ROC) curve. Results: For patients with Ccr less than or equal to 10 ml/min, correlation between the urine protein excretion in 24-h collections and the P/C in first morning urine specimens was not significant. For patients with Ccr > 10 ml/min, the correlation was highly significant. Similar results were obtained for random urine specimens. By ROC curve analysis, the P/C of 0.94 and 2.84 g/gcr in first morning urine specimens represent the best threshold to detect urine protein excretion of 1 and 3 g in 24-h collections, respectively. There is a good correlation between P/C in first morning urine specimens and random urine specimens from inpatients and outpatients. But the P/C in random specimens is significantly higher than that in first morning specimens in outpatients. Conclusion: The P/C in spot urine samples could be used as an alternative to urine protein excretion in 24-h collections in patients with Ccr >10 ml/min. The P/C in first morning urine samples is better than that in random specimens, especially for outpatients. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:35 / 39
页数:5
相关论文
共 8 条
[1]   Proteinuria, albuminuria, risk, assessment, detection, elimination (PARADE): A position paper of the national kidney foundation [J].
Keane, WF ;
Eknoyan, G .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1999, 33 (05) :1004-1010
[2]   Prediction of 24-hour protein excretion in pregnancy with a single voided urine protein-to-creatinine ratio [J].
Neithardt, AB ;
Dooley, SL ;
Borensztajn, J .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2002, 186 (05) :883-886
[3]   QUANTITATION OF PROTEINURIA BY THE USE OF PROTEIN-TO-CREATININE RATIOS IN SINGLE URINE SAMPLES [J].
SCHWAB, SJ ;
CHRISTENSEN, RL ;
DOUGHERTY, K ;
KLAHR, S .
ARCHIVES OF INTERNAL MEDICINE, 1987, 147 (05) :943-944
[4]  
STEINHAUSLIN F, 1995, CLIN NEPHROL, V43, P110
[5]   The urine protein to creatinine ratio (P/C) as a predictor of 24-hour urine protein excretion in renal transplant patients [J].
Torng, S ;
Rigatto, C ;
Rush, DN ;
Nickerson, P ;
Jeffery, JR .
TRANSPLANTATION, 2001, 72 (08) :1453-1456
[6]   Application of an improved biuret method to the determination of total protein in urine and cerebrospinal fluid without concentration step by use of Hitachi 7170 auto-analyzer [J].
Xu, GB ;
Jiao, LL ;
Zhu, LH ;
Xia, T .
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2001, 15 (04) :161-164
[7]   Proteinuria is still useful for the screening and diagnosis of overt diabetic nephropathy [J].
Zelmanovitz, T ;
Gross, JL ;
Oliveira, J ;
de Azevedo, MJ .
DIABETES CARE, 1998, 21 (07) :1076-1079
[8]   The receiver operating characteristics curve in the evaluation of a random urine specimen as a screening test for diabetic nephropathy [J].
Zelmanovitz, T ;
Gross, JL ;
Oliveira, JR ;
Paggi, A ;
Tatsch, M ;
Azevedo, MJ .
DIABETES CARE, 1997, 20 (04) :516-519