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Jornal Brasileiro de Nefrologia

versão impressa ISSN 0101-2800

J. Bras. Nefrol. vol.34 no.1 São Paulo jan./mar. 2012

http://dx.doi.org/10.1590/S0101-28002012000100010 

ORIGINAL ARTICLE

 

Urinary protein/creatinine ratio versus 24-hour proteinuria in the evaluation of lupus nephritis

 

 

Grace Tamara Moscoso SolorzanoI; Marcus Vinicius Madureira e SilvaI; Sílvia Regina MoreiraII; Sonia Kiyomi NishidaIII; Gianna Mastroianni KirsztajnI

IGlomerulopathy sector at Universidade Federal de São Paulo – UNIFESP
IICentral laboratory of Hospital do Rim
IIILaboratory of Glomerulopathy and Renal Immunopathology of the Glomerulopathy sector at UNIFESP

Correspondence to

 

 


ABSTRACT

INTRODUCTION: The urinary protein/creatinine ratio has been used instead of 24-hour proteinuria in Nephrology practice for the follow-up of glomerular diseases, considering the advantages of collection and the low cost. However, there are still doubts as to its applicability both for an isolated evaluation and for the follow-up of patients with lupus nephritis.
OBJECTIVE: To evaluate 24-hour proteinuria determinations and random urine samples, performing urinary creatinine correction and urinary protein/creatinine ratio in subjects with lupus nephritis.
METHODS: 24-hour proteinuria and urinary protein/creatinine ratio were determined by conventional methods (automated Pyrogallol for proteinuria and alkaline picrate for creatinine).
RESULTS: Seventy-eight urine samples of 41 patients diagnosed with systemic lupus erythematosus, according to the American Rheumatology Association, with lupus nephritis, were analyzed, and a good correlation between 24-hour proteinuria and urinary protein/creatinine ratio (r = 0.9010 and r² = 0.813) was observed. However, a poor correlation between random proteinuria (without creatinine correction) versus 24-hour proteinuria (r = 0.635 and r² = 0.403) or versus urinary protein/creatinine ratio (r = 0.754 and r² = 0.569) was seen.
CONCLUSION: 24-hour proteinuria and urinary protein/creatinine ratio were useful in the follow-up of each case. However, we observed that the absolute values were different, which did not allow the replacement of one for the other during follow-up, especially when this result is used to define the activity of the disease. Based on these results, we suggest a period of intersection from one to the other (two to three determinations by both methods) and the choice of one marker for proteinuria follow-up, if necessary.

Keywords: Lupus Nephritis. Proteinuria. Lupus Erythematosus, Systemic. Diagnostic Tests, Routine.


 

 

INTRODUCTION

The quantification of proteinuria is a valuable test to analyze kidney diseases, thus being considered as a diagnostic and prognostic marker, besides being essential for the follow-up of treatments for glomerulopathy.

Gold standard is 24-hour proteinuria (24hP), due to the great variation in the concentration of urinary protein throughout the day – for different reasons –, which impedes the dosage in a random sample.

However, it is worth to mention that 24hP determination is associated with some difficulties, such as patient adherence and the adequate collection and handling of this material in the laboratory.

In the past few years, the use of protein/creatinine ratio has been spread in random urine samples as a proper test for the quantification of proteinuria.1 It has been demonstrated that P/C ratio is an accurate and reliable method to estimate the protein in the urine of pregnant women, kidney-transplanted patients and those with diabetic nephropaty, as well as in children.2-6 However, there are doubts as to the reliability to use this index both for the isolated evaluation and for the follow-up of patients with lupus nephritis.

In this study, 24hP determinations and random urine samples were analyzed with the urinary creatinine correction by the P/C ratio in patients with lupus nephritis. The objective was to evaluate the possibility that the second test can replace the first one for the follow-up of these patients.

 

MATERIAL AND METHODS

Forty-one patients in the outclinic patient of glomerulopathies at Universidade Federal de São Paulo (UNIFESP) with systemic erythematosus lupus were evaluated according to the criteria of the American Association of Rheumatology. They all had clinical and laboratory diagnosis of lupus nephritis; eight did not have a biopsy (six patients) or the material was not adequate (two patients); the others had lupus nephritis classified according to the World Health Organization (WHO) in classes III (3), IV (18), V (11) and VI (1). One patient underwent two renal biopsies during follow-up (the first showed class V, and the second, class IV, but here we considered class V). Other characteristics of the studied population are demonstrated in Table 1.

Patients collected 24-hour urine samples for examinations and, when delivering this material to the laboratory, they collected an additional random urine sample.

In order to determine 24hP and proteinuria in a random urine sample, the automated Pyrogallol method was used; urinary creatinine was measured by the alkaline picrate method. Besides the tests in this protocol, patients underwent the examinations for the routine evaluation of their disease.

 

RESULTS

Patients with lupus nephritis presented with mean serum creatinine of 1.0 mg/dL (minimum: 0.7; maximum: 4.7 mg/dL). Proteinuria values are presented in Table 2.

Seventy eight urine samples of patients with lupus nephritis were compared, showing a good correlation between 24hP and P/C ratio (r = 0.901 and r2 = 0.813, Graph 1). When comparing values of proteinuria in a random sample with 24hP (r = 0.635 and r2 = 0.403, Graph 2), and with the P/C ratio (r = 0.754 and r2 = 0.569, Graph 3), the correlation between variables was lower.

 

 

 

 

 

 

DISCUSSION

It is important to consider that 24hP remains as gold standard to diagnose proteinuric diseases, and it is the most used parameter for syndromic definitions concerning glomerular diseases. The P/C ratio in a random urine sample is a simple test, which is low-cost and easy to perform. It does not require timed collection of urine, since it can be collected any time of the day, although there are some controversies as to the quality of the sample. Some problems were found concerning the use of this examination: the lack of knowledge on its applicability and, from the practical point of view, the frequent inexistence of specific codes in clinical laboratories to facilitate its performance, when ordered by the doctors.

Even though it is hard for nephrologists to understand how difficult it is to provide an examination that depends only on dividing the result of protein dosage in a urine sample by the result of creatinine in the same sample, using the same measurement, apparently it is not possible to charge for such examination in most national laboratories, since it is not part of the list of examinations performed by health insurance companies.

Since this argument is frequently used as a reason, it is possible to display its importance together with some simple measures that can facilitate the availability of this examination with time. The authors believe that some factors can contribute with the inclusion of this test in the laboratories: the personal contact between the assistant doctor and the clinical pathologist; the repetition of requirements to determine protein/creatinine ratio due to the need to count on this examination; and, in the first stage, the additional requirement of separate doses of protein and creatinine in the random urine sample (together with the order for protein/creatinine ratio, emphasizing the need to insert the calculation of this ratio), as collaboration, to facilitate charging for these examinations. In order to interpret the results, it is worth to mention the values in this marker, which are used to define response to treatment, for example, are similar to the ones used for 24hP; results between zero and 0.2, or 0.3 g/g2 are considered normal.

In this study, a great correlation between 24hP and P/C ratio was observed in a random sample among patients with lupus nephritis, which is in accordance with prior studies performed with other subgroups (pregnant women, kidney transplanted patients and patients with diabetic nephropathy).2-4,6 For instance, Khan et al.6 noticed an excellent correlation (r = 0.96, p < 0.001) between both parameters among patients with kidney diseases, and not such a good one with proteinuria in a random sample without urinary creatinine correction (0.52), whose use may define errors of interpretation of proteinuria in the clinical context.

In the group of lupus nephritis, it is possible to say that every marker, alone, was useful to determine proteinuria. However, absolute values of both exams were different in each case, which did not enable the replacement of one for the other during follow-up, especially when this result should be used to define the activity of the disease, particularly such polymorph glomerular disease lupus nephritis.

Because of that, if it is necessary to replace one test for the other during follow-up of a specific patient, the suggestion is a period of intersection (two to three determination by both methods) before any change is defined.

Finally, it is important to say that the isolated collection of the random urine sample to determine the P/C ratio has some advantages concerning facility, reliability, accuracy, and diagnostic speed; it could also be used as the preferential marker in subgroups of subjects with more difficult to properly collect urine in 24 hours, such as children, elderly patients and those with intellectual disabilities; or when the collection is incompatible with the professional activities of the patient, in case of refusing to do this examination or at the suspicion of lack of adherence.

 

REFERENCES

1. Mastroianni Kirsztajn G, Pereira AB. The clinical pathology laboratory and the screening of renal diseases. J Bras Nefrol 2007;29:13-7.         [ Links ]

2. Morales JV, Vaisbich MH, Heilberg IP, Mastroianni Kirsztajn G, Barros EJG. Urine random samples versus 24-hour collections their role in clinical practice. J Bras Nefrol 2006;28:33-40.         [ Links ]

3. Ramos JGL, Martins-Costa SH, Mathias MM, Guerin YLS, Barros EG. Urinary protein/creatinine ratio in hypertensive pregnant women. Hypertens Pregnancy 1999;18:209-18.         [ Links ]

4. Ruggenenti P, Gaspari F, Perna A, Remuzzi G. Cross sectional longitudinal study of spot morning urine protein: creatinine ratio, 24 hour urine protein excretion rate, glomerular filtration rate, and end stage renal failure in chronic renal disease in patients without diabetes. British Med J 1998;316:504-9.         [ Links ]

5. Mastroianni Kirsztajn G. Proteinuria: mais do que um simples exame. J Bras Patol Med Lab 2010;46:168-9.         [ Links ]

6. Khan DA, Ahmad TM Qureshil AH, Halim A, Ahmad M, Afzal S. Assessment of proteinuria by using protein: creatinine index in random urine sample. J Pak Med Assoc 2005;55:428-31.         [ Links ]

 

 

Correspondence to:
Gianna Mastroianni Kirsztajn
Setor de Glomerulopatias, Disciplina de Nefrologia, UNIFESP-EPM
Rua Botucatu, 740
São Paulo – SP – Brasil
Zip code 04023-900
E-mail: giannamk@uol.com.br

Submitted on: 10/29/2011
Approved on: 11/28/2011

 

 

This study was undertaken at UNIFESP.
The authors report no conflict of interest.