Background
Microalbuminuria is a risk factor of renal dysfunction [
1‐
4], cardiovascular disease [
1‐
6], death [
1‐
3,
5], and dementia [
7] in lifestyle-related diseases. Investigation of proteinuria typically begins with the detection of proteinuria via dipstick measurements [
8]. The Kidney Disease Improving Global Outcomes (KDIGO) 2012 clinical practice guideline for the evaluation and management of chronic kidney disease recommends the urine albumin-to-creatinine ratio (uACR), urine protein-to-creatinine ratio (uPCR), reagent strip urinalysis for total protein with automated reading, and reagent strip urinalysis for manual reading (in that order) be evaluated for the initial testing of proteinuria [
3].
Albuminuria measurement is covered by insurance once every three months in Japan, if incipient diabetic nephropathy is suspected; however, albuminuria measurement is not covered for non-diabetic lifestyle-related diseases. Diabetes and hypertension are the two main causes of end-stage kidney disease worldwide, although the causes in general vary significantly among countries. According to a statistical survey of the Japanese Society for Dialysis Therapy, diabetic nephropathy was the most common primary disease among incident dialysis patients in Japan, followed by nephrosclerosis, the rate of which has been increasing [
9].
Lifestyle-related diseases include type 2 diabetes, obesity, metabolic syndrome, non-familial dyslipidemia, hypertension, hyperuricemia, myocardial infarction, stroke, liver disease, cancer, etc., the onset and progression of which are related to lifestyle habits such as eating habits (e.g. excessive intake of salt or sugar), lack of exercise, smoking, and excessive alcohol intake. Lifestyle-related disease had been proposed as a disease name, by clarifying the cause as being an unhealthy lifestyle, and was officially recognized in 1996 in Japan, with this name having been used so that everyone can definitely work on prevention. This study targeted lifestyle-related diseases excluding cancer, etc., that cause CKD such as type 2 diabetes, hypertension, obesity, metabolic syndrome, dyslipidemia, and hyperuricemia.
Advances are also being made with regard to treatment for chronic kidney disease [
10]. The prompt detection of microalbuminuria is considered necessary, in order to intervene in patients with lifestyle-related diseases at an early stage.
The urine dipstick is useful for screening uACR ≥ 30 mg/gCr [
11‐
14], with a few limitations having been reported [
12,
13]. While it is recommended to diagnose microalbuminuria based on positive results in two of three tests [
3], the accuracy and optimal cut-off(CO) for the prediction of microalbuminuria via three dipstick tests are not clear.
Although a CKD classification of A, defined as with a uPCR < 0.15 g/gCr for A1 and 0.15 to 0.49 g/gCr for A2 [
2] is more useful for predicting uACR 30-300 mg/gCr than the dipstick test, this is also not sufficient [
15]. The uPCR is useful for predicting uACR ≥ 30 mg/gCr [
14,
16‐
18] and microalbuminuria in cases of lifestyle-related diseases [
18]. Therefore, in the present study, we compared the utility of dipstick measurements and the uPCR for detecting microalbuminuria. Furthermore, the effect of qualitative proteinuria findings on the optimal CO and accuracy of uPCR in the prediction of microalbuminuria, including its utility for predicting microalbuminuria in proteinuria-negative cases, was unclear, meriting a further examination. In addition to the utility of the uPCR for the detection of microalbuminuria, in cases with negative proteinuria, the effects of urine specific gravity and urine creatinine were also examined.
Methods
The subjects included Japanese patients ≥ 18 years old who visited Yuurinkousekusei Fuji Hospital from October 2017 to May 2021 for lifestyle-related diseases or CKD due to diseases or aging and who had an estimated glomerular filtration rate (eGFR) of ≥ 15 ml/min/1.73 m2 and a uPCR of < 0.5 g/gCr at initiation. Patients with urinary tract infection, nephritis, hereditary renal disease, paraproteinemia, or cancer and kidney transplanted patients were excluded. We interviewed the patients in order to obtain their family history of hereditary diseases, and medical history of infectious diseases and kidney transplants. Urine protein, hematuria, urinary glucose, and urinary sediment were assessed by midstream urine examination for all patients. For those with proteinuria, hematuria, urine dysmorphic erythrocytes or urine cellular casts, ASO, serum IgA, antinuclear antibody, anti-DNA antibody, complements, MPO-ANCA, PR3-ANCA, and cryoglobulin were measured; while those suspected of having nephritis and collagen disease underwent a renal biopsy. Those with proteinuria, hematuria, and purpura, along with IgA vasculitis by skin biopsy were excluded. Serum and urine immunoelectrophoresis was performed in elderly individuals who were positive for proteinuria in order to examine the presence or absence of M protein and Bence-Jones protein, while amyloidosis and multiple myeloma were excluded. An echo examination of the renal urinary tract was performed in all cases and postrenal renal failure, tumors in organs such as kidney, ureter, bladder, and prostate, and polycystic kidney disease were excluded. For cases with negative urine protein and renal dysfunction of unknown causes, tubulointerstitial markers such as urine NAG, urine β2microglobulin, or urine L-FABP were examined, with a renal biopsy performed if necessary, while renal disorders due to interstitial nephritis and sarcoidosis were excluded. A renal biopsy was performed in diabetic patients with proteinuria and hematuria and suspected nephritis, while cases with nephritis were excluded.
A urine dipstick evaluation and uPCR, and uACR measurements were performed in the same urine samples three times per case on different days within one year with the second and third measurements performed using early morning spot urine samples [
3]. Patients whose proteinuria had increased to ≥ 0.5 g/gCr at the second or third measurement were not excluded. Patients whose eGFR had decreased by ≥ 30% within 3 months were excluded. The average eGFR during the period was used to determine the GFR category [
2].
Negative proteinuria (-) as 0, ( ±) trace as 0.5, ( +) as 1, 2 ( +) as 2, 3 ( +) as 3 were used to determine the dipstick proteinuria score. The sum of the three urine protein dipstick scores for both non-diabetic and diabetic patients showed a significant positive correlation with the sum of the three uPCRs (Supplemental Fig.
1a, b), which was used as the sum of the urine protein dipstick scores (SuPDS).
The three dipstick proteinuria evaluations were classified as proteinuria(-) of 0, proteinuria ≥ ( ±) of 1, or proteinuria( ±)(-) of 0, proteinuria ≥ ( +) of 1, using dummy variables, in order to examine the usefulness of differentiating micro- and macroalbuminuria by qualitative proteinuria using a binomial logistic regression.
The A1 caregory (uPCR < 0.15 g/gCr) is divided into three equal parts: A1L (uPCR 0–0.05 g/gCr), A1M (uPCR 0.06–0.10 g/gCr), and A1H (uPCR 0.11–0.14 g/gCr) in order to examine the association between dipstick proteinuria, uPCR and uACR.
Microalbuminuria was defined as a uACR of 30–299 mg/gCr for at least 2 of 3 measurements, while normoalbuminuria was defined as a uACR of < 30 mg/gCr for at least 2 of 3 measurements, and macroalbuminuria was defined as a uACR of ≥ 300 mg/gCr for at least 2 of 3 measurements. When the uACR was < 30 mg/gCr, 30–299 mg/gCr, and ≥ 300 mg/gCr, once at each measurement, the condition was defined as microalbuminuria in this study.
The c that met the minimum value of [(1 - sensitivity(c))
2 + (1 - specificity(c))
2)]
1/2 of the receiver operating characteristic (ROC) curve was defined as the optimal CO according to the distance (D). The c* that met the maximum of [sensitivity(c*) + specificity(c*) - 1] of ROC curve was defined as the Youden's Index (YI). The optimal CO according to the D and YI were described as CO (D) and CO (YI), respectively [
19].
Supplemental Fig.
2a, b shows a graph of the relationship between the CO of uPCR and sensitivity, specificity, YI, and 1—D, which was created from the ROC curve, in order to clarify the effect of the dipstick proteinuria findings on the ability of the uPCR to differentiate uACR ≥ 30 mg/gCr or microalbuminuria.
A urine dipstick was performed to determine the pH, specific gravity, protein, hematuria and glucose levels using a Clinitek Nouvus Automated urine chemistry analyzer (SIEMENS, Berlin, German). Proteinuria was measured using the pyrogallol red method (AR WAKO microTP-AR; FUJIFILM Wako Pure Chemical Industries, Osaka, Japan), urinary albumin was measured using an immunoturbimetric method (Auto Wako Microalbumin; FUJIFILM Wako Pure Chemical Industries), and serum and urine creatinine were measured using the enzyme method (L type WAKO CRE M; FUJIFILM Wako Pure Chemical Corporation) with an autoanalyzer (TBA-FX8, Canon medical systems corporation, Tochigi, Japan).
The correlation between two factors was examined by a simple regression analysis. The relationship between the log uPCR and log median uACR was analyzed by a restricted cubic spline. The chi-squared test, Mann–Whitney U test and Kruskal–Wallis and Steel–Dwass tests were used to compare clinical symptoms and the laboratory values for each category.
The factors differentiating uACR ≥ 30 mg/gCr or microalbuminuria were obtained using the logistic model, while the prediction probability was determined using λ = logit p, p = 1/(1 + exp(-λ)).
All statistical analyses were performed using the BellCurve for Excel (Social Survey Research Information Co., Ltd., Tokyo, Japan), SigmaStat Statistics (Systat Software, Inc., CA, USA), and Stata MP version16 (StataCorp LP, College Station, TX, USA) software programs.
Discussion
Regarding the detection of uACR ≥ 30 mg/gCr by a single dipstick measurement, the sensitivity + specificity—1 value was the highest in non-diabetic and diabetic patients with more than trace proteinuria, as shown in Supplemental Table
2. Findings in previous reports have varied, reporting values of “sensitivity 37.1%, specificity 97.3%, positive predictive value (PPV) 71.4%, negative predictive value (NPV) 89.5%” [
11]; “sensitivity 69.4%, specificity 86.8%, PPV 27.1%, NPV 97.6%” [
12]; and “sensitivity 43.6% specificity 93.6%, PPV 34.6%, NPV 95.5%” [
13] for more than trace proteinuria. This difference is believed to be due to the fact that there are many cases of advanced CKD, as the subjects in this study were outpatients with lifestyle-related diseases, and because dipstick evaluations are affected by the urine concentration and test reagents [
20]. Although it is necessary to confirm the results when the PPV is low, even if the sensitivity of uACR ≥ 30 mg/gCr is high [
12,
13], this study indicated that the PPV was high and suggested the utility of dipstick test, even if a dipstick proteinuria evaluation showed low sensitivity. However, as the NPV was relatively low, a uACR of ≥ 30 mg/gCr cannot be ruled out in cases of negative proteinuria.
When the utility of a single dipstick evaluation was compared with that of the uPCR for detecting of uACR ≥ 30 mg/gCr, the uPCR was shown to be more useful, with a high sensitivity and NPV as well as an almost equivalent specificity and PPV.
It is recommended that microalbuminuria be diagnosed, even when a single uACR measurement is ≥ 30 mg/gCr, if another examination shows uACR ≥ 30 mg/gCr among 2 subsequent early-morning urine tests [
3]. Regarding the significance of the three-time dipstick measurement, if the CO of 1 measurement is trace proteinuria, 3 measurements are more useful than 1 measurement, with the CO of 3 measurements indicating sensitivity 55.5% and specificity 79.7% when trace or more proteinuria is shown even once out of 3 times. If the CO of microalbuminuria is set at trace or more proteinuria two out of three times or 1( +) or more proteinuria one out of three times, the sensitivity for detecting microalbuminuria is reduced in non-diabetic patients, and therefore when the dipstick test shows trace levels or higher proteinuria once, it is desirable to confirm the result by measuring either uPCR or uACR at that time.
The sum of three uPCRs in non-diabetic patients was useful for differentiating microalbuminuria and indicated a CO (D, YI) of 0.23 g/gCr, which is approximately 3 times the CO of a single uPCR measurement. However, for qualitative proteinuria measurements, the CO (D, YI) was set at a trace finding being obtained at least one out of three times. The reason for this may be because the median uACRs of trace proteinuria in non-diabetic and diabetic patients were 56 and 73 mg/gCr, respectively, while the first quartiles were at 32.5 and 42 mg/gCr, respectively, which were higher than 30 mg/gCr.
The uPCR was useful for differentiating between uACR < 30 mg/dl and ≥ 30 mg/dl, when we limited our studies to dipstick-negative proteinuria. Furthermore, a single uPCR measurement was useful for predicting microalbuminuria, even when evaluating proteinuria-negative cases via the dipstick test three times in a row, with the sum of three uPCRs also being useful. While proteinuria is generally quantified after detection of proteinuria by a dipstick examination [
8], measuring the uPCR, even wnen the result is negative, seems useful for the early detection of microalbuminuria in lifestyle-related diseases.
The CO (YI) of uPCR that differentiates uACR ≥ 30 mg/dl in non-diabetic lifestyle-related diseases remained unchanged from the CO of negative proteinuria, with the values for G1-3a and G3b-4 being 0.07 g/gCr and 0.10 g/gCr, respectively, even when more than trace proteinuria was included. The sensitivity at the same uPCR and AUC increased while the specificity showed a small decrease when more than trace proteinuria was included. This is believed to be due to the fact that the COs is in A1M, while the uACR is mostly ≥ 30 mg/gCr in A1H and A2, along with the fact that the high fraction ratio of uPCR increases with the increase in qualitative proteinuria findings.
Regarding the difference in CO (YI) between G1-3a and 3b-4, the specificity of G1-3a increased more rapidly with the increase in the CO of the uPCR than did that of G3b-4, whereas G3b-4 had a slower decrease in sensitivity than G1-3a. This difference is attributed to the significant difference in the number of cases with uACR < 30 mg/gCr and ≥ 30 mg/gCr by uPCR category between G1-3a and G3b-4, meaning that G1-3a had higher proteinuria selectivity than G3b-4 or tubular protein in the urine may be increased in G3b-4.
The predictive probability of uACR ≥ 30 mg/gCr based on a logistic model using uPCR and the uSG or uCr in both non-diabetic and diabetic patients with negative proteinuria was significantly better than the uPCR alone for differentiating of uACR ≥ 30 mg/gCr. This appears to be due to the fact that the uSG, uCr and uACR exhibit a negative correlation at the same uPCR value of ≤ 0.10 g/gCr, suggesting that the uACR may be increased in diluted urine and decreased in concentrated urine. While the reason for this is unclear, the reabsorption of filtered albumin in the renal proximal tubules [
21] may be increased in concentrated urine compared with nonalbumin protein in the urine.
The KDIGO CKD guideline [
3] recommended that even if a uACR ≥ 30 mg/gCr is noted in a single spot urine measurement, the results should be confirmed by measuring the uACR using early-morning urine in order to exclude the possibility of postural proteinuria. Another reason for using the early morning urine based on the findings of this study is that the uACR of the specimen may have been reduced, as early-morning urine is expected to be more concentrated than spot urine. When predicting the uACR from the uPCR, it may also be desirable to use early-morning urine, although the uPCR itself is a major predictive factor of microalbuminuria.
The uACR estimates the daily albuminuria excretion under the assumption that the daily urinary creatinine excretion is 1 g, with a good correlation reportedly having been shown in patients with a normal renal function [
22]. It appears that the significance thereof in G3b and G4 is unclear. The urinary Cr excretion per unit time is expressed as (serum Cr value × GFR + amount of creatinine secreted by renal tubules). As renal dysfunction progresses, the tubular secretion of creatinine per unit nephron increases, while the number of functional nephrons is expected to decrease. While serum creatinine increases as eGFR decreases, this study found that the median age at stages G1, 2, 3a, 3b and 4 indicated 46.4, 60.6, 71.0, 77.3 and 79.5 years old for non-diabetic patients, respectively, and 55.0, 65.7, 75.0, 76.1 and 76.0 years old for diabetic patients, respectively, with significantly more elderly patients showed a decreased renal function than younger patients (Kruskal–Wallis test
P < 0.001, respectively). In addition to aging, a study on CKD patients with minimal dietary interventions reported that patients with lower creatinine clearance had a spontaneous decrease in dietary protein intake, reduced 24-h urine Cr excretion [
23], and prevalence of sarcopenia is increased as CKD progressed [
24]. Judging from the above, it is predicted that muscle mass will decrease in patients with a decreased renal function, with serum Cr value × GFR also potentially decreasing. With respect to improving the limitations of the daily albuminuria excretion prediction by uACR, it has been reported that the estimated albumin excretion rate, calculated by multiplying the spot uACR value by the estimated urinary creatinine excretion rate (g/24 h), improved the prediction of the measured 24-h albumin excretion [
25]. Nonalbuminuric renal dysfunction have been reported in type 2 diabetic patients and the general population [
26,
27], so it is necessary to investigate the estimated albumin excretion rate and the estimated protein excretion rate for predicting it in cases of a decreased renal function.
The BMI and abdominal circumference were higher in diabetic patients than in non-diabetic patients, and while significant positive correlations between the BMI and uPCR and the BMI and uACR were noted in non-diabetic patients, no such correlations were noted in diabetic patients. The lack of correlations in diabetic patients may be due to a small number of this study. It is reported that high waist-to-hip ratio and BMI are independently positively associated with albuminuria due to intraglomerular haemodynamics resulting from excess adiposity [
28]. uACR and uPCR were higher in hypertensive cases than in non-hypertensive cases among non-diabetic patients in this study. There is the possibility that hypertension and obesity correlate with the severity of global nephrosclerosis in non-diabetic nephrosclerosis [
29], and it is speculated that systemic and intraglomerular hypertension cause glomerular sclerosis, resulting in high uACR and uPCR values in non-diabetic hypertensive or obese patients. In addition, glomerular lesions, which are typically found in diabetic nephropathy (diabetic glomerulopathy) [
29], may be involved in the increase in uACR and uPCR in diabetic patients.
In this study, uPCR was useful for determining microalbuminuria in both non-diabetic and diabetic patients, even when testing negative using a dipstick test, and the CO of uPCR for microalbuminuria in cases with three consecutive negative proteinuria findings for both groups was 0.06 g/gCr. In Japan, the measurement of albuminuria is covered by insurance only when incipient diabetic nephropathy is supposed. Obesity [
30] and metabolic syndrome [
31] are risk factors for diabetes. uACR and uPCR were high in obese and hypertensive cases of non-diabetic patients in this study. Therefore, in the group at high-risk for diabetes, even if the patient is found to be a proteinuria-negative case based on the findings of a dipstick test, it is desirable to measure uPCR, and by maintaining uPCR at a level of ≤ 0.05 g/gCr, it is possible for the albuminuria to remain in the normal range, even if diabetes has already developed. Should microalbuminuria be suspected, then encouraging the patient to make changes in their lifestyle may reduce albuminuria, decrease the risk of a progression to diabetes, and also prevent the development of nephrosclerotic lesions in cases that have developed diabetes.
Albuminuria is a risk factor for renal dysfuction and cardiovascular disease in diabetic patients [
4], and this study targeted patients with normo- and microalbuminuria. Exacerbation of albuminuria indicates an increasing risk of renal dysfunction and cardiovascular disease, while amelioration from macroalbuminuria to microalbuminuria or microalbuminuria to normoalbuminuria indicates a reduced risk following the onset of diabetes [
4,
6,
32]. This study indicated that changes in uACR and uPCR exhibited a significant positive correlation even if urinary protein was negative three times via the dipstick test, with changes in uACR appearing to be predictable from changes in uPCR. When the dipstick proteinuria was negative three times, the increase/decrease in uACR per uPCR 0.01 g/gCr was approximately 3 mg/gCr, which tended to be lower than approximately 5–6 mg/gCr which included trace or more urinary protein qualitative findings. This is probably because uPCR values in cases of positive dipstick protein findings are higher than the uPCR values in cases of negative proteinuria, and the ratio of albumin in total proteinuria increases as uPCR increases. In Japan, uACR measurement is covered by insurance only once in three months for diabetic patients, so uPCR may be able to evaluate the therapeutic effect and detect deterioration at an early stage during that period.
It has been reported that the use of RAAi (such as ACEi, ARB, and MRB) [
10,
33,
34] and SGLT2i [
10,
35] reduces albuminuria and the accompanying renal dysfunction and cardiovascular disease in patients with chronic kidney disease with or without diabetic patients. Although the use of ACEi and ARB has been reported to be associated with high uACR/uPCR levels [
36], the effects of SGLT2i are unclear. This study indicated that the CO of uPCR, which distinguishes uACR 30 mg/gCr or more in cases using SGLT2i, tended to be higher than that in non-use cases (Supplemental Table
14), so the effect of taking SGLT2i on uACR/uPCR and the CO of microalbuminuria shall be investigated going forward.
The inconsistency between the CO (D) and CO (YI) was recognized in differentiating uACR ≥ 30 mg/gCr in proteinuria-negative cases among non-diabetic patients with G3b-4 and microalbuminuria in triple proteinuria-negative cases of G1-3a. The CO (YI) is reportedly preferable because it maximizes the overall rate of correct classification when the criteria do not agree [
19]. However, D
2 = min [-2(sensitivity + specificity -1) + (sensitivity
2 + specificity
2)], and (sensitivity
2 + specificity
2) is smallest at the CO where the sensitivity and specificity are equal and when (sensitivity + specificity) is constant. In cases of lifestyle-related diseases, the risk of cardiovascular disease increases starting at uACR < 30 mg/gCr [
5], so there is little disadvantage in intervening in patients with normoalbuminuria. As high sensitivity for detecting microalbuminuria is considered necessary for early prevention of cardiovascular disease, the CO (D) seems useful in that it takes into consideration both the accuracy and the balance between sensitivity and specificity.
One limitation associated with this study was its single-center setting, with different results potentially being obtained depending on the target patient, dipstick test, proteinuria, albumin quantification measurement conditions, and measurement methods [
20]. In addition, the number of patients was relatively small, but there have been no reports evaluating the factors for microalbuminuria based on urine dipstick, uPCR, and uACR measurements in the same urine sample three times. The median time between the three uACR measurements was about four to five months, which was relatively long, so the results may have been affected by the treatment of lifestyle-related diseases during this period, although the KDIGO guideline recommends a further two measurements of the uACR within two months after the first measurement [
3].
The main results of this study were summarized in Table
5.
Table 5
Summary of prediction of microalbuminuria from urine dipstick and uPCR in non-diabetic and diabetic life-style related disease
prediction of microalbuminuria |
urine dipstick | A one-time dipstick proteinuria examination is useful for predicting microalubuminuria, with uPCR or uACR having to be measured and confirmed at ≥ trace( ±) |
Three-time dipstick proteinuria examinations are more useful for predicting microalubuminuria than the one-time dipstick examination, with uPCR or uACR having to be measured and confirmed upon the first ≥ trace( ±) |
uPCR | Among all proteinuria findings on urine dipsticks, uPCR is useful for predicting microalbuminuria |
Even if the urinary protein tests negative using a urine dipstick, measuring uPCR is useful for the early detection of microalbuminuria |
By maintaining the value of the one-time uPCR at ≤ 0.05 g/gCra, as well as the sum of the three-time uPCRs at ≤ 0.22 g/gCrb, it may be possible to maintain normoalbuminuria |
It may be microalbuminuria if the one-time uPCR is ≥ 0.06 g/gCr or the sum of the three-time uPCRs is ≥ 0.23 g/gCr, requiring intervention such as confirmation by measuring uACR or further improvement in lifestyle |
prediction of change in uACR |
| Among all proteinuria findings on urine dipsticks, including dipstick proteinuria negative, an increase or decrease in uACR can be predicted by an increase or decrease in uPCR |
sample | A spot first-morning urine sample is desirable, which is relatively concentrated and is not influenced by postural proteinuria |