Cystatin C and beta2-microglobulin: markers of glomerular filtration in critically ill children

Glomerular filtration rate (GFR) is difficult to measure in clinical practice [1‐4]. The ideal laboratory marker should be of endogen synthesis, regular production rate, eliminated only by glomerular filtration, and without tubular secretion or reabsorption [4‐6]. Creatinine clearance (CrC) using a 24-hour urine sample and serum creatinine (Cr) are the most commonly used parameters to estimate GFR in clinical practice [2, 4, 5, 7, 8], although not the most accurate. However, there are limitations to their use. Cr could be affected by factors other than renal function (for example, muscle mass, protein intake, inflammatory illness, or hepatic disease) [2, 4, 9‐12]. Moreover, Cr is partially secreted by renal tubules [2, 4, 10, 13] and frequently overestimates GFR [1, 2, 4, 5, 13]. On the other hand, CrC requires urine collection over a 24-hour period with a steady-state situation [1, 2, 4, 11, 14]. Mathematical formulas using Cr serum levels to estimate GFR (Schwartz formula is the most widely used and is based on Cr, age, and height) have been developed [15, 16].

To overcome the problems of measuring GFR, an extensive search is being conducted to find a serum marker able to detect renal function impairment, especially at the initial phase. Cystatin C and beta2-microglobulin (B2M) are low-molecular-weight proteins freely filtered by the glomerulus [1, 6, 11, 12]. Their serum concentrations, especially that of cystatin C, are less dependent on extra renal factors than in the case of Cr [1, 5, 6, 10, 11, 13, 14, 17, 18]. Early detection of renal function impairment in paediatric intensive care would be of great value, allowing accurate treatment, adjustment of drug dose, and prevention of more severe renal damage [3, 7, 9]. Previous studies demonstrated the superiority of serum cystatin C compared with creatinine in the evaluation of GFR [1, 5, 8, 11, 13, 17‐19], especially when there is a minor reduction in GFR [1, 5, 6, 8, 12, 13]. We have not found any medical literature evaluating these low-molecular-weight proteins in critically ill children. The aim of this study was to evaluate the accuracies of serum Cr, serum cystatin C, and B2M as markers of GFR in critically ill children by comparing their results with CrC and Schwartz.

Twenty-five children admitted to our paediatric intensive care unit (PICU) were included in the study. All patients between the ages of 1 month and 14 years who were admitted due to an acute illness and who had a bladder catheter were included. The presence of previous renal or thyroideal pathology and the need of renal replacement therapy were considered exclusion criteria. Demographic and clinical conditions of the children were recorded. A serum sample was taken regularly from each patient in the morning (between 7 and 8 a.m.) for creatinine measurement. Cystatin C and B2M were measured in this sample. A 24-hour urine sample was obtained just before the serum sample to calculate the CrC adjusted to adult body surface area by means of the following formula: CrC (in millilitres/minute per 1.73 m²) = [(urine volume × urine Cr)/(serum Cr × 1,440)] × (1.73 m²/body surface). Schwartz CrC rate was calculated using the following formula: (height × k)/Cr, where height is calculated in centimetres, k = 0.44 for children under two years old and 0.55 for children over two years, and Cr is serum creatinine. Blood and urine samples were obtained 2.8 days (range, 1 to 6 days) after admission to the PICU. Serum and urine creatinine levels were measured using standard laboratory methods. Renal dysfunction was defined as CrC or as CrC estimation by Schwartz less than 80 ml/minute per 1.73 m². Serum cystatin C and B2M levels were determined by endpoint nephelometry in a BN-II device (Dade Behring Marburg GmbH, Marburg, Germany).

Statistical analysis was performed using SPSS 11.0 (SPSS Inc., Chicago, IL, USA) and EPIDAT 3.0 (Xunta de Galicia, Galicia, Spain, and World Health Organization, 2003) for Windows. Data are expressed as a mean value and 95% confidence interval (CI) unless indicated otherwise. Inverses of Cr, cystatin C, and B2M were correlated with CrC and with Schwartz. We used the inverses of creatinine, cystatin C, and B2M to obtain a direct correlation with CrC and Schwartz formula. Correlations between age and CrC, Schwartz, creatinine, cystatin C, and B2M were performed. The diagnostic value of Cr, cystatin C, and B2M for identifying CrC or Schwartz less than 80 ml/minute per 1.73 m² was evaluated using receiver operating characteristic (ROC) curve analysis. Sensitivity, specificity, and positive likelihood ratio were calculated. A p value of less than 0.05 was considered statistically significant. Each patient's determinations were made with the informed consent of their parents.

The mean age was 2.9 years (95% CI, 1.4 to 4.3 years) with a range of 0.1 to 13.9 years and a median of 1.3 years. Male/female ratio was 1.27:1. Mean height was 86.3 cm (range, 53.0 to 151.0 cm). Mean body surface area was 0.5 m² (range, 0.2 to 1.5 m²). Mean paediatric risk of mortality (PRISM) [20] (standard deviation [SD]) scores 24 hours after admission were 15.0 (11.3). The patients' clinical conditions and the treatments they received are summarized in Table 1.

The mean CrC was 76.3 ml/minute per 1.73 m² (95% CI, 58.4 to 94.1 ml/minute per 1.73 m²) and the mean Schwartz was 104.5 ml/minute per 1.73 m² (95% CI, 88.3 to 120.8 ml/minute per 1.73 m²). The mean serum Cr concentration was 0.42 mg/dl (95% CI, 0.36 to 0.48 mg/dl), the mean serum cystatin C concentration was 0.69 mg/l (95% CI, 0.57 to 0.81 mg/l), and the mean serum B2M concentration was 2.12 mg/l (95% CI, 1.66 to 2.57 mg/l). There were no significant differences between male and female regarding CrC (79.9 versus 71.7 ml/minute per 1.73 m²), Schwartz (103.7 versus 105.5 ml/minute per 1.73 m²), serum Cr (0.43 versus 0.42 mg/dl), serum cystatin C (0.65 versus 0.75 mg/l), and serum B2M (2.23 versus 1.97 mg/l).

Fourteen out of the 25 patients enrolled in the study (56.0%) had a CrC less than 80 ml/minute per 1.73 m², and 9 patients (36%) had a Schwartz less than 80 ml/minute per 1.73 m². CrC, Schwartz, serum Cr, serum cystatin C, and serum B2M values are listed in Table 2, separating patients in two groups: renal dysfunction (CrC less than 80 ml/minute per 1.73 m²) and normal renal function. Schwartz, CrC, serum Cr, serum cystatin C, and serum B2M are listed in Table 3, separating patients in two groups: renal dysfunction (Schwartz less than 80 ml/minute per 1.73 m²) and normal renal function.

Mean PRISM (SD) scores were 13.5 (14.5) in the group with CrC less than 80 ml/minute per 1.73 m² and 10.2 (5.1) in the group with CrC greater than 80 ml/minute per 1.73 m² (differences not significant [NS]). Mean PRISM (SD) scores were 15.9 (16.5) in the group with Schwartz less than 80 ml/minute per 1.73 m² and 9.6 (5.7) in the group with Schwartz greater than 80 ml/minute per 1.73 m² (differences NS).

The correlation with CrC was better for the inverse of serum B2M (r = 0.477, p < 0.05) than for the inverse of cystatin C (r = 0.390, p = 0.054). The inverse of Cr showed the worse correlation with CrC (r = 0.104, differences NS). The correlation with Schwartz was also better for the inverse of serum B2M (r = 0.697, p < 0.01) than for the inverse of cystatin C (r = 0.586, p < 0.01). The inverse of Cr showed the worse correlation with Schwartz (r = 0.442, p < 0.05).

Patient age in the renal dysfunction group was significantly lower than in the normal renal function group, 1.6 years (95% CI, 0.3 to 2.8 years) versus 4.7 years (95% CI, 1.8 to 7.5 years) if GFR was estimated with CrC and 0.9 years (95% CI, 0.3 to 1.5 years) versus 4.1 years (95% CI, 1.9 to 6.2 years) if GFR was estimated with Schwartz. Age had a lineal correlation with CrC (r = 0.42, p < 0.05), Schwartz (r = 0.41, p < 0.05), and Cr (r = 0.54, p < 0.01), but not with cystatin C (r = 0.10, differences NS) and B2M (r = 0.23, differences NS).

ROC curves for detecting renal dysfunction are shown in Figures 1 and 2. To diagnose CrC less than 80 ml/minute per 1.73 m², the areas under the curve were 0.633 (95% CI, 0.403 to 0.863) for serum Cr, 0.851 (95% CI, 0.698 to 1.003) for serum cystatin C, and 0.802 (95% CI, 0.628 to 0.976) for serum B2M. To diagnose Schwartz less than 80 ml/minute per 1.73 m², the areas under the curve were 0.625 (95% CI, 0.403 to 0.847) for serum Cr, 0.792 (95% CI, 0.598 to 0.986) for serum cystatin C, and 0.799 (95% CI, 0.622 to 0.976) for serum B2M.

The diagnosis efficacy of each marker we studied to detect renal dysfunction is shown in Tables 4 and 5. For each variable, the cutoff level with best sensitivity and specificity was chosen.

Gold standard techniques to assess GFR are based on exogenous substance clearance (inulin, iodine 125-iothalamate, technetium 99m-DTPA [diethylenetriaminepentaacetic acid], chromium 51-EDTA [ethylenediaminetetraacetic acid], ...) [1‐4, 21]. However, these methods are difficult to apply in clinical practice [1, 3, 7, 10, 13, 14, 21, 22]. We chose CrC and Schwartz formula as gold standards because they are commonly used in clinical practice. Because urine collection technique during 24 hours is a limiting factor in children, we included only those children who had a bladder catheter in place. Serum Cr level is frequently used in daily practice [2, 4, 5, 7, 8]. However, only two criteria of an ideal GFR marker are accomplished by serum Cr: endogenous substance and free glomerular filtration [11]. Serum Cr level is affected by circumstances other than renal ones [2, 4, 9‐12, 21] and it is secreted by the renal tubules [2, 4, 10, 13]. This leads to an overestimation of GFR, especially when a moderate GFR descent is present [1, 2, 4, 5, 13, 21]. Serum Cr could not detect renal failure until GFR decreases more than 50% [10, 12]. Our results showed that serum Cr levels were not statistically different in the groups with a level higher or lower than 80 ml/minute per 1.73 m², confirming the low sensitivity of serum Cr to detect renal dysfunction. In critically ill children, there would be a muscle loss and a relative malnutrition; in these cases, serum Cr could also indicate GFR values higher than the actual levels [2, 10, 12, 23].

Cystatin C and B2M are low-molecular-weight proteins produced by all nucleated cells at a constant rate [1, 2, 4‐6, 8, 9, 11‐14, 18, 24]. They are freely filtered by the glomerulus and reabsorbed and catabolized by proximal tubular cells [2, 4‐6, 8, 9, 11‐14, 18, 23, 24]. Therefore, their serum values could be a better marker of GFR than serum Cr level [1, 6, 24].

The molecular weight of cystatin C is 13.3 kDa [1, 2, 4, 5, 8, 9, 11, 14, 18, 22, 24]. Its concentration is more dependent on renal function in comparison with serum Cr [1, 14, 21, 23]. However, some authors found that serum cystatin C concentration could increase in hyperthyroidism or in patients who are receiving corticosteroids [3, 8, 11, 18, 21, 23], although other studies did not find this association [1, 15, 25].

The molecular weight of B2M is 11.8 kDa [6, 22]. It is not influenced by age [5, 17], gender, or muscle mass [12, 19]. However, unlike production of cystatin C, that of B2M increases in infectious or inflammatory process, proliferative syndromes, and hepatic and autoimmune illnesses [1, 5, 6, 12, 26].

Several studies have demonstrated the capacity of cystatin C to estimate GFR [8, 9, 11, 13, 14, 18, 19, 24] and that its ability to detect moderate acute kidney injury was better than that of Cr [1, 5, 6, 8, 13, 19, 23, 24]. Cystatin C values will be abnormally high when GFR decreases to 88 to 95 ml/minute per 1.73 m² [6, 13, 19]. Therefore, cystatin C could detect renal dysfunction one to two days before Cr [8]. Cystatin C was also superior to Cr in children and patients with muscle loss [5, 14, 18]. Recent studies have developed formulas that include cystatin C [15, 16]. Some of them also include serum Cr and other factors like age, weight, and height, improving diagnostic accuracy. Other authors have shown that parameters such as urinary neutrophil gelatinase-associated lipocalin and interleukin-18 were superior to serum Cr for acute kidney injury diagnosis [27‐29]. However, new evaluations will be needed. B2M also increases before Cr [12, 19]. Some studies found B2M to be less adequate than cystatin C as a GFR marker [18, 24, 26], but one other did not show any differences [6].

It has been demonstrated that low-molecular-weight proteins have greater diagnostic sensitivity than serum Cr in children [17, 25] and critically ill adults [7, 9, 23]. However, to date, no studies have been performed in critically ill children.

We found CrC less than 80 ml/minute per 1.73 m² in 56% and Schwartz less than 80 ml/minute per 1.73 m² in 37.5% of the cases, similar to other studies with critically ill patients [7, 9]. Patients with CrC less than 80 ml/minute per 1.73 m² and with Schwartz less than 80 ml/minute per 1.73 m² were younger than patients with normal renal function. Like previous studies [1, 12, 17‐19, 25], we did not find gender differences in cystatin C and B2M levels.

As shown in Figures 1 and 2, we found that the capacities of cystatin C and B2M to detect acute kidney injury were better than that of serum Cr. Filler and colleagues [17] obtained similar results to detect patients with GFR less than 90 ml/minute per 1.73 m² in 225 children with different chronic renal diseases; the areas under the ROC curve were 0.840, 0.943, and 0.899 for serum Cr, cystatin C, and B2M, respectively. Our study showed worse figures for serum Cr, with areas under the ROC curve of 0.633 and 0.625. The probable explanation is that our patients were critically ill. In these patients, serum Cr demonstrated an insufficient sensibility to detect early acute kidney injury. Hoste and colleagues [7] and Delanaye and colleagues [23] found normal levels of serum Cr in critically ill adults when 46.4% and 42% of them, respectively, had CrC less than 80 ml/minute per 1.73 m². Villa and colleagues [9] and Delanaye and colleagues [23] found a better correlation of CrC with the inverse of cystatin C than with the inverse of Cr (r = 0.832 versus 0.426 and r = 0.68 versus 0.4, respectively). They also found a higher cystatin C sensitivity to detect CrC less than 80 ml/minute per 1.73 m² (areas under the ROC curve, 0.927 versus 0.694 and 0.833 versus 0.789, respectively). Le Bricon and colleagues [14] found the same results in critically ill adults.

In critically ill children, early diagnosis of renal impairment is very important for making therapeutic decisions [3, 7, 9]. Therefore, we tried to determine the best marker to detect CrC and Schwartz less than 80 ml/minute 1.73 m². Cystatin C and B2M had a better area under the ROC curve than Cr. Cystatin C and B2M had better diagnostic efficiency values than Cr (Tables 4 and 5). As previously shown in other groups of patients [5], in our experience serum cystatin C and B2M are better markers than serum Cr to detect acute kidney injury in critically ill children. One possible explanation is that GFR in critically ill children can change rapidly, but changes in serum Cr take more time.

We obtained cutoff values to differentiate patients with CrC and with Schwartz less than 80 ml/minute 1.73 m² that were considered normal in previous studies [5, 11, 17, 18, 30]. A possible explanation was the early determination of the biological markers at the beginning of renal dysfunction. Longitudinal assessment of GFR markers over a period of time will be useful to determine their value for the early diagnosis of GFR decrease.

Patients with CrC and Schwartz less than 80 ml/minute 1.73 m² were younger. Age correlates with Cr but not with cystatin C and B2M. Therefore, age did not influence the higher cystatin C concentration found in patients with low CrC or low Schwartz.

Our study has limitations. The main problem is the 'gold standard' against which low-molecular-weight proteins can be calibrated. CrC using a 24-hour urine sample and Schwartz formula based on serum Cr and height were considered the gold standard because, despite the controversy, they are used in clinical practice. Another limitation of our study was the size of the sample and the difference in the ages of the patients. Because of the small size of the sample, we cannot compare children older than one year and those younger than one year.

In our experience, serum cystatin C and B2M were confirmed as simple and useful markers, better than serum Cr, to detect acute kidney injury in critically ill children. However, new studies with a bigger sample of patients and more accurate gold standards to use for comparisons will be necessary to establish cystatin C or B2M as biochemical markers for monitoring GFR in unstable critically ill children.