Acute kidney injury (AKI) is a syndrome of sudden organ damage, often secondary to other primary diseases. The early stage of injury itself is not always associated with obvious organ dysfunction, which makes diagnosis challenging. Unfortunately, even a mild, subclinical kidney injury can lead to severe consequences, such as acute kidney failure or chronic kidney disease (12). This condition, underestimated in horses in the past, is quite common, especially in patients undergoing intensive care (6, 19). The most common causes of AKI in horses are haemodynamic changes (dehydration or hypovolaemia), endotoxaemia or systemic inflammatory response syndrome, and the use of potentially nephrotoxic drugs (especially aminoglycosides and nonsteroidal anti-inflammatory drugs – NSAIDs) (1, 11, 25). Since the early stages of AKI do not give specific clinical signs and manifest only in exacerbation of the primary disease, non-specific urinary abnormalities and slight to no change in ultrasound, there is a need to identify sensitive and specific biomarkers of this condition (22). Currently, the diagnosis is mainly based on detection of an increase in the serum creatinine concentration, which occurs relatively late in the AKI process and is dependent on many non-renal factors. In human medicine, many serum and urinary biomarkers are used to detect AKI. These include dysfunction and injury biomarkers such as cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) (30). In equine medicine such biomarkers are not in widespread use, and in the
literature there are only limited studies which investigated cystatin C and NGAL for evaluation of renal function in horses (1, 9, 27).
The main goal of this study was to report and compare the concentrations of serum and urinary cystatin C and NGAL in healthy horses, horses at risk of AKI and horses with clinical AKI. The secondary goal was to assess the relationship between these and more conventional renal dysfunction biomarkers such as serum creatinine and urea, urinary protein, the gamma-glutamyl transpeptidase (GGT) to creatinine ratio, and fractional excretion of sodium (FENa). Additionally, this research sought to establish which biomarkers could be used to detect AKI and examine how potentially nephrotoxic factors such as gastrointestinal diseases and drugs affect the kidneys.
For this investigation, samples from a previously published study were used. A detailed description of the study design, group constitution and additional results was provided by Siwińska
Evaluation of NGAL and cystatin C from frozen serum and urine samples was undertaken in the Department of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine of the Wroclaw University of Environmental and Life Sciences, Poland. Following thawing, the samples were mixed thoroughly and centrifuged briefly. Undiluted serum and urine were used to measure NGAL (ng/mL) and cystatin C (mg/L) levels with commercially available ELISA kits (MyBioSource, USA, catalogue numbers MBS087573 and MBS022947), according to the manufacturer’s instructions. These kits were developed and validated by the manufacturer for use with serum and urine samples of equine origin. The plates were washed with an ELx50 Automatic Plate Washer (BioTek Instruments, USA), and the absorbance was assessed with a Multiskan EX photometer (Thermo Scientific, USA). For each measurement, the 620 nm background absorbance was subtracted from the 450 nm absorbance, and a four-parameter curve fitting was employed to calculate the analyte concentration. All measurements were performed in duplicate.
The results concerning basic blood and urinary parameters were previously published by Siwińska
Concentration of serum and urinary cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) measured in healthy horses (non-acute kidney injury (AKI) group), horses at risk of acute kidney injury (AKI-risk group; divided into colic sufferers, recipients of nonsteroidal anti-inflammatory drugs (NSAIDs) and recipients of gentamicin) and horses diagnosed with acute kidney injury (AKI group)
AKI-risk group (n = 30) | |||||||||||||
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Parameter | Non-AKI group (n = 30) Colic (n = 10) | NSAIDS (n = 10) | Gentamicin (n = 10) | All | AKI | group (n = 11) | |||||||
Min–max | Me (Q1– n’ Q3) | Min–max | Me (Q1– n’ Q3) | Min–max | Me (Q1– n’ Q3) | Min–max | Me (Q1– n’ Q3) | Min–max | Me (Q1–Q3) n’ | Min–max | Me (Q1–Q3) n’ | ||
NGAL | Serum | 25.00– 95.20 | 50.50 (38.80– 0 58.80) | 30.70– 201.90 | 73.00 (54.50– 3 129.70) | 27.20– 74.20 | 45.80 (33.70– 0 61.10) | 31.10–91.20 | 48.30 (40.40– 0 57.30) | 27.20– 201.90 | 51.10 (40.40– 3 66.90) | 50.60– 277.60 | 98.10 (59.40– 6 128.20) |
(ng/mL) | Urine | 8.50– 41.70 | 20.70 (17.90– 4 24.50) | 12.90– 112.10 | 53.40 (31.10– 7 64.20) | 18.80– 59.80 | 30.20 (23.10– 3 47.80) | 12.80–60.90 | 29.80 (25.20– 2 33.00) | 12.80– 112.10 | 32.30 (23.70– 12 55.80) | 19.10– 223.00 | 36.60 (26.80– 7 89.90) |
Cystatin | Serum C | 0.13–0.71 | 0.25 (0.19– 2 0.37) | 0.09–1.01 | 0.36 (0.19– 3 0.60) | 0.08–0.40 | 0.24 (0.15– 0 0.26) | 0.06–0.55 | 0.19 (0.13– 1 0.26) | 0.06–1.01 | 0.23 (0.15– 0.37) 4 | 0.07–1.71 | 0.61 (0.37– 7 1.13) |
(mg/L) | Urine | 0.06–0.50 | 0.10 (0.07– 2 0.13) | 0.02–0.43 | 0.25 (0.10– 5 0.35) | 0.07–0.19 | 0.13 (0.12– 0 0.13) | 0.05–0.34 | 0.14 (0.08– 1 0.19) | 0.02–0.43 | 0.13 (0.10– 6 0.19) | 0.10–0.50 | 0.34 (0.22– 9 0.37) |
Me – median; Q1 – first quartile; Q3 – third quartile; S – serum; U – urine; n’ – number of horses with elevated parameter above cut-off value
The correlations between NGAL/cystatin C and conventional serum/urine biomarkers of renal dysfunction are presented in Table 3. Only in the case of urinary cystatin C was there a low positive correlation with serum creatinine. A low correlation with serum urea was demonstrated by serum NGAL and serum and urinary cystatin C. Urinary cystatin C and NGAL also showed a low positive correlation with urine protein. All tested biomarkers presented low positive correlations with the GGT to creatinine ratio, except for serum cystatin C. Urinary NGAL was the only biomarker which revealed a low positive correlation with FENa.
Significant differences in serum and urine biomarkers between healthy horses (non-acute kidney injury (AKI) group), horses at risk of kidney injury (AKI-risk group; divided into colic sufferers, recipients of nonsteroidal anti-inflammatory drugs (NSAIDs) and recipients of gentamicin) and horses diagnosed with acute kidney injury (AKI group)
Parameter | Non-AKI |
AKI-risk colic |
AKI-risk NSAIDs |
AKI-risk gentamicin |
||||
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AKI | Non-AKI | AKI | Non-AKI | AKI | Non-AKI | AKI | ||
NGAL (ng/mL) | Serum | 0.0030 | - | - | - | 0.0030 | - | 0.0200 |
Urine | 0.0050 | 0.0050 | - | - | - | - | - | |
Cystatin C (mg/L) | Serum | 0.0400 | - | - | - | 0.0400 | - | 0.0200 |
Urine | 0.0001 | 0.0400 | - | - | 0.0400 | - | 0.0300 |
NGAL – neutrophil gelatinase-associated lipocalin
Table 4 and Figs 3 and 4 contain the results of the ROC analysis of the concentration of NGAL and cystatin C to detect acute kidney dysfunction in the examined horses.
Spearman’s correlation between the analysed biomarkers and selected conventional renal dysfunction biomarkers
Parameter | NGAL | Cystatin C | |||
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Serum | Urine | Serum | Urine | ||
Serum | Urea | rs = 0.360 | NS | rs = 0.300 | rs = 0.340 |
P = 0.002 | P = 0.014 | P = 0.004 | |||
Creatinine | NS | NS | NS | rs = 0.300 | |
P = 0.013 | |||||
Urine | Protein | NS | rs = 0.360 | NS | rs = 0.400 |
P < 0.005 | P < 0.001 | ||||
GGT : Creatinine ratio | rs = 0.300 | rs = 0.390 | NS | rs = 0.370 | |
P = 0.012 | P < 0.001 | P < 0.005 | |||
FENa | NS | rs = 0.33 | NS | NS | |
P = 0.005 |
NGAL – neutrophil gelatinase-associated lipocalin; rs – Spearman’s correlation coefficient; GGT – Gamma-glutamyltransferase; FENa – Fractional sodium excretion; NS – statistically nonsignificant
The receiver operating characteristic (ROC) analysis of serum and urinary cystatin C and neutrophil gelatinase-associated lipocalin (NGAL) relative to kidney dysfunction in horses
Parameter | Cut-off value | Sensitivity | Specificity | Positive predictive value | Negative predictive value | AUC | |
---|---|---|---|---|---|---|---|
NGAL | Serum | 95.20 | 0.54 | 0.93 | 0.60 | 0.92 | 0.73 |
Urine | 33.10 | 0.64 | 0.71 | 0.30 | 0.90 | 0.66 | |
Cystatin C | Serum | 0.53 | 0.64 | 0.85 | 0.44 | 0.93 | 0.67 |
Urine | 0.20 | 0.82 | 0.85 | 0.50 | 0.96 | 0.84 |
AUC – area under the ROC
The best cut-off values for the evaluated biomarkers were 95.2 for serum NGAL, 33.1 for urinary NGAL, 0.53 for serum cystatin C, and 0.2 for urinary cystatin C. The highest sensitivity for the detection of AKI was demonstrated by urinary cystatin C and the highest specificity was shown by serum NGAL. All biomarkers proved more effective in detecting negative rather than positive results. The best ability to distinguish between normal and abnormal results was demonstrated by urinary cystatin C, whereas in the case of serum NGAL this ability was fair, and for serum cystatin C and urine NGAL it was moderate.
The conducted study presents the results of serum and urine cystatin C and serum and urine NGAL measured in healthy horses, horses at risk of AKI, and horses with AKI. To the authors’ knowledge, this is the first study assessing NGAL and cystatin C in preclinical and clinical AKI in horses. The authors also assessed how selected biomarker concentrations corresponded to the concentrations of the more conventional biomarkers used as a standard indicator of renal function. The few current reports on new renal biomarkers in equine medicine focus mainly on serum biomarkers, while the present study assessed selected biomarkers in equine urine.
Neutrophil gelatinase-associated lipocalin is a small extracellular protein molecule the expression of which is rapidly induced in the nephron in response to renal epithelial hypoxia, injury and inflammation (13). Increased NGAL concentrations are seen in human patients with suspicion of AKI (14, 24). In horses, NGAL was identified in postmortem specimens of laminitic hoof lamellar tissue, necrotic cecum, inflamed salivary glands and wounds (3, 10). So far, there are only two reports on serum NGAL concentration in healthy horses and horses with renal problems (9, 27). Compared to the serum NGAL concentration in healthy horses reported by Jacobsen
Increased urinary NGAL, in contrast to serum NGAL, indicates inadequate renal reabsorption ability (21). Since there are no published reference concentrations for urinary NGAL in horses, the results of this study were compared to those in the human medical literature. The urinary NGAL median concentration in non-AKI horses was similar to that recorded for humans, but the maximum values are lower (20). Interestingly, a few healthy horses had a urinary NGAL concentration above the cut-off value. In the AKI-risk group, the NGAL concentration was lower than those observed in people at risk of AKI (20). However, in colic horses urinary NGAL concentration was higher than in healthy horses, but the maximum concentration in this subgroup did not reach the values of the AKI group. This result can be compared to those in humans, where lower urinary NGAL values are observed in individuals at risk than in patients with clinical AKI (20). It can be concluded that urinary NGAL concentration increases with the transition of the renal disease from subclinical to clinical. Similarly to the other groups, urinary NGAL concentrations in AKI horses were lower than those reported in humans and their maximum concentrations did not reach human sufferer levels (20). Only seven AKI horses showed urinary NGAL concentration above the cut-off value. In humans, not all patients with clinical AKI had elevated NGAL urinary concentration, patients with stage 3 AKI having lower NGAL concentrations than those with stages 1 and 2 (20). This implies that urinary NGAL is elevated during early kidney disease and decreases with disease progression. This may also explain the lack of correlation between serum creatinine/urea and NGAL. In the examined equine subjects, there were horses with urinary NGAL above and serum NGAL below the cut-off value. It is possible that the concentration of NGAL increases in urine before it does in serum. Urinary NGAL showed greater sensitivity than the serum NGAL and the values obtained in the ROC analysis of this parameter are very similar to those obtained in humans (20).
Cystatin C is a protease inhibitor that is expressed in all nucleated cells and is excreted exclusively by the kidneys. Its concentrations are closely related to renal function (7) and AKI is predicted by elevated plasma cystatin C levels in critically ill patients (8). Only one study has researched cystatin C in horses (1). Our research documented serum cystatin C concentrations in the non-AKI group similar to those recorded in dogs and cats (2, 16, 17). In the group of AKI-risk horses, serum cystatin C concentrations were no different from those in non-AKI horses. There were individuals with serum cystatin C concentration above the cut-off value. The highest concentration of serum cystatin C was achieved in the AKI horse group; however, while being the highest in the study, the reported concentrations in AKI horses were lower than those determined for other species with clinical renal disease, except cats (17). As in the case of NGAL, only some horses from this group showed values of this parameter above the cut-off value. Similar observations were made by Braun
Cystatin C is present in very negligible amounts in normal urine (15) and urinary concentrations of this protein for all examined horses in previous research were similar to the normal human range (15). In the AKI-risk group, five colic horses had urinary cystatin C concentrations above the cut-off value and in this subgroup this parameter was higher than in healthy horses. This may indicate the detection of early AKI in this group. In the AKI group of horses, as in the case of serum NGAL and cystatin C, urinary cystatin C concentration was also the highest. Nine horses from this group had urine cystatin C values above the cut-off value. That elevated values were not common to all horses may be due to the different advancement of the renal dysfunction process in different individuals, as observed in humans (15). In our study, a correlation between cystatin C and serum creatinine was observed. Of all the tested biomarkers, urinary cystatin C had the highest sensitivity and diagnostic power.
Potential nephrotoxic side effects from colic and administration of nephrotoxic drugs are well documented in horses (1, 11, 26). In the AKI-risk group, an increase in tested biomarkers was observed mainly in colic horses. An increase in several biomarkers in this group may indicate the occurrence of kidney dysfunction or organ injury. Since gastrointestinal diseases are associated with a higher number of changes in the animal – haemodynamic changes, endotoxemia and systematic inflammatory response syndrome – they have a potentially more significant negative impact on renal function (28). In horses receiving potentially nephrotoxic drugs, no changes in the novel biomarker were seen, compared to healthy horses. Complications associated with the use of nephrotoxic medication have been observed mainly in foals, young horses and horses with dehydration or endotoxaemia (5).
One of the study limitations was that the animals selected for the study were not homogeneous with respect to AKI aetiology or pathogenesis. This could influence the results of biomarker assays. However, under clinical conditions, AKI is polyaetiological in many patients (12). AKI itself may be associated with independent kidney injury with or without dysfunction. Moreover, a variety of biomarkers assess organ function and the degree of tissue damage. An optimally reliable predictive score for AKI may include a panel of different biomarkers rather than a single indicator. However, more research into the expression of selected biomarkers both in healthy and diseased horses is needed before they can be routinely used in practice. The second limitation of the study was the lack of renal histology, which would have allowed an assessment of the real degree of kidney injury in the examined horses. Due to the lack of available alternatives, serum creatinine was used as the gold standard to evaluate kidney function. Unfortunately, serum creatinine concentration is not an indicator capable of completely ruling out early AKI. The next limitation of the study was that biomarker concentrations were assessed only once. Each biomarker has its own concentration versus time curve. Finally, the storage of biological material, freezing or centrifugation of the sample may have affected the levels of the selected biomarkers. Due to the lack of other possibilities, the authors decided to use commercially available validated tests. The next interesting step would be to perform NGAL analyses with two different tests: those used by the authors and the ones used in the previous publications referred to. More research is needed to validate cystatin C and NGAL levels as biomarkers in horses at different stages of kidney disease progression.
In conclusion, in this study, horses with AKI had a higher median concentration of all biomarkers compared to healthy horses. None of the single selected biomarkers recognised azotaemia in all affected horses. In every study group there were individuals with values below and above the cut-off value, however the urinary NGAL and cystatin C concentrations were higher in AKI-risk horses with colic compared to healthy ones, which indicates that those parameters may be suitable for the detection of subclinical AKI. Gastrointestinal diseases had a greater impact on the changes in selected biomarkers, and thus in the kidneys. Since primary diseases can affect these biomarker concentrations, their use for recognising AKI may be limited. Urinary cystatin C showed the greatest diagnostic power as well as high sensitivity and specificity, which recommends further research be undertaken on this biomarker in horses. The obtained results indicate the need to create a serum and urinary biomarker panel to detect AKI instead of using a single selected biomarker.