Printer Friendly

Toward noninvasive diagnosis of IgA nephropathy: a pilot urinary metabolomic and proteomic study.

1. Introduction

Diagnosis of many kidney diseases and assessment of the severity of renal injury currently requires a renal biopsy for examination of the histological features. Although renal biopsy entails a risk of morbidity due to bleeding complications [1, 2], it is currently the only tool for reliable diagnosis of glomerular diseases. Therefore, noninvasive tests based on analysis of serum or urine specimens are needed [36]. Ideally, such a test would enable monitoring of disease progression and assessment of responses to treatment [7]. Efforts in this direction have identified clinical and molecular biomarkers capable of predicting outcomes in chronic kidney diseases; yet their introduction into clinical practice remains a challenge [8-10].

In this study, we assessed the utility of several analytical techniques to identify urinary compounds that are differentially present in the urine samples from patients with IgA nephropathy (IgAN) versus renal-disease controls and healthy controls. The tested markers included urinary proteins and low-molecular-mass compounds [11], such as products of oxidative stress formed during oxidative damage of phospholipids, proteins, and nucleic acids. The panel of biomarkers was selected based on data from our mass spectrometric untargeted metabolomics profiling and targeted proteomic analysis, using available database and software solutions. Our statistical approaches using ANOVA eliminated analytes that have not statistically contributed to the separation of the groups with p < 0.05. The panel of biomarkers was selected from all tested analytes based on the capacity of various combinations to differentiate the tested samples into three groups: healthy controls, patients with IgAN, and disease controls.

2. Materials and Methods

2.1. Urine Samples. Spot urine samples were collected from 19 healthy controls and 19 patients with biopsy-proven IgAN or non-IgAN renal disease. Samples from the patients with kidney diseases were collected on the day of renal biopsy, before the biopsy was performed. The urine samples were stored in aliquots at -80[degrees]C until assayed. Clinical and laboratory data for patients with biopsy-proven nephropathy [IgAN, membranous nephropathy, lupus nephritis, antineutrophilic cytoplasmic antibody (ANCA) vasculitis-associated kidney disease, and diabetic nephropathy] are summarized in Table 1. The study was approved by the Ethics Committee of the General Teaching Hospital in Prague, Czech Republic. Written informed consent was obtained from all participants.

2.2. Determination of Protein Biomarkers: Immunomagnetic Isolation Followed by MALDI-TOF MS Analysis

2.2.1. Immunomagnetic Isolation. We followed our previously published protocol [12] with the antibodies detailed below. Candidate urinary biomarkers [6, 11] were isolated by using polyclonal affinity-purified antibodies specific for human proteins IL-6, IL-8, IgA, IgA-uromodulin complex, monocyte chemotactic protein-1 (MCP-1), epidermal growth factor (EGF), [alpha]1-antitrypsin, LG3 fragment of endorepellin, soluble transferrin receptor, tumstatin, endostatin, and heparan sulfate (purchased from Antibody Technology Inc.; MALDI matrix 1,2-dimethoxy-4-hydroxycinnamic (sinapinic acid) and other chemicals were purchased from Sigma-Aldrich (St. Louis, MO, USA) and chemical solvents were purchased from Merck (Darmstadt, Germany).


Buffer A: 0.1 M sodium-phosphate buffer pH 7.4.

Buffer B: phosphate-buffered saline (PBS) pH 7.4 with 0.1% (w/v) bovine serum albumin (BSA).

Buffer C: 0.2 M Tris pH 8.5 with 0.1% (w/v) BSA.

Buffer D: 100 mM glycine (pH 2.5).

Dynabeads[R] M-280, tosyl-activated superparamagnetic polystyrene beads coated with polyurethane, were washed twice in Buffer A to remove sodium azide (NaN3) using magnetic particle concentrator following the manufacturer's protocol (Thermo Fisher Scientific, Waltham, MA, USA). Antibodies listed above (500 [micro]g each) were dissolved in 100 [micro]L of Buffer A and added to 100 [micro]L suspension of Dynabeads, mixed for 1min, followed by 24-hour incubation at 37[degrees]C with mixing. Then, the supernatant was removed and the particles were washed twice with Buffer B (500 [micro]L) at 4[degrees]C. Free tosyl groups on the beads were blocked with Buffer C (500 [micro]L; 4 h, 37[degrees]C), followed by washing with Buffer B (500 [micro]L; 5 min, 4[degrees]C).

Each individual preparation of the antibody-coated magnetic beads was resuspended in a 0.5 mL aliquot of a urine sample and incubated with shaking for 1 h at 37[degrees]C. The supernatants were then removed and the beads were washed five times with Buffer B (500 [micro]L; 4[degrees]C, 5 min, vortexing). The captured antigens were eluted with Buffer D (50 [micro]L; 4[degrees]C, 1 min, vortexing) and the beads were magnetically separated. The eluates were desalted using C18 ZipTip (EMD Millipore, Billerica, MA, USA) before analysis by matrix-assisted laser-desorption ionization-time-of-flight mass spectrometry (MALDI-TOF MS). The beads were washed five times with Buffer B (500 [micro]L-4[degrees]C, 5 min, vortexing) and then resuspended in 500 [micro]L of Buffer A before the next immunomagnetic separation.

2.2.2. MALDI-TOF MS Analysis. MALDI-TOF MS data were acquired on Autoflex mass spectrometer (Bruker Daltonics, Germany) with MALDI sample target (600 [micro]m Chip[TM]; Bruker Daltonics). Ionization was achieved by irradiation with a nitrogen laser (337 nm) operating at 4 Hz. Ions were accelerated at 20 kV with 250 ns of pulsed ion extraction delay. Each spectrum was detected in linear positive mode and externally calibrated using a mixture of peptide/protein standards. Freshly prepared 1,2-dimethoxy-4-hydroxycinnamic acid was used as matrix (10 mg/mL) in 50% acetonitrile 0.1% (v/v) of trifluoroacetic acid. The instrument's parameters and laser energy were kept constant during a series of experiments performed on the same day for the comparison of intensity values (cps).

The urinary protein candidate biomarkers were analyzed by MALDI-TOF MS using several different concentrations of samples to determine the linearity and detection limit. Standard proteins were also analyzed using several different concentrations. The protonated molecular ion peak (MH+) for each protein was detectable to a sub-pmol level with a signalto-noise ratio >50. This detection limit was comparable with immunochemical assays. MALDI-TOF MS is a semiquantitative method; however, using rigorous sample preparation and the data acquisition method, the intensity of the MH+ peak(s) increased linearly with increasing quantities of each protein from a nanomolar to picomolar range. Therefore, in this concentration range, the protein biomarkers could be analyzed in a quantitative manner.

The identification of galactose-deficient IgA1 in each urine sample was accomplished after derivatization of the immunoaffinity-isolated IgA1. Reducing-end labeling based on hydrazone-linkage enabled derivatization of the sample directly on MALDI target plates. For quantitative evaluation of selected ion candidates, molecular ions of derivatized monomeric IgA1, an in-house-developed software tool was used. Naturally galactose-deficient IgA1 protein purified from human plasma was used as a standard for calibration. Uromodulin-IgA complex (Antibody Technology Inc.) was used for calibration of the complex of IgA with uromodulin.

2.3. Antibody Microarrays. Custom-designed antibody microarrays were used to confirm MS data by comparing the relative content of different analytes in the samples. Polyclonal affinity-purified antibodies specific for human proteins IL-6, IL-8, IgA-uromodulin complex, MCP-1, EGF, a1-antitrypsin, LG3 fragment of endorepellin, soluble transferrin receptor, tumstatin, and endostatin were obtained from Antibody Technology Inc. The antibodies were spotted on the arrays using contact printing technology (NanoPrint[TM] 2, Arrayit Corp., Sunnyvale, CA, USA) under a controlled environment with advanced 3-axis linear drives, Warp2 controllers, and 0.5 [micro]m positional resolution. Each antibody was printed in triplicate. After the antibody spotting, the microarrays were blocked (5mL blocking buffer Arrayit; 3 x 5 min, room temperature, gently shaking) and washed with washing buffer (Arrayit; 5 mL, room temperature, 3 x 2 min). The design of the assay included fluorescent detection at 540 nm, based on using urine protein samples labeled with a green fluorescent dye, Cyanine 3. Briefly, the urine samples were desalted and concentrated and then labeled using a protein-labeling kit, following the manufacturer's instructions (Arrayit). The labeled samples were then diluted with 5 mL of reaction buffer (Arrayit) and added to the corresponding compartment of a microarray reaction tray. After 1-hour binding reactions (37[degrees]C, gently shaking), microarrays were washed using four wash cycles (3 min, 4 mL wash buffer per well). All preparation steps and the reactions with fluorescent reagents were carried out in the dark to prevent photobleaching. After the final wash, the microarrays were dried and images were acquired using a laser scanner (GenePix 4000B, 540 nm; Molecular Devices, LLC, Sunnyvale, CA, USA) and analyzed using GenePix[R] Pro software and Acuity[R] Microarray Informatics Software. The raw data were processed using an open-source software Rstudio ( with an incorporated limma package [13].

2.4. Analysis of Oxidative-Stress Biomarkers by Liquid Chromatography/Tandem Mass Spectrometry. Analysis of markers of oxidative stress was performed using liquid chromatography/mass spectrometry (LC-MS) system consisting of quaternary pump, Accela 600, Accela autosampler (Thermo Fisher Scientific) linked with a triple quadrupole mass spectrometer equipped with electrospray ionization (HESI) (TSQ Vantage, Thermo Fisher Scientific). To implement multimarker screening, we performed two types of analyses, one to detect compounds containing amino group(s) and the second to detect compounds with aldehyde and carboxylic groups. These two separate analyses used different conditions of derivatization reactions (acid versus alkaline environment) and the LC conditions (different composition of the mobile phase and different chromatographic columns). For the detection, tandem mass spectrometry was used, as detailed below.

2.4.1. Determination of Amino Compounds. The compounds with an amino group [(o-tyrosine (o-Tyr), 3-nitrotyrosine (3-N[O.sub.2]-Tyr), 3-chlorotyrosine (3-Cl-Tyr), 8-hydroxyguanosine (8-OHG), and 8-hydroxy-2'-deoxyguanosine (8-OHdG)] were derivatized using 3-aminopyridyl-N-hydroxysuccinimidyl carbamate (APDS). Deuterium-labeled analogues of the analytes served as standards. To 500 [micro]L of each urine sample supplemented with the deuterium-labeled standards, 450 [micro]L of borate buffer (pH 8.5) and 50 [micro]L of APDS derivatization agent (1 mg/mL, acetonitrile) were added. Derivatization reactions were carried out for 10 min at room temperature and then the samples were heated to 55[degrees] C, to decompose the excess of the derivatization agent. The sample was then subjected to liquid chromatography electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) analysis on a chromatographic column XTerra[R] MS (C18 50 x 1mm x 3.5 mm) (Waters, Republic of Ireland), using an isocratic elution method with a mobile phase consisting of acetonitrile :water (60 :40, v/v) with 0.1% formic acid. The temperature of the column was kept at 25[degrees]C and the flow rate was 150 [micro]L/min. Assay parameters were optimized for use in neutral-loss mode in the interval 250-500 Da (Q1) [right arrow] 130-380 Da (Q3) (Table 2) with collision-induced dissociation (CID) energy 15 eV in the negative electrospray ionization ([ESI.sup.-]) mode.

2.4.2. Determination of Aldehydes and Carboxylic Acids. Derivatization of aldehydes [n-aliphatic aldehydes (C6-C12), malondialdehyde (MDA), 4-hydroxynonenal (4-HNE), and 4-hydroxyhexenal (4-HHE)] and compounds with a carboxyl group in the structure [8-isoprostane (8-iso-[PGF.sub.2[alpha]]), cysteinyl leukotrienes C, D, and E (Cys-LTs), and leukotriene [B.sub.4] (LTB4)] was carried out using derivatization with Girard's reagent T (GirT) in the presence of N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride and N-hydroxysuccinimide. Deuterium-labeled analogues of the analytes served as standards. To a 100 [micro]L aliquot of each urine sample supplemented with the deuterium-labeled standards, 10 [micro]L of derivatization reagent GirT and 10 [micro]L of N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride together with 10 [micro]L sulfo-N-hydroxysuccinimide, 10 [micro]L of 1% hydrochloric acid, and 270 [micro]L of propan-2-ol were added. Derivatization proceeded for 30 min and the derivatized sample was immediately analyzed by LC-ESI-MS/MS. The chromatographic Thermo Hypercarb column (100 x 21 mm x 5 mm) with a Hypercarb precolumn (Thermo Fisher Scientific) was used with an isocratic elution (methanol : water (40 : 60, v/v) with pH adjusted with ammonium hydroxide to pH 9). The flow rate was 150 [micro]L/min. The column was kept at constant temperature 30[degrees]C, and 10 [micro]L volume of each sample was injected. Mass spectrometer parameters were capillary voltage 3,000 V, capillary inlet temperature 300[degrees]C, HESI evaporator temperature 300[degrees]C, sheath gas (nitrogen) pressure 45 psi, and auxiliary gas (nitrogen) 10 ArbU. Measurement parameters were optimized for the use in neutral-loss mode in the interval 150-750 Da (Q1) [right arrow] 91-691 Da (Q3) (Table 3) with CID energy 16.5 eV in the positive electrospray ionization (ESI+) mode.

2.5. Statistical Analyses

2.5.1. ANOVA. A one-way analysis of variance (ANOVA) was used to test whether two or more means were equal and whether the value of a single variable differed significantly among two or more levels of a factor and multiple observations at each level. In this study, the factor is "disease" at three levels: (1) healthy controls, (2) IgAN, and (3) non-IgAN renal disease. ANOVA statistical analysis was performed using Excel standard procedure for all 33 markers tested.

2.5.2. Cluster Analysis. Cluster analysis is an exploratory data analysis tool for identifying homogenous groups of objects called clusters [14]. Objects in a specific cluster share many characteristics but significantly differ in objects not belonging to this cluster. Each object should be characterized by the value of (experimental) variables (features, parameters). By selecting a specific clustering procedure, one determines how clusters are to be formed. There are many different clustering procedures and also many ways of classifying them. In this study, we used hierarchical agglomerative clustering. In this method, clusters are consecutively formed from objects. Initially, this type of procedure starts with each object representing an individual cluster. These clusters are then sequentially merged according to their similarity (or dissimilarity). As a measure of association between the objects (distance metrics), the Euclidean distance was used in this work. All calculations were done by program XLSTAT (

2.5.3. Discriminant Analysis. Discriminant analysis predicts a membership in a group or category based on observed values of several continuous variables [14]. Specifically, discriminant analysis predicts a classification X variable (i.e., three diagnoses) based on known continuous responses Y (i.e., 33 biomarkers). The data for a discriminant analysis consists of a sample of observations with known group membership together with their values on the continuous variables. In this study, we used discriminant analysis with transformed variables, the so-called principal components, to reduce the dimensionality of the problem and provide a better graphical view of the output. To verify the correct discriminant function, confusion matrix has been used, which resulted in classifying each of the objects in those categories. Another result of the discriminant analysis is a so-called confusion matrix that is actually a contingency table. It is possible to estimate selectivity and specificity of the biomarker test from the confusion matrix for two diagnoses. For samples from subjects with different diagnoses, it is possible to estimate accuracy of distribution of patients into three or more groups. Our suggestion is to calculate "partial" selectivity and specificity from the confusion matrix, that is, in this study, specificity and selectivity between groups 1 versus 2,1 versus 3, and 2 versus 3. For perfect distribution in our study, partial selectivity and/or specificity are equal to 1. Another advantage is that individual biomarker tests could have an unsatisfactory specificity (selectivity), but their combination can be satisfactory or excellent, as in our case. This is called a "synergic" effect. All calculations were done by program XLSTAT (

3. Results

In this pilot project, we assessed potential urinary biomarkers using a small cohort of subjects that included 19 patients with different renal diseases (IgAN, membranous nephropathy, lupus nephritis, ANCA vasculitis-associated kidney disease, and diabetic nephropathy; Table 1) and 19 healthy controls. We used three different experimental techniques (immunoaffinity-MALDI MS, protein-array, and LC-MS/MS analyses) for quantitative marker assessment. The testing of urinary samples included an untargeted analysis of low-molecular-mass metabolites using selective reaction monitoring LC-MS/MS with conditions detailed in Tables 2 and 3 and a targeted analysis of selected proteins and heparan sulfate [15-19].

Table 4 provides mean concentrations of all detected analytes in the urine samples from healthy controls (group 1, n = 19), patients with IgAN (group 2, n = 11), and patients with other kidney diseases (disease controls; group 3, n = 8). Analysis of variance (ANOVA) and ROC curve analysis indicated that no individual biomarker completely differentiated the three groups and, thus, we next assessed the utility of several markers combined into a panel of biomarkers.

We evaluated all variables within the three individual groups by ANOVA and found that the measured markers can be divided into two groups. The first group of markers differentiated subjects in group 1 (healthy controls) from subjects in group 2 (IgAN patients) and/or group 3 (disease controls). However, these markers did not differentiate group 2 (IgAN patients) from group 3 (disease controls) (Box 1).

The second group of markers differentiated the three groups of subjects from each other. Discriminant analysis revealed that these markers included three metabolites (dodecanal, 8-hydroxyguanosine, and leukotriene C4), three proteins (a1-antitrypsin, IgA-uromodulin complex, and galactose-deficient IgA1), and heparan sulfate (Box 2, Figure 1). The conclusion on the utility of these seven markers was reproduced after normalization to urinary creatinine concentration (Table 5, Figure 2).

4. Discussion

Recent expansion in knowledge of the complex nature of molecular interactions has led to a better understanding of the physiological and pathological processes necessary for better diagnostic tests and treatment of various diseases. Novel and more precise analytical instruments have facilitated identifying and measuring levels of not only new individual biological markers (biomarkers) but also assessing their complex interactions that define disease pathogenesis. Molecular biomarkers are now used across many disciplines. A biomarker can be any molecule, part of a molecule, or even a particular configuration that is both detectable and measurable, where the presence, amount, or another characteristic is indicative of a particular biological state. Most diagnostic tests have been based on a single biomarker or a combination of a few biomarkers, often leading to false-positive data. To minimize this problem, multiplexing of biomarkers (i.e., signatures or panels comprised of multiple components) is now used to improve sensitivity and specificity for the diagnosis and characterization of a disease.
BOX 1: Urinary markers differentiating subjects in group 1 (healthy
controls) from subjects in group 2 (IgAN patients) and/or group
3 (disease controls). These markers did not differentiate group 2
(IgAN patients) from group 3 (disease controls).

Metabolomic markers
  3-Chlorotyro sine
  Leukotriene B4
Proteomic markers
  Leukotriene D4
  Interleukin 6
  Interleukin 8
  Monocyte chemotactic protein-1
  Epidermal growth factor
  Soluble transferrin receptor
  LG3 fragment of endorepellin

BOX 2: Urinary markers that differentiated all groups of subjects:
group 1 (healthy controls), group 2 (IgAN patients), and group 3
(disease controls). This panel of markers differentiated the groups of
subjects from each other (see also Figure 1). Discriminant analysis
for this set of markers (see Table 5 for full list) confirmed the
perfect distribution within the three groups of subjects.

Metabolomic markers
Leukotriene [C.sub.4]
Proteomic markers
Galactose-deficient IgA1
Heparan sulfate

In our pilot study, we found that a panel of seven biomarkers (dodecanal, 8-hydroxyguanosine, leukotriene C4, [alpha]1-antitrypsin, IgA-uromodulin complex, galactose-deficient IgA1, and heparan sulfate) differentiated patients with IgAN from patients with other kidney diseases and healthy controls. However, none of the measured markers alone was specific.

Some of the seven components of our panel play a role in pathogenesis of IgAN or renal injury [16]. For example, serum levels of galactose-deficient IgA1 are elevated in many patients with IgAN [15, 20, 21]. Moldoveanu et al. [22] found elevated serum levels of galactose-deficient IgA1 in IgAN patients compared to healthy controls of Caucasian ancestry, and other studies showed similar results for patients of Asian and African-American ancestry [23]. In children with IgAN, including Caucasians and African Americans, serum levels of galactose-deficient IgA1 were elevated, but not associated with proteinuria [24]. Other investigators have shown that high serum levels of galactose-deficient IgA1 are associated with progressive loss of renal clearance function [25].

Uromodulin, also known as Tamm-Horsfall glycoprotein, is the most abundant protein in normal urine [17]. It is produced by the thick ascending limb of the loop of Henle [17] and may serve as a unique renal regulatory glycoprotein, specifically binding several cytokines, including IL-1 and TNF. Other studies found elevated levels of a fragment of uromodulin in the urine of patients with IgAN compared to that of healthy controls and patients with other glomerulonephritides [19]. A complex of uromodulin and IgA may be a diagnostic marker of IgAN; its value may be in the diagnosis of patients with an early phase of the disease with an ongoing inflammatory activity [17]. Other investigators have found increased urinary levels of complexes composed of IgA and IgG in patients with IgAN [18] or uromodulin fragments [19].

8-Hydroxyguanosine is a biomarker of nucleic acid oxidation and dodecanal is a marker of lipid peroxidation. Signs of altered oxidation have been detected in sera of patients with IgAN, including increased levels of lipoperoxide or malondialdehyde and reduced activity of superoxide dismutase, catalase, and glutathione peroxidase [26]. Recent data suggest that the nephrotoxicity of galactose-deficient IgA1-containing immune complexes in patients with IgAN is potentiated in the presence of systemic oxidation; furthermore, the intensity of the oxidative stress alters expression and progression of the disease [27].

Leukotrienes are a family of eicosanoid inflammatory mediators produced in leukocytes by the enzymatic oxidation of two essential fatty acids, arachidonic acid and eicosapentaenoic acid. The involvement of metabolites of leukotrienes in the inflammatory component of IgAN has been described [28]. Inhibitors of proliferation of mesangial cells, for example, leukotriene antagonists, may offer therapeutic options for the treatment of proliferative glomerular diseases [29].

Tubulointerstitial alterations of heparan sulfate proteoglycans that may affect inflammatory responses were observed in IgAN and other kidney diseases [30]. Other data showed increased binding of a leukocyte adhesion molecule, L-selectin, and MCP-1 to heparan sulfate proteoglycans of tubular epithelial cells in proteinuric diseases, including membranous nephropathy, IgAN, and lupus nephritis [32]. An increased expression of IL-8 on tubular epithelial cells of proteinuric patients and an increase of luminal protein may activate tubular epithelial cells to increase expression of L-selectin and MCP-1 [31]. Moreover, tubular heparan sulfate proteoglycans provide a docking platform for activation of the alternative pathway of the complement cascade via properdin, which may play a role in proteinuric renal damage [32]. Such data suggested that tubulointerstitial alterations of heparan sulfate proteoglycans in primary kidney diseases, including IgAN, may affect the inflammatory response associated with the progressive damage [31].

Elevated urinary levels of profibrotic cytokines such as IL-6, MCP-1, and soluble transferrin have been detected in patients with IgAN in contrast to the results of our study [33-35]. Another study detected elevated urinary levels of [alpha]1-gantitrypsin in patients with IgAN, contrary to our results [36]. Urinary levels of epidermal growth factor, IL-6, and MCP-1 might act as predictor markers of renal function outcome in IgAN [37], which was not confirmed in our study.

We identified two groups of patients with different diagnoses in which individual biomarkers had unsatisfactory specificity (selectivity) but the "synergic" effect of the combination of several biomarkers was satisfactory. One of the aims of our pilot study was to suggest a new approach to test the evaluation of grouped biomarkers, implying a synergic effect of the combination of individual biomarkers to be utilized in the monitoring of disease activity and/or treatment effectiveness. This approach is also suitable for the evaluation of more diagnoses all at once.

Our preliminary data showed that combining several urinary compounds in a panel of biomarkers differentiated patients with IgAN from patients with other renal diseases and healthy controls. Further studies are needed to validate these initial findings in a larger cohort.

5. Conclusions

In conclusion, our pilot project found that a panel comprised of seven urinary biomarkers (8-hydroxyguanosine, dodecanal, leukotriene [C.sub.4], [alpha]1-antitrypsin, IgA-uromodulin complex, galactose-deficient IgA1, and heparan sulfate) differentiated patients with IgAN from patients with other renal diseases and healthy controls. Such data need to be validated in a larger study. Moreover, a future prospective study should assess whether these biomarkers have prognostic significance and determine the power of these urinary markers for assessment of responses to therapy. 10.1155/2016/3650909

Competing Interests

The authors declare that there are no competing interests concerning their work in this study.


The authors (Jan Novak, Colin Reily, and Bruce A. Julian) have been supported in part by Grants DK106341, DK079337, DK078244, DK082753, and GM098539 from the National Institutes of Health and a gift from the IGA Nephropathy Foundation of America and the authors (Dita Maixnerova, Michaela Neprasova, Miloslav Suchanek, Petr Kacer, and Vladimir Tesar) by Grants LH15168 and LH12116 from the Ministry of Education, Youth and Sports of the Czech Republic. The authors (Dita Maixnerova, Michaela Neprasova, and Vladimir Tesar) were supported by PRVOUKP25/LF1/2. This work was also supported by the "Operational Programme Prague Competitiveness" (CZ.2.16/3.1.00/22197) and "National Program of Sustainability" (NPU I LO1215), MSMT-34870/2013; the Operational Programme Prague Competitiveness (CZ.2.16/3.1.00/21537) and "National Program of Sustainability" (NPU I LO1601) MSMT-43760/2015); the Operational Programme Prague Competitiveness (CZ.2.16/ 3.1.00/24501), and "National Program of Sustainability" (NPU I LO1613), MSMT-43760/2015.


[1] M. Eiro, T. Katoh, and T. Watanabe, "Risk factors for bleeding complications in percutaneous renal biopsy," Clinical and Experimental Nephrology, vol. 9, no. 1, pp. 40-45, 2005.

[2] A. E. Parrish, "Complications of percutaneous renal biopsy: a review of 37 years' experience," Clinical Nephrology, vol. 38, no. 3, pp. 135-141, 1992.

[3] D. Fliser, J. Novak, V. Thongboonkerd et al., "Advances in urinary proteome analysis and biomarker discovery," Journal of the American Society of Nephrology, vol. 18, no. 4, pp. 1057-1071, 2007.

[4] W. K. Han, S. S. Waikar, A. Johnson et al., "Urinary biomarkers in the early diagnosis of acute kidney injury," Kidney International, vol. 73, no. 7, pp. 863-869, 2008.

[5] M. C. Hastings, Z. Moldoveanu, H. Suzuki et al., "Biomarkers in IgA nephropathy: relationship to pathogenetic hits," Expert Opinion on Medical Diagnostics, vol. 7, no. 6, pp. 615-627, 2013.

[6] B. A. Julian, H. Suzuki, Y. Suzuki, Y. Tomino, G. Spasovski, and J. Novak, "Sources of urinary proteins and their analysis by urinary proteomics for the detection of biomarkers of disease," Proteomics--Clinical Applications, vol. 3, no. 9, pp. 1029-1043, 2009.

[7] S. M. Hewitt, J. Dear, and R. A. Star, "Discovery of protein biomarkers for renal diseases," Journal of the American Society of Nephrology, vol. 15, no. 7, pp. 1677-1689, 2004.

[8] H. Mischak, G. Allmaier, R. Apweiler et al., "Recommendations for biomarker identification and qualification in clinical proteomics," Science Translational Medicine, vol. 2, no. 46, Article ID 46ps42, 2010.

[9] H. Mischak, J. P. A. Ioannidis, A. Argiles et al., "Implementation of proteomic biomarkers: making it work," European Journal of Clinical Investigation, vol. 42, no. 9, pp. 1027-1036, 2012.

[10] C. Pontillo, L. Jacobs, J. A. Staessen et al., "A urinary proteome-based classifier for the early detection of decline in glomerular filtration," Nephrology Dialysis Transplantation, 2016.

[11] D. Maixnerova, C. Reily, Q. Bian, M. Neprasova, J. Novak, and V. Tesar, "Markers for the progression of IgA nephropathy," Journal of Nephrology, vol. 29, no. 4, pp. 535-541, 2016.

[12] G. Schlosser, P. Kacer, M. Kuzma et al., "Coupling immunomagnetic separation on magnetic beads with matrix-assisted laser desorption ionization-time of flight mass spectrometry for detection of staphylococcal enterotoxin B," Applied and Environmental Microbiology, vol. 73, no. 21, pp. 6945-6952, 2007.

[13] M. E. Ritchie, B. Phipson, D. Wu et al., "Limma powers differential expression analyses for RNA-sequencing and microarray studies," Nucleic Acids Research, vol. 43, no. 7, article e47, 2015.

[14] B. G. M. Vandeginste, Handbook of Chemometrics and Qualimetrics, PartB, 1998.

[15] H. Yanagawa, H. Suzuki, Y. Suzuki et al., "A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases," PLoS ONE, vol. 9, no. 5, Article ID e98081, 2014.

[16] J. Novak, M. B. Renfrow, A. G. Gharavi, and B. A. Julian, "Pathogenesis of IgA nephropathy. Invited review," Current Opinion in Nephrology and Hypertension, vol. 22, pp. 287-294, 2013.

[17] T. Obara, S. Mizoguchi, Y. Shimozuru, T. Sato, and O. Hotta, "The complex of immunoglobulin A and uromodulin as a diagnostic marker for immunoglobulin A nephropathy," Clinical and Experimental Nephrology, vol. 16, no. 5, pp. 713-721, 2012.

[18] K. Matousovic, J. Novak, T. Yanagihara et al., "IgA-containing immune complexes in the urine of IgA nephropathy patients," Nephrology Dialysis Transplantation, vol. 21, no. 9, pp. 2478-2484, 2006.

[19] J. Wu, N. Wang, J. Wang et al., "Identification of a uromodulin fragment for diagnosis of IgA nephropathy," Rapid Communications in Mass Spectrometry, vol. 24, no. 14, pp. 1971-1978, 2010.

[20] J. Nakata, Y. Suzuki, H. Suzuki et al., "Changes in nephritogenic serum galactose-deficient IgA1 in IgA nephropathy following tonsillectomy and steroid therapy," PLoS ONE, vol. 9, no. 2, article e89707, 2014.

[21] H. Suzuki, M. Raska, K. Yamada et al., "Cytokines alter IgA1 O-glycosylation by dysregulating C1GalT1 and ST6GalNAc-II enzymes," The Journal of Biological Chemistry, vol. 289, no. 8, pp. 5330-5339, 2014.

[22] Z. Moldoveanu, R. J. Wyatt, J. Y. Lee et al., "Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels," Kidney International, vol. 71, no. 11, pp. 1148-1154, 2007.

[23] M. C. Hastings, Z. Moldoveanu, B. A. Julian et al., "Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability," Clinical Journal of the American Society of Nephrology, vol. 5, no. 11, pp. 2069-2074, 2010.

[24] M. C. Hastings, S. Afshan, J. T. Sanders et al., "Serum galactose- deficient IgA1 level is not associated with proteinuria in children with IgA nephropathy," International Journal of Nephrology, vol. 2012, Article ID 315467, 7 pages, 2012.

[25] N. Zhao, P. Hou, J. Lv et al., "The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression," Kidney International, vol. 82, no. 7, pp. 790-796, 2012.

[26] R. Coppo, R. Camilla, A. Amore, and L. Peruzzi, "Oxidative stress in IgA nephropathy," Nephron Clinical Practice, vol. 116, no. 3, pp. c196-c199, 2010.

[27] R. Camilla, H. Suzuki, V Dapra et al., "Oxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy," Clinical Journal of the American Society of Nephrology, vol. 6, no. 8, pp. 1903-1911, 2011.

[28] B. McMahon, D. Mitchell, R. Shattock, F. Martin, H. R. Brady, and C. Godson, "Lipoxin, leukotriene, and PDGF receptors cross-talk to regulate mesangial cell proliferation," The FASEB Journal, vol. 16, no. 13, pp. 1817-1819, 2002.

[29] Y. Kurogi, "Mesangial cell proliferation inhibitors for the treatment of proliferative glomerular disease," Medicinal Research Reviews, vol. 23, no. 1, pp. 15-31, 2003.

[30] J. W. Celie, R. M. Reijmers, E. M. Slot et al., "Tubulointerstitial heparan sulfate proteoglycan changes in human renal diseases correlate with leukocyte influx and proteinuria," American Journal of Physiology--Renal Physiology, vol. 294, no. 1, pp. F253-F263, 2008.

[31] A. M. Zivkovic, J. Yang, K. Georgi et al., "Serum oxylipin profiles in IgA nephropathy patients reflect kidney functional alterations," Metabolomics, vol. 8, no. 6, pp. 1102-1113, 2012.

[32] A. Zaferani, R. R. Vives, P. Van Der Pol et al., "Identification of tubular heparan sulfate as a docking platform for the alternative complement component properdin in proteinuric renal disease," Journal of Biological Chemistry, vol. 286, no. 7, pp. 5359-5367, 2011.

[33] M. Stangou, A. Papagianni, C. Bantis et al., "Up-regulation of urinary markers predict outcome in IgA nephropathy but their predictive value is influenced by treatment with steroids and azathioprine," Clinical Nephrology, vol. 80, no. 3, pp. 203-210, 2013.

[34] P. Kalliakmani, L. Nakopoulou, S. Tsakas, M. Gerolymos, M. Papasotiriou, and D. S. Goumenos, "Urinary interleukin6 (IL-6) and transforming growth factor (TGF-[beta]) levels in corticosteroidtreated patients with IgA nephropathy," Clinical Nephrology, vol. 76, no. 2, pp. 144-150, 2011.

[35] Y. Li, J. Wang, X. Zhu, Q. Feng, X. Li, and X. Feng, "Urinary protein markers predict the severity of renal histological lesions in children with mesangial proliferative glomerulonephritis," BMC Nephrology, vol. 13, article 29, 2012.

[36] P.-G. Moon, J.-E. Lee, S. You et al., "Proteomic analysis of urinary exosomes from patients of early IgA nephropathy and thin basement membrane nephropathy," Proteomics, vol. 11, no. 12, pp. 2459-2475, 2011.

[37] M. Stangou, E. Alexopoulos, A. Papagianni et al., "Urinary levels of epidermal growth factor, interleukin-6 and monocyte chemoattractant protein-1 may act as predictor markers of renal function outcome in immunoglobulin A nephropathy," Nephrology, vol. 14, no. 6, pp. 613-620, 2009.

Michaela Neprasova, (1) Dita Maixnerova, (1) Jan Novak, (2) Colin Reily, (2) Bruce A. Julian, (2) Jan Boron, (3,4) Petr Novotny, (4) Miloslav Suchanek, (3) Vladimir Tesar, (1) and Petr Kacer (3)

(1) First Faculty of Medicine, Department of Nephrology, Charles University and General University Hospital in Prague, Prague 2, Czech Republic

(2) Departments of Microbiology and Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA

(3) University of Chemistry and Technology, Technicka 5,166 28 Prague 6, Czech Republic

(4) Essence Line, Plzemka 130/221,150 00 Prague 5, Czech Republic

Correspondence should be addressed to Dita Maixnerova;

Received 6 May 2016; Revised 2 August 2016; Accepted 18 August 2016

Academic Editor: Kishore Chaudhry

Caption: FIGURE 1: The graphical output from discriminant analysis for seven urinary markers (see also Box 2). F1 and F2, artificial axes (principal component reduction of seven selected markers into a two-dimensional space); group 1 (healthy controls, blue); group 2 (patients with IgAN, green); group 3 (disease controls, red-brown); yellow circles show centroids for each group; 95% confidentialinterval ellipses are around centroids for each group.

Caption: FIGURE 2: The graphical output from discriminant analysis for seven urinary markers listed in Box 2 normalized to urinary creatinine (see also Table 5) for the two groups of patients with renal disease. The same discrimination power was found for normalized markers as for nonnormalized. Group 2 (patients with IgAN, green), group 3 (disease controls, red-brown).
TABLE 1: Clinical and laboratory data for patients with renal diseases.

Dg     N          S-urea              S-Cr                 PU
                 (mmol/L)        ([micro]mol/L)          (g/d)

IgAN   11    9.8 [+ or -] 4.7    158 [+ or -] 70   1.54 [+ or -] 1.28
MN     2    10.4 [+ or -] 0.5    156 [+ or -] 4    5.92 [+ or -] 1.75
LN     2    16.1 [+ or -] 0.5    283 [+ or -] 15   3.88 [+ or -] 3.18
DN     2    29.6 [+ or -] 9.1    293 [+ or -] 19   2.24 [+ or -] 0.59
ANCA   2    17.2 [+ or -] 10.7   460 [+ or -] 68   2.86 [+ or -] 2.55

Dg             PU                Age         M/F         eGFR
             (g/L)              (yrs)                 (mL/s/1.73

IgAN   0.85 [+ or -] 0.61   49 [+ or -] 18   10/1   53 [+ or -] 30
MN     2.97 [+ or -] 1.44   56 [+ or -] 18   1/1    35 [+ or -] 6
LN     2.82 [+ or -] 1.43   33 [+ or -] 4    1/1    20 [+ or -] 6
DN     1.31 [+ or -] 0.23   62 [+ or -] 14   0/2    14 [+ or -] 1
ANCA   0.93 [+ or -] 0.25   42 [+ or -] 14   1/1    12 [+ or -] 5

Dg           U-Cr

IgAN   7.9 [+ or -] 5.0
MN     5.7 [+ or -] 1.3
LN     7.1 [+ or -] 1.7
DN     3.6 [+ or -] 1.1
ANCA   6.2 [+ or -] 0.8

Dg, diagnosis; IgAN, IgA nephropathy; MN, membranous nephropathy; LN,
lupus nephritis; DN, diabetic nephropathy; ANCA, antineutrophilic
cytoplasmic antibody vasculitis-associated kidney disease; N, number
of patients; S-urea, concentration of serum urea; S-Cr, serum
creatinine; PU, proteinuria; yrs, years; M-F, male-female; eGFR,
estimated glomerular filtration rate (MDRD formula); U-Cr, urinary
creatinine. Data are shown as mean values [+ or -] SD.

TABLE 2: Selected reaction monitoring transitions of compounds
derivatized with 3-aminopyridyl-N-hydroxysuccinimidyl
carbamate reagent.

Analyte                          SRM transition        CID
                               Q1 [right arrow] Q3    energy

o-Tyrosine                    300 [right arrow] 180     15
3-Chlorotyrosine              334 [right arrow] 214     16
3-Nitrotyrosine               345 [right arrow] 225     14
8-Hydroxyguanosine            418 [right arrow] 298     15
8-Hydroxy-2'-deoxyguanosine   402 [right arrow] 282     15

Q1, precursor ion; Q3, product ion; SRM, selected reaction
monitoring; CID, collision-induced dissociation.

TABLE 3: Selected reaction monitoring transitions of compounds
derivatized with Girard's reagent T.

Analyte                               SRM transition        CID
                                    Q1 [right arrow] Q2    energy

Hexanal                            214 [right arrow] 155     16
Heptanal                           228 [right arrow] 169     16
Oktanal                            242 [right arrow] 183     16
Nonanal                            256 [right arrow] 197     16
Decanal                            270 [right arrow] 211     16
Undecanal                          284 [right arrow] 225     16
Dodecanal                          298 [right arrow] 239     17
Malondialdehyde                    169 [right arrow] 101     8
4-Hydroxynonenal                   273 [right arrow] 214     15
4-Hydroxyhexenal                   231 [right arrow] 172     15
8-Isoprostane-[PGF.sub.2[alpha]]   471 [right arrow] 412     15
Leukotriene [B.sub.4]              454 [right arrow] 395     17
Leukotriene [C.sub.4]              744 [right arrow] 685     14
Leukotriene [D.sub.4]              615 [right arrow] 556     15
Leukotriene [E.sub.4]              558 [right arrow] 499     15

Q1, precursor ion; Q3, product ion; SRM, selected reaction monitoring;
CID, collision-induced dissociation; Girard's reagent T, (carboxymethyl)
trimethylammonium chloride hydrazide.

TABLE 4: Mean values for all analytes in the three groups of subjects.

Analyte ((1) ng/mL,                            Mean
(2) pg/mL,
(3) [micro]g/mL)                    Group 1   Group 2   Group 3

Metabolomic markers
  Malondialdehyde (1)                22.1      32.3      31.2
  4-Hydroxyhexenal (1)               13.1      29.4      28.9
  4-Hydroxynonenal (1)               23.9      33.3      35.8
  Hexanal (1)                        15.4      28.3      24.2
  Heptanal1                          22.5      32.1      28.9
  Oktanal (1)                         9.0      15.1      13.6
  Nonanal (1)                        12.2      15.3      14.6
  Decanal (1)                         9.0      13.8      12.6
  Undodecanal (1)                     5.6       7.2       6.9
  Dodecanal (1)                       6.6       8.1       7.5
  3-Nitrotyrosine (2)                52.5      76.4      74.6
  8-Hydroxy-2'-deoxyguanosine (2)    190.2     341.8     303.3
  8-Hydroxyguanosine (2)             190.2     337.9     284.1
  5-Hydroxymethyluracil (2)          90.1      168.0     156.8
  o-Tyrosine (2)                     54.6      91.4      82.6
  3-Chlortyrosine (2)                23.8      50.2      44.5
  Leukotriene B4 (2)                 151.3     381.2     293.1
  8-Isoprostane (2)                  20.5      43.4      38.6
  Leukotriene [E.sub.4] (2)          120.0     135.5     126.0
  Leukotriene [D.sub.4] (2)          55.6      65.1      62.8
  Leukotriene [C.sub.4] (2)          63.9      76.4      71.6
Proteomic markers
  Interleukin 6 (2)                  38.8      110.5     78.8
  Interleukin 8 (2)                  18.3      97.4      60.6
  Monocyte chemotactic                1.6       5.2       4.9
    protein-1 (1)
  Epidermal growth factor (1)         5.1       2.9       3.2
  a1-Antitrypsin (1)                 16.0      55.0      40.6
  IgA-Uromodulin (1)                 53.8      518.0     221.9
  Galactose-deficient IgA1 (1)       49.8      186.7     141.3
  Soluble transferrin                10.0      41.2      37.5
    receptor (1)
  LG3 fragment of                    14.0      53.2      63.9
    endorepellin (1)
  Tumstatin (2)                      72.5      158.5     167.8
  Endostatin (2)                     75.2      192.7     178.1
Heparan sulfate (3)                   0.1       2.1       1.1

Group 1 (healthy controls), group 2 (IgAN patients), and group 3
(disease controls, patients with membranous nephropathy, lupus
nephritis, antineutrophilic cytoplasmic antibody
vasculitis-associated kidney disease, or diabetic nephropathy).

TABLE 5: Mean values of concentrations of measured urinary
analytes normalized to urinary creatinine for patients with IgAN and
disease controls.

Analyte                                    IgAN   Disease

  Metabolomic markers
  Malondialdehyde (ng/mg)                  6.3      6.2
  4-Hydroxyhexenal (ng/mg)                 5.9      5.5
  4-Hydroxynonenal (ng/mg)                 6.6      7.2
  Hexanal (ng/mg)                          5.5      4.6
  Heptanal (ng/mg)                         6.2      5.6
  Oktanal (ng/mg)                          3.0      2.6
  Nonanal (ng/mg)                          2.9      2.9
  Decanal (ng/mg)                          2.7      2.4
  Undodecanal (ng/mg)                      1.4      1.3
  8-Hydroxyguanosine (pg/mg)               65.6     54.6
  5-Hydroxymethyluracil (pg/mg)            32.6     30.2
  o-Tyrosine (pg/mg)                       18.1     16.0
  3-Chlorotyrosine (pg/mg)                 10.0     8.6
  Leukotriene [B.sub.4] (pg/mg)            75.8     56.1
  8-Isoprostane (pg/mg)                    8.4      7.4
  Leukotriene [E.sub.4] (pg/mg)            26.0     24.5
  Leukotriene [D.sub.4] (pg/mg)            12.4     12.3
  Leukotriene [C.sub.4] (pg/mg)            14.5     14.0
Proteomic markers
  Interleukin 6 (pg/mg)                    22.4     16.0
  Interleukin 8 (pg/mg)                    20.1     11.5
  Monocyte chemotactic protein-1 (ng/mg)   1.1      0.9
  EGF (ng/mg)                              0.5      0.6
  [alpha]1-Antitrypsin (ng/mg)             10.8     7.8
  IgA-Uromodulin (ng/mg)                   99.1     40.3
  Galactose-deficient IgA1 (ng/mg)         35.5     28.1
  Soluble transferrin receptor (ng/mg)     7.8      7.1
  LG3 fragment of endorepellin (ng/mg)     9.8      12.3
  Tumstatin (pg/mg)                        30.6     31.9
  Endostatin (pg/mg)                       36.4     35.7
Heparan sulfate ([micro]g/mg)              0.4      0.2
COPYRIGHT 2016 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2016 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:Neprasova, Michaela; Maixnerova, Dita; Novak, Jan; Reily, Colin; Julian, Bruce A.; Boron, Jan; Novot
Publication:Disease Markers
Date:Jan 1, 2016
Previous Article:WISP1 is increased in intestinal mucosa and contributes to inflammatory cascades in inflammatory bowel disease.
Next Article:Interplay between matrix metalloproteinase-9, matrix metalloproteinase-2, and interleukins in multiple sclerosis patients.

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |