Novel Urinary Protein Biomarkers Predicting the Development of Microalbuminuria and Renal Function Decline in Type 1 Diabetes
- Daniela Schlatzer, BS1,
- David M. Maahs, MD, PHD2,
- Mark R. Chance, PHD1,
- Jean-Eudes Dazard, PHD1,
- Xiaolin Li, MS1,
- Fred Hazlett, MS1,
- Marian Rewers, MD, PHD2 and
- Janet K. Snell-Bergeon, PHD2⇓
- 1Center for Proteomics, Case Western Reserve University, Cleveland, Ohio
- 2Barbara Davis Center for Childhood Diabetes, University of Colorado Denver, Aurora, Colorado
- Corresponding author: Janet K. Snell-Bergeon, .
OBJECTIVE To define a panel of novel protein biomarkers of renal disease.
RESEARCH DESIGN AND METHODS Adults with type 1 diabetes in the Coronary Artery Calcification in Type 1 Diabetes study who were initially free of renal complications (n = 465) were followed for development of micro- or macroalbuminuria (MA) and early renal function decline (ERFD, annual decline in estimated glomerular filtration rate of ≥3.3%). The label-free proteomic discovery phase was conducted in 13 patients who progressed to MA by the 6-year visit and 11 control subjects, and four proteins (Tamm-Horsfall glycoprotein, α-1 acid glycoprotein, clusterin, and progranulin) identified in the discovery phase were measured by enzyme-linked immunosorbent assay in 74 subjects: group A, normal renal function (n = 35); group B, ERFD without MA (n = 15); group C, MA without ERFD (n = 16); and group D, both ERFD and MA (n = 8).
RESULTS In the label-free analysis, a model of progression to MA was built using 252 peptides, yielding an area under the curve (AUC) of 84.7 ± 5.3%. In the validation study, ordinal logistic regression was used to predict development of ERFD, MA, or both. A panel including Tamm-Horsfall glycoprotein (odds ratio 2.9, 95% CI 1.3–6.2, P = 0.008), progranulin (1.9, 0.8–4.5, P = 0.16), clusterin (0.6, 0.3–1.1, P = 0.09), and α-1 acid glycoprotein (1.6, 0.7–3.7, P = 0.27) improved the AUC from 0.841 to 0.889.
CONCLUSIONS A panel of four novel protein biomarkers predicted early renal damage in type 1 diabetes. These findings require further validation in other populations for prediction of renal complications and treatment monitoring.
Despite tremendous progress in treatment, patients with type 1 diabetes still live 15 years shorter, experience excess morbidity, and have medical costs over 10 times higher than the general population (1). Modification of traditional risk factors has made only limited impact on development of renal complications in these patients (2). Improved glycemic control reduces progression to early stages of microvascular complications in type 1 diabetes even years later (2), but the risk of diabetic nephropathy is not completely abolished by improved glycemic control (3) or lowering blood pressure (4). Whereas rates of end-stage renal disease have declined over recent years, after 30 years of diabetes duration, the cumulative incidence of end-stage renal disease is 7.8% among patients with type 1 diabetes (5). Further, the presence of microvascular complications is associated with increased risk of developing cardiovascular disease (6,7), which remains the leading cause of death in people with type 1 diabetes.
The development of renal complications and eventual end-stage renal disease in people with diabetes has been thought to follow a linear path involving the development of microalbuminuria, progressing to frank proteinuria. It was thought that renal function only declines once proteinuria is present and that regression of microalbuminuria indicates reversal of the disease progress. However, clinical trials have recently demonstrated that this dogma may be incorrect (4,8,9). First, renal function as measured by glomerular filtration rate (GFR) declines before the development of proteinuria, demonstrating that there is an earlier phase of kidney damage that could be detected and targeted with interventions. Second, kidney damage can progress even when microalbuminuria has regressed (10). The identification of novel biomarkers for early renal disease is therefore a high priority.
Urine is an easily accessible biological matrix for which to identify new biomarkers. The urinary proteome is very complex, containing 1,000 of proteins and peptides that are derived from filtration/secretion/reabsorption processes within the kidney (11,12). Many of these proteins are sensitive to alterations in the kidney, and urinary proteomics provides a platform from which to simultaneously quantify hundreds of urinary proteins.
In this analysis, we have performed a longitudinal label-free protein expression study to discover early biomarkers of diabetic kidney damage before the onset of disease. Here we describe a label-free protein expression analysis in adults with type 1 diabetes who developed microalbuminuria or a significant decline in estimated glomerular filtration rate (eGFR) over 6 years of follow-up. The purpose of this study was to define a panel of proteins that can serve as novel biomarkers of early development of renal disease. In addition, we verified a selected panel of proteins identified from the discovery analysis via enzyme-linked immunosorbent assay (ELISA) in a larger cohort of patients with type 1 diabetes who developed MA and/or early renal decline.
RESEARCH DESIGN AND METHODS
Between April 2000 and April 2002, the Coronary Artery Calcification in Type 1 Diabetes (CACTI) study enrolled 652 type 1 diabetic patients meeting the following criteria: age 19–56 years; no history of myocardial infarction, angioplasty, coronary artery bypass graft, or angina; currently on insulin therapy; diagnosed before age 30 year or a clinical course consistent with type 1 diabetes; on insulin therapy within the first year after diagnosis; and longstanding type 1 diabetes (range of duration 4–52 years). This cohort represents nearly 40% of eligible patients in the Denver metro area. Study participants were examined at baseline, 3 years, and 6 years.
There were 465 study participants with type 1 diabetes who were normoalbuminuric at baseline. Over 6 years of follow-up, 25 study participants with type 1 diabetes who were initially normoalbuminuric developed micro- or macroalbuminuria (MA), defined by albumin excretion rate (AER) ≥20 μg/min or albumin-to-creatinine ratio ≥30 mg/g in two overnight urine collections at the 6-year visit. We randomly selected half (n = 13) of these study participants to conduct a proteomic discovery phase. Participants with type 1 diabetes who remained normoalbuminuric (AER <7.5 μg/min) at all three study visits in both overnight urine samples were frequency matched on age and diabetes duration (n = 11). A total of 72 samples for the 24 study participants were included in this study, where each visit was considered an individual sample.
ELISA validation study.
This validation study analyzed urine from 74 patients with type 1 diabetes at the baseline visit (visit 1). All subjects with the development of new MA from baseline to either visit 2 or visit 3 who were not previously included in the label-free analysis (n = 24) and all subjects with early renal function decline (ERFD) from baseline to visit 2 or visit 3 were included in the validation study. ERFD was defined using the method outlined by Perkins and Krolewski (13), defined as a decline in cystatin C–based eGFR of ≥3.3% per year. There were 23 subjects in the CACTI study who experienced ERFD, and all were selected for the ELISA validation study. There were 35 subjects with type 1 diabetes who completed all three study visits, had baseline urine samples available, and remained normoalbuminuric (AER <7.5 μg/min) and did not experience ERFD over the course of the study. All of these subjects were included as a control group with normal renal function. Study participants were categorized into groups as follows: group A, normal renal function (n = 35); group B, ERFD but no MA (n = 15); group C, MA but no ERFD (n = 16); and group D, both ERFD and MA (n = 8).
Overnight urine collections.
Study subjects were asked to collect two overnight timed urine collections at each visit. Subjects were asked to record the time at night that they last voided their bladder and to collect all urine produced overnight and first thing in the morning. The total time of the collection and the volume were recorded, and AER was calculated. In the event that subjects were unable to complete both timed samples, a spot urine sample was collected and albumin-to-creatinine ratio was calculated as an estimate of AER.
Four milliliters of urine from the CACTI study subjects was desalted using a Microcon concentrator. Each sample was buffer exchanged three times using 3 mL of 50 mmol/L Tris, pH 8.8, to a final volume of ∼100 μL, and protein concentrations were determined by a 2D Quant Kit (GE Healthcare, Piscataway, NJ). Ten micrograms of each sample was loaded onto a one-dimensional SDS-PAGE gel (4–20% Tris-HCl) as a quality-control measure for the desalting step. Subsequent to digestion, each sample was adjusted to 10 μg in 50 μL. Ten microliters of 0.2% Rapigest (Waters, Milford, MA) and dithiothreitol was added to a final concentration of 5 mmol/L. The samples were reduced at 80°C for 15 min and cooled to room temperature before alkylation with iodacetamide at a final concentration of 10 mmol/L for 30 min. Proteolytic digestion was performed with endopeptidase Lys C (Wako Chemicals, Richmond, VA) with a final enzyme-to-protein ratio of 1:10 (w/w) for 18 h at 37°C.
Liquid chromatography and mass spectrometry.
A total of 100 nanograms of each sample was analyzed by liquid chromatography/mass spectrometry/mass spectrometry (LC/MS/MS), and the order of sample injections was randomized over all samples. Separation and detection of peptides was performed as previously published (14). Raw LC/MS/MS data were processed via Proteomarker software (Infochromics, Toronto, Canada).
Data processing: qualitative and quantitative.
The raw data for each run were first extracted to provide MS/MS peak lists for identification- and intensity-based profile peak lists for quantification. The MS/MS peak lists were subsequently searched by Mascot version 2.2.0 (Matrix Science, London, U.K.). The database used was the human International Protein Index (68,020 sequences). Search settings were as follows: no enzyme specificity, mass accuracy window for precursor ion, 10 ppm; mass accuracy window for fragment ions, 0.8 Da; and variable modification, including only carbamidomethylation of cysteines and oxidation of methionine. The criteria for peptide identification were a mass accuracy of ≤10 ppm and an expectation value of P ≤ 0.05. Proteins that had two or more peptides matching the above criteria were considered confirmed assignments, whereas proteins identified with one peptide regardless of the Mascot score were highlighted as tentative assignments. Automated differential quantification of peptides in a set of samples was accomplished with Proteomarker as previously described (14).
Data quality control: prefiltering, imputation, and normalization.
Subsequent to raw data acquisition and processing, data quality control and prefiltering were done for this study as previously described (14). In brief, three-step prefiltering was performed to resolve some of the peak misalignment issues and remove those peptides in the abundance matrix that received poor quality identifications or no qualitative identification at all. A peptide was rejected if 1) its consensus sequence was not assigned at all or 2) the consensus peptide sequence score was below the 74th percentile of all scores (Mascot score of ≤21.125). Next, intensity summaries of identical sequence peptides were integrated with annotations retained from the diffset with the least number of missing values (including retention time, charge/mass ratio, sequence, score, and protein annotation). A final prefiltering procedure was carried out to retain those peptides only for which the observed missing count per peptide was strictly <50% per experimental unit while maximizing the total number of peptides remaining after selection. The final number of peptides retained was P = 2,584 (1,360 proteins).
Missing value imputation.
Missing values in LC/MS data arise because of imperfect detection and alignment of peak intensities or by true absence of expression. To account for the nonrandom nature of the “missingness mechanism” at play (nonignorable left-censoring) and its extent in this type of data (nonignorable left-censoring), we used a probability model adapted from Wang et al. (15) that describes “artifactual missing events.” This model makes inferences on the missing values of one sample on the basis of the information from other similar samples (technical replicates or nearest neighbors). It substitutes a missing measurement of intensity with its expected value of the true intensity, given that it is unobservable. Estimation of the imputation parameters was done to minimize the percentage of remaining missing values. The initial number of missing values after the above prefiltering was 60.8%. Remaining missing values after imputation (42.2%) represent truly absent peptides in the samples and were typically imputed by taking an estimate of the background noise.
Variance stabilization of the data features.
To remove sources of systematic variation due to experimental artifacts in the measured intensities and to ensure that the usual assumptions for statistical inferences are met (normality, homoscedasticity), we applied a variance stabilization and normalization transformation on the variables (peptides). We used the joint adaptive mean variance regularization procedure recently introduced by Dazard and Rao (16). This method overcomes the lack of degrees of freedom and issues with variance-mean dependency common in high-dimensional proteomics datasets where the number of variables dominates the number of samples.
Potential groups and outliers among the samples were checked by a principal component analysis (Supplementary Fig. 1) (17). Clustering analysis was performed using complete linkage hierarchical clustering and the gap statistics to estimate the real number of clusters in the data.
Predictive proteomics model.
Patients were relabeled at visit 1 with their MA status at visit 3. This new response variable was then regressed onto all peptide expression levels at visit 1 by fitting a generalized (logistic) linear model via penalized maximum likelihood (elastic net regularization) (18). Fitting was carried out by fourfold cross-validation with the help of the R implementation in the “glmnet” CRAN package (http://cran.r-project.org). This step allowed the selection of peptide predictors as early as visit 1 with best predictive value of progression toward MA at visit 3, as well as the determination of individual probability of MA progression by the patient.
ELISA verification of target urine biomarkers.
Four putative urine biomarkers identified in the label-free proteomic analysis as having significant abundance at visit 1 were selected for verification via ELISA, and an additional protein progranulin was examined, which was identified in the analysis but not found significant at visit 1. Urine samples collected at visit 1 from a total of 74 study subjects were analyzed. The five biomarkers were measured by commercially available ELISA kits according to the manufacturer’s instructions: Tamms-Horsfall glycoprotein (THP) (MD Biosciences, St. Paul, MN); human progranulin (R&D Systems, Minneapolis, MN); clusterin (BioVendor, Chandler, NC); human α-1 acid glycoprotein (AGP) (Assaypro, St. Charles, MO), and prostaglandin D synthase (ProstD) (BioVendor). All kits have inter- and intra-assay coefficients of variation of <15%.
Label-free expression analysis
Study participants in the label-free expression analysis who developed MA did not differ from those who remained normoalbuminuric over the 6 years of the study in terms of age, diabetes duration, sex, HbA1c, or baseline AER.
The sample preparation protocol was reproducible across individual samples and yielded sufficient protein concentrations with ranges of 0.206 to 39 μg/μL. Reproducible protein patterns via one-dimensional SDS-PAGE were observed across all samples (data not shown). These samples were subsequently digested and analyzed by LC/MS/MS as described in research design and methods. Distinct chromatographic differences were observed in normoalbuminuric and MA samples (Supplementary Fig. 2). Good proteome coverage was observed with 1,115 tentative protein assignments (at least one peptide sequenced with reproducible chromatographic entities) and 246 confirmed protein assignments (at least two or more peptide sequenced). However, two samples were excluded from subsequent analyses because of poor LC/MS/MS data acquisition, leaving 22 samples for predictive model building.
To build a predictive model of the progression to MA among normoalbuminuric patients, we used data from visit 1 (252 peptides corresponding to 183 proteins) as predictors and the MA status at visit 3 as the outcome. This step formed the basis of a predictive proteomics model, which determines the individual probability of MA progression by the patient, whether the patient has already been observed or is incoming (new). The model yielded an area under the receiver operating curve (AUC) of 84.7 ± 5.3% with a true positive rate of 84.7 ± 12.7%, which corresponded to 19 of 22 correctly classified at visit 1. An equal distribution of increasing and decreasing peptide abundances was observed in patients who progressed to MA compared with patients who did not develop MA. Overall, 148 peptides decreased in abundance in the MA group, while 104 peptides increased.
Good correlation was observed between albumin peptide abundance and label-free albumin measures at visit 1 with values of AER measured previously in the urine samples. The median AER value for the control and MA groups was 5.64 and 9.42, respectively, whereas the label-free median peptide intensities (normalized and transformed scale) were 0.67 for the control subjects and 0.85 for the MA group. Additional example proteins that were found to be significant in the MA group at visit 1 were AGP, THP, clusterin, and ProstD (Supplementary Fig. 3). In addition, progranulin that was detected in the LC/MS/MS analysis was included in the verification analysis, since it has a similar expression profile to THP in the kidney tubule, and we detected changes in abundances of this protein in type 1 diabetic patients with MA (data not shown) (19).
ELISA protein analysis.
Characteristics of study participants at the baseline exam were examined in patients with type 1 diabetes who remained normoalbuminuric and had normal renal function (group A, n = 35), patients with type 1 diabetes who developed ERFD without MA (group B, n = 15), patients with type 1 diabetes who went on to develop MA but not ERFD (group C, n = 16), and patients with type 1 diabetes who went on to develop both MA and ERFD (group D, n = 8) (Table 1). There were no differences in age, diabetes duration, sex, systolic or diastolic blood pressure, total or HDL cholesterol, or waist-to-hip ratio (WHR) across groups. HbA1c was significantly lower in group A than in group C, and the use of antihypertensive medication was significantly lower in group A than in group D, whereas lipid medication use was significantly lower in group A than in group C. Baseline AER was significantly lower in group A than in groups C and D and in group B than in group D. There were no differences in baseline cystatin C or eGFR by group, but as per the study design, follow-up eGFR was significantly lower in the group with ERFD (group B) than in patients with normal renal function and no albuminuria (group A), and in the group with both ERFD and albuminuria (group D) than in the group with only albuminuria (group C).
Levels of THP, progranulin, clusterin, AGP, and ProstD were compared in groups A, B, C, and D, adjusted for age and urine creatinine (Table 2). THP was significantly higher in group D than in all other groups. AGP and ProstD were significantly higher in group B than in group A.
Standardized z scores were calculated for all proteins and were examined by group, adjusting for baseline age, diabetes duration, baseline AER, HbA1c, cystatin C, and uric acid. Significant differences were observed between groups A and D for THP and progranulin and groups A and B for AGP (Fig. 1). Both THP and progranulin followed a stepwise pattern, with the lowest levels in patients who maintained normal renal function and normoalbuminuria (group A), increasing nonsignificantly in patients with either ERFD (group B) or MA (group C) and significantly increased in patients with both ERFD and MA (group D). AGP was also lowest among patients who maintained normal renal function (group A), but was significantly increased only in patients who developed ERFD with normoalbuminuria (group B). No group differences were observed for clusterin or ProstD (data not shown).
In multivariable ordinal logistic regression modeling with study group as the outcome, THP and progranulin were significantly predictive of ERFD and MA in patients with type 1 diabetes, adjusting for baseline age, diabetes duration, uric acid and cystatin C, total and HDL cholesterol, and systolic blood pressure as well as factors [baseline AER, BMI, ever smoking, WHR × 10, and log(HbA1c) × 10] previously found to predict microalbuminuria in multiple cohorts with type 1 diabetes (20) (Table 3). AGP was marginally (P = 0.07) predictive of ERFD and MA. In a model using stepwise selection to determine the most parsimonious model and including model 1, THP, progranulin, and clusterin were selected. Finally, a model was considered that included THP, progranulin, clusterin, and AGP. In this model, THP was significantly associated with renal outcomes, but clusterin, progranulin, and AGP were not statistically significantly predictive of the development of ERFD and MA. The C-statistic, a measure of model fit, increased from 0.841 in model 1 (without any urinary proteins except for AER) to 0.857 with progranulin, 0.871 with THP, and 0.888 in the stepwise selection model, which included model 1 + THP, progranulin, and clusterin, and to 0.889 in the final model, which included also AGP.
In this validation study using ELISA, we were able to confirm the value of several proteins previously identified through the label-free protein expression as potential predictors of early diabetic nephropathy and that added to the model fit above and beyond previously identified risk markers. Discovery-based quantitative proteomics provide a powerful technique for identification and quantification in large-scale protein profiling for biomarker discovery, and multiple proteomic techniques are available (21–23). To date, most proteomic approaches have used two-dimensional gel electrophoresis or capillary electrophoresis–mass spectrometry to classify type 1 diabetes and its complications (24–26).
Label-free protein expression is a peptide-based proteomic technique that capitalizes on the highly reproducible chromatography and accurate mass accuracy available in current LC/MS systems. This platform quantifies a peptide by its intensity and groups each peptide across individual samples on the basis of its accurate mass and retention time (27,28). These intensities associated with specific mass and retention time values are organized into peptide array tables that may be further processed using statistical techniques. The label-free protein expression analysis in the current study provided a comprehensive view of proteomic changes during the development of microalbuminuria from which predictive models could be derived. The models highlight a number of clinically relevant proteins, as well as novel indicators of disease.
THP, which is produced in the thick ascending limb and the early distal convoluted tubule of the kidney, is the most abundant protein in normal urine. THP is the protein product encoded by the uromodulin gene (UMOD), which has been identified in genome-wide association scans with chronic kidney disease and GFR estimated from serum creatinine (29). Urinary THP has been suggested as a useful marker of renal damage and has been reported to be decreased in patients with type 1 diabetes (30–32) and in patients with kidney damage with and without diabetes (33). In the current study, we found that levels of THP were significantly increased in patients who developed both ERFD and albuminuria. Köttgen et al. (34) also found that higher levels of THP were associated with chronic kidney disease in a case-control study, with an odds ratio for chronic kidney disease of 1.72 per 1 SD increase in THP.
AGP has previously been reported as increasing in patients with diabetic nephropathy (35,36) and may serve as both an early marker of diabetic nephropathy as well as a marker of diabetic nephropathy progression. Prostaglandin D synthase, which was not predictive of renal outcomes in the current study, was previously reported to be increased in patients with type 2 diabetes who had increased permeability of glomerular capillary walls, and higher levels of prostaglandin D synthase predicted albuminuria (37).
Other proteins included in the model (clusterin and progranulin), while not directly associated with diabetic nephropathy, were observed to be associated with renal toxicity and/or renal damage. Clusterin is a glycoprotein that may have a role in repairing kidney damage, since low levels of clusterin have been found to predict worse recovery from renal ischemia-reperfusion injury in mice (38). Clusterin may have a role in protecting organisms from apoptosis because of oxidative stress (39) and may prevent glomerulopathy associated with aging (40). Progranulin is a growth factor involved in wound healing and is known to have an anti-inflammatory effect (41). On the other hand, when progranulin is degraded into peptides by proteases, it has been shown to have a proinflammatory effect (42).
The current study provided important preliminary data on a panel of proteins that could be used to predict the early signs of diabetic nephropathy, including the development of micro- and macroalbuminuria as well as significant renal function decline. Further validation of this protein panel is needed in other populations to verify their predictive ability for the development of both renal function decline and urinary albumin and to determine whether these could be used as biomarkers of disease progression and response to treatment.
This study was performed at the Barbara Davis Center for Childhood Diabetes in Denver, CO, and at the Case Center for Proteomics and Bioinformatics at Case Western Reserve University, Cleveland, OH. Support was provided by the National Institutes of Health (NIH) National Heart, Lung and Blood Institute grants R01 HL61753 and R01 HL079611, American Diabetes Association postdoctoral fellowship 7-09-CVD-06 (mass spectrometry), American Diabetes Association Junior Faculty Award 1-10-JF-50 (J.K.S.-B.), and Diabetes Endocrinology Research Center Clinical Investigation Core P30 DK57516. The study was performed at the Clinical Translational Research Center at the University of Colorado Denver, supported by NIH Grant M01 RR000051. Support was also provided in part from the Cleveland Center for Translational Science Collaborative of the NIH (UL1-RR024989).
No potential conflicts of interest relevant to this article were reported.
D.S. researched data and wrote the manuscript. D.M.M. and M.R.C. contributed to the discussion and reviewed and edited the manuscript. J.-E.D., X.L., and F.H. researched data and reviewed and edited the manuscript. M.R. reviewed and edited the manuscript. J.K.S.-B. researched data, wrote the manuscript, and contributed to the discussion. J.K.S.-B. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
The article contains Supplementary Data online at http://care.diabetesjournals.org/lookup/suppl/doi:10.2337/dc11-1491/-/DC1.
- Received August 9, 2011.
- Accepted November 22, 2011.
- © 2012 by the American Diabetes Association.
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