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novel plasma peptide markers involved in the pathology of ckd identified using mass spectrometric approach
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نویسنده
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gajjala prathibha r. ,bruck heike ,noels heidi ,heinze georg ,ceccarelli francesco ,kribben andreas ,saez-rodriguez julio ,marx nikolaus ,zidek walter ,jankowski joachim ,jankowski vera
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منبع
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journal of molecular medicine - 2019 - دوره : 97 - شماره : 10 - صفحه:1451 -1463
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چکیده
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Chronic kidney disease (ckd) progress to end-stage renal disease (esrd) at different pace. early markers of disease progression could facilitate and improve patient management. however, conventional blood and urine chemistry have proven unable to predict the progression of disease at early stages. therefore, we performed untargeted plasma peptidome analysis to select the peptides involved in progression, which are suitable for long prospective studies in future. the study consists of non-ckd (n = 66) and ckd (n = 106) patients with different stages. we performed plasma peptidomics on these subjects using chromatography and mass spectrometric approaches. initially, we performed lc-esi-ms and applied least absolute shrinkage and selection operator logistic regressions to select the peptides that are differentially expressed and we generated a peptidomic score for each subject. later, we identified and sequenced the peptides with maldi-ms/ms and also performed univariate and multivariate analyses with the clinical variables and peptidomic score to reveal their association with progression of renal disease. a logistic regression model selected 14 substances showing different concentrations according to renal function, of which seven substances were most likely occur in ckd patients. the peptidomic model had a global p value of < 0.01 with r2 of 0.466, and the area under the curve was 0.87 (95% ci, 0.8149–0.9186; p < 0.0001). the predicted score was significantly higher in ckd than in non-ckd patients (2.539 ± 0.2637 vs − 0.9382 ± 0.1691). the model was also able to predict stages of ckd: the spearman correlation coefficient of the linear predictor with ckd stages was 0.83 with concordance indices of 0.899 (95% ci 0.863–0.927). in univariate analysis, the most consistent association of peptidomic score in ckd patients was with c-reactive protein, sodium level, and uric acid, which are unanticipated substances. peptidomic analysis enabled to list some unanticipated substances that have not been extensively studied in the context of ckd but were associated with ckd progression, thus revealing interesting candidate markers or mediators of ckd of potential use in ckd progression management. • conventional blood and urine chemistry have proven unable to predict the progression of disease at early stages of chronic kidney disease (ckd). • we performed untargeted plasma peptidome analysis to select the peptides involved in progression. • a logistic regression model selected 14 substances showing different concentrations according to renal function. • these peptides are unanticipated substances that have not been extensively studied in the context of ckd but were associated with ckd progression, thus revealing markers or mediators of ckd of potential use in ckd progression management.
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کلیدواژه
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chronic kidney disease ,end-stage renal disease ,disease progression ,systems medicine ,proteomics ,peptidomics
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آدرس
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university hospital rwth aachen, institute of molecular cardiovascular research, germany, helios hospital krefeld, department of internal medicine, germany, university hospital rwth aachen, institute of molecular cardiovascular research, germany, medical university of vienna, section for clinical biometrics, center for medical statistics, austria, rwth aachen university, joint research centre for computational biomedicine, germany, university hospital essen, university of duisburg-essen, department of nephrology, germany, rwth aachen university, joint research centre for computational biomedicine, germany. heidelberg university, institute for computational biomedicine, faculty of medicine bioquant, germany, university hospital aachen, department of internal medicine i, germany, charité-universitätsmedizin berlin, germany, university hospital rwth aachen, institute of molecular cardiovascular research, germany. university of maastricht, cardiovascular research institute maastricht (carim), netherlands, university hospital rwth aachen, institute of molecular cardiovascular research, germany
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Authors
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