Identification of novel mechanistic markers with prognostic value in clinical course of chronic kidney disease (CKD) will provide a better understanding of disease process and improve care of the patients by identification of high risk groups at earlier stages. Importantly, identification of mechanistic pathways will be amenable to novel preventive or therapeutic interventions. This study is aimed at comparing the predictive power of ANCUAL (Amino acids, Nucleotides, intermediates of Citric acid and Urea cycles, Acylcarnitines, and Lipids) metabolic panel to predict progression of CKD by comparing their area under Receiver Operating Characteristics (ROC) curves with those of the traditional markers (serum creatinine, urinary protein, eGFR) at early stage. We also aim to explore the link between the proposed metabolic markers with the renal tissue expression level of genes involved in regulation of these markers. Methods: This will be a nested case-cohort study. Study populations consist of participants of Chronic Renal Insufficiency Cohort (CRIC) for measurement of metabolites, and Clinical Phenotyping Resource and Biobank Core (CPROBE) for transcriptomics- metabolomics integrative analysis. Inclusion criteria are entry age of 21 to 74 years with eGFR of 30-70 for CRIC participants, and entry eGFR of 30 mL/min or higher for CPROBE participants. Exclusion criteria are the same as CRIC and CPROBE core studies. Sampling: From CRIC participants; case group is defined as 100 patients who have progressed to ESRD including 50 patients with diabetes and 50 patients without diabetes. Control group will be 100 patients matched by age, sex, race, diabetes, and baseline eGFR (N=200). This sampling will be replicated to get another 200 patients from CRIC in the validation phase (total=400). From CPROBE participants; 42 participants with available gene expression data obtained from kidney biopsy will be selected. Data collection: Starting with CRIC, fasting serum samples from baseline will be collected. First, samples will be subjected to targeted metabolomics analysis by mass spectrometry (MS) for quantification of ANCUAL panel, in the first 200 CRIC participants. This will be followed by an untargeted metabolomic analysis for expansion of the initial panel, followed by an orthogonal quantification of the newly identified prognostic metabolites to validate the discovery of the new compounds from untargeted platform. The expanded ANCUAL panel will then undergo replication in a targeted platform in another 200 independent samples from CIRC to validate the final panel. At last step the final panel will be quantified in the baseline serum samples of CPROBE participants in an attempt to integrate with their transcriptomics data. Predictors are the expanded ANCUAL panel derived from MS. Outcome is incident ESRD. Covariates include demographics, laboratory values, comorbidities, physical examination findings and anthropometric measures from the time of sample collection. Analysis: Multiple logistic regression analysis will be applied to identify the independent components of a multi panel marker among the differentially expressed baseline panel. C-statistics will be applied to compare the area under Receiver Operating Characteristics (ROC) curve of the multi-panel marker with that if the traditional biomarkers for discrimination of progressors from non-progressors. Integrated discrimination improvement, net reclassification index, and C-statistics will be applied to assess the classification improvement of the expanded panel compared to baseline panel. Risk of ESRD by quartiles of the proposed panel will be estimated using logistic regression adjusting for relevant prognostic covariates. Gene and metabolic set enrichment analysis will be applied to test enrichment of differentially regulated metabolic pathways. Bioinformatics tools will be used for pathway recognition.

Public Health Relevance

Lack of prognostic biomarkers predictive of outcome at early stages of CKD necessitates shift of paradigm from exclusive reliance on traditional biomarkers to mechanistically driven approaches for identification and validation of prognostic biomarkers in CKD and their incorporation in clinical care. This study is aimed at comparing the predictive power of proposed panel of biomarkers to predict progression of CKD to ESRD with the traditional biomarkers such as serum creatinine, urinary protein excretion and eGFR, using a mass- spectrometry based metabolomics approach through a nested case-cohort design. We also aim at exploring the signature of progression in kidney tissue by exploring the relationship between the proposed metabolic panels with the renal tissue expression level of corresponding genes. As metabolic derangements start at early CKD, identification of novel biomarkers representative of kidney injury and its progression may provide the opportunities for detecting high risk patients and developing targeted preventive and therapeutic interventions at early stage with ultimate goal of improving care and outcome of the patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
1K08DK106523-01
Application #
8949489
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Rankin, Tracy L
Project Start
2015-09-17
Project End
2020-07-31
Budget Start
2015-09-17
Budget End
2016-07-31
Support Year
1
Fiscal Year
2015
Total Cost
$147,449
Indirect Cost
$10,922
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Afshinnia, Farsad; Rajendiran, Thekkelnaycke M; Wernisch, Stefanie et al. (2018) Lipidomics and Biomarker Discovery in Kidney Disease. Semin Nephrol 38:127-141
Jadoon, Adil; Mathew, Anna V; Byun, Jaeman et al. (2018) Gut Microbial Product Predicts Cardiovascular Risk in Chronic Kidney Disease Patients. Am J Nephrol 48:269-277
Afshinnia, Farsad; Zeng, Lixia; Byun, Jaeman et al. (2018) Elevated lipoxygenase and cytochrome P450 products predict progression of chronic kidney disease. Nephrol Dial Transplant :
Wernisch, Stefanie; Afshinnia, Farsad; Rajendiran, Thekkelnaycke et al. (2018) Probing the application range and selectivity of a differential mobility spectrometry-mass spectrometry platform for metabolomics. Anal Bioanal Chem 410:2865-2877
Afshinnia, Farsad; Rajendiran, Thekkelnaycke M; Soni, Tanu et al. (2018) Impaired ?-Oxidation and Altered Complex Lipid Fatty Acid Partitioning with Advancing CKD. J Am Soc Nephrol 29:295-306
Bria, Carmen R M; Afshinnia, Farsad; Skelly, Patrick W et al. (2018) Asymmetrical flow field-flow fractionation for improved characterization of human plasma lipoproteins. Anal Bioanal Chem :
Afshinnia, Farsad; Zeng, Lixia; Byun, Jaeman et al. (2017) Myeloperoxidase Levels and Its Product 3-Chlorotyrosine Predict Chronic Kidney Disease Severity and Associated Coronary Artery Disease. Am J Nephrol 46:73-81
Mazidi, M; Pennathur, S; Afshinnia, F (2017) Link of dietary patterns with metabolic syndrome: analysis of the National Health and Nutrition Examination Survey. Nutr Diabetes 7:e255
Ding, Fangrui; Wickman, Larysa; Wang, Su Q et al. (2017) Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome. Kidney Int 92:1515-1525
Shamsaeefar, Alireza; Shafiee, Mohammad; Nikeghbalian, Saman et al. (2017) Biliary reconstruction in liver transplant patients with primary sclerosing cholangitis, duct-to-duct or Roux-en-Y? Clin Transplant 31:

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