Cardiovascular mortality is the leading cause of death in Chronic kidney disease patients and traditional risk factors do not fully explain the 10-40 times increased risk in kidney patients. We use our expertise in metabolomics and proteomics on animal and clinical studies to demonstrate the role of heme enzyme myeloperoxidase in oxidizing vascular wall proteins and high density lipoprotein making them dysfunctional.
Salt sensitivity and hypertension are risk factors for Chronic Kidney Disease progression, but very little evidence exists on the metabolic basis and role of salt sensitivity in kidney disease. We aim to delineate the metabolic markers associated with salt sensitivity in kidney patients using targeted metabolomics in animal and clinical studies.
Diabetic kidney disease remains the primary cause of end-stage renal disease. We explore the metabolic determinants of the diabetic kidney disease using a targeted metabolomics and mechanistic animal metabolic flux studies to demonstrate the patho-physiological roles of these metabolites in disease process.
NIH, National Heart Lung and Blood Institute
George O'Brien Michigan Kidney Translational Core Center Pilot and Feasibility Grant
Michigan Nutrition and Obesity Research Center Pilot and Feasibility Grant
Michigan Proteomics Resource Facility Pilot and Feasibility Grant
University of Michigan ADVANCE program Elizabeth Caroline Crosby Award
University of Michigan Geriatric and Palliative Care Medicine -Pilot and Exploratory Studies Core (PESC)
Michigan Institute for Clinical and Health Research (MICHR)
Michigan Taubman Institute
Michigan Biology of Cardiovascular Aging (MBoCA)
Dr. Subramaniam Pennathur (Neph)
Dr. Pavan Reddy (Hem-Onc)
Dr. Rajiv Saran (Neph)
Dr. Brenda Gillespie (SPH)
Dr. Rodica Pop-Busui (MEND)
Dr. Farsad Afshinnia (Neph)
Dr. Laura Mariani (Neph)
Dr. Mathias Kretzler (Neph)
Dr. Robert Brooks (Cardiology)
Dr. Kumar Sharma (UTHSCSA)
Dr. Anne-Emiliee Decleves (Universite de Mons, Belgium)