Chronic Kidney Disease (CKD) is a global health epidemic and patients with CKD suffer from increased mortality and cardiovascular disease. Despite the severity of the disease, there are limited treatment options to hinder its progression. Tubular injury (TI) is a common finding on many kidney biopsies from patients with CKD, and there is mechanistic data supporting that TI can lead to interstitial fibrosis and tubular atrophy. While interstitial fibrosis and tubular atrophy are the strongest known pathologic predictor of progression of CKD, we have limited understand of how TI contributes to this progression. Hypoxia Inducible Factor-1? (HIF-1?) has been shown in animal studies to impact the severity of TI and is also known to trigger a fibrotic cascade, but there is limited data regarding its overall activity in kidney tissue, its cell type specific activity, its association with pathologic features or patient outcomes. It is of utmost importance to better understand this pathway as several Prolyl Hydroxylase inhibitors, which are novel therapeutic agents that increase the expression of HIF- 1?, are currently in clinical trial testing to treat anemia of CKD.
The first aim of this proposal is to develop a measure of HIF-1? pathway activity that enables evaluation of clinical and morphologic features and cell-type specificity. Specifically, the candidate will a) Identify clinical and pathologic descriptors associated with increased HIF-1? pathway activity score and b) Determine the cell-type specific expression level of HIF-1? and its downstream components in tubular cells using single-cell RNA-sequencing.
The second aim of this proposal is to determine the association of increased HIF-1? activity with outcomes and identify patients with increased HIF-1? activity non-invasively using biomarkers. Specifically, the candidate will a) Determine the association of increased HIF-1? activity score with patient outcomes and b) Identify serum or urine biomarkers that detect increased HIF-1? pathway activity in patients. The candidate will analyze data from 3 cohorts to accomplish these aims: Nephrotic Syndrome Study Network (NEPTUNE), Clinical Phenotyping Resource and Biobank Core (C-PROBE) and the Native Americans with Type 2 Diabetes cohort (formerly known as the Pima Indian cohort). These investigations will allow us to monitor HIF-1? activity non-invasively in trials where patients receive novel drug agents, such as Prolyl Hydroxylase Inhibitors. The candidate will obtain formal training in analysis of gene expression data, single cell RNA- sequencing and machine learning techniques during the course of the award period to successfully integrate gene expression data, pathology data and clinical data. She will be mentored by an expert team with complementary experience in nephrology, tubular injury biology, systems biology and bioinformatics. The long-term goal of these investigations is to ultimately be able to better sub-type patients with tubular injury based on mechanistic terms.

Public Health Relevance

Chronic Kidney Disease is a global health epidemic and is associated with increased mortality, but we do not have a detailed understanding of why this disease progresses. Identifying sub-types of patients who progress by the same molecular mechanism is important to identify patients for future clinical trials. This project aims to use gene expression data from kidney biopsies to identify patients who will respond differently to medications that increase the expression of Hypoxia Inducible Factor-1 alpha.

National Institute of Health (NIH)
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Clinical Investigator Award (CIA) (K08)
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Kidney, Urologic and Hematologic Diseases D Subcommittee (DDK)
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Rankin, Tracy L
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University of Michigan Ann Arbor
Internal Medicine/Medicine
Schools of Medicine
Ann Arbor
United States
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