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Pilot & Feasibility
Pilot & Feasibility Program Application Abstract
Multi-scale imaging tools to map pathology and gene expression in the human kidney
(Saint Louis, MO)
Pilot & Feasibility Program
The goal of this pilot and feasibility study is to develop a multi-scale framework to evaluate the human kidney, to provide an improved understanding of diabetic kidney disease. Pathologies associated with kidney disease are highly heterogeneous, with wide variability in presentation within and between subjects. This heterogeneity limits the ability of histopathology derived from biopsies due to sampling bias, despite recent significant advances in histologic analysis. In diabetic patients, even kidney biopsies are not normally performed to detect progression to diabetic kidney disease (DKD), and noninvasive imaging biomarkers are early in development. Thus, there is a lack in knowledge about 1) Early microstructural biomarkers that could predict which diabetic patients progress to DKD or end stage kidney disease and 2) How pathology relates to structure, function, and gene expression across the entire kidney. Here we bridge the gap between anatomical structure, microstructural features, and gene expression to provide a multi-scale, three-dimensional map of the whole, intact human kidney. These preliminary studies will be performed in donor kidneys from a local organ procurement organization, not accepted for transplantation. We will investigate kidneys from both healthy and diabetic kidneys to establish preliminary data to guide future work. In Aim 1 we will combine three-dimensional, multi-parametric MRI with image-guided site directed biopsy to correlate imaging features with histopathology and measure the level of intra- and inter-kidney heterogeneity present in typical tissue. We will also investigate how these parameters relate to vascular, glomerular, and pyramidal morphology. In Aim 2 we will investigate how both single-cell and bulk RNA profiles vary within and between kidneys and how these are related to gross microstructural features. We will compare parameters measured in Aims 1-2 between kidneys from the healthy and diabetic donors. Together, this work will establish the image acquisition and processing framework to evaluate the human kidney across the scales from gross anatomy to gene expression. It will also provide preliminary data to support studies to understand heterogeneous pathology and its etiology during development of DKD.
Data for this report has not yet been released.
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Please acknowledge all posters, manuscripts or scientific materials that were generated in part or whole using funds from the Diabetic Complications Consortium(DiaComp) using the following text:
Financial support for this work provided by the NIDDK Diabetic Complications Consortium (RRID:SCR_001415, www.diacomp.org), grants DK076169 and DK115255
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