Rationale and design of the Kidney Precision Medicine Project. Author Ian de Boer, Charles Alpers, Evren Azeloglu, Ulysses Balis, Jonathan Barasch, Laura Barisoni, Kristina Blank, Andrew Bomback, Keith Brown, Pierre Dagher, Ashveena Dighe, Michael Eadon, Tarek El-Achkar, Joseph Gaut, Nir Hacohen, Yongqun He, Jeffrey Hodgin, Sanjay Jain, John Kellum, Krzysztof Kiryluk, Richard Knight, Zoltan Laszik, Chrysta Lienczewski, Laura Mariani, Robyn McClelland, Steven Menez, Dennis Moledina, Sean Mooney, John O'Toole, Paul Palevsky, Chirag Parikh, Emilio Poggio, Sylvia Rosas, Matthew Rosengart, Minnie Sarwal, Jennifer Schaub, John Sedor, Kumar Sharma, Becky Steck, Robert Toto, Olga Troyanskaya, Katherine Tuttle, Miguel Vazquez, Sushrut Waikar, Kayleen Williams, Francis Wilson, Kun Zhang, Ravi Iyengar, Matthias Kretzler, Jonathan Himmelfarb, Kidney Precision Medicine Project Publication Year 2021 Type Journal Article Abstract Chronic kidney disease (CKD) and acute kidney injury (AKI) are common, heterogeneous, and morbid diseases. Mechanistic characterization of CKD and AKI in patients may facilitate a precision-medicine approach to prevention, diagnosis, and treatment. The Kidney Precision Medicine Project aims to ethically and safely obtain kidney biopsies from participants with CKD or AKI, create a reference kidney atlas, and characterize disease subgroups to stratify patients based on molecular features of disease, clinical characteristics, and associated outcomes. An additional aim is to identify critical cells, pathways, and targets for novel therapies and preventive strategies. This project is a multicenter prospective cohort study of adults with CKD or AKI who undergo a protocol kidney biopsy for research purposes. This investigation focuses on kidney diseases that are most prevalent and therefore substantially burden the public health, including CKD attributed to diabetes or hypertension and AKI attributed to ischemic and toxic injuries. Reference kidney tissues (for example, living-donor kidney biopsies) will also be evaluated. Traditional and digital pathology will be combined with transcriptomic, proteomic, and metabolomic analysis of the kidney tissue as well as deep clinical phenotyping for supervised and unsupervised subgroup analysis and systems biology analysis. Participants will be followed prospectively for 10 years to ascertain clinical outcomes. Cell types, locations, and functions will be characterized in health and disease in an open, searchable, online kidney tissue atlas. All data from the Kidney Precision Medicine Project will be made readily available for broad use by scientists, clinicians, and patients. Keywords Humans, Proteomics, Adult, Kidney, Prospective Studies, Precision Medicine, Acute Kidney Injury, Renal Insufficiency, Chronic Journal Kidney Int Volume 99 Issue 3 Pages 498-510 Date Published 2021 Mar ISSN Number 1523-1755 DOI 10.1016/j.kint.2020.08.039 Alternate Journal Kidney Int PMCID PMC8330551 PMID 33637194 PubMedPubMed CentralGoogle ScholarBibTeXEndNote X3 XML