Rationale and design of the Kidney Precision Medicine Project

肾脏疾病 医学 急性肾损伤 重症监护医学 肾病科 内科学 病理 生物信息学 生物
作者
Ian H. de Boer,Charles E. Alpers,Evren U. Azeloglu,Ulysses G. Balis,Jonathan Barasch,Laura Barisoni,Kristina N. Blank,Andrew S. Bomback,Keith Brown,Pierre C. Dagher,Ashveena Dighe,Michael T. Eadon,Tarek M. El‐Achkar,Joseph P. Gaut,Nir Hacohen,Yongqun He,Jeffrey B. Hodgin,Sanjay Jain,John A. Kellum,Krzysztof Kiryluk,Richard Knight,Zoltán Lászik,Chrysta Lienczewski,Laura Mariani,Robyn L. McClelland,Steven Menez,Dennis G. Moledina,Sean D. Mooney,John F. O’Toole,Paul M. Palevsky,Chirag R. Parikh,Emilio D. Poggio,Sylvia E. Rosas,Matthew R. Rosengart,Minnie Sarwal,Jennifer A. Schaub,John R. Sedor,Kumar Sharma,Becky Steck,Robert D. Toto,Olga G. Troyanskaya,Katherine R. Tuttle,Miguel A. Vázquez,Sushrut S. Waikar,Kayleen Williams,F. Perry Wilson,Kun Zhang,Ravi Iyengar,Matthias Kretzler,Jonathan Himmelfarb,Richard Knight,Stewart H. Lecker,Isaac E. Stillman,Sushrut S. Waikar,Gearoid M. McMahon,Astrid Weins,Samuel Short,Nir Hacohen,Paul Hoover,Mark P. Aulisio,Leslie Cooperman,Leal Herlitz,John F. O’Toole,Emilio D. Poggio,John R. Sedor,Stacey E. Jolly,Paul S. Appelbaum,Olivia Balderes,Jonathan Barasch,Andrew S. Bomback,Pietro A. Canetta,Vivette D. D’Agati,Krzysztof Kiryluk,Satoru Kudose,Karla Mehl,Jai Radhakrishnan,Chen-hua Weng,Laura Barisoni,Theodore Alexandrov,Tarek Ashkar,Daria Barwinska,Pierre C. Dagher,Kenneth W. Dunn,Michael T. Eadon,Michael J. Ferkowicz,Katherine J. Kelly,Timothy A. Sutton,Seth Winfree,Steven Menez,Chirag R. Parikh,Avi Z. Rosenberg,Pam Villalobos,Rubab F. Malik,Derek M. Fine,Mohammed Atta,Jose Manuel Monroy Trujillo,Alison Slack,Sylvia E. Rosas,Mark Williams,Evren U. Azeloglu,Cijang He,Ravi Iyengar,Jens Hansen,Samir V. Parikh,Brad H. Rovin,Chris Anderton,Ljiljana Paša‐Tolić,Dušan Veličković,Jessica Lukowski,George Oliver,Joseph Ardayfio,Jack Bebiak,Keith Brown,Taneisha Campbell,Catherine E. Campbell,Lynda Hayashi,Nichole Jefferson,Robert Koewler,Glenda V. Roberts,John Saul,Anna Shpigel,Edith Christine Stutzke,Lorenda Wright,Leslie Miegs,Roy Pinkeney,Rachel Sealfon,Olga G. Troyanskaya,Katherine R. Tuttle,Deján Dobi,Yury Goltsev,Blue B. Lake,Kun Zhang,Maria Joanes,Zoltán Lászik,Andrew Schroeder,Minnie Sarwal,Tara K. Sigdel,Ulysses G. Balis,Victoria M. Blanc,Oliver He,Jeffrey B. Hodgin,Matthias Kretzler,Laura Mariani,Rajasree Menon,Edgar A. Otto,Jennifer A. Schaub,Becky Steck,Chrysta Lienczewski,Sean Eddy,Michele Elder,Daniel E. Hall,John A. Kellum,Mary Kruth,Raghav Murugan,Paul M. Palevsky,Parmjeet Randhawa,Matthew R. Rosengart,Sunny Sims-Lucas,Mary Stefanick,Stacy Stull,Mitchell Tublin,Charles E. Alpers,Ian H. de Boer,Ashveena Dighe,Jonathan Himmelfarb,Robyn L. McClelland,Sean D. Mooney,Stuart J. Shankland,Kayleen Williams,Kristina N. Blank,Jonas Carson,Frederick Dowd,Zach Drager,Chris Park,Kumar Sharma,Guanshi Zhang,Shweta Bansal,Manjeri A. Venkatachalam,Asra Kermani,Simon Lee,Christopher Y. Lu,Tyler Miller,Orson W. Moe,Harold S. Park,Kamalanathan K. Sambandam,Francisco Javier Carrasco Sánchez,José Torrealba,Robert Toto,Miguel A. Vázquez,Nancy Wang,Joe Gaut,Sanjay Jain,Anitha Vijayan,Randy L. Luciano,Dennis G. Moledina,Ugwuowo Ugochukwu,F. Perry Wilson,Sandy Alfano
出处
期刊:Kidney International [Elsevier BV]
卷期号:99 (3): 498-510 被引量:98
标识
DOI:10.1016/j.kint.2020.08.039
摘要

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. 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. Patient perspectives and involvement in precision medicine researchKidney InternationalVol. 99Issue 3PreviewThe Kidney Precision Medicine Project will advance understanding of chronic kidney disease attributed to diabetes or hypertension and acute kidney injury through a protocol kidney biopsy used for deep phenotyping with state-of-the-art methodology. To guide scientific inquiry toward clinically meaningful benefit, patients are equal partners for priority setting, study design and conduct, and dissemination of findings. Patients from stakeholder organizations, recruitment sites, tissue interrogation sites, and the Central Hub are represented on the Community Engagement Committee. Full-Text PDF

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