Literature DB >> 35372952

Initial Validation of a Machine Learning-Derived Prognostic Test (KidneyIntelX) Integrating Biomarkers and Electronic Health Record Data To Predict Longitudinal Kidney Outcomes.

Kinsuk Chauhan1, Girish N Nadkarni1, Fergus Fleming2, James McCullough2, Cijiang J He1, John Quackenbush3, Barbara Murphy1, Michael J Donovan4, Steven G Coca1, Joseph V Bonventre5.   

Abstract

Background: Individuals with type 2 diabetes (T2D) or the apolipoprotein L1 high-risk (APOL1-HR) genotypes are at increased risk of rapid kidney function decline (RKFD) and kidney failure. We hypothesized that a prognostic test using machine learning integrating blood biomarkers and longitudinal electronic health record (EHR) data would improve risk stratification.
Methods: We selected two cohorts from the Mount Sinai BioMe Biobank: T2D (n=871) and African ancestry with APOL1-HR (n=498). We measured plasma tumor necrosis factor receptors (TNFR) 1 and 2 and kidney injury molecule-1 (KIM-1) and used random forest algorithms to integrate biomarker and EHR data to generate a risk score for a composite outcome: RKFD (eGFR decline of ≥5 ml/min per year), or 40% sustained eGFR decline, or kidney failure. We compared performance to a validated clinical model and applied thresholds to assess the utility of the prognostic test (KidneyIntelX) to accurately stratify patients into risk categories.
Results: Overall, 23% of those with T2D and 18% of those with APOL1-HR experienced the composite kidney end point over a median follow-up of 4.6 and 5.9 years, respectively. The area under the receiver operator characteristic curve (AUC) of KidneyIntelX was 0.77 (95% CI, 0.75 to 0.79) in T2D, and 0.80 (95% CI, 0.77 to 0.83) in APOL1-HR, outperforming the clinical models (AUC, 0.66 [95% CI, 0.65 to 0.67] and 0.72 [95% CI, 0.71 to 0.73], respectively; P<0.001). The positive predictive values for KidneyIntelX were 62% and 62% versus 46% and 39% for the clinical models (P<0.01) in high-risk (top 15%) stratum for T2D and APOL1-HR, respectively. The negative predictive values for KidneyIntelX were 92% in T2D and 96% for APOL1-HR versus 85% and 93% for the clinical model, respectively (P=0.76 and 0.93, respectively), in low-risk stratum (bottom 50%). Conclusions: In patients with T2D or APOL1-HR, a prognostic test (KidneyIntelX) integrating biomarker levels with longitudinal EHR data significantly improved prediction of a composite kidney end point of RKFD, 40% decline in eGFR, or kidney failure over validated clinical models.
Copyright © 2020 by the American Society of Nephrology.

Entities:  

Keywords:  APOL1 protein; HAVCR1 protein; TNFRSF1A protein; apolipoprotein L1; area under curve; biologic specimen banks; clinical nephrology; diabetes mellitus; electronic health records; follow-up studies; glomerular filtration rate; hepatitis A virus cellular receptor 1; human; prognosis; receptors; tumor necrosis factor; tumor necrosis factors; type 2; type I

Mesh:

Substances:

Year:  2020        PMID: 35372952      PMCID: PMC8815746          DOI: 10.34067/KID.0002252020

Source DB:  PubMed          Journal:  Kidney360        ISSN: 2641-7650


  38 in total

1.  APOL1 risk variants, race, and progression of chronic kidney disease.

Authors:  Afshin Parsa; W H Linda Kao; Dawei Xie; Brad C Astor; Man Li; Chi-yuan Hsu; Harold I Feldman; Rulan S Parekh; John W Kusek; Tom H Greene; Jeffrey C Fink; Amanda H Anderson; Michael J Choi; Jackson T Wright; James P Lash; Barry I Freedman; Akinlolu Ojo; Cheryl A Winkler; Dominic S Raj; Jeffrey B Kopp; Jiang He; Nancy G Jensvold; Kaixiang Tao; Michael S Lipkowitz; Lawrence J Appel
Journal:  N Engl J Med       Date:  2013-11-09       Impact factor: 91.245

2.  Risk Prediction for Early CKD in Type 2 Diabetes.

Authors:  Daniela Dunkler; Peggy Gao; Shun Fu Lee; Georg Heinze; Catherine M Clase; Sheldon Tobe; Koon K Teo; Hertzel Gerstein; Johannes F E Mann; Rainer Oberbauer
Journal:  Clin J Am Soc Nephrol       Date:  2015-07-14       Impact factor: 8.237

3.  GFR Slope as a Surrogate End Point for Kidney Disease Progression in Clinical Trials: A Meta-Analysis of Treatment Effects of Randomized Controlled Trials.

Authors:  Lesley A Inker; Hiddo J L Heerspink; Hocine Tighiouart; Andrew S Levey; Josef Coresh; Ron T Gansevoort; Andrew L Simon; Jian Ying; Gerald J Beck; Christoph Wanner; Jürgen Floege; Philip Kam-Tao Li; Vlado Perkovic; Edward F Vonesh; Tom Greene
Journal:  J Am Soc Nephrol       Date:  2019-07-10       Impact factor: 10.121

4.  Circulating TNF receptors 1 and 2 predict stage 3 CKD in type 1 diabetes.

Authors:  Tomohito Gohda; Monika A Niewczas; Linda H Ficociello; William H Walker; Jan Skupien; Florencia Rosetti; Xavier Cullere; Amanda C Johnson; Gordon Crabtree; Adam M Smiles; Tanya N Mayadas; James H Warram; Andrzej S Krolewski
Journal:  J Am Soc Nephrol       Date:  2012-01-19       Impact factor: 10.121

5.  Circulating TNF receptors 1 and 2 predict ESRD in type 2 diabetes.

Authors:  Monika A Niewczas; Tomohito Gohda; Jan Skupien; Adam M Smiles; William H Walker; Florencia Rosetti; Xavier Cullere; John H Eckfeldt; Alessandro Doria; Tanya N Mayadas; James H Warram; Andrzej S Krolewski
Journal:  J Am Soc Nephrol       Date:  2012-01-19       Impact factor: 10.121

6.  Incorporating temporal EHR data in predictive models for risk stratification of renal function deterioration.

Authors:  Anima Singh; Girish Nadkarni; Omri Gottesman; Stephen B Ellis; Erwin P Bottinger; John V Guttag
Journal:  J Biomed Inform       Date:  2014-11-15       Impact factor: 6.317

7.  The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.

Authors:  Catherine A McCarty; Rex L Chisholm; Christopher G Chute; Iftikhar J Kullo; Gail P Jarvik; Eric B Larson; Rongling Li; Daniel R Masys; Marylyn D Ritchie; Dan M Roden; Jeffery P Struewing; Wendy A Wolf
Journal:  BMC Med Genomics       Date:  2011-01-26       Impact factor: 3.063

8.  Association of Soluble TNFR-1 Concentrations with Long-Term Decline in Kidney Function: The Multi-Ethnic Study of Atherosclerosis.

Authors:  Pavan K Bhatraju; Leila R Zelnick; Michael Shlipak; Ronit Katz; Bryan Kestenbaum
Journal:  J Am Soc Nephrol       Date:  2018-10-04       Impact factor: 10.121

9.  Soluble Tumor Necrosis Factor Receptor 1 Is Associated with Glomerular Filtration Rate Progression and Incidence of Chronic Kidney Disease in Two Community-Based Cohorts of Elderly Individuals.

Authors:  Axel C Carlsson; Lina Nordquist; Tobias E Larsson; Juan-Jesús Carrero; Anders Larsson; Lars Lind; Johan Ärnlöv
Journal:  Cardiorenal Med       Date:  2015-07-31       Impact factor: 2.041

10.  Empagliflozin and Progression of Kidney Disease in Type 2 Diabetes.

Authors:  Christoph Wanner; Silvio E Inzucchi; John M Lachin; David Fitchett; Maximilian von Eynatten; Michaela Mattheus; Odd Erik Johansen; Hans J Woerle; Uli C Broedl; Bernard Zinman
Journal:  N Engl J Med       Date:  2016-06-14       Impact factor: 91.245

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  3 in total

1.  The Next Frontier: Biomarkers and Artificial Intelligence Predicting Cardiorenal Outcomes in Diabetic Kidney Disease.

Authors:  Gregory L Braden; Daniel L Landry
Journal:  Kidney360       Date:  2022-09-29

2.  Course Corrections for Clinical AI.

Authors:  Alex J DeGrave; Joseph D Janizek; Su-In Lee
Journal:  Kidney360       Date:  2021-09-27

3.  Cohort design and natural language processing to reduce bias in electronic health records research.

Authors:  Shaan Khurshid; Christopher Reeder; Lia X Harrington; Pulkit Singh; Gopal Sarma; Samuel F Friedman; Paolo Di Achille; Nathaniel Diamant; Jonathan W Cunningham; Ashby C Turner; Emily S Lau; Julian S Haimovich; Mostafa A Al-Alusi; Xin Wang; Marcus D R Klarqvist; Jeffrey M Ashburner; Christian Diedrich; Mercedeh Ghadessi; Johanna Mielke; Hanna M Eilken; Alice McElhinney; Andrea Derix; Steven J Atlas; Patrick T Ellinor; Anthony A Philippakis; Christopher D Anderson; Jennifer E Ho; Puneet Batra; Steven A Lubitz
Journal:  NPJ Digit Med       Date:  2022-04-08
  3 in total

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