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Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes Mellitus..docx (136.97 kB)

Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes.

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posted on 2022-09-28, 08:46 authored by Morgan E Grams, Nigel J Brunskill, Shoshana H Ballew, Yingying Sang, Josef Coresh, Kunihiro Matsushita, Aditya Surapaneni, Samira Bell, Juan J Carrero, Gabriel Chodick, Marie Evans, Hiddo JL Heerspink, Lesley A Inker, Kunitoshi Iseki, Philip A Kalra, H Lester Kirchner, Brian J Lee, Adeera Levin, Rupert W Major, James Medcalf, Girish N Nadkarni, David MJ Naimark, Ana C Ricardo, Simon Sawhney, Manish M Sood, Natalie Staplin, Nikita Stempniewicz, Benedicte Stengel, Keiichi Sumida, Jamie P Traynor, Jan van den Brand, Chi-Pang Wen, Mark Woodward, Jae Won Yang, Angela Yee-Moon Wang, Navdeep Tangri, CKD Prognosis Consortium, John Chalmers, Chi-Yuan Hsu, Amanda Anderson, Panduranga Rao, Harold Feldman, Alex R Chang, Kevin Ho, Jamie Green, Moneeza Siddiqui, Colin Palmer, Varda Shalev, Marie Metzger, Martin Flamant, Pascal Houillier, Jean-Philippe Haymann, John Cuddeback, Elizabeth Ciemins, Csaba P Kovesdy, Marco Trevisan, Carl Gustaf Elinder, Björn Wettermark, Philip Kalra, Rajkumar Chinnadurai, James Tollitt, Darren Green, Ron T Gansevoort, Orlando Gutierrez, Tsuneo Konta, Anna Köttgen, Andrew S Levey, Kevan Polkinghorne, Elke Schäffner, Luxia Zhang, Jingsha Chen

Objective

To predict adverse kidney outcomes for use in optimizing medical management and clinical trial design.

Research design and methods

In this meta-analysis of individual participant data, 43 cohorts (N = 1,621,817) from research studies, electronic medical records, and clinical trials with global representation were separated into development and validation cohorts. Models were developed and validated within strata of diabetes mellitus (presence or absence) and estimated glomerular filtration rate (eGFR; ≥60 or <60 mL/min/1.73 m2) to predict a composite of ≥40% decline in eGFR or kidney failure (i.e., receipt of kidney replacement therapy) over 2-3 years.

Results

There were 17,399 and 24,591 events in development and validation cohorts, respectively. Models predicting ≥40% eGFR decline or kidney failure incorporated age, sex, eGFR, albuminuria, systolic blood pressure, antihypertensive medication use, history of heart failure, coronary heart disease, atrial fibrillation, smoking status, and BMI, and, in those with diabetes, hemoglobin A1c, insulin use, and oral diabetes medication use. The median C-statistic was 0.774 (interquartile range [IQR] = 0.753, 0.782) in the diabetes and higher-eGFR validation cohorts; 0.769 (IQR = 0.758, 0.808) in the diabetes and lower-eGFR validation cohorts; 0.740 (IQR = 0.717, 0.763) in the no diabetes and higher-eGFR validation cohorts; and 0.750 (IQR = 0.731, 0.785) in the no diabetes and lower-eGFR validation cohorts. Incorporating the previous 2-year eGFR slope minimally improved model performance, and then only in the higher-eGFR cohorts.

Conclusions

Novel prediction equations for a decline of ≥40% in eGFR can be applied successfully for use in the general population in persons with and without diabetes with higher or lower eGFR.

Funding

The CKD Prognosis Consortium (CKD-PC) Data Coordinating Center is funded in part by a program grant from the US National Kidney Foundation and the National Institute of Diabetes and Digestive and Kidney Diseases (Grant R01DK100446)

History

Author affiliation

Department of Cardiovascular Sciences, University of Leicester

Version

  • AM (Accepted Manuscript)

Published in

Diabetes care

Volume

45

Issue

9

Pagination

2055 - 2063

Publisher

American Diabetes Association

issn

0149-5992

eissn

1935-5548

Copyright date

2022

Available date

2022-09-28

Spatial coverage

United States

Language

eng

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