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

Authors :
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 J L, 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 M J, 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
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
Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET)
Groningen Kidney Center (GKC)
Source :
Diabetes Care, 45, 9, pp. 2055-2063, Diabetes Care, 45(9), 2055-2063. AMER DIABETES ASSOC, Diabetes Care, 45, 2055-2063
Publication Year :
2022
Publisher :
AMER DIABETES ASSOC, 2022.

Abstract

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 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.

Details

Language :
English
ISSN :
19355548 and 01495992
Volume :
45
Issue :
9
Database :
OpenAIRE
Journal :
Diabetes Care
Accession number :
edsair.doi.dedup.....00f7d045f621eb8b8780b2cc124c1cf0