Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes.
Journal
Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975
Informations de publication
Date de publication:
01 09 2022
01 09 2022
Historique:
received:
10
04
2022
accepted:
16
05
2022
pubmed:
21
7
2022
medline:
9
9
2022
entrez:
20
7
2022
Statut:
ppublish
Résumé
To predict adverse kidney outcomes for use in optimizing medical management and clinical trial design. 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. 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. 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.
Identifiants
pubmed: 35856507
pii: 147251
doi: 10.2337/dc22-0698
pmc: PMC9472501
doi:
Banques de données
figshare
['10.2337/figshare.20061143']
Types de publication
Journal Article
Meta-Analysis
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2055-2063Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK100446
Pays : United States
Investigateurs
John Chalmers
(J)
Mark Woodward
(M)
Chi-Yuan Hsu
(CY)
Ana C Ricardo
(AC)
Amanda Anderson
(A)
Panduranga Rao
(P)
Harold Feldman
(H)
Alex R Chang
(AR)
Kevin Ho
(K)
Jamie Green
(J)
H Lester Kirchner
(HL)
Samira Bell
(S)
Moneeza Siddiqui
(M)
Colin Palmer
(C)
Varda Shalev
(V)
Gabriel Chodick
(G)
Benedicte Stengel
(B)
Marie Metzger
(M)
Martin Flamant
(M)
Pascal Houillier
(P)
Jean-Philippe Haymann
(JP)
Nikita Stempniewicz
(N)
John Cuddeback
(J)
Elizabeth Ciemins
(E)
Csaba P Kovesdy
(CP)
Keiichi Sumida
(K)
Juan J Carrero
(JJ)
Marco Trevisan
(M)
Carl Gustaf Elinder
(CG)
Björn Wettermark
(B)
Philip Kalra
(P)
Rajkumar Chinnadurai
(R)
James Tollitt
(J)
Darren Green
(D)
Josef Coresh
(J)
Shoshana H Ballew
(SH)
Alex R Chang
(AR)
Ron T Gansevoort
(RT)
Morgan E Grams
(ME)
Orlando Gutierrez
(O)
Tsuneo Konta
(T)
Anna Köttgen
(A)
Andrew S Levey
(AS)
Kunihiro Matsushita
(K)
Kevan Polkinghorne
(K)
Elke Schäffner
(E)
Mark Woodward
(M)
Luxia Zhang
(L)
Shoshana H Ballew
(SH)
Jingsha Chen
(J)
Josef Coresh
(J)
Morgan E Grams
(ME)
Kunihiro Matsushita
(K)
Yingying Sang
(Y)
Aditya Surapaneni
(A)
Mark Woodward
(M)
Informations de copyright
© 2022 by the American Diabetes Association.
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