New Creatinine- and Cystatin C-Based Equations to Estimate GFR without Race.
Détails
Télécharger: Inker et al New creatinine- and cystatin C–based equations to esti- mate GFR without race NEJM 2021.pdf (2683.81 [Ko])
Etat: Public
Version: Final published version
Licence: Non spécifiée
Etat: Public
Version: Final published version
Licence: Non spécifiée
Document(s) secondaire(s)
Télécharger: Inker et al New creatinine- and cystatin C–based equations to esti- mate GFR without race Suppl NEJM 2021.pdf (3478.26 [Ko])
Etat: Public
Version: Supplementary document
Licence: Non spécifiée
Etat: Public
Version: Supplementary document
Licence: Non spécifiée
ID Serval
serval:BIB_D550EFCE6824
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
New Creatinine- and Cystatin C-Based Equations to Estimate GFR without Race.
Périodique
The New England journal of medicine
Collaborateur⸱rice⸱s
Chronic Kidney Disease Epidemiology Collaboration
Contributeur⸱rice⸱s
Andresdottir M.B., Gudmundsdottir H., Indridason O.S., Palsson R., Kasiske B., Weir M., Pesavento T., Kalil R., Feldman H., Anderson A., Go A., Hsu C.Y., Chapman A.B., Landsittel D.P., Mrug M., Yu ASL, Steffes M., Braffett B.H., Wyatt C., Krishnasami Z., Hellinger J., Abraham A., Lieske J.C., Shafi T., Post W., Rossing P., Rossert J., Stengel B., Galecki A., Spino C., Mauer M., Karger A., Zinman B., Klein R., Parving H.H., Looker H.C., Knowler W.C., Klintmalm G.B., Velez R., Selvin E., Wang D.
ISSN
1533-4406 (Electronic)
ISSN-L
0028-4793
Statut éditorial
Publié
Date de publication
04/11/2021
Peer-reviewed
Oui
Volume
385
Numéro
19
Pages
1737-1749
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural
Publication Status: ppublish
Publication Status: ppublish
Résumé
Current equations for estimated glomerular filtration rate (eGFR) that use serum creatinine or cystatin C incorporate age, sex, and race to estimate measured GFR. However, race in eGFR equations is a social and not a biologic construct.
We developed new eGFR equations without race using data from two development data sets: 10 studies (8254 participants, 31.5% Black) for serum creatinine and 13 studies (5352 participants, 39.7% Black) for both serum creatinine and cystatin C. In a validation data set of 12 studies (4050 participants, 14.3% Black), we compared the accuracy of new eGFR equations to measured GFR. We projected the prevalence of chronic kidney disease (CKD) and GFR stages in a sample of U.S. adults, using current and new equations.
In the validation data set, the current creatinine equation that uses age, sex, and race overestimated measured GFR in Blacks (median, 3.7 ml per minute per 1.73 m <sup>2</sup> of body-surface area; 95% confidence interval [CI], 1.8 to 5.4) and to a lesser degree in non-Blacks (median, 0.5 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 0.0 to 0.9). When the adjustment for Black race was omitted from the current eGFR equation, measured GFR in Blacks was underestimated (median, 7.1 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 5.9 to 8.8). A new equation using age and sex and omitting race underestimated measured GFR in Blacks (median, 3.6 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 1.8 to 5.5) and overestimated measured GFR in non-Blacks (median, 3.9 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 3.4 to 4.4). For all equations, 85% or more of the eGFRs for Blacks and non-Blacks were within 30% of measured GFR. New creatinine-cystatin C equations without race were more accurate than new creatinine equations, with smaller differences between race groups. As compared with the current creatinine equation, the new creatinine equations, but not the new creatinine-cystatin C equations, increased population estimates of CKD prevalence among Blacks and yielded similar or lower prevalence among non-Blacks.
New eGFR equations that incorporate creatinine and cystatin C but omit race are more accurate and led to smaller differences between Black participants and non-Black participants than new equations without race with either creatinine or cystatin C alone. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases.).
We developed new eGFR equations without race using data from two development data sets: 10 studies (8254 participants, 31.5% Black) for serum creatinine and 13 studies (5352 participants, 39.7% Black) for both serum creatinine and cystatin C. In a validation data set of 12 studies (4050 participants, 14.3% Black), we compared the accuracy of new eGFR equations to measured GFR. We projected the prevalence of chronic kidney disease (CKD) and GFR stages in a sample of U.S. adults, using current and new equations.
In the validation data set, the current creatinine equation that uses age, sex, and race overestimated measured GFR in Blacks (median, 3.7 ml per minute per 1.73 m <sup>2</sup> of body-surface area; 95% confidence interval [CI], 1.8 to 5.4) and to a lesser degree in non-Blacks (median, 0.5 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 0.0 to 0.9). When the adjustment for Black race was omitted from the current eGFR equation, measured GFR in Blacks was underestimated (median, 7.1 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 5.9 to 8.8). A new equation using age and sex and omitting race underestimated measured GFR in Blacks (median, 3.6 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 1.8 to 5.5) and overestimated measured GFR in non-Blacks (median, 3.9 ml per minute per 1.73 m <sup>2</sup> ; 95% CI, 3.4 to 4.4). For all equations, 85% or more of the eGFRs for Blacks and non-Blacks were within 30% of measured GFR. New creatinine-cystatin C equations without race were more accurate than new creatinine equations, with smaller differences between race groups. As compared with the current creatinine equation, the new creatinine equations, but not the new creatinine-cystatin C equations, increased population estimates of CKD prevalence among Blacks and yielded similar or lower prevalence among non-Blacks.
New eGFR equations that incorporate creatinine and cystatin C but omit race are more accurate and led to smaller differences between Black participants and non-Black participants than new equations without race with either creatinine or cystatin C alone. (Funded by the National Institute of Diabetes and Digestive and Kidney Diseases.).
Mots-clé
Adult, African Continental Ancestry Group, Aged, Algorithms, Continental Population Groups, Creatinine/blood, Cystatin C/blood, Datasets as Topic, Female, Glomerular Filtration Rate, Humans, Male, Middle Aged, Renal Insufficiency, Chronic/blood, Renal Insufficiency, Chronic/epidemiology, Renal Insufficiency, Chronic/ethnology, Renal Insufficiency, Chronic/physiopathology, United States/epidemiology
Pubmed
Web of science
Open Access
Oui
Création de la notice
01/10/2021 16:33
Dernière modification de la notice
18/10/2023 6:10