Black and White Adults With CKD Hospitalized With Acute Kidney Injury: Findings From the Chronic Renal Insufficiency Cohort (CRIC) Study.
Adult
Humans
Acute Kidney Injury
/ epidemiology
Angiotensin-Converting Enzyme Inhibitors
Angiotensins
Apolipoprotein L1
Cohort Studies
Creatinine
Glomerular Filtration Rate
/ physiology
Hospitalization
Prospective Studies
Renal Insufficiency, Chronic
/ epidemiology
Risk Factors
Sickle Cell Trait
Black People
White People
Acute kidney injury (AKI)
Black race
CRIC
White race
chronic kidney disease (CKD)
clinical risk factors
health care inequity
hospitalization
racial disparities
serum creatinine (Scr)
Journal
American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
received:
13
10
2021
accepted:
21
02
2022
pubmed:
12
4
2022
medline:
26
10
2022
entrez:
11
4
2022
Statut:
ppublish
Résumé
Few studies have investigated racial disparities in acute kidney injury (AKI), in contrast to the extensive literature on racial differences in the risk of kidney failure. We sought to study potential differences in risk in the setting of chronic kidney disease (CKD). Prospective cohort study. We studied 2,720 self-identified Black or White participants with CKD enrolled in the Chronic Renal Insufficiency Cohort (CRIC) Study from July 1, 2013, to December 31, 2017. Self-reported race (Black vs White). Hospitalized AKI (≥50% increase from nadir to peak serum creatinine). Cox regression models adjusting for demographics (age and sex), prehospitalization clinical risk factors (diabetes, blood pressure, cardiovascular disease, estimated glomerular filtration rate, proteinuria, receipt of angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers), and socioeconomic status (insurance status and education level). In a subset of participants with genotype data, we adjusted for apolipoprotein L1 gene (APOL1) high-risk status and sickle cell trait. Black participants (n = 1,266) were younger but had a higher burden of prehospitalization clinical risk factors. The incidence rate of first AKI hospitalization among Black participants was 6.3 (95% CI, 5.5-7.2) per 100 person-years versus 5.3 (95% CI, 4.6-6.1) per 100 person-years among White participants. In an unadjusted Cox regression model, Black participants were at a modestly increased risk of incident AKI (HR, 1.22 [95% CI, 1.01-1.48]) compared with White participants. However, this risk was attenuated and no longer significant after adjusting for prehospitalization clinical risk factors (adjusted HR, 1.02 [95% CI, 0.83-1.25]). There were only 11 AKI hospitalizations among individuals with high-risk APOL1 risk status and 14 AKI hospitalizations among individuals with sickle cell trait. Participants were limited to research volunteers and potentially not fully representative of all CKD patients. In this multicenter prospective cohort of CKD patients, racial disparities in AKI incidence were modest and were explained by differences in prehospitalization clinical risk factors.
Identifiants
pubmed: 35405207
pii: S0272-6386(22)00583-2
doi: 10.1053/j.ajkd.2022.02.021
pmc: PMC9547036
mid: NIHMS1800770
pii:
doi:
Substances chimiques
Angiotensin-Converting Enzyme Inhibitors
0
Angiotensins
0
APOL1 protein, human
0
Apolipoprotein L1
0
Creatinine
AYI8EX34EU
Types de publication
Multicenter Study
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
610-618.e1Subventions
Organisme : NCATS NIH HHS
ID : UL1 TR002548
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK060963
Pays : United States
Organisme : NIDDK NIH HHS
ID : U2C DK114886
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024131
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061022
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK119199
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000003
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000439
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK060990
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK114857
Pays : United States
Organisme : NIDDK NIH HHS
ID : K24 DK092291
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR029879
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061028
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000433
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL153161
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK119562
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK060984
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061021
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK060990
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK060980
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000424
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR016500
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM109036
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK060902
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK114014
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK120811
Pays : United States
Investigateurs
Lawrence J Appel
(LJ)
Jing Chen
(J)
Debbie L Cohen
(DL)
James P Lash
(JP)
Robert G Nelson
(RG)
Mahboob Rahman
(M)
Panduranga S Rao
(PS)
Vallabh O Shah
(VO)
Mark L Unruh
(ML)
Informations de copyright
Copyright © 2022 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.
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