Kidney Outcomes with Sodium-Glucose Cotransporter-2 Inhibitor Initiation after Acute Kidney Injury among Veterans with Diabetic Kidney Disease.


Journal

Kidney360
ISSN: 2641-7650
Titre abrégé: Kidney360
Pays: United States
ID NLM: 101766381

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 01 09 2023
accepted: 22 01 2024
medline: 30 1 2024
pubmed: 30 1 2024
entrez: 30 1 2024
Statut: aheadofprint

Résumé

The effect of SGLT2i on kidney function after acute kidney injury (AKI) is unknown. The study population was drawn from a retrospective cohort of Veterans with diabetes mellitus type 2 (DM2) and proteinuria. The study exposure was time-varying use of SGLT2i after an index AKI hospitalization. The two study outcomes were time-to- 1) a sustained decrease in eGFR over at least three months to <60 mL/minute/1.73 m2 and ≥30% below a post-AKI-updated eGFR and 2) recurrent hospitalization with AKI. AKI was defined as a rise in serum creatinine concentration to ≥50% above a moving outpatient creatinine baseline. DM2 was defined by ≥2 billing codes related to DM2 prior to the index AKI; proteinuria was defined by the most recent albuminuria, proteinuria, or urinalysis test. Veterans were required to have a baseline eGFR and an eGFR 3-12 months after the index AKI hospitalization ≥30 mL/minute/1.73 m2. 10,036 Veterans met study inclusion criteria. 2,794 (28%) received a SGLT2i. 775 (8%) had CKD progression and 1,816 (18%) had recurrent AKI over a median follow-up of 1.8 and 1.7 years, respectively, which began one year after the index AKI hospitalization. SGLT2i use was associated with lower risk for CKD progression [adjusted hazard ratio (aHR) 0.72 (95% confidence interval (CI): 0.57-0.91)] and for recurrent AKI [aHR 0.75 (95% CI: 0.65-0.88)]. SGLT2i use was associated with a lower risk for CKD progression and for recurrent AKI among those with diabetic kidney disease and recent AKI.

Sections du résumé

BACKGROUND BACKGROUND
The effect of SGLT2i on kidney function after acute kidney injury (AKI) is unknown.
METHODS METHODS
The study population was drawn from a retrospective cohort of Veterans with diabetes mellitus type 2 (DM2) and proteinuria. The study exposure was time-varying use of SGLT2i after an index AKI hospitalization. The two study outcomes were time-to- 1) a sustained decrease in eGFR over at least three months to <60 mL/minute/1.73 m2 and ≥30% below a post-AKI-updated eGFR and 2) recurrent hospitalization with AKI. AKI was defined as a rise in serum creatinine concentration to ≥50% above a moving outpatient creatinine baseline. DM2 was defined by ≥2 billing codes related to DM2 prior to the index AKI; proteinuria was defined by the most recent albuminuria, proteinuria, or urinalysis test. Veterans were required to have a baseline eGFR and an eGFR 3-12 months after the index AKI hospitalization ≥30 mL/minute/1.73 m2.
RESULTS RESULTS
10,036 Veterans met study inclusion criteria. 2,794 (28%) received a SGLT2i. 775 (8%) had CKD progression and 1,816 (18%) had recurrent AKI over a median follow-up of 1.8 and 1.7 years, respectively, which began one year after the index AKI hospitalization. SGLT2i use was associated with lower risk for CKD progression [adjusted hazard ratio (aHR) 0.72 (95% confidence interval (CI): 0.57-0.91)] and for recurrent AKI [aHR 0.75 (95% CI: 0.65-0.88)].
CONCLUSIONS CONCLUSIONS
SGLT2i use was associated with a lower risk for CKD progression and for recurrent AKI among those with diabetic kidney disease and recent AKI.

Identifiants

pubmed: 38287468
doi: 10.34067/KID.0000000000000375
pii: 02200512-990000000-00327
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology.

Auteurs

Daniel P Murphy (DP)

Department of Medicine, Medical School, University of Minnesota, Minneapolis, MN.

Julian Wolfson (J)

Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN.

Scott Reule (S)

Department of Medicine, Medical School, University of Minnesota, Minneapolis, MN.
Section of Nephrology, Minneapolis Veterans Affairs Health Care System, Minneapolis, MN.

Kirsten L Johansen (KL)

Department of Medicine, Medical School, University of Minnesota, Minneapolis, MN.
Division of Nephrology, Hennepin Healthcare, Minneapolis, MN.
Chronic Disease Research Group, Hennepin Healthcare Research Institute, Minneapolis, MN.

Areef Ishani (A)

Department of Medicine, Medical School, University of Minnesota, Minneapolis, MN.
Section of Nephrology, Minneapolis Veterans Affairs Health Care System, Minneapolis, MN.

Paul E Drawz (PE)

Department of Medicine, Medical School, University of Minnesota, Minneapolis, MN.

Classifications MeSH