Acute Kidney Injury, Systemic Inflammation and Long-term Cognitive Function: ASSESS-AKI.


Journal

Clinical journal of the American Society of Nephrology : CJASN
ISSN: 1555-905X
Titre abrégé: Clin J Am Soc Nephrol
Pays: United States
ID NLM: 101271570

Informations de publication

Date de publication:
10 May 2024
Historique:
received: 07 11 2023
accepted: 07 05 2024
medline: 10 5 2024
pubmed: 10 5 2024
entrez: 10 5 2024
Statut: aheadofprint

Résumé

Cognitive dysfunction is a well-known complication of chronic kidney disease, but it is less known whether cognitive decline occurs in survivors after acute kidney injury (AKI). We hypothesized that an episode of AKI is associated with poorer cognitive function, mediated, at least in part, by persistent systemic inflammation. ASSESS-AKI enrolled patients surviving three months after hospitalization with and without AKI matched based on demographics, comorbidities, and baseline kidney function. A subset underwent cognitive testing using the modified mini-mental status examination (3MS) at 3, 12, and 36 months. We examined the association of AKI with 3MS scores using mixed linear models and assessed the proportion of risk mediated by systemic inflammatory biomarkers. Among 1538 participants in ASSESS-AKI, 1420 (92%) completed the 3MS assessment at 3 months and had a corresponding matched participant. Participants with AKI had lower 3MS scores at three years (difference -1.1 (95% CI: -2.0, -0.3) P=0.009) compared to participants without AKI. A higher proportion of AKI participants had a clinically meaningful (≥ 5 point) reduction in 3MS scores at three years compared to participants without AKI (14% vs. 10%, P=0.04). In mediation analyses, plasma soluble tumor necrosis factor receptor-1 (sTNFR-1) at three months after AKI mediated 35% (P=0.02) of the AKI related risk for 3MS scores at three years. AKI was associated with lower 3MS scores and sTNFR-1 concentrations appeared to mediate a significant proportion of the risk of long-term cognitive impairment. Further work is needed to determine if AKI is causal or a marker for cognitive impairment.

Sections du résumé

BACKGROUND BACKGROUND
Cognitive dysfunction is a well-known complication of chronic kidney disease, but it is less known whether cognitive decline occurs in survivors after acute kidney injury (AKI). We hypothesized that an episode of AKI is associated with poorer cognitive function, mediated, at least in part, by persistent systemic inflammation.
METHODS METHODS
ASSESS-AKI enrolled patients surviving three months after hospitalization with and without AKI matched based on demographics, comorbidities, and baseline kidney function. A subset underwent cognitive testing using the modified mini-mental status examination (3MS) at 3, 12, and 36 months. We examined the association of AKI with 3MS scores using mixed linear models and assessed the proportion of risk mediated by systemic inflammatory biomarkers.
RESULTS RESULTS
Among 1538 participants in ASSESS-AKI, 1420 (92%) completed the 3MS assessment at 3 months and had a corresponding matched participant. Participants with AKI had lower 3MS scores at three years (difference -1.1 (95% CI: -2.0, -0.3) P=0.009) compared to participants without AKI. A higher proportion of AKI participants had a clinically meaningful (≥ 5 point) reduction in 3MS scores at three years compared to participants without AKI (14% vs. 10%, P=0.04). In mediation analyses, plasma soluble tumor necrosis factor receptor-1 (sTNFR-1) at three months after AKI mediated 35% (P=0.02) of the AKI related risk for 3MS scores at three years.
CONCLUSIONS CONCLUSIONS
AKI was associated with lower 3MS scores and sTNFR-1 concentrations appeared to mediate a significant proportion of the risk of long-term cognitive impairment. Further work is needed to determine if AKI is causal or a marker for cognitive impairment.

Identifiants

pubmed: 38728094
doi: 10.2215/CJN.0000000000000473
pii: 01277230-990000000-00386
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Division of Diabetes, Endocrinology, and Metabolic Diseases
ID : K23DK116967
Organisme : Division of Diabetes, Endocrinology, and Metabolic Diseases
ID : R01DK133177

Informations de copyright

Copyright © 2024 by the American Society of Nephrology.

Auteurs

Pavan K Bhatraju (PK)

Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington.
Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington.

Leila R Zelnick (LR)

Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington.

Ian B Stanaway (IB)

Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington.

T Alp Ikizler (TA)

Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN.

Steven Menez (S)

Division of Nephrology, School of Medicine, Johns Hopkins University, Baltimore, MD.

Vernon M Chinchilli (VM)

Department of Public Health Sciences, Penn State College of Medicine, Hershey, PA.

Steve G Coca (SG)

Section of Nephrology, Department of Internal Medicine, Mount Sinai School of Medicine, New York, NY.

James S Kaufman (JS)

Division of Nephrology, New York University School of Medicine, New York, NY and Division of Nephrology, VA New York Harbor Healthcare System, New York, NY.

Paul L Kimmel (PL)

National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.

Chirag R Parikh (CR)

Division of Nephrology, School of Medicine, Johns Hopkins University, Baltimore, MD.

Alan S Go (AS)

Division of Nephrology, Department of Medicine, University of California, San Francisco, CA.
Division of Research, Kaiser Permanente Northern California, Oakland, CA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, CA.

Edward D Siew (ED)

Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN.

Mark M Wurfel (MM)

Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington.
Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington.

Jonathan Himmelfarb (J)

Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington.

Classifications MeSH