Evidence map›Paper›PMID 39843671›Full record

ArticleJournal of general internal medicine2025

Kidney Function, Cognitive Impairment, and Trajectories: A Longitudinal Biracial Study.

Katharine L Cheung, Miguel Arce Renteria, Peter W Callas, Manjula Kurella Tamura, Orlando M Gutierrez, Mary Cushman, Michael LaMantia

Abstract read
In one paragraph

Article in Journal of general internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Katharine L CheungUniversity of Vermont College of Medicine, Burlington, VT, USA. klcheung@med.uvm.edu.ORCID 0000-0002-2282-4778
Miguel Arce RenteriaColumbia University, New York, NY, USA.
Peter W CallasUniversity of Vermont College of Medicine, Burlington, VT, USA.
Manjula Kurella TamuraStanford University School of Medicine, Stanford, CA, USA.
Orlando M GutierrezThe University of Alabama at Birmingham School of Medicine, Birmingham, AL, USA.
Mary CushmanUniversity of Vermont College of Medicine, Burlington, VT, USA.
Michael LaMantiaVeterans Administration Healthcare System, Portland, OR, USA.

Funding

VCID and Stroke in a Bi-racial National CohortU01NS041588 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CUSHMAN, MARY, HOWARD, GEORGE · 2002 to 2022
$96.0M
Vermont Center for Cardiovascular and Brain HealthP20GM135007 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Kathryn H Morelli · 2020 to 2026
$17.4M
Mentored patient-oriented research in disparities in cardiovascular and kidney diseaseK24DK116180 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M · 2018 to 2022
$749k
A Mentoring Program in Kidney Care for Older AdultsK24AG073615 · NIA · STANFORD UNIVERSITY · PI MANJULA KURELLA TAMURA · 2022 to 2026
$651k
NIA NIH HHS K24AG073615NIDDK NIH HHS K24DK116180NIGMS NIH HHS P20 GM135007NINDS NIH HHS U01 NS041588
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) is associated with incident cognitive impairment (ICI) and disproportionately affects older adults and Black persons.

objectiveTo determine (1) whether age or race differences exist in the association of CKD and ICI and (2) whether cognitive trajectories differ in people with and without CKD.

designNationwide cohort study.

participantsA total of 22,435 Black and White adults age ≥ 45 years without baseline cognitive impairment. MEASUREMENTS: Creatinine-cystatin C-based eGFR and albumin-to-creatinine ratio (ACR). Six-item screener (SIS) of global cognition every 6 months, three cognitive domain tests (memory, semantic, and letter fluencies) every 2 years for 10 years. Logistic regression for risk of CI and latent growth curve models for trajectory analysis.

resultsParticipants were 56% female, 37% Black, 56% hypertensive, and 19% had diabetes. Overall, 13% (n = 2959) developed ICI over 10 years. In mid-life (age 45- < 65), the OR (95% CI) of ICI for eGFR < 45 vs eGFR ≥ 90 was 1.9 (1.2, 3.0); in late-life (≥ 65), the OR was 0.9 (0.7, 1.1), p interaction < 0.001. For ACR > 300 vs ACR < 10, in mid-life and late-life, the ORs were 1.6 (1.0, 2.6) and 1.0 (0.7, 1.4), p interaction 0.02. Compared to those with eGFR ≥ 60, eGFR < 60 was associated with lower initial cognitive domains scores, worse in mid-life than late-life, but the slopes did not differ. Compared to ACR < 30, ACR ≥ 30 had lower initial cognitive domain scores, which were similar in mid and late-life, and a steeper decline for memory scores. No differences by race were observed.

conclusionsKidney disease was more strongly linked to cognitive impairment in mid-life than in late-life. Albuminuria was associated with steeper decline in memory function, especially in mid-life. PRIMARY FUNDING SOURCE: NIGMS.

Indexed as

Cognition DisordersCognitive DysfunctionRenal Insufficiency, ChronicAgedAged, 80 and overBlack or African AmericanCohort StudiesFemaleGlomerular Filtration RateHumansKidney Function TestsLongitudinal StudiesMaleMiddle AgedWhite

Identifiers

PMID39843671
PMCPMC12586251

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.