Evidence map›Paper›PMID 41278313›Full record

ArticleKidney international reports2025

Uric Acid Trajectories and CKD Progression in the African American Study of Kidney Disease and Hypertension.

Yoojin Lee, Michael S Lipkowitz, Jeffrey B Kopp, Cheryl A Winkler, Sung Kweon Cho

Abstract read
In one paragraph

Article in Kidney international reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Yoojin LeeExperimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institute of Health, Bethesda, Maryland, USA.
Michael S LipkowitzDepartment of Medicine, Georgetown University School of Medicine, Washington, District of Columbia, USA.
Jeffrey B KoppKidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Cheryl A WinklerBasic Research Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.
Sung Kweon ChoBasic Research Program, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.

Funding

NCI NIH HHS HHSN261201500003CNCI NIH HHS HHSN261201500003I
6 · The paper itself

Abstract

Introduction: Serum uric acid levels increase with progressive kidney disease, and chronic elevations may contribute to chronic kidney disease (CKD) progression. We analyzed data from the African American Study of Kidney Disease and Hypertension (AASK) to examine the hypothesis that individuals with declining serum urate levels during follow-up would experience slower loss of kidney function. Methods: The AASK recruited 1094 African-American individuals with reduced estimated glomerular filtration rate (eGFR) and followed up with them for up to 12 years. The eGFR and defined end-stage kidney disease (ESKD) composite score were used to establish CKD stages. We employed a Cox proportional hazards model to investigate the association between uric acid trajectories and the composite ESKD outcome. Results: Compared with the normo-increasing uric acid group (i.e., those who had the lowest overall serum uric acid levels), the high-stable (hazard ratio [HR] = 2.28, Conclusion: Uric acid trajectories are associated with ESKD incidence in African Americans with CKD. Tracking temporal changes in uric acid improves the assessment of ESKD risk in CKD progression.

Indexed as

end-stage kidney disease (ESKD)hyperuricemiatrajectory analysisuric acid

Identifiers

PMID41278313
PMCPMC12640014

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.