Evidence map›Paper›PMID 42081475›Full record

ArticlePLOS digital health2026

Dynamically predicting renal failure after development of diabetes across biobanks.

Aubrey Jensen, Sayera Dhaubhadel, Jonathan Hori, Nabil Alami, Gang Li, Hua Zhou, Sridharan Raghavan, Benjamin H McMahon, Peter Reaven, Jin J Zhou

Abstract read
In one paragraph

Article in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Aubrey JensenDepartment of Biostatistics, University of California, Los Angeles, California, United States of America.
Sayera DhaubhadelLos Alamos National Laboratory, Los Alamos, New Mexico, United States of America.ORCID https://orcid.org/0000-0003-1683-634X
Jonathan HoriDepartment of Biostatistics, University of California, Los Angeles, California, United States of America.
Nabil AlamiCentraleSupélec, Université Paris-Saclay, Gif-sur-Yvette, France.
Gang LiDepartment of Biostatistics, University of California, Los Angeles, California, United States of America.
Hua ZhouDepartment of Biostatistics, University of California, Los Angeles, California, United States of America.
Sridharan RaghavanSection of Academic Primary Care, United States of America Department of Veterans Affairs Eastern Colorado Health Care System, Aurora, Colorado, United States of America.
Benjamin H McMahonLos Alamos National Laboratory, Los Alamos, New Mexico, United States of America.
Peter ReavenPhoenix VA Health Care System, Phoenix, Arizona, United States of America.
Jin J ZhouDepartment of Biostatistics, University of California, Los Angeles, California, United States of America.ORCID https://orcid.org/0000-0001-7983-0274

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

End-stage renal disease (ESRD) remains a major complication of diabetes, yet existing static risk scores may lose accuracy as patient profiles evolve and competing mortality risks change over time. We developed and externally validated a landmark-based ESRD Dynamic Risk Score (ESRD-DRS) that updates individual risk estimates at 1, 5, and 10 years after diabetes diagnosis using routinely collected EHR data. We assembled a retrospective cohort of 708,435 U.S. Veterans with newly diagnosed diabetes in the Veterans Health Administration (VHA). At 1, 5, and 10 years after diabetes diagnosis (LM1, LM5, and LM10), we fit penalized Fine-Gray subdistribution hazard models, drawing from more than 400 demographic, medication, comorbidity, and laboratory variables. Models were evaluated over 1-, 5-, and 10-year horizons for discrimination (area under the time-dependent receiver operating characteristic curve [AUROC]) and calibration (Brier score), and compared with the established RECODe and 4-variable KFRE risk equations. External validation was performed in an independent All of Us (AoU) cohort (n = 13,223). In the VHA cohort (median follow-up 7.6 years), 8,955 patients (1.26%) developed ESRD, and 136,666 (19.3%) died without ESRD. At LM1, ESRD-DRS achieved AUROCs of 0.93, 0.90, and 0.85 for 1-, 5-, and 10-year risk, respectively, and Brier scores ranging from 0.00098 to 0.0162. In the AoU cohort, corresponding AUROCs were 0.94, 0.91, and 0.86, with similar calibration performance. RECODe and KFRE yielded lower discrimination and poorer calibration. Top risk predictors, including estimated glomerular filtration rate, albuminuria, systolic blood pressure, and age, were consistent across landmarks and cohorts. ESRD-DRS, a scalable landmark approach that accounts for competing mortality and evolving patient profiles, outperformed existing static equations. Embedding ESRD-DRS into EHR workflows may support more timely, individualized ESRD risk assessment in patients with diabetes.

Identifiers

PMID42081475
PMCPMC13138643

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.