Evidence map›Paper›PMID 42176190›Full record

ArticleJournal of medical systems2026

Machine Learning-Predicted Risk Trajectories for Incident Chronic Kidney Disease and Associations with Post-CKD Outcomes.

Aaron Boussina, Amy M Sitapati, Soo-Young Yoon, Sripad Karne, Jongwoo Seo, Woo-Jung Kim, Hyeon Seok Hwang

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Article in Journal of medical systems, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Aaron Boussina *Division of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, USA.
Amy M Sitapati *Division of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, USA.
Soo-Young YoonDivision of Nephrology, Department of Internal Medicine, Kyung Hee University Hospital, Seoul, Korea.
Sripad KarneDivision of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, USA.
Jongwoo SeoAI Research Laboratory, Department of Nephrology, Kyung Hee University Medical Center, Seoul, Republic of Korea.
Woo-Jung KimDivision of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, USA.
Hyeon Seok HwangDivision of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, San Diego, CA, USA. hwanghsne@gmail.com.

Funding

George M. O'Brien Kidney Resource Alliance 5U24DK137318Patient-Centered Clinical Research Coordinating Center (PACEN) RS-2025-25394255
6 · The paper itself

Abstract

Chronic kidney disease (CKD) is a progressive condition where risk accumulates before clinical onset. However, strategies for evaluating CKD risk remain limited, and the trajectories of risk over time are poorly understood. We enrolled 51,156 individuals without CKD in the University of California health system between 2012 and 2024. A debiased XGBoost model was developed to predict CKD risk, and the predicted probabilities from this model at each visit were used to derive risk trajectories through latent class growth mixture modeling. The model achieved a time-dependent area under the curve of 0.95 (95% confidence interval (CI), 0.94-0.96), a C-index of 0.93 (0.92-0.94), and a Brier score of 0.027 (0.026-0.028) for predicting 5-year CKD occurrence. Similar predictive performance was observed for 1 to 4 years. Longitudinal patterns of predicted CKD risk revealed three distinct trajectories: gradual (75.9%), progressive (10.1%), and rapid increase (14.0%). Compared to the gradual trajectory, the progressive trajectory was associated with a higher risk of estimated glomerular filtration rate (eGFR) decline of ≥ 25% (adjusted hazard ratio (HR) 1.31; 95% CI, 1.06-1.61) and ≥ 50% (HR 1.59; 95% CI, 1.09-2.31) following CKD onset. The progressive and rapid trajectory was linked to an increased risk of cardiovascular events (HR 1.84; 95% CI 1.18-2.91) and all-cause mortality (HR 2.36; 95% CI 1.49-3.73). Our machine learning model demonstrated strong predictive performance for incident CKD risk and identified three distinct risk trajectories that were associated with different post-CKD outcomes, highlighting the importance of early risk monitoring.

Indexed as

Machine LearningRenal Insufficiency, ChronicAgedBoosting Machine Learning AlgorithmsCaliforniaDisease ProgressionFemaleGlomerular Filtration RateHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRisk AssessmentRisk FactorsCardiovascular eventsChronic kidney diseaseExtreme gradient boostingRisk trajectory

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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.