Evidence map›Paper›PMID 42133311›Full record

ArticleJAMA network open2026

New-Onset Atrial Fibrillation and Accelerated Kidney Function Decline in Working-Age Adults.

Yuichiro Mori, Keita Hirano, Tatsuyoshi Ikenoue, Arisa Kobayashi, Motoko Yanagita, Shingo Fukuma

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Article in JAMA network open, 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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1 · What the graph read from it

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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

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3 · Its place in the literature

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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

6 authors.

Yuichiro MoriDepartment of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Keita HiranoDepartment of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Tatsuyoshi IkenoueDepartment of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Arisa KobayashiDepartment of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Motoko YanagitaDepartment of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Shingo FukumaDepartment of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Early identification of cardiovascular-kidney-metabolic (CKM) syndrome is essential for preventing subsequent organ failure. While atrial fibrillation (AF) is often incidentally detected in working-age adults and such detection is a risk for heart failure development, its specific impact on kidney function decline is yet to be elucidated in this young population. Objective: To investigate the association of new-onset AF with subsequent kidney function decline in working-age adults. Design, Setting, and Participants: This retrospective cohort study was conducted using annual health screening records (serial electrocardiogram and estimated glomerular filtration rate [eGFR]) and insurance claims data from April 1, 2015, to March 31, 2023, in Japan. Participants included screening attendees aged 35 to 59 years (working-age population) in sinus rhythm without prior AF, cardiovascular comorbidities, or end-stage kidney disease. Data were analyzed from April 1, 2024, to November 1, 2025. Exposure: Individuals who developed new-onset AF during the annual screening interval were matched 1:5 to those who did not. Main Outcomes: The primary outcome was annual rate of eGFR decline, estimated using linear mixed-effects models. The secondary outcome was a 30% or greater decline in eGFR from baseline, assessed using a Cox proportional hazards model. Results: Among 7 717 526 individuals with sinus rhythm at baseline, 141 060 adults were matched (mean [SD] age, 49.8 [6.6] years; 81.8% male; median [IQR] follow-up, 4.73 [3.50-6.22] years). New-onset AF was associated with a greater annual rate of eGFR decline (-1.23 [95% CI, -1.26 to -1.21] mL/min/1.73 m2) than that of individuals who did not develop AF (-0.94 [95% CI, -0.95 to -0.93] mL/min/1.73 m2), with a difference of -0.29 (95% CI, -0.32 to -0.26) mL/min/1.73 m2 (P < .001). Also, new-onset AF was associated with an increased incidence of a 30% or greater eGFR decline (hazard ratio, 2.91; 95% CI, 2.72-3.11; P < .001). Conclusions and Relevance: In this retrospective cohort study of working-age adults, new-onset AF was associated with an acceleration in kidney function decline. Further investigation is warranted to clarify the impact of AF burden on the decline and to determine the effectiveness of AF treatments for improving kidney outcomes.

Indexed as

Atrial FibrillationAdultFemaleGlomerular Filtration RateHumansJapanMaleMiddle AgedRetrospective StudiesRisk Factors

Identifiers

PMID42133311
PMCPMC13177024

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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.