Evidence map›Paper›PMID 41542113›Full record

ArticleKidney international reports2026

Heterogeneity of Estimated GFR Slopes According to Etiology, Estimated GFR and Urinary Albumin-to-Creatinine Ratio in a Large Cohort of Patients With CKD.

Charlotte Behning, Ulla T Schultheiss, Jennifer Nadal, Heike Meiselbach, Sebastian Schönherr, Lukas Forer, Elke Schaeffner, Vera Krane, Markus P Schneider, Matthias Schmid and 5 more

Abstract read
In one paragraph

Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

15 authors.

Charlotte BehningDepartment of Medical Biometry, Informatics, and Epidemiology, University Hospital Bonn, Bonn, Germany.
Ulla T SchultheissFaculty of Medicine and Medical Center, Institute of Epidemiology and Prevention, University of Freiburg, Freiburg, Germany.
Jennifer NadalDepartment of Medical Biometry, Informatics, and Epidemiology, University Hospital Bonn, Bonn, Germany.
Heike MeiselbachDepartment of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Sebastian SchönherrInstitute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.
Lukas ForerInstitute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.
Elke SchaeffnerInstitute of Public Health, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Vera KraneDepartment of Clinical Research and Epidemiology, German Heart Failure Center, University Hospital Würzburg, Würzburg, Germany.
Markus P SchneiderDepartment of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Matthias SchmidDepartment of Medical Biometry, Informatics, and Epidemiology, University Hospital Bonn, Bonn, Germany.
Florian KronenbergInstitute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.
Anna KöttgenFaculty of Medicine and Medical Center, Institute of Epidemiology and Prevention, University of Freiburg, Freiburg, Germany.
Kai-Uwe EckardtDepartment of Nephrology and Hypertension, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Fruzsina KotsisFaculty of Medicine and Medical Center, Institute of Epidemiology and Prevention, University of Freiburg, Freiburg, Germany.
GCKD study investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The rate of decline in estimated glomerular filtration rate (GFR, eGFR) is increasingly recognized as a quantitative marker of chronic kidney disease (CKD) progression. However, data on eGFR slopes have mainly been reported in cohorts enriched for fast progression and the heterogeneity of eGFR slopes across the spectrum of CKD remains poorly defined. Methods: In 5214 participants of the German CKD (GCKD) study, we modeled eGFR slopes using per-protocol and clinical measurements. We used linear-mixed effects models, with eGFR slope as the outcome and baseline demographics as independent variables to (i) describe eGFR slope heterogeneity; (ii) assess differences by CKD etiology, eGFR and urinary albumin-to-creatinine ratio (UACR) categories, sex, and age; and (iii) determine associations of slopes with estimated eGFR decline (30%, 40%, and 57%) and observed end points (kidney failure with replacement therapy, mortality). Results: On average, 9 eGFR values per participant (interquartile range: 7-12) over 6.5 years were used for slope calculation. The adjusted mean annual eGFR slope was -1.43 ml/min per 1.73 m Conclusion: In conclusion, though the average eGFR slope was low, it varied considerably, depending on CKD etiology and UACR. This data may help to put slope estimates in individual patients and defined subpopulations into perspective.

Indexed as

CKD progressioneGFR slopeetiologyheterogeneity

Identifiers

PMID41542113
PMCPMC12800589

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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.