Evidence map›Paper›PMID 37901700›Full record

ArticleGlomerular diseases

CureGN-Diabetes Study: Rationale, Design, and Methods of a Prospective Observational Study of Glomerular Disease Patients with Diabetes.

Amy K Mottl, Andrew S Bomback, Laura H Mariani, Gaia Coppock, J Charles Jennette, Salem Almaani, Debbie S Gipson, Sara Kelley, Jason Kidd, Louis-Philippe Laurin and 9 more

Abstract read
In one paragraph

Article in Glomerular diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

19 authors.

Amy K MottlUNC Kidney Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Andrew S BombackDivision of Nephrology, Columbia University Medical Center, New York, NY, USA.
Laura H MarianiDivision of Nephrology, University of Michigan, Ann Arbor, MI, USA.
Gaia CoppockRenal, Electrolyte and Hypertension Division, University of Pennsylvania, Philadelphia, PA, USA.
J Charles JennetteDivision of Nephropathology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Salem AlmaaniDivision of Nephrology, The Ohio State University Medical Center, Columbus, OH, USA.
Debbie S GipsonDepartment of Pediatrics, Division of Nephrology, University of Michigan, Ann Arbor, MI, USA.
Sara KelleyUNC Kidney Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Jason KiddDivision of Nephrology, Virginia Commonwealth University, Richmond, VA, USA.
Louis-Philippe LaurinCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Faculté de Médecine, Centre affilié à l'Université de Montréal, Montréal, QC, Canada.
Krzysztof MuchaDepartment of Immunology, Transplantology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.
Andrea OliverioDivision of Nephrology, University of Michigan, Ann Arbor, MI, USA.
Matthew PalmerDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Dana RizkDivision of Nephrology, University of Alabama, Birmingham, AL, USA.
Neil SanghaniDivision of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, TN, USA.
M Barry StokesDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
Katalin SusztakRenal, Electrolyte and Hypertension Division, University of Pennsylvania, Philadelphia, PA, USA.
Shikha WadhwaniDivision of Nephrology and Hypertension, Northwestern University, Chicago, IL, USA.
Cynthia C NastDepartment of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Funding

The Impact of Diabetes on Patients with Glomerular Disease: CureGN-DiabetesR01DK126959 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Andrew Stephen Bomback, Gaia Muallem Coppock · 2021 to 2026
$3.2M
Developing a decision aid for reproductive health for women with kidney diseaseK23DK123413 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OLIVERIO, ANDREA L · 2020 to 2024
$1.1M
NIDDK NIH HHS K23 DK123413NIDDK NIH HHS R01 DK126959
6 · The paper itself

Abstract

Glomerular diseases (GDs) represent the third leading cause of end-stage kidney disease (ESKD) in the US Diabetes was excluded from the CureGN Study, an NIH/NIDDK-sponsored observational cohort study of four leading primary GDs: IgA nephropathy (IgAN), membranous nephropathy (MN), focal segmental glomerulosclerosis (FSGS), and minimal change disease (MCD). CureGN-Diabetes, an ancillary study to CureGN, seeks to understand how diabetes influences the diagnosis, treatment, and outcomes of GD. It is a multicenter, prospective cohort study, targeting an enrollment of 300 adults with prevalent type 1 or type 2 diabetes and MCD, FSGS, MN, or IgAN, with first kidney biopsy obtained within 5 years of enrollment in 80% (20% allowed if biopsy after 2010). CureGN and Transformative Research in DiabEtic NephropaThy (TRIDENT) provide comparator cohorts. Retrospective and prospective clinical data and patient-reported outcomes are obtained. Blood and urine specimens are collected at study visits annually. Kidney biopsy reports and digital images are obtained, and standardized pathologic evaluations performed. Light microscopy images are uploaded to the NIH pathology repository. Outcomes include relapse and remission rates, changes in proteinuria and estimated glomerular filtration rate, infections, cardiovascular events, malignancy, ESKD, and death. Multiple analytical approaches will be used leveraging the baseline and longitudinal data to compare disease presentation and progression across subgroups of interest. With 300 patients and an average of 3 years of follow-up, the study has 80% power to detect a HR of 1.4-1.8 for time to complete remission of proteinuria, a rate ratio for hospitalizations of 1.18-1.56 and difference in eGFR slope of 6.0-8.6 mL/min/year between two groups of 300 participants each. CureGN-Diabetes will enhance our understanding of diabetes as a modifying factor of the pathology and outcomes of GDs and support studies to identify disease mechanisms and improve patient outcomes in this understudied patient population.

Indexed as

Cure Glomerulonephropathy NetworkDiabetesFocal segmental glomerulosclerosisGlomerular diseaseIgA nephropathyIgA vasculitisMembranous nephropathyMinimal change disease

Identifiers

PMID37901700
PMCPMC10601908

What OpenQuestion holds

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Registered trials

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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.