Evidence map›Paper›PMID 39991191›Full record

ArticleGlomerular diseases

RESOLVE: Recurrence Posttransplant Observational Study in Focal Segmental Glomerulosclerosis and Minimal Change Disease.

Eloise C Salmon, Ashley E Rahimi, Hailey E Desmond, Nathaniel M Putnam, Elena Martinelli, Elizabeth M Hendren, Susan F Massengill, Priya S Verghese, Simone Sanna-Cherchi, Matthias Kretzler and 3 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

13 authors.

Eloise C SalmonDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Ashley E RahimiDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Hailey E DesmondDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Nathaniel M PutnamDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Elena MartinelliDivision of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.
Elizabeth M HendrenDivision of Nephrology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Susan F MassengillDepartment of Pediatrics/Pediatric Nephrology, Levine Children's Hospital at Atrium Health, Charlotte, NC, USA.
Priya S VergheseDepartment of Pediatrics, Division of Nephrology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
Simone Sanna-CherchiDivision of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.
Matthias KretzlerDivision of Nephrology, Department of Internal Medicine, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Abhijit S NaikDivision of Nephrology, Department of Internal Medicine, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Howard TrachtmanDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.
Zubin J ModiDivision of Nephrology, Department of Pediatrics, Michigan Medicine, University of Michigan, Ann Arbor, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The morbidity of recurrent focal segmental glomerulosclerosis (FSGS) and minimal change disease (MCD) after transplant is well recognized. Additional collaborative research is necessary to advance understanding of recurrence epidemiology, mechanisms, interventions, and outcomes, particularly in children. Methods: RESOLVE is a multicenter, observational cohort study examining the posttransplant course of patients with FSGS and MCD across the lifespan. Multiple enrollment options will facilitate both retrospective and prospective collection of biospecimens, self-report items, and electronic health record data across pediatric and adult participants. The study offers a unique mobile health option for participants to enroll and engage with the study remotely. Logistic regression using a log link function will evaluate recurrence risk within 3 months of transplant based on clinical characteristics and assess the impact of social determinants of health on time to graft failure, following adjustment. Cox proportional hazards models with primary outcome of graft failure with competing risk of death will evaluate the impact of recurrence therapy and access to preventative versus reactive recurrence therapy. Independent logistic regression will evaluate the impact of recurrence therapy and endophenotypes on proteinuric outcomes. Conclusion: Multiple enrollment approaches and tailored site participation are needed while studying recurrent FSGS (rFSGS) due to its rarity and phenotypic variability. RESOLVE provides a framework for international collaboration to unravel the course of rFSGS through a biospecimen and data repository. It also explores the potential for mobile health tools to enhance recruitment of participants and to promote cooperation among researchers to advance understanding of recurrence mechanisms and treatments.

Indexed as

Focal segmental glomerular sclerosisRecurrenceTransplant

Identifiers

PMID39991191
PMCPMC11842035

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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.